US20200123117A1 - Androgen receptor modulators and methods for their use - Google Patents

Androgen receptor modulators and methods for their use Download PDF

Info

Publication number
US20200123117A1
US20200123117A1 US16/657,625 US201916657625A US2020123117A1 US 20200123117 A1 US20200123117 A1 US 20200123117A1 US 201916657625 A US201916657625 A US 201916657625A US 2020123117 A1 US2020123117 A1 US 2020123117A1
Authority
US
United States
Prior art keywords
alkyl
optionally substituted
halogen
alkenyl
alkynyl
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US16/657,625
Other languages
English (en)
Inventor
Han-Jie Zhou
Peter VIRSIK
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
ESSA Pharma Inc
Original Assignee
ESSA Pharma Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by ESSA Pharma Inc filed Critical ESSA Pharma Inc
Priority to US16/657,625 priority Critical patent/US20200123117A1/en
Assigned to ESSA PHARMA, INC. reassignment ESSA PHARMA, INC. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: VIRSIK, PETER, ZHOU, HAN-JIE
Priority to US16/852,810 priority patent/US11059795B2/en
Publication of US20200123117A1 publication Critical patent/US20200123117A1/en
Priority to US17/363,534 priority patent/US20220380325A1/en
Abandoned legal-status Critical Current

Links

Images

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
    • C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
    • C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
    • C07D261/10—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
    • C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
    • C07D263/30—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D263/34—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D263/46—Sulfur atoms
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4164—1,3-Diazoles
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/42—Oxazoles
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/42—Oxazoles
    • A61K31/421—1,3-Oxazoles, e.g. pemoline, trimethadione
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4245—Oxadiazoles
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00—Drugs for disorders of the urinary system
    • A61P13/08—Drugs for disorders of the urinary system of the prostate
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/30—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
    • C07D207/34—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/30—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
    • C07D207/34—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D207/36—Oxygen or sulfur atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/72—Nitrogen atoms
    • C07D213/76—Nitrogen atoms to which a second hetero atom is attached
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D231/18—One oxygen or sulfur atom
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D231/38—Nitrogen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D231/38—Nitrogen atoms
    • C07D231/40—Acylated on said nitrogen atom
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/64—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D233/72—Two oxygen atoms, e.g. hydantoin
    • C07D233/74—Two oxygen atoms, e.g. hydantoin with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to other ring members
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D233/72—Two oxygen atoms, e.g. hydantoin
    • C07D233/76—Two oxygen atoms, e.g. hydantoin with substituted hydrocarbon radicals attached to the third ring carbon atom
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D233/72—Two oxygen atoms, e.g. hydantoin
    • C07D233/80—Two oxygen atoms, e.g. hydantoin with hetero atoms or acyl radicals directly attached to ring nitrogen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D233/84—Sulfur atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D233/88—Nitrogen atoms, e.g. allantoin
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
    • C07D237/02—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
    • C07D237/06—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D237/10—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D237/20—Nitrogen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/32—One oxygen, sulfur or nitrogen atom
    • C07D239/38—One sulfur atom
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/32—One oxygen, sulfur or nitrogen atom
    • C07D239/42—One nitrogen atom
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
    • C07D241/02—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings
    • C07D241/10—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D241/14—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D241/20—Nitrogen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
    • C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
    • C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
    • C07D261/08—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
    • C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
    • C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
    • C07D261/10—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D261/12—Oxygen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
    • C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
    • C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
    • C07D261/10—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D261/14—Nitrogen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
    • C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
    • C07D263/30—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D263/32—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
    • C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
    • C07D263/30—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D263/34—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
    • C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
    • C07D263/30—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D263/34—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D263/36—One oxygen atom
    • C07D263/38—One oxygen atom attached in position 2
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
    • C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
    • C07D263/30—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D263/34—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D263/36—One oxygen atom
    • C07D263/40—One oxygen atom attached in position 4
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
    • C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
    • C07D263/30—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D263/34—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D263/48—Nitrogen atoms not forming part of a nitro radical
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D271/00—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms
    • C07D271/02—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms not condensed with other rings
    • C07D271/06—1,2,4-Oxadiazoles; Hydrogenated 1,2,4-oxadiazoles
    • C07D271/07—1,2,4-Oxadiazoles; Hydrogenated 1,2,4-oxadiazoles with oxygen, sulfur or nitrogen atoms, directly attached to ring carbon atoms, the nitrogen atoms not forming part of a nitro radical
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D271/00—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms
    • C07D271/02—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms not condensed with other rings
    • C07D271/10—1,3,4-Oxadiazoles; Hydrogenated 1,3,4-oxadiazoles
    • C07D271/113—1,3,4-Oxadiazoles; Hydrogenated 1,3,4-oxadiazoles with oxygen, sulfur or nitrogen atoms, directly attached to ring carbon atoms, the nitrogen atoms not forming part of a nitro radical
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
    • C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D277/36—Sulfur atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
    • C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D277/38—Nitrogen atoms
    • C07D277/42—Amino or imino radicals substituted by hydrocarbon or substituted hydrocarbon radicals
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
    • C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D277/56—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
    • C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D307/56—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D307/64—Sulfur atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
    • C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D307/56—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D307/66—Nitrogen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
    • C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
    • C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
    • C07D333/26—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D333/30—Hetero atoms other than halogen
    • C07D333/34—Sulfur atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/04—Ortho-condensed systems
    • C07D491/044—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
    • C07D491/052—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being six-membered

Definitions

  • the present disclosure generally relates to tricyclic compounds and their use for treatment of various indications.
  • the disclosure relates to tricyclic compounds and their use for treatment of various cancers, for example prostate cancer, including but not limited to, primary/localized prostate cancer (newly diagnosed), locally advanced prostate cancer, recurrent prostate cancer, non-metastatic castration-resistant prostate cancer, metastatic prostate cancer, metastatic castration-resistant prostate cancer (CRPC), and hormone-sensitive prostate cancer.
  • This invention also relates to tricyclic compounds and their use for modulating androgen receptor (AR) activity, including truncated AR.
  • AR androgen receptor
  • Androgens mediate their effects through the androgen receptor (AR). Androgens play a role in a wide range of developmental and physiological responses and are involved in male sexual differentiation, maintenance of spermatogenesis, and male gonadotropin regulation (R. K. Ross, G. A. Coetzee, C. L. Pearce, J. K. Reichardt, P. Bretsky, L. N. Kolonel, B. E. Henderson, E. Lander, D. Altshuler & G. Daley, Eur Urol 35, 355-361 (1999); A. A. Thomson, Reproduction 121, 187-195 (2001); N. Tanji, K. Aoki & M. Yokoyama, Arch Androl 47, 1-7 (2001)).
  • prostate cancer does not develop if humans or dogs are castrated before puberty (J. D. Wilson & C. Roehrborn, J Clin Endocrinol Metab 84, 4324-4331 (1999); G. Wilding, Cancer Surv 14, 113-130 (1992)). Castration of adult males causes involution of the prostate and apoptosis of prostatic epithelium while eliciting no effect on other male external genitalia (E. M. Bruckheimer & N. Kyprianou, Cell Tissue Res 301, 153-162 (2000); J. T. Isaacs, Prostate 5, 545-557 (1984)). This dependency on androgens provides the underlying rationale for treating prostate cancer with chemical or surgical castration (androgen ablation), also known as androgen ablation therapy (ABT) or androgen depravation therapy (ADT).
  • ABT androgen ablation therapy
  • ADT androgen depravation therapy
  • Androgens also play a role in female diseases such as polycystic ovary syndrome as well as cancers.
  • ovarian cancer where elevated levels of androgens are associated with an increased risk of developing ovarian cancer (K. J. Helzlsouer, A. J. Alberg, G. B. Gordon, C. Longcope, T. L. Bush, S. C. Hoffman & G. W. Comstock, JAMA 274, 1926-1930 (1995); R. J. Edmondson, J. M. Monaghan & B. R. Davies, Br J Cancer 86, 879-885 (2002)).
  • the AR has been detected in a majority of ovarian cancers (H. A.
  • prostate cancer can eventually grow again in the absence of testicular androgens (castration-resistant disease) (Huber et al 1987 Scand J. Urol Nephrol. 104, 33-39). Castration-resistant prostate cancer that is still driven by AR is biochemically characterized before the onset of symptoms by a rising titre of serum PSA (Miller et al 1992 J. Urol. 147, 956-961). Once the disease becomes castration-resistant most patients succumb to their disease within two years.
  • the AR has distinct functional domains that include the carboxy-terminal ligand-binding domain (LBD), a DNA-binding domain (DBD) comprising two zinc finger motifs, and an N-terminus domain (NTD) that contains two transcriptional activation units (tau1 and tau5) within activation function-1 (AF-1). Binding of androgen (ligand) to the LBD of the AR results in its activation such that the receptor can effectively bind to its specific DNA consensus site, termed the androgen response element (ARE), on the promoter and enhancer regions of “normally” androgen regulated genes, such as PSA, to initiate transcription.
  • LBD carboxy-terminal ligand-binding domain
  • DBD DNA-binding domain
  • NTD N-terminus domain
  • AF-1 activation function-1
  • the AR can be activated in the absence of androgen by stimulation of the cAMP-dependent protein kinase (PKA) pathway, with interleukin-6 (IL-6) and by various growth factors (Culig et al 1994 Cancer Res. 54, 5474-5478; Nazareth et al 1996 J. Biol. Chem. 271, 19900-19907; Sadar 1999 J. Biol. Chem. 274, 7777-7783; Ueda et al 2002 A J. Biol. Chem. 277, 7076-7085; and Ueda et al 2002 B J. Biol. Chem. 277, 38087-38094).
  • PKA cAMP-dependent protein kinase pathway
  • IL-6 interleukin-6
  • the mechanism of ligand-independent transformation of the AR has been shown to involve: 1) increased nuclear AR protein suggesting nuclear translocation; 2) increased AR/ARE complex formation; and 3) the AR-NTD (Sadar 1999 J. Biol. Chem. 274, 7777-7783; Ueda et al 2002 A J Biol. Chem. 277, 7076-7085; and Ueda et al 2002 B J. Biol. Chem. 277, 38087-38094).
  • the AR can be activated in the absence of testicular androgens by alternative signal transduction pathways in castration-resistant disease, which is consistent with the finding that nuclear AR protein is present in secondary prostate cancer tumors (Kim et al 2002 Am. J. Pathol. 160, 219-226; and van der Kwast et al 1991 Inter. J. Cancer 48, 189-193).
  • Clinically available inhibitors of the AR include nonsteroidal antiandrogens such as apalutamide, darolutamide, bicalutamide (CasodexTM), nilutamide, flutamide, and enzalutamide.
  • nonsteroidal antiandrogens such as apalutamide, darolutamide, bicalutamide (CasodexTM), nilutamide, flutamide, and enzalutamide.
  • steroidal antiandrogens such as cyproterone acetate and spironolactone. Both steroidal and non-steroidal antiandrogens target the LBD of the AR and predominantly fail presumably due to poor affinity and mutations that lead to activation of the AR by these same antiandrogens (Taplin, M. E., Bubley, G. J., Kom Y. J., Small E.
  • AR degraders such as niclosamide (Liu C et al 2014), galeterone (Njar et al 2015; Yu Z at al 2014), and ARV-330/Androgen receptor PROTAC (Neklesa et al 2016 J Clin Oncol 34 suppl 2S; abstr 267); AR DBD inhibitor VPC-14449 (Dalal K et al 2014 J Biol Chem.
  • the AR-NTD is also a target for drug development (e.g. WO 2000/001813; Myung et al. J. Clin. Invest 2013, 123, 2948), since the NTD contains Activation-Function-1 (AF-1) which is the essential region required for AR transcriptional activity (Jenster et al 1991 . Mol Endocrinol. 5, 1396-404).
  • AF-1 Activation-Function-1
  • the AR-NTD importantly plays a role in activation of the AR in the absence of androgens (Sadar, M. D. 1999 J Biol. Chem. 274, 7777-7783; Sadar M D et al 1999 Endocr Relat Cancer. 6, 487-502; Ueda et al 2002 J Biol. Chem.
  • the AR-NTD is important in hormonal progression of prostate cancer as shown by application of decoy molecules (Quayle et al 2007 , Proc Natl Acad Sci USA. 104, 1331-1336).
  • Compounds that modulate AR, potentially through interaction with NTD domain include the bisphenol compounds disclosed in published PCT Nos: WO 2010/000066, WO 2011/082487; WO 2011/082488; WO 2012/145330; WO 2012/139039; WO 2012/145328; WO 2013/028572; WO 2013/028791; WO 2014/179867; WO 2015/031984; WO 2016/058080; WO 2016/058082; WO 2016/112455; WO 2016/141458; WO 2017/177307; WO 2017/210771; and WO 2018/045450, and which are hereby incorporated by reference in their entireties.
  • AR mechanisms of resistance to ADT include: overexpression of AR (Visakorpi, T. et al Nature Genetics 1995, 9, 401-406; Koivisto, P. et al Scandinavian Journal of Clinical and Laboratory Investigation Supplementum 1996, 226, 57-63); gain-of-function mutations in the AR LBD (Culig Z.
  • AR-Vs AR splice variants
  • LBD ligand-binding domain
  • Anti-androgens such as bicalutamide and enzalutamide target AR LBD, but have no effect on truncated constitutively active AR-Vs such as AR-V7 (Li Y. et al Cancer Research 2013, 73, 483-489). Expression of AR-V7 is associated with resistance to current hormone therapies (Li Y. et al Cancer Research 2013, 73, 483-489; Antonarakis E. S. et al The New England Journal of Medicine 2014, 371, 1028-1038).
  • the compounds of the present disclosure are androgen receptor modulators which may be useful in treating various diseases and conditions as disclosed herein.
  • the present disclosure provides compounds comprising the structure of formula (IIIA):
  • the present disclosure provides compounds comprising the structure of formula (IVA):
  • C is 5- to 10-membered heteroaryl or aryl. In some embodiments, C is 5- to 7-membered heteroaryl comprising 1, 2, or 3 heteroatoms selected from O, S, or N as a ring member.
  • C, which is substituted with (R 3 )n3, is pyrazole, imidazole, oxazole, oxadiazole, oxazolone, isoxazole, thiazole, pyridyl, pyrazine, furan or pyrimidyl. In some embodiments, C, which is substituted with (R 3 )n3, is selected from
  • R 3a is C 1 -C 3 alkyl.
  • R 1 and R 2 are each independently C 1 , —CN, —CF 3 , —OH, methyl, methoxy, or —CONH 2 .
  • the present disclosure provides compounds comprising the structure of formula (A-I):
  • At least one R 3 is selected from —CN, C 1 -C 3 alkoxy, —CONH 2 , —NHSO 2 CH 3 , —N(CH 3 )SO 2 CH 3 , —NHSO 2 CH 2 CH 3 , —N(CH 3 )SO 2 CH 2 CH 3 , or —SO 2 CH 3 and the other R 3 , if present, is selected from —CN, —CF 3 , C 1 -C 3 alkyl, C 2 -C 3 alkenyl, C 2 -C 3 alkynyl, C 1 -C 3 alkoxy, —S(C 1 -C 3 alkyl), —SO 2 (C 1 -C 3 alkyl), —NH 2 , —(C 1 -C 3 alkyl)NH 2 , —NHSO 2 CH 3 , —NHSO 2 CF 3 , —N(CH 3 )SO 2 CH 3 , —NHSO
  • the present disclosure provides compounds comprising the structure of formula (G-II):
  • At least one R 3 is selected from —NHSO 2 CH 3 , —NHSO 2 CH 2 CH 3 , or —SO 2 CH 3 and the other R 3 , if present, is selected from —CN, C 1 -C 3 alkyl, C 1 -C 3 alkoxy, —SO 2 (C 1 -C 3 alkyl), —NH 2 , —(C 1 -C 3 alkyl)NH 2 , —NHSO 2 CH 3 , —N(CH 3 )SO 2 CH 3 , —NHSO 2 CH 2 CH 3 , —N(CH 3 )SO 2 CH 2 CH 3 , —SO 2 NH 2 , —CONH 2 , —CON(C 1 -C 3 alkyl) 2 , —CONH(C 1 -C 3 alkyl), —NHCO(C 1 -C 3 alkyl), —N(CH 3 )COO(C 1 -C 3
  • the present disclosure provides Compounds A1-A96, A98-A116, A118-A159, A161-A175, and A177-A234, or a pharmaceutically acceptable salt, tautomer, stereoisomer or prodrug thereof.
  • the present disclosure provides Compounds A13, A57, A74, A93, A109, A112, A122, A126, A131, A134, A136, A137, A164, A168, A169, A170, A171, A172, A184, A185, A195, and/or A204, or a pharmaceutically acceptable salt, tautomer, stereoisomer or prodrug thereof.
  • the present disclosure provides a pharmaceutical composition comprising any one of the compound of formula (IIIA), or a pharmaceutically acceptable salt, tautomer, stereoisomer or prodrug thereof, and a pharmaceutically acceptable carrier.
  • the present disclosure provides a pharmaceutical composition comprising any one of the compound of formula (IVA), or a pharmaceutically acceptable salt, tautomer, stereoisomer or prodrug thereof, and a pharmaceutically acceptable carrier.
  • the present disclosure provides a pharmaceutical composition comprising any one of the compound of formula (A-I), or a pharmaceutically acceptable salt, tautomer, stereoisomer or prodrug thereof, and a pharmaceutically acceptable carrier.
  • the present disclosure provides a pharmaceutical composition comprising any one of the compound of formula (G-II), or a pharmaceutically acceptable salt, tautomer, stereoisomer or prodrug thereof, and a pharmaceutically acceptable carrier.
  • the present disclosure provides a pharmaceutical composition
  • a pharmaceutical composition comprising any one of Compounds A1-A96, A98-A116, A118-A159, A161-A175, and A177-A234, or a pharmaceutically acceptable salt, tautomer, stereoisomer or prodrug thereof, and a pharmaceutically acceptable carrier.
  • the present disclosure provides a pharmaceutical composition
  • a pharmaceutical composition comprising any one of Compounds A13, A57, A74, A93, A109, A112, A122, A126, A131, A134, A136, A137, A164, A168, A169, A170, A171, A172, A184, A185, A195, and A204, or a pharmaceutically acceptable salt, tautomer, stereoisomer or prodrug thereof, and a pharmaceutically acceptable carrier.
  • the present disclosure provides a method for treating cancer, comprising administering any one of the compound of formula (IIIA), (IVA), (A-I), or (G-II), and Compounds A1-A96, A98-A116, A118-A159, A161-A175, or A177-A234, or a pharmaceutically acceptable salt, tautomer, stereoisomer or prodrug thereof, to a subject in need thereof.
  • the cancer is prostate cancer.
  • the prostate cancer is metastatic castration-resistant prostate cancer.
  • the prostate cancer expresses full-length androgen receptor or truncated androgen receptor splice variant.
  • the present disclosure provides a method for treating cancer, comprising administering any one of Compounds A13, A57, A74, A93, A109, A112, A122, A126, A131, A134, A136, A137, A164, A168, A169, A170, A171, A172, A184, A185, A195, and A204, or a pharmaceutically acceptable salt, tautomer, stereoisomer or prodrug thereof.
  • FIG. 1 shows a dose-dependent curve of PSA-luciferase activities in response to representative compounds in transiently transfected LNCaP cells treated with synthetic androgen (R1881).
  • FIG. 2A shows the percent PSA-luciferase activities of representative compounds in LNCaP cells transiently transfected with the PSA (6.1 kb)-luciferase reporter and treated without or with R1881.
  • FIG. 2B shows the percent PSA-luciferase activities of representative compounds in LNCaP cells co-transfected with an expression vector for AR-V7 and the PSA-luciferase reporter and treated without or with R1881.
  • FIG. 3 shows concentration of representative compounds in plasma of male CD-1 mice after a single dose PO (oral) dose.
  • FIG. 4 shows change in tumor volume in male NCG mice bearing LNCaP tumors after oral administration of representative compounds.
  • FIG. 5 shows change in % body weight in male NCG mice bearing LNCaP tumors after oral administration of representative compounds.
  • FIG. 6 shows individual tumor volume change from baseline measured at the end of experiment for oral administration of representative compounds to male NCG mice bearing LNCaP tumors.
  • FIG. 7 shows concentration dependent effects on cell proliferation of LNCaP, PC3, and LNCaP95 cells treated with Compound A13.
  • the terms “about” and/or “approximately” may be used in conjunction with numerical values and/or ranges.
  • the term “about” is understood to mean those values near to a recited value.
  • the phrases “less than about [a value]” or “greater than about [a value]” should be understood in view of the definition of the term “about” provided herein.
  • the terms “about” and “approximately” may be used interchangeably.
  • ranges are provided for certain quantities. It is to be understood that these ranges comprise all subranges therein. Thus, the range “from 50 to 80” includes all possible ranges therein (e.g., 51-79, 52-78, 53-77, 54-76, 55-75, 60-70, etc.). Furthermore, all values within a given range may be an endpoint for the range encompassed thereby (e.g., the range 50-80 includes the ranges with endpoints such as 55-80, 50-75, etc.).
  • a androgen receptor modulator refers to one or more androgen receptor modulators or at least one androgen receptor modulator.
  • the terms “a” (or “an”), “one or more” and “at least one” are used interchangeably herein.
  • reference to “an inhibitor” by the indefinite article “a” or “an” does not exclude the possibility that more than one of the inhibitors is present, unless the context clearly requires that there is one and only one of the inhibitors.
  • the verb “comprise” as is used in this description and in the claims and its conjugations are used in its non-limiting sense to mean that items following the word are included, but items not specifically mentioned are not excluded.
  • the present invention may suitably “comprise”, “consist of”, or “consist essentially of”, the steps, elements, and/or reagents described in the claims.
  • salts includes both acid and base addition salts.
  • Pharmaceutically acceptable salts include those obtained by reacting the active compound functioning as a base, with an inorganic or organic acid to form a salt, for example, salts of hydrochloric acid, sulfuric acid, phosphoric acid, methanesulfonic acid, camphorsulfonic acid, oxalic acid, maleic acid, succinic acid, citric acid, formic acid, hydrobromic acid, benzoic acid, tartaric acid, fumaric acid, salicylic acid, mandelic acid, carbonic acid, etc.
  • acid addition salts may be prepared by reaction of the compounds with the appropriate inorganic or organic acid via any of a number of known methods.
  • treating means one or more of relieving, alleviating, delaying, reducing, improving, or managing at least one symptom of a condition in a subject.
  • the term “treating” may also mean one or more of arresting, delaying the onset (i.e., the period prior to clinical manifestation of the condition) or reducing the risk of developing or worsening a condition.
  • the compounds of the invention, or their pharmaceutically acceptable salts can contain one or more asymmetric centers and can thus give rise to enantiomers, diastereomers, and other stereoisomeric forms that can be defined, in terms of absolute stereochemistry, as (R)— or (S)— or, as (D)- or (L)- for amino acids.
  • the present disclosure is meant to include all such possible isomers, as well as their racemic and optically pure forms whether or not they are specifically depicted herein.
  • Optically active (+) and ( ⁇ ), (R)- and (S)-, or (D)- and (L)-isomers can be prepared using chiral synthons or chiral reagents, or resolved using conventional techniques, for example, chromatography and fractional crystallization.
  • Conventional techniques for the preparation/isolation of individual enantiomers include chiral synthesis from a suitable optically pure precursor or resolution of the racemate (or the racemate of a salt or derivative) using, for example, chiral high pressure liquid chromatography (HPLC).
  • HPLC high pressure liquid chromatography
  • stereoisomer refers to a compound made up of the same atoms bonded by the same bonds but having different three-dimensional structures, which are not interchangeable.
  • the present disclosure contemplates various stereoisomers and mixtures thereof and includes “enantiomers”, which refers to two stereoisomers whose molecules are nonsuperimposable mirror images of one another.
  • a “tautomer” refers to a proton shift from one atom of a molecule to another atom of the same molecule.
  • the present disclosure includes tautomers of any said compounds.
  • a “prodrug” refers to a derivative of a compound of the present disclosure that will be converted to the compound in vivo.
  • a prodrug includes a compound of formula (I), (IA), (IB), (IC), (II), (IIA), (IIIA), (IIB), (III), (IV), (V), (VA), (VI), (A), (A-I), (B)-(D), (E), (E-I)-(E-VII), (F), (G), (G-I), (G-II), (H), and (H-I), having a free hydroxyl group (—OH) that is acetylated (—OCOMe) at one or more positions.
  • an “effective amount” means the amount of a formulation according to the invention that, when administered to a patient for treating a state, disorder or condition is sufficient to effect such treatment.
  • the “effective amount” will vary depending on the active ingredient, the state, disorder, or condition to be treated and its severity, and the age, weight, physical condition and responsiveness of the mammal to be treated.
  • terapéuticaally effective applied to dose or amount refers to that quantity of a compound or pharmaceutical formulation that is sufficient to result in a desired clinical benefit after administration to a patient in need thereof.
  • a “subject” can be a human, non-human primate, mammal, rat, mouse, cow, horse, pig, sheep, goat, dog, cat and the like.
  • the subject can be suspected of having or at risk for having a cancer, such as prostate cancer, breast cancer, ovarian cancer, salivary gland carcinoma, or endometrial cancer, or suspected of having or at risk for having acne, hirsutism, alopecia, benign prostatic hyperplasia, ovarian cysts, polycystic ovary disease, precocious puberty, spinal and bulbar muscular atrophy, or age-related macular degeneration.
  • a cancer such as prostate cancer, breast cancer, ovarian cancer, salivary gland carcinoma, or endometrial cancer, or suspected of having or at risk for having acne, hirsutism, alopecia, benign prostatic hyperplasia, ovarian cysts, polycystic ovary disease, precocious puberty, spinal and bulbar muscular atrophy
  • Diagnostic methods for various cancers such as prostate cancer, breast cancer, ovarian cancer, bladder cancer, pancreatic cancer, hepatocellular cancer, salivary gland carcinoma, or endometrial cancer, and diagnostic methods for acne, hirsutism, alopecia, benign prostatic hyperplasia, ovarian cysts, polycystic ovary disease, precocious puberty, spinal and bulbar muscular atrophy, or age-related macular degeneration and the clinical delineation of cancer, such as prostate cancer, breast cancer, ovarian cancer, bladder cancer, pancreatic cancer, hepatocellular cancer, salivary gland carcinoma, or endometrial cancer, diagnoses and the clinical delineation of acne, hirsutism, alopecia, benign prostatic hyperplasia, ovarian cysts, polycystic ovary disease, precocious puberty, spinal and bulbar muscular atrophy, or age-related macular degeneration are known to those of ordinary skill in the art.
  • “Mammal” includes humans and both domestic animals such as laboratory animals (e.g., mice, rats, monkeys, dogs, etc.) and household pets (e.g., cats, dogs, swine, cattle, sheep, goats, horses, rabbits), and non-domestic animals such as wildlife and the like.
  • laboratory animals e.g., mice, rats, monkeys, dogs, etc.
  • household pets e.g., cats, dogs, swine, cattle, sheep, goats, horses, rabbits
  • non-domestic animals such as wildlife and the like.
  • substantially refers to the complete or nearly complete extent or degree of an action, characteristic, property, state, structure, item, or result.
  • an object that is “substantially” enclosed would mean that the object is either completely enclosed or nearly completely enclosed.
  • the exact allowable degree of deviation from absolute completeness may in some cases depend on the specific context. However, generally speaking, the nearness of completion will be so as to have the same overall result as if absolute and total completion were obtained.
  • the use of “substantially” is equally applicable when used in a negative connotation to refer to the complete or near complete lack of action, characteristic, property, state, structure, item, or result.
  • compositions that is “substantially free of” other active agents would either completely lack other active agents, or so nearly completely lack other active agents that the effect would be the same as if it completely lacked other active agents.
  • a composition that is “substantially free of” an ingredient or element or another active agent may still contain such an item as long as there is no measurable effect thereof
  • Amino refers to the —NH 2 radical.
  • Halo or “halogen” refers to bromo, chloro, fluoro or iodo radical, including their radioisotopes.
  • 123 I refers to the radioactive isotope of iodine having atomic mass 123.
  • the compounds of Formula I can comprise at least one 123 I moiety. Throughout the present application, where structures depict a 123 I moiety at a certain position it is meant that the I moiety at this position is enriched for 123 I. In other words, the compounds contain more than the natural abundance of 123 I at the indicated position(s). It is not required that the compounds comprise 100% 123 I at the indicated positions, provided 123 I is present in more than the natural abundance.
  • the 123 I isotope is enriched to greater than 50%, greater than 60%, greater than 70%, greater than, 80% or greater than 90%, relative to 127 I.
  • 18 F refers to the radioactive isotope of fluorine having atomic mass 18.
  • F or 19 F refers to the abundant, non-radioactive fluorine isotope having atomic mass 19.
  • the compounds of Formula I can comprise at least one 18 F moiety. Throughout the present application, where structures depict a 18 F moiety at a certain position it is meant that the F moiety at this position is enriched for 18 F. In other words, the compounds contain more than the natural abundance of 18 F at the indicated position(s).
  • the compounds comprise 100% 18 F at the indicated positions, provided 18 F is present in more than the natural abundance.
  • 18 F isotope is enriched to greater than 50%, greater than 60%, greater than 70%, greater than 80% or greater than 90%, relative to 19 F.
  • Niro refers to the —NO 2 radical.
  • Oxo refers to the ⁇ O substituent.
  • Thioxo refers to the ⁇ S substituent.
  • Alkyl or “alkyl group” refers to a fully saturated, straight or branched hydrocarbon chain radical having from one to twelve carbon atoms, and which is attached to the rest of the molecule by a single bond. Alkyls comprising any number of carbon atoms from 1 to 12 are included. An alkyl comprising up to 12 carbon atoms is a C 1 -C 12 alkyl, an alkyl comprising up to 10 carbon atoms is a C 1 -C 10 alkyl, an alkyl comprising up to 6 carbon atoms is a C 1 -C 6 alkyl and an alkyl comprising up to 5 carbon atoms is a C 1 -C 5 alkyl.
  • a C 1 -C 5 alkyl includes C 5 alkyls, C 4 alkyls, C 3 alkyls, C 2 alkyls and C 1 alkyl (i.e., methyl).
  • a C 1 -C 6 alkyl includes all moieties described above for C 1 -C 5 alkyls but also includes C 6 alkyls.
  • a C 1 -C 10 alkyl includes all moieties described above for C 1 -C 5 alkyls and C 1 -C 6 alkyls, but also includes C 7 , C 8 , C 9 and C 10 alkyls.
  • a C 1 -C 12 alkyl includes all the foregoing moieties, but also includes C 11 and C 12 alkyls.
  • Non-limiting examples of C 1 -C 12 alkyl include methyl, ethyl, n-propyl, i-propyl, sec-propyl, n-butyl, i-butyl, sec-butyl, t-butyl, n-pentyl, t-amyl, n-hexyl, n-heptyl, n-octyl, n-nonyl, n-decyl, n-undecyl, and n-dodecyl.
  • an alkyl group can be optionally substituted.
  • Alkylene or “alkylene chain” refers to a fully saturated, straight or branched divalent hydrocarbon chain radical, and having from one to twelve carbon atoms.
  • C 1 -C 12 alkylene include methylene, ethylene, propylene, n-butylene, ethenylene, propenylene, n-butenylene, propynylene, n-butynylene, and the like.
  • the alkylene chain is attached to the rest of the molecule through a single bond and to the radical group through a single bond. The points of attachment of the alkylene chain to the rest of the molecule and to the radical group can be through one carbon or any two carbons within the chain. Unless stated otherwise specifically in the specification, an alkylene chain can be optionally substituted.
  • Alkenyl or “alkenyl group” refers to a straight or branched hydrocarbon chain radical having from two to twelve carbon atoms, and having one or more carbon-carbon double bonds. Each alkenyl group is attached to the rest of the molecule by a single bond. Alkenyl group comprising any number of carbon atoms from 2 to 12 are included.
  • An alkenyl group comprising up to 12 carbon atoms is a C 2 -C 12 alkenyl
  • an alkenyl comprising up to 10 carbon atoms is a C 2 -C 10 alkenyl
  • an alkenyl group comprising up to 6 carbon atoms is a C 2 -C 6 alkenyl
  • an alkenyl comprising up to 5 carbon atoms is a C 2 -C 5 alkenyl.
  • a C 2 -C 5 alkenyl includes C 5 alkenyls, C 4 alkenyls, C 3 alkenyls, and C 2 alkenyls.
  • a C 2 -C 6 alkenyl includes all moieties described above for C 2 -C 5 alkenyls but also includes C 6 alkenyls.
  • a C 2 -C 10 alkenyl includes all moieties described above for C 2 -C 5 alkenyls and C 2 -C 6 alkenyls, but also includes C 7 , C 8 , C 9 and C 10 alkenyls.
  • a C 2 -C 12 alkenyl includes all the foregoing moieties, but also includes C 11 and C 12 alkenyls.
  • Non-limiting examples of C 2 -C 12 alkenyl include ethenyl (vinyl), 1-propenyl, 2-propenyl (allyl), iso-propenyl, 2-methyl-1-propenyl, 1-butenyl, 2-butenyl, 3-butenyl, 1-pentenyl, 2-pentenyl, 3-pentenyl, 4-pentenyl, 1-hexenyl, 2-hexenyl, 3-hexenyl, 4-hexenyl, 5-hexenyl, 1-heptenyl, 2-heptenyl, 3-heptenyl, 4-heptenyl, 5-heptenyl, 6-heptenyl, 1-octenyl, 2-octenyl, 3-octenyl, 4-octenyl, 5-octenyl, 6-octenyl, 7-octenyl, 1-nonenyl, 2-nonenyl, 3-nonenyl, 4-noneny
  • alkenylene or “alkenylene chain” refers to a straight or branched divalent hydrocarbon chain radical, having from two to twelve carbon atoms, and having one or more carbon-carbon double bonds.
  • C 2 -C 12 alkenylene include ethene, propene, butene, and the like.
  • the alkenylene chain is attached to the rest of the molecule through a single bond and to the radical group through a single bond.
  • the points of attachment of the alkenylene chain to the rest of the molecule and to the radical group can be through one carbon or any two carbons within the chain. Unless stated otherwise specifically in the specification, an alkenylene chain can be optionally substituted.
  • Alkynyl or “alkynyl group” refers to a straight or branched hydrocarbon chain radical having from two to twelve carbon atoms, and having one or more carbon-carbon triple bonds. Each alkynyl group is attached to the rest of the molecule by a single bond. Alkynyl group comprising any number of carbon atoms from 2 to 12 are included.
  • An alkynyl group comprising up to 12 carbon atoms is a C 2 -C 12 alkynyl
  • an alkynyl comprising up to 10 carbon atoms is a C 2 -C 10 alkynyl
  • an alkynyl group comprising up to 6 carbon atoms is a C 2 -C 6 alkynyl
  • an alkynyl comprising up to 5 carbon atoms is a C 2 -C 5 alkynyl.
  • a C 2 -C 5 alkynyl includes C 5 alkynyls, C 4 alkynyls, C 3 alkynyls, and C 2 alkynyls.
  • a C 2 -C 6 alkynyl includes all moieties described above for C 2 -C 5 alkynyls but also includes C 6 alkynyls.
  • a C 2 -C 10 alkynyl includes all moieties described above for C 2 -C 5 alkynyls and C 2 -C 6 alkynyls, but also includes C 7 , C 8 , C 9 and C 10 alkynyls.
  • a C 2 -C 12 alkynyl includes all the foregoing moieties, but also includes C 11 and C 12 alkynyls.
  • Non-limiting examples of C 2 -C 12 alkenyl include ethynyl, propynyl, butynyl, pentynyl and the like. Unless stated otherwise specifically in the specification, an alkyl group can be optionally substituted.
  • Alkynylene or “alkynylene chain” refers to a straight or branched divalent hydrocarbon chain radical, having from two to twelve carbon atoms, and having one or more carbon-carbon triple bonds.
  • C 2 -C 12 alkynylene include ethynylene, propargylene and the like.
  • the alkynylene chain is attached to the rest of the molecule through a single bond and to the radical group through a single bond. The points of attachment of the alkynylene chain to the rest of the molecule and to the radical group can be through one carbon or any two carbons within the chain. Unless stated otherwise specifically in the specification, an alkynylene chain can be optionally substituted.
  • Alkoxy refers to a radical of the formula —OR a where R a is an alkyl, alkenyl or alknyl radical as defined above containing one to twelve carbon atoms. Unless stated otherwise specifically in the specification, an alkoxy group can be optionally substituted.
  • Alkylamino refers to a radical of the formula —NHR a or —NR a R a where each R a is, independently, an alkyl, alkenyl or alkynyl radical as defined above containing one to twelve carbon atoms. Unless stated otherwise specifically in the specification, an alkylamino group can be optionally substituted.
  • Alkylcarbonyl refers to the —C( ⁇ O)R a moiety, wherein R a is an alkyl, alkenyl or alkynyl radical as defined above.
  • R a is an alkyl, alkenyl or alkynyl radical as defined above.
  • a non-limiting example of an alkyl carbonyl is the methyl carbonyl (“acetal”) moiety.
  • Alkylcarbonyl groups can also be referred to as “Cw-Cz acyl” where w and z depicts the range of the number of carbon in R a , as defined above.
  • C 1 -C 10 acyl refers to alkylcarbonyl group as defined above, where R a is C 1 -C 10 alkyl, C 1 -C 10 alkenyl, or C 1 -C 10 alkynyl radical as defined above. Unless stated otherwise specifically in the specification, an alkyl carbonyl group can be optionally substituted.
  • Aryl refers to a hydrocarbon ring system radical comprising hydrogen, 6 to 18 carbon atoms and at least one aromatic ring.
  • the aryl radical can be a monocyclic, bicyclic, tricyclic or tetracyclic ring system, which can include fused or bridged ring systems.
  • Aryl radicals include, but are not limited to, aryl radicals derived from aceanthrylene, acenaphthylene, acephenanthrylene, anthracene, azulene, benzene, chrysene, fluoranthene, fluorene, as-indacene, s-indacene, indane, indene, naphthalene, phenalene, phenanthrene, pleiadene, pyrene, and triphenylene.
  • aryl is meant to include aryl radicals that are optionally substituted.
  • Alkyl or “arylalkyl” refers to a radical of the formula —R b —R c where R b is an alkylene group as defined above and R c is one or more aryl radicals as defined above, for example, benzyl, diphenylmethyl and the like. Unless stated otherwise specifically in the specification, an aralkyl group can be optionally substituted.
  • alkenyl or “arylalkenyl” refers to a radical of the formula —R b —R c where R b is an alkenylene o group as defined above and R c is one or more aryl radicals as defined above. Unless stated otherwise specifically in the specification, an aralkenyl group can be optionally substituted.
  • Alkynyl or “arylalkynyl” refers to a radical of the formula —R b —R c where R b is an alkynylene group as defined above and R c is one or more aryl radicals as defined above. Unless stated otherwise specifically in the specification, an aralkynyl group can be optionally substituted.
  • Carbocyclyl “carbocyclic ring” or “carbocycle” refers to a rings structure, wherein the atoms which form the ring are each carbon. Carbocyclic rings can comprise from 3 to 20 carbon atoms in the ring. Carbocyclic rings include aryls and cycloalkyl, cycloalkenyl and cycloalkynyl as defined herein. Unless stated otherwise specifically in the specification, a carbocyclyl group can be optionally substituted.
  • Cycloalkyl refers to a stable non-aromatic monocyclic or polycyclic fully saturated hydrocarbon radical consisting solely of carbon and hydrogen atoms, which can include fused or bridged ring systems, having from three to twenty carbon atoms, preferably having from three to ten carbon atoms, and which is attached to the rest of the molecule by a single bond.
  • Monocyclic cycloalkyl radicals include, for example, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, and cyclooctyl.
  • Polycyclic cycloalkyl radicals include, for example, adamantyl, norbornyl, decalinyl, 7,7-dimethyl-bicyclo[2.2.1]heptanyl, and the like. Unless otherwise stated specifically in the specification, a cycloalkyl group can be optionally substituted.
  • “Cycloalkenyl” refers to a stable non-aromatic monocyclic or polycyclic hydrocarbon radical consisting solely of carbon and hydrogen atoms, having one or more carbon-carbon double bonds, which can include fused or bridged ring systems, having from three to twenty carbon atoms, preferably having from three to ten carbon atoms, and which is attached to the rest of the molecule by a single bond.
  • Monocyclic cycloalkenyl radicals include, for example, cyclopentenyl, cyclohexenyl, cycloheptenyl, cycloctenyl, and the like.
  • Polycyclic cycloalkenyl radicals include, for example, bicyclo[2.2.1]hept-2-enyl and the like. Unless otherwise stated specifically in the specification, a cycloalkenyl group can be optionally substituted.
  • Cycloalkynyl refers to a stable non-aromatic monocyclic or polycyclic hydrocarbon radical consisting solely of carbon and hydrogen atoms, having one or more carbon-carbon triple bonds, which can include fused or bridged ring systems, having from three to twenty carbon atoms, preferably having from three to ten carbon atoms, and which is attached to the rest of the molecule by a single bond.
  • Monocyclic cycloalkynyl radicals include, for example, cycloheptynyl, cyclooctynyl, and the like. Unless otherwise stated specifically in the specification, a cycloalkynyl group can be optionally substituted.
  • Cycloalkylalkyl refers to a radical of the formula —R b —R d where R b is an alkylene, alkenylene, or alkynylene group as defined above and R d is a cycloalkyl, cycloalkenyl, cycloalkynyl radical as defined above. Unless stated otherwise specifically in the specification, a cycloalkylalkyl group can be optionally substituted.
  • Haloalkyl refers to an alkyl radical, as defined above, that is substituted by one or more halo radicals, as defined above, e.g., trifluoromethyl, difluoromethyl, trichloromethyl, 2,2,2-trifluoroethyl, 1,2-difluoroethyl, 3-bromo-2-fluoropropyl, 1,2-dibromoethyl, and the like. Unless stated otherwise specifically in the specification, a haloalkyl group can be optionally substituted.
  • Haloalkenyl refers to an alkenyl radical, as defined above, that is substituted by one or more halo radicals, as defined above, e.g., 1-fluoropropenyl, 1,1-difluorobutenyl, and the like. Unless stated otherwise specifically in the specification, a haloalkenyl group can be optionally substituted.
  • Haloalkynyl refers to an alkynyl radical, as defined above, that is substituted by one or more halo radicals, as defined above, e.g., 1-fluoropropynyl, 1-fluorobutynyl, and the like. Unless stated otherwise specifically in the specification, a haloalkenyl group can be optionally substituted.
  • Heterocyclyl refers to a stable 3- to 20-membered non-aromatic, partially aromatic, or aromatic ring radical which consists of two to twelve carbon atoms and from one to six heteroatoms selected from the group consisting of nitrogen, oxygen and sulfur. Heterocyclyl or heterocyclic rings include heteroaryls as defined below.
  • the heterocyclyl radical can be a monocyclic, bicyclic, tricyclic or tetracyclic ring system, which can include fused or bridged ring systems; and the nitrogen, carbon or sulfur atoms in the heterocyclyl radical can be optionally oxidized; the nitrogen atom can be optionally quaternized; and the heterocyclyl radical can be partially or fully saturated.
  • heterocyclyl radicals include, but are not limited to, dioxolanyl, thienyl[1,3]dithianyl, decahydroisoquinolyl, imidazolinyl, imidazolidinyl, isothiazolidinyl, isoxazolidinyl, morpholinyl, octahydroindolyl, octahydroisoindolyl, 2-oxopiperazinyl, 2-oxopiperidinyl, 2-oxopyrrolidinyl, oxazolidinyl, piperidinyl, piperazinyl, 4-piperidonyl, pyrrolidinyl, pyrazolidinyl, quinuclidinyl, thiazolidinyl, tetrahydrofuryl, trithianyl, tetrahydropyranyl, thiomorpholinyl, thiamorpholinyl, 1-oxo-thio
  • Heterocyclylalkyl refers to a radical of the formula —R b —R e where R b is an alkylene group as defined above and Re is a heterocyclyl radical as defined above. Unless stated otherwise specifically in the specification, a heterocycloalkylalkyl group can be optionally substituted.
  • Heterocyclylalkenyl refers to a radical of the formula —R b —R e where R b is an alkenylene group as defined above and Re is a heterocyclyl radical as defined above. Unless stated otherwise specifically in the specification, a heterocycloalkylalkenyl group can be optionally substituted.
  • Heterocyclylalkynyl refers to a radical of the formula —R b —Re where R b is an alkynylene group as defined above and Re is a heterocyclyl radical as defined above. Unless stated otherwise specifically in the specification, a heterocycloalkylalkynyl group can be optionally substituted.
  • N-heterocyclyl refers to a heterocyclyl radical as defined above containing at least one nitrogen and where the point of attachment of the heterocyclyl radical to the rest of the molecule is through a nitrogen atom in the heterocyclyl radical. Unless stated otherwise specifically in the specification, a N-heterocyclyl group can be optionally substituted.
  • Heteroaryl refers to a 5- to 20-membered ring system radical comprising hydrogen atoms, one to thirteen carbon atoms, one to six heteroatoms selected from the group consisting of nitrogen, oxygen and sulfur, and at least one aromatic ring.
  • the heteroaryl radical can be a monocyclic, bicyclic, tricyclic or tetracyclic ring system, which can include fused or bridged ring systems; and the nitrogen, carbon or sulfur atoms in the heteroaryl radical can be optionally oxidized; the nitrogen atom can be optionally quaternized.
  • Examples include, but are not limited to, azepinyl, acridinyl, benzimidazolyl, benzothiazolyl, benzindolyl, benzodioxolyl, benzofuranyl, benzooxazolyl, benzothiazolyl, benzothiadiazolyl, benzo[b][1,4]dioxepinyl, 1,4-benzodioxanyl, benzonaphthofuranyl, benzoxazolyl, benzodioxolyl, benzodioxinyl, benzopyranyl, benzopyranonyl, benzofuranyl, benzofuranonyl, benzothienyl (benzothiophene), benzotriazolyl, benzo[4,6]imidazo[1,2-a]pyridinyl, carbazolyl, cinnolinyl, dibenzofuranyl, dibenzothiophene, furanyl,
  • N-heteroaryl refers to a heteroaryl radical as defined above containing at least one nitrogen and where the point of attachment of the heteroaryl radical to the rest of the molecule is through a nitrogen atom in the heteroaryl radical. Unless stated otherwise specifically in the specification, an N-heteroaryl group can be optionally substituted.
  • Heteroarylalkyl refers to a radical of the formula —R b —R f where R b is an alkylene chain as defined above and R f is a heteroaryl radical as defined above. Unless stated otherwise specifically in the specification, a heteroarylalkyl group can be optionally substituted.
  • Heteroarylalkenyl refers to a radical of the formula —R b —R f where R b is an alkenylene, chain as defined above and R f is a heteroaryl radical as defined above. Unless stated otherwise specifically in the specification, a heteroarylalkenyl group can be optionally substituted.
  • Heteroarylalkynyl refers to a radical of the formula —R b —R f where R b is an alkynylene chain as defined above and R f is a heteroaryl radical as defined above. Unless stated otherwise specifically in the specification, a heteroarylalkynyl group can be optionally substituted.
  • Ring refers to a cyclic group which can be fully saturated, partially saturated, or fully unsaturated.
  • a ring can be monocyclic, bicyclic, tricyclic, or tetracyclic. Unless stated otherwise specifically in the specification, a ring can be optionally substituted.
  • Thioalkyl refers to a radical of the formula —SR a where R a is an alkyl, alkenyl, or alkynyl radical as defined above containing one to twelve carbon atoms. Unless stated otherwise specifically in the specification, a thioalkyl group can be optionally substituted.
  • substituted means any of the above groups (i.e., alkyl, alkylene, alkenyl, alkenylene, alkynyl, alkynylene, alkoxy, alkylamino, alkylcarbonyl, thioalkyl, aryl, aralkyl, carbocyclyl, cycloalkyl, cycloalkenyl, cycloalkynyl, cycloalkylalkyl, haloalkyl, heterocyclyl, N-heterocyclyl, heterocyclylalkyl, heteroaryl, N-heteroaryl and/or heteroarylalkyl) wherein at least one hydrogen atom is replaced by a bond to a non-hydrogen atoms such as, but not limited to: a halogen atom such as F, Cl, Br, and I; an oxygen atom in groups such as hydroxyl groups, alkoxy groups, and ester groups; a sulfur atom in groups such as hydroxyl groups
  • “Substituted” also means any of the above groups in which one or more hydrogen atoms are replaced by a higher-order bond (e.g., a double- or triple-bond) to a heteroatom such as oxygen in oxo, carbonyl, carboxyl, and ester groups; and nitrogen in groups such as imines, oximes, hydrazones, and nitriles.
  • a higher-order bond e.g., a double- or triple-bond
  • nitrogen in groups such as imines, oximes, hydrazones, and nitriles.
  • substituted includes any of the above groups in which one or more hydrogen atoms are replaced with —NR g R h , —NR g C( ⁇ O)R h , —NR g C( ⁇ O)NR g R h , —NR g C( ⁇ O)OR h , —NR g SO 2 R h , —OC( ⁇ O)NR g R h , —OR g , —SR g , —SOR g , —SO 2 R g , —OSO 2 R g , —SO 2 OR g , ⁇ NSO 2 R g , and —SO 2 NR g R h .
  • “Substituted also means any of the above groups in which one or more hydrogen atoms are replaced with —C( ⁇ O)R g , —C( ⁇ O)OR g , —C( ⁇ O)NR g R h , —CH 2 SO 2 R g , —CH 2 SO 2 NR g R h .
  • R g and R h are the same or different and independently hydrogen, alkyl, alkenyl, alkynyl, alkoxy, alkylamino, thioalkyl, aryl, aralkyl, cycloalkyl, cycloalkenyl, cycloalkynyl, cycloalkylalkyl, haloalkyl, haloalkenyl, haloalkynyl, heterocyclyl, N-heterocyclyl, heterocyclylalkyl, heteroaryl, N-heteroaryl and/or heteroarylalkyl.
  • “Substituted” further means any of the above groups in which one or more hydrogen atoms are replaced by a bond to an amino, cyano, hydroxyl, imino, nitro, oxo, thioxo, halo, alkyl, alkenyl, alkynyl, alkoxy, alkylamino, thioalkyl, aryl, aralkyl, cycloalkyl, cycloalkenyl, cycloalkynyl, cycloalkylalkyl, haloalkyl, haloalkenyl, haloalkynyl, heterocyclyl, N-heterocyclyl, heterocyclylalkyl, heteroaryl, N-heteroaryl and/or heteroarylalkyl group.
  • each of the foregoing substituents can also be optionally substituted with one or more of the above substituents.
  • a point of attachment bond denotes a bond that is a point of attachment between two chemical entities, one of which is depicted as being attached to the point of attachment bond and the other of which is not depicted as being attached to the point of attachment bond.
  • fused refers to any ring structure described herein which is fused to an existing ring structure in the compounds of the invention.
  • the fused ring is a heterocyclyl ring or a heteroaryl ring
  • any carbon atom on the existing ring structure which becomes part of the fused heterocyclyl ring or the fused heteroaryl ring can be replaced with a nitrogen atom.
  • the compound of the present disclosure can be useful for modulating androgen receptor (AR). Further, the compound of the present disclosure can be useful for treating various diseases and conditions including, but not limited to, cancer.
  • the cancer is prostate cancer or breast cancer.
  • the present disclosure provides compounds comprising the structure of formula (I):
  • the present disclosure provides compounds comprising the structure of formula (II):
  • the present disclosure provides compounds comprising the structure of formula (IIA):
  • the present disclosure provides compounds comprising the structure of formula (IIB):
  • the present disclosure provides compounds comprising the structure of formula (III):
  • the present disclosure provides compounds comprising the structure of formula (IIIA):
  • the present disclosure provides compounds comprising the structure of formula (IV):
  • the present disclosure provides compounds comprising the structure of formula (V):
  • the present disclosure provides compounds comprising the structure of formula (VA):
  • the present disclosure provides compounds comprising the structure of formula (VI):
  • the present disclosure provides compounds comprising the structure of formula (A):
  • the present disclosure provides compounds comprising the structure of formula (B)
  • —V-L is —CH 2 CH 2 C 1 , —CH 2 CH 2 CH 2 C 1 , —CH 2 CH 2 NH 2 , or —CH 2 CH 2 CH 2 NH 2 .
  • —Y—W— is a bond, —OCH 2 —, —OCH 2 CH 2 —, —OCH(CH 3 )—, —NH—, —NHCH 2 —, —NHC( ⁇ O)—, or —C( ⁇ O)NH—.
  • X is a bond, —CH 2 —, —C(CH 3 )H—, —C(CH 3 ) 2 —, or —CH 2 CH 2 —.
  • the present disclosure provides compounds comprising the structure of formula (C):
  • the present disclosure provides compounds comprising the structure of formula (D):
  • the present disclosure provides compounds comprising the structure of formula (E):
  • R 3 is selected from hydrogen, F, Cl, Br, I, —CN, —CF 3 , —OH, methyl, methoxy, —S(C 1 -C 3 alkyl), —SO 2 (C 1 -C 3 alkyl), —NH 2 , —NHSO 2 CH 3 , —NHSO 2 CF 3 , —N(CH 3 )SO 2 CH 3 , —SO 2 NH 2 , —CONH 2 , —CON(C 1 -C 3 alkyl) 2 , —CONH(C 1 -C 3 alkyl), —NHCO(C 1 -C 3 alkyl), or —NHCO(C 1 -C 3 alkyl).
  • the present disclosure provides compounds comprising the structure of formula (F):
  • the present disclosure provides compounds comprising the structure of formula (G):
  • the present disclosure provides compounds comprising the structure of formula (G-II)
  • the present disclosure provides compounds comprising the structure of formula (H):
  • R 2A and R 2B are not both Cl.
  • R 2A and R 2B are Cl, then the other of R 2A and R 2B is not —CN.
  • R 2A and R 2B are not both Cl.
  • a and B are each independently 5- or 6-membered aryl or heteroaryl.
  • a and B are each independently selected from phenyl, pyridyl, pyrimidyl, or thiophene.
  • a and B are each phenyl.
  • A has a meta or para connectivity with X and Y.
  • B has a meta or para connectivity with X and Z.
  • a and B are phenyl and has one of the connectivity as shown:
  • C is aryl or heteroaryl.
  • C is 5- to 10-membered aryl or heteroaryl.
  • C is aryl.
  • C is phenyl or naphthyl.
  • C is aryl.
  • C is phenyl.
  • C is heteroaryl.
  • C monocyclic or bicyclic heteroaryl.
  • C is monocyclic heteroaryl.
  • C is 5- or 10-membered heteroaryl.
  • C is 5- or 6-membered heteroaryl, which is optionally substituted with 1, 2, 3, 4, or 5 R 3 .
  • C is 5- or 6-membered heteroaryl containing 1, 2, or 3 heteroatoms selected from O, S, or N, wherein the heteroaryl is optionally substituted with 1, 2, 3, 4, or 5 R 3 .
  • C is 5- or 6-membered heteroaryl containing 1 or 2 heteroatoms selected from O, S, or N, wherein the heteroaryl is optionally substituted with 1, 2, 3, 4, or 5 R 3 .
  • C is pyrazole, imidazole, oxazole, oxadiazole, oxazolone, isoxazole, thiazole, pyridyl, or pyrimidyl, which are each optionally substituted with 1, 2, 3, 4, or 5 R 3 .
  • C, which is substituted with (R 3 )n3, is pyrazole, imidazole, oxazole, oxadiazole, oxazolone, isoxazole, thiazole, pyridyl, pyrazine, furan or pyrimidyl.
  • C is pyrazole, imidazole, oxazole, oxadiazole, oxazolone, isoxazole, thiazole, pyridyl, pyrazine, furan or pyrimidyl, which are each substituted with 1, 2, 3, 4, or 5 R 3 .
  • C is selected from
  • R 3a is C 1 -C 3 alkyl.
  • C is selected from
  • R 3a is C 1 -C 3 alkyl.
  • C is
  • C is
  • C is heterocyclyl.
  • C is saturated or partially saturated heterocycle.
  • C is monocyclic or bicyclic.
  • C is 5- to 7-membered heterocyclyl comprising 1, 2, or 3 heteroatoms selected from O, S, or N as a ring member.
  • C is imidazolidine, imidazolidine-dione, or dihydrooxazole. In one embodiment, C is selected from
  • C is
  • D is —O—, —NH— or —NR 3 —; and U is each independently O, S, or NR 16 .
  • D is —NH— or —NR 3 —.
  • at least one U is O.
  • each U is O.
  • at least one R 3 is —SO 2 CH 3 , —NHSO 2 CH 3 , —CH 2 NHSO 2 CH 3 , —SO 2 NH 2 , —CONH 2 , or —NHCOCH 3 .
  • C is aryl. In some embodiments, C is phenyl or naphthyl. In one embodiment of the compounds of formula (I)-(VA) or (A), C is phenyl.
  • C is bicyclic heteroaryl or heterocyclyl. In one embodiment, C is
  • Z is a bond, —(CR 8 R 9 ) m —, —O—, —C( ⁇ O)—, —S—, —S( ⁇ O)—, —SO 2 —, or —NR 7 —.
  • Z is —(CR 8 R 9 ) m —, —O—, —C( ⁇ O)—, —S—, —S( ⁇ O)—, —SO 2 —, or —NR 7 —.
  • Z is —C( ⁇ O)—.
  • Z is a bond, —CH 2 —, —C(CH 3 )H—, —O—, —S—, —NH—, —NCH 3 —, or —N(COCH 3 )—.
  • Z is —CH 2 —, —C(CH 3 )H—, —O—, —S—, —NH—, —NCH 3 —, or —N(COCH 3 )—.
  • Z is a bond, —CH 2 —, —O—, or —NCH 3 —.
  • Z is a bond, —CH 2 —, —O—, or —NH—.
  • Z is —O—.
  • “compounds of formula (I)-(IV) and (A)-(H-I)” refers to compounds of formula (I), (IA), (IB), (IC), (II), (IIA), (IIIA), (IIB), (III), (IV), (IVA), (V), (VA), (VI), (A), (A-I), (B)-(D), (E), (E-I)-(E-VII), (F), (G), (G-I), (G-II), (H), and (H-I).
  • Y is a bond, —(CR 8 R 9 ) m —, —O—, —C( ⁇ O)—, —S—, —S( ⁇ O)—, —SO 2 —, or —NR 7 —.
  • Y is —(CR 8 R 9 ) m —, —O—, —C( ⁇ O)—, —S—, —S( ⁇ O)—, —SO 2 —, or —NR 7 —.
  • Y is —C( ⁇ O)—.
  • Y is a bond, —CH 2 —, —C(CH 3 )H—, —O—, —S—, —NH—, —NCH 3 —, or —N(COCH 3 )—.
  • Y is —CH 2 —, —C(CH 3 )H—, —O—, —S—, —NH—, —NCH 3 —, or —N(COCH 3 )—.
  • Y is a bond, —CH 2 —, —O—, or —NCH 3 —.
  • Y is a bond, —CH 2 —, —O—, or —NH—. In some embodiments of the compounds of formula (I)-(VI) and (A)-(H-I), Y is —O—.
  • V is a bond, —(CR 8a R 9a ) m —, or —C( ⁇ O)—. In some embodiments, V is bond, or —(CR 8a R 9a ) m —.
  • V is —(CR 8a R 9a ) m —, wherein m is 1, 2, or 3.
  • V is —(CR 8a R 9a ) m —, wherein R 8a and R 8b are each independently hydrogen, —OH, halogen, optionally substituted C 1 -C 3 alkyl, optionally substituted C 2 -C 3 alkenyl, optionally substituted C 2 -C 3 alkynyl, C 1 -C 3 alkoxy, —NR 13 R 14 , optionally substituted —(C 1 -C 3 alkyl)-NR 13 R 14 , —NR 14 COR 16 , optionally substituted —(C 1 -C 3 alkyl)-NR 14 COR 16 , —CONR 14 R 15 , or optionally
  • V is —(CR 8a R 9a ) m —, wherein R 8a and R 8b are each independently hydrogen, —OH, halogen, C 1 -C 3 alkyl, C 2 -C 3 alkenyl, C 2 -C 3 alkynyl, C 1 -C 3 alkoxy, —NR 13 R 14 , —(C 1 -C 3 alkyl)-NR 13 R 14 , —NR 14 COR 16 , —(C 1 -C 3 alkyl)-NR 14 COR 16 , —CONR 14 R 15 , or —(C 1 -C 3 alkyl)-CONR 14 R 15 ; or R 8a and R 8b , on the same carbon atom or on a different carbon atom, taken together form an optionally substituted 3- to 6-membered carbocyclyl or heterocyclyl.
  • V is —CH 2 —, —CH 2 CH 2 —, —CH(CH 3 )CH 2 —, —CH 2 CH(CH 3 )—, or —CH 2 CH 2 CH 2 —.
  • V is —CH 2 —, —CH 2 CH 2 —, or —CH 2 CH 2 CH 2 —, each optionally substituted with one or more of —OH, halogen, or C 1 -C 3 alkyl.
  • V is —CH 2 —, —CH 2 CH 2 —, —CH 2 CH(OH)CH 2 — or —CH 2 CH 2 CH 2 —.
  • V is —CH 2 —, —CH 2 CH 2 —, or —CH 2 CH 2 CH 2 —.
  • V is —CH 2 — or —CH 2 CH 2 —.
  • V is —CH 2 — and L is halogen, —NH 2 , or —CF 3 ; or V is —CH 2 CH 2 — and L is halogen or —NH 2 .
  • L is hydrogen, halogen, —CF 2 H, —CF 3 , —CN, —O(C 1 -C 3 alkyl), —NR 11 R 12 , or —CONR 11 R 12 .
  • L is hydrogen, halogen, —CF 2 H, —CF 3 , —CN, —O(C 1 -C 3 alkyl), —NH 2 , —NH(C 1 -C 3 alkyl), —N(C 1 -C 3 alkyl) 2 , —CONH 2 , —CONH(C 1 -C 3 alkyl), or —CON(C 1 -C 3 alkyl) 2 .
  • L is hydrogen, halogen, —CF 3 , or —NH 2 .
  • L is halogen, —CCl 3 , —CCl 2 , —CF 3 , or —NH 2 .
  • L is halogen, —CF 3 , or —NH 2 .
  • L is hydrogen or halogen.
  • L is halogen.
  • L is Cl, or Br.
  • L is Cl.
  • W is a bond.
  • W is —(CR 8a R 9a ) m —, —C( ⁇ O)—, —N(R′)CO—, —CONR 7 —, or —NSO 2 R 7 —.
  • W is —(CR 8a R 9a ) m —, wherein m is 1, 2, or 3.
  • W is a bond, —CH 2 —, —C(CH 3 )H—, —C( ⁇ O)—, —N(R 7 )CO—, or —CONR 7 —, wherein R 7 is H or C 1 -C 6 alkyl. In some embodiments, W is a bond, —CH 2 —, —C(CH 3 )H—, —C( ⁇ O)—, —N(R 7 )CO—, or —CONR 7 —, wherein R 7 is H or C 1 -C 3 alkyl.
  • W is a bond, —CH 2 —, —C(CH 3 )H—, —C( ⁇ O)—, —NHCO—, —N(C 1 -C 3 alkyl)CO—, —CONH—, or —CON(C 1 -C 3 alkyl)-.
  • W is a bond, —CH 2 —, or —C(CH 3 )H—.
  • W is a —CH 2 — or —C(CH 3 )H—.
  • —Y—W— is a bond, —OCH 2 —, —OCH 2 CH 2 —, —OCH(CH 3 )—, —NH—, —NHCH 2 —, —NHC( ⁇ O)—, or —C( ⁇ O)NH—.
  • —Y—W— is —OCH 2 —, —OCH 2 CH 2 —, or —OCH(CH 3 )—.
  • —Z—V-L is —Z—CH 2 CH 2 C 1 , —Z—CH 2 CH 2 CH 2 C 1 , —Z—CH 2 CH 2 NH 2 , or —Z—CH 2 CH 2 CH 2 NH 2 , wherein Z is a bond, —O—, —NH—, or —N(COCH 3 )—.
  • —Z—V-L is —OCH 3 .
  • —Z—V-L is —O—CH 2 CH 2 Cl or —O—CH 2 CH 2 CH 2 Cl.
  • —V-L is —CH 2 CH 2 C 1 , —CH 2 CH 2 CH 2 C 1 , —CH 2 CH 2 NH 2 , or —CH 2 CH 2 CH 2 NH 2 . In one embodiment, —V-L is —CH 3 .
  • X is a bond, —(CR 5 R 6 ) t —, —O—, —C( ⁇ O)—, —S—, —S( ⁇ O)—, —SO 2 —, or —NR 7 —.
  • X is a bond, —(CR 5 R 6 ) t —, —O—, —C( ⁇ O)—, —S—, —S( ⁇ O)—, —SO 2 —, or —NR 7 —, wherein R 7 is H or C 1 -C 6 alkyl.
  • X is a bond, —(CR 5 R 6 ) t —, or —NR 7 —. In some embodiments, X is a bond or —(CR 5 R 6 ) t —. In some embodiments, X is a bond, —CH 2 —, —C(CH 3 )H—, —C(CH 3 ) 2 —, —CH 2 CH 2 —, —NH—, or —N(C 1 -C 6 alkyl)-.
  • X is a bond, —CH 2 —, —C(CH 3 )H—, —C(CH 3 ) 2 —, —CH 2 CH 2 —, —NH—, —N(CH 3 )—, —N(CH 2 CH 3 )—, —N(iPr)—, or —N(tBu)-.
  • X is a bond, —CH 2 —, —C(CH 3 )H—, —C(CH 3 ) 2 —, or —CH 2 CH 2 —.
  • X is —CH 2 —, —C(CH 3 )H—, or —C(CH 3 ) 2 -. In one embodiment, X is —C(CH 3 ) 2 -.
  • R 1 and R 2 are each independently halogen, —CN, —CF 3 , —OH, C 1 -C 3 alkyl, C 1 -C 3 alkoxy, —(C 1 -C 3 alkyl)-(C 1 -C 3 alkoxy), —(C 1 -C 3 alkyl)-OH, —NR 13 R 14 , —(C 1 -C 3 alkyl)-NR 13 R 14 , —NR 14 SO 2 R 16 , —(C 1 -C 3 alkyl)NR 14 SO 2 R 16 , —NR 14 COR 16 , —(C 1 -C 3 alkyl)-NR 14 COR 16 , —CONR 14 R 15 , —(C 1 -C 3 alkyl)-CONR 14 R 15 , —SO 2 NR 14 R 15 , —(C 1 -C 3 alkyl)
  • R 1 and R 2 are each independently hydrogen, halogen, —CN, —CF 3 , —OH, optionally substituted C 1 -C 6 alkyl, optionally substituted C 1 -C 6 alkoxy, optionally substituted —(C 1 -C 6 alkyl)-(C 1 -C 6 alkoxy), optionally substituted —(C 1 -C 6 alkyl)-OH, —NR 13 R 14 , optionally substituted —(C 1 -C 6 alkyl)-NR 13 R 14 , —NR 14 SO 2 R 16 , optionally substituted —(C 1 -C 6 alkyl)NR 14 SO 2 R 16 , —NR 14 COR 16 , optionally substituted —(C 1 -C 6 alkyl)-NR 14 COR 16 , —CONR 14 R 15 , optionally substituted —(C 1 -C 6 alkyl)-NR 14 COR 16 , —CONR 14 R 15 , optionally substituted
  • R 1 and R 2 are each independently hydrogen, halogen, —CN, —CF 3 , —OH, optionally substituted C 1 -C 3 alkyl, C 1 -C 3 alkoxy, optionally substituted —(C 1 -C 3 alkyl)-(C 1 -C 3 alkoxy), optionally substituted —(C 1 -C 3 alkyl)-OH, —NR 13 R 14 , —(C 1 -C 3 alkyl)-NR 13 R 14 , —NR 14 SO 2 R 16 , optionally substituted —(C 1 -C 3 alkyl)NR 14 SO 2 R 16 , —NR 14 COR 16 , optionally substituted —(C 1 -C 3 alkyl)-NR 14 COR 16 , —CONR 14 R 15 , optionally substituted —(C 1 -C 3 alkyl)-CONR 14 R 15 , —SO 2 NR 14 R 15 , optionally substituted —(C
  • R 1 and R 2 are each independently hydrogen, halogen, —CN, —CF 3 , —OH, C 1 -C 3 alkyl, C 1 -C 3 alkoxy, —(C 1 -C 3 alkyl)-(C 1 -C 3 alkoxy), —(C 1 -C 3 alkyl)-OH, —NR 13 R 14 , —(C 1 -C 3 alkyl)-NR 13 R 14 , —NR 14 SO 2 R 16 , —(C 1 -C 3 alkyl)NR 14 SO 2 R 16 , —NR 14 COR 16 , —(C 1 -C 3 alkyl)-NR 14 COR 16 , —CONR 14 R 15 , —(C 1 -C 3 alkyl)-CONR 14 R 15 , —SO 2 NR 14 R 15 , —(C 1 -C 3 alkyl)-CONR 14 R 15 , —SO 2 NR 14 R 15 , —(
  • R 1 and R 2 are each independently hydrogen, halogen, —CN, —CF 3 , —OH, C 1 -C 3 alkyl, or —CONR 14 R 15 .
  • R 1 and R 2 are each independently hydrogen, halogen, —CN, —CF 3 , —OH, methyl, methoxy, or —CONH 2 .
  • R 1 and R 2 are each independently hydrogen, C 1 , —CN, —CF 3 , —OH, methyl, methoxy, or —CONH 2 .
  • R 1 and R 2 are each independently hydrogen, halogen, —CN, —CF 3 , —OH, or methyl. In one embodiment, R 1 and R 2 are each independently C 1 , —CN, —CF 3 , —OH, methyl, methoxy, or —CONH 2 . In one embodiment of the compounds of formula (I)-(VI), R 1 and R 2 are each independently halogen, —CN, —CF 3 , —OH, or methyl.
  • R 1 and R 2 are each halogen, methyl, —CF 3 , or —CN. In one embodiment of the compounds of formula (I)-(VI) and (A)-(F), R 1 and R 2 are each halogen or —CN. In one embodiment of the compounds of formula (I)-(VI) and (A)-(H-I), at least one of R 1 and R 2 is Cl or —CN. In one embodiment of the compounds of formula (I)-(VI) and (A)-(H-I), at least two of R 1 and R 2 are each independently Cl or —CN. In one embodiment of the compounds of formula (I)-(VI) and (A)-(H-I), R 1 and R 2 are each Cl or —CN.
  • R 1 and R 2 are each independently optionally substituted carbocyclyl, optionally substituted heterocyclyl, optionally substituted aryl, or optionally substituted heteroaryl. In one embodiment, R 1 and R 2 are each independently 3- to 7-membered carbocyclyl, 3- to 7-membered heterocyclyl, phenyl, or 5- to 6-membered heteroaryl.
  • R 1 have one of the connectivity as shown below with respect to X and Y:
  • R 2 have one of the connectivity as shown below with respect to X and Z:
  • n1 is 0, 1, or 2. In some embodiments, n1 is 0 or 1. In other embodiments, n1 is 0. In some embodiments, n1 is 1. In one embodiment, the sum of n1 and n2 is 0, 1, 2, 3, or 4. In some embodiments, the sum of n1 and n2 is 1, 2, 3, or 4. In one embodiment, the sum of n1 and n2 is 2.
  • n2 is 0, 1, or 2. In some embodiments, n2 is 1 or 2. In other embodiments, n2 is 0. In some embodiments, n2 is 1. In some embodiments, n2 is 2.
  • n3 is 1, 2, 3, 4, or 5. In some embodiments, n3 is 1, 2, 3, or 4. In one embodiment, n3 is 1, 2, or 3. In one embodiment, n3 is 1 or 2.
  • R 3 is selected from hydrogen, halogen, oxo, ⁇ S, ⁇ NR 16 , —CN, —CF 3 , —OH, —SR 16 , optionally substituted C 1 -C 6 alkyl, optionally substituted C 2 -C 6 alkenyl, optionally substituted C 2 -C 6 alkynyl, optionally substituted C 1 -C 6 alkoxy, optionally substituted —(C 1 -C 6 alkyl)-(C 1 -C 6 alkoxy), optionally substituted —(C 1 -C 6 alkyl)-OH, —NR 13 R 14 , optionally substituted —(C 1 -C 6 alkyl)-NR 13 R 14 , —NR 14 SO 2 R 16 , optionally substituted —(C 1 -C 6 alkyl)NR 14 SO 2 R 16 , —NR 14
  • R 3 is selected from hydrogen, halogen, oxo, ⁇ S, ⁇ NR 16 , —CN, —CF 3 , —OH, —SR 16 , optionally substituted C 1 -C 6 alkyl, optionally substituted C 2 -C 6 alkenyl, optionally substituted C 2 -C 6 alkynyl, optionally substituted C 1 -C 6 alkoxy, optionally substituted —(C 1 -C 6 alkyl)-(C 1 -C 6 alkoxy), optionally substituted —(C 1 -C 6 alkyl)-OH, —NR 13 R 14 , optionally substituted —(C 1 -C 6 alkyl)-NR 13 R 14 , —NR 14 SO 2 R 16 , optionally substituted —(C 1 -C 6 alkyl)NR 14 SO 2 R 16 , —NR 14 COR 16 , optionally substituted —(C 1 -C 6 alkyl)-NR 14
  • R 3 is hydrogen, halogen, oxo, ⁇ S, ⁇ NR 16 , —CN, —CF 3 , —OH, —SR 16 , optionally substituted C 1 -C 3 alkyl, optionally substituted C 2 -C 3 alkenyl, optionally substituted C 2 -C 3 alkynyl, optionally substituted C 1 -C 3 alkoxy, optionally substituted —(C 1 -C 3 alkyl)-(C 1 -C 3 alkoxy), optionally substituted —(C 1 -C 3 alkyl)-OH, —NR 13 R 14 , optionally substituted —(C 1 -C 3 alkyl)-NR 13 R 14 , —NR 14 SO 2 R 16 , optionally substituted —(C 1 -C 3 alkyl)NR 14 SO 2 R 16 , —NR 14 COR 16 , optionally substituted —(C 1 -C 3 alkyl)-NR 14 COR 16 , optional
  • R 3 is selected from —NR 14 SO 2 R 16 , optionally substituted —(C 1 -C 6 alkyl)NR 14 SO 2 R 16 , or optionally substituted —SO 2 R 16 ; wherein R 16 is hydrogen, optionally substituted C 1 -C 3 alkyl, optionally substituted C 2 -C 3 alkenyl, optionally substituted C 2 -C 3 alkynyl, C 3 -C 6 cycloalkyl, or phenyl.
  • R 3 is selected from —NR 14 SO 2 R 16 , —(C 1 -C 6 alkyl)NR 14 SO 2 R 16 , or —SO 2 R 16 ; wherein R 16 is hydrogen, C 1 -C 3 alkyl, —(C 1 -C 3 alkyl)-NH 2 , C 3 -C 6 cycloalkyl, or phenyl.
  • R 3 is selected from hydrogen, halogen, oxo, ⁇ S, ⁇ NR 16 , —CN, —CF 3 , —OH, —S(C 1 -C 3 alkyl), C 1 -C 3 alkyl, C 2 -C 3 alkenyl, C 2 -C 3 alkynyl, C 1 -C 3 alkoxy, —(C 1 -C 3 alkyl)-(C 1 -C 3 alkoxy), —(C 1 -C 3 alkyl)-OH, —NR 13 R 14 , —(C 1 -C 3 alkyl)-NR 13 R 14 , —NR 14 SO 2 R 16 , —(C 1 -C 3 alkyl)NR 14 SO 2 R 16 , —NR 14 COR 16 , —(C 1 -C 6 alkyl)-NR 14 COR 16 , —(C 1 -C 6 alkyl)-NR 14 COR 16 , —(C 1
  • R 3 is selected from hydrogen, F, Cl, Br, I, oxo, ⁇ S, ⁇ NR 16 , —CN, —CF 3 , —OH, C 1 -C 3 alkyl, C 2 -C 3 alkenyl, C 2 -C 3 alkynyl, —S(C 1 -C 3 alkyl), —SO(C 1 -C 3 alkyl), —SO 2 (C 1 -C 3 alkyl), —NHSO 2 CH 3 , —N(CH 3 )SO 2 CH 3 , —NHSO 2 CH 2 CH 3 , —N(CH 3 )SO 2 CH 2 CH 3 , —CH 2 NHSO 2 CH 3 , —CH 2 N(CH 3 )SO 2 CH 3 , —SO 2 NH 2 , —CONH 2 , —CON(C 1 -C 3 alkyl) 2 , —CONH(C 1 -C 3 alkyl), —NHCO(
  • R 3 is selected from hydrogen, F, Cl, Br, I, oxo, ⁇ S, ⁇ NR 16 , —CN, —CF 3 , —OH, C 1 -C 3 alkyl, C 2 -C 3 alkenyl, C 2 -C 3 alkynyl, —S(C 1 -C 3 alkyl), —SO(C 1 -C 3 alkyl), —SO 2 (C 1 -C 3 alkyl), —NHSO 2 CH 3 , —N(CH 3 )SO 2 CH 3 , —CH 2 NHSO 2 CH 3 , —CH 2 N(CH 3 )SO 2 CH 3 , —SO 2 NH 2 , —CONH 2 , —CON(C 1 -C 3 alkyl) 2 , —CONH(C 1 -C 3 alkyl), —NHCO(C 1 -C 3 alkyl), or —N(CH 3 )CO(C 1 -C 3 alkyl),
  • R 3 is selected from hydrogen, F, Cl, Br, I, oxo, ⁇ S, ⁇ NR 16 , —CN, —CF 3 , —OH, methyl, —SCH 3 , —SO 2 CH 3 , —NHSO 2 CH 3 , —NHSO 2 CH 2 CH 3 , —CH 2 NHSO 2 CH 3 , —SO 2 NH 2 , —CONH 2 , or —NHCOCH 3 .
  • R 3 is selected from hydrogen, F, Cl, Br, I, oxo, ⁇ S, ⁇ NR 16 , —CN, —CF 3 , —OH, methyl, —SCH 3 , —SO 2 CH 3 , —NHSO 2 CH 3 , —CH 2 NHSO 2 CH 3 , —SO 2 NH 2 , —CONH 2 , or —NHCOCH 3 .
  • R 3 is selected from F, Cl, Br, I, oxo, ⁇ S, ⁇ NR 16 , —CN, —CF 3 , —OH, C 1 -C 3 alkyl, C 2 -C 3 alkenyl, C 2 -C 3 alkynyl, —S(C 1 -C 3 alkyl), —SO(C 1 -C 3 alkyl), —SO 2 (C 1 -C 3 alkyl), —NHSO 2 CH 3 , —N(CH 3 )SO 2 CH 3 , —CH 2 NHSO 2 CH 3 , —CH 2 N(CH 3 )SO 2 CH 3 , —SO 2 NH 2 , —CONH 2 , —CON(C 1 -C 3 alkyl) 2 , —CONH(C 1 -C 3 alkyl), —NHCO(C 1 -C 3 alkyl), or —N(CH 3 )CO(C 1 -C 3 alkyl), or
  • R 3 is selected from F, Cl, Br, I, oxo, ⁇ S, ⁇ NR 16 , —CN, —CF 3 , —OH, C 1 -C 3 alkyl, C 2 -C 3 alkenyl, C 2 -C 3 alkynyl, —S(C 1 -C 3 alkyl), —SO(C 1 -C 3 alkyl), —SO 2 (C 1 -C 3 alkyl), —NHSO 2 CH 3 , —N(CH 3 )SO 2 CH 3 , NHSO 2 CH 2 CH 3 , —N(CH 3 )SO 2 CH 2 CH 3 , —CH 2 NHSO 2 CH 3 , —CH 2 N(CH 3 )SO 2 CH 3 , —SO 2 NH 2 , —CONH 2 , —CON(C 1 -C 3 alkyl) 2 , —CONH(C 1 -C 3 alkyl), —NHCO(C 1 -
  • R 3 is selected from F, Cl, Br, I, oxo, ⁇ S, ⁇ NR 16 , —CN, —CF 3 , —OH, methyl, —SCH 3 , —SO 2 CH 3 , —NHSO 2 CH 3 , —CH 2 NHSO 2 CH 3 , —SO 2 NH 2 , —CONH 2 , or —NHCOCH 3 .
  • R 3 is —SO 2 CH 3 , —NHSO 2 CH 3 , —CH 2 NHSO 2 CH 3 , —SO 2 NH 2 , —CONH 2 , or —NHCOCH 3 .
  • R 3 is oxo, ⁇ S, ⁇ NR 16 , C 1 -C 3 alkyl, —SO 2 (C 1 -C 3 alkyl), or —NHSO 2 (C 1 -C 3 alkyl). In one embodiment, at least one of R 3 is oxo, ⁇ S, or ⁇ NR 16 . In one embodiment, at least one of R 3 is oxo, ⁇ S, or ⁇ NR 16 , wherein R 16 is H or C 1 -C 3 alkyl.
  • R 3 is selected from hydrogen, F, Cl, Br, I, oxo, —CN, —CF 3 , —OH, C 1 -C 3 alkyl, C 2 -C 3 alkenyl, C 2 -C 3 alkynyl, C 1 -C 3 alkoxy, —S(C 1 -C 3 alkyl), —SO 2 (C 1 -C 3 alkyl), —NH 2 , —NHSO 2 CH 3 , —NHSO 2 CF 3 , —N(CH 3 )SO 2 CH 3 , —NHSO 2 CH 2 CH 3 , —N(CH 3 )SO 2 CH 2 CH 3 , —CH 2 NHSO 2 CH 3 , —CH 2 N(CH 3 )SO 2 CH 3 , —SO 2 NH 2 , —CONH 2 , —CON(C 1 -C 3 alkyl)
  • R 3 is selected from hydrogen, F, Cl, Br, I, oxo, —CN, —CF 3 , —OH, C 1 -C 3 alkyl, C 2 -C 3 alkenyl, C 2 -C 3 alkynyl, C 1 -C 3 alkoxy, —S(C 1 -C 3 alkyl), —SO 2 (C 1 -C 3 alkyl), —NH 2 , —NHSO 2 CH 3 , —NHSO 2 CF 3 , —N(CH 3 )SO 2 CH 3 , —CH 2 NHSO 2 CH 3 , —CH 2 N(CH 3 )SO 2 CH 3 , —SO 2 NH 2 , —CONH 2 , —CON(C 1 -C 3 alkyl) 2 , —CONH(C 1 -C 3 alkyl), —NHCO(C 1 -
  • R 3 on a sp 3 carbon is each selected from hydrogen, halogen, oxo, ⁇ S, ⁇ NR 16 , —CN, —CF 3 , —OH, —S(C 1 -C 3 alkyl), C 1 -C 3 alkyl, C 2 -C 3 alkenyl, C 2 -C 3 alkynyl, C 1 -C 3 alkoxy, —(C 1 -C 3 alkyl)-(C 1 -C 3 alkoxy), —(C 1 -C 3 alkyl)-OH, —NR 13 R 14 , —(C 1 -C 3 alkyl)-NR 13 R 14 , —NR 14 SO 2 R 16 , —(C 1 -C 3 alkyl)NR 14 SO 2 R 16 , —NR 14 COR 16 , —(C 1 -C 6 alkyl
  • R 3 on a sp 2 carbon is each selected from hydrogen, halogen, —CN, —CF 3 , —OH, —S(C 1 -C 3 alkyl), C 1 -C 3 alkyl, C 2 -C 3 alkenyl, C 2 -C 3 alkynyl, C 1 -C 3 alkoxy, —(C 1 -C 3 alkyl)-(C 1 -C 3 alkoxy), —(C 1 -C 3 alkyl)-OH, —NR 13 R 14 , —(C 1 -C 3 alkyl)-NR 13 R 14 , —NR 14 SO 2 R 16 , —(C 1 -C 3 alkyl)NR 14 SO 2 R 16 , —NR 14 COR 16 , —(C 1 -C 6 alkyl)-NR 14 COR 16 , —CONR
  • R 3 on a nitrogen atom is each selected from C 1 -C 3 alkyl, C 2 -C 3 alkenyl, C 2 -C 3 alkynyl, C 1 -C 3 alkoxy, —(C 1 -C 3 alkyl)-(C 1 -C 3 alkoxy), —(C 1 -C 3 alkyl)-OH, —(C 1 -C 3 alkyl)-NR 13 R 14 , —(C 1 -C 3 alkyl)NR 14 SO 2 R 16 , —(C 1 -C 6 alkyl)-NR 14 COR 16 , —CONR 14 R 15 , —(C 1 -C 3 alkyl)-CONR 14 R 15 , —(C 1 -C 3 alkyl)-SO 2 NR 14 R 15 , or —(C 1 -C 6 alkyl)
  • At least one R 3 is selected from —CN, C 1 -C 3 alkoxy, —CONH 2 , —NHSO 2 CH 3 , —N(CH 3 )SO 2 CH 3 , —NHSO 2 CH 2 CH 3 , —N(CH 3 )SO 2 CH 2 CH 3 , or —SO 2 CH 3 and the other R 3 , if present, is selected from —CN, —CF 3 , C 1 -C 3 alkyl, C 2 -C 3 alkenyl, C 2 -C 3 alkynyl, C 1 -C 3 alkoxy, —S(C 1 -C 3 alkyl), —SO 2 (C 1 -C 3 alkyl), —NH 2 , —(C 1 -C 3 alkyl)NH 2 , —NHSO 2 CH 3 , —NHSO 2 CF 3 , —N(CH
  • At least one R 3 is selected from —NHSO 2 CH 3 , —NHSO 2 CH 2 CH 3 , or —SO 2 CH 3 and the other R 3 , if present, is selected from —CN, C 1 -C 3 alkyl, C 1 -C 3 alkoxy, —SO 2 (C 1 -C 3 alkyl), —NH 2 , —(C 1 -C 3 alkyl)NH 2 , —NHSO 2 CH 3 , —N(CH 3 )SO 2 CH 3 , —NHSO 2 CH 2 CH 3 , —N(CH 3 )SO 2 CH 2 CH 3 , —SO 2 NH 2 , —CONH 2 , —CON(C 1 -C 3 alkyl) 2 , —CONH(C 1 -C 3 alkyl), —NHCO(C 1 -C 3 alkyl), —N(CH 3 )COO(C 1 -C 3 alkyl), —NHCO(C 1 -
  • R 3 is not hydrogen
  • At least one R 3 is —SO 2 CH 3 , —NHSO 2 CH 3 , —NCH 3 SO 2 CH 3 , —NHSO 2 CH 2 CH 3 , or —N(CH 3 )SO 2 CH 2 CH 3 . In one embodiment of the compounds of formula (I)-(VI) and (A)-(G-II), at least one R 3 is —SO 2 CH 3 , —NHSO 2 CH 3 , or —NCH 3 SO 2 CH 3 .
  • R 3 is heterocyclyl
  • R 3 is heterocyclyl selected from
  • R 3 is —NR 14 SO 2 R 16 , wherein R 14 and R 16 together form a 5 or 6 membered ring including the nitrogen and sulfur atoms.
  • R 3 is —NR 14 SO 2 R 16 , wherein R 16 is optionally substituted C 1 -C 6 alkyl.
  • R 3 is —NR 14 SO 2 R 16 , wherein R 16 is C 1 -C 6 alkyl optionally substituted with one or more groups selected from halogen, —CN, —CF 3 , —OH, C 1 -C 3 alkyl, C 1 -C 3 alkoxy, —NH 2 , —NH(C 1 -C 3 alkyl), —N(C 1 -C 3 alkyl) 2 , —SCH 3 .
  • R 3 is —NR 14 SO 2 R 16 , wherein R 16 is C 1 -C 3 alkyl substituted with —NH 2 .
  • R 5 and R 6 are each independently hydrogen, halogen, —OH, C 1 -C 3 alkyl, C 2 -C 3 alkenyl, C 2 -C 3 alkynyl, or C 1 -C 3 alkoxy; or R 5 and R 6 taken together form an optionally substituted 3- to 6-membered carbocyclyl or heterocyclyl.
  • R 5 and R 6 are each independently hydrogen, halogen, —OH, optionally substituted C 1 -C 6 alkyl, optionally substituted C 2 -C 6 alkenyl, optionally substituted C 2 -C 6 alkynyl.
  • R 5 and R 6 are hydrogen, halogen, —OH, or C 1 -C 3 alkyl. In one embodiment, R 5 and R 6 are each independently hydrogen, F, —OH, or C 1 -C 3 alkyl. In one embodiment, R 5 and R 6 are each independently, hydrogen, F, —OH, or methyl. In one embodiment, R 5 and R 6 are each H. In one embodiment, R 5 and R 6 are each methyl. In one embodiment of the compounds of formula (I)-(VI) and (A)-(H-I), R 5 and R 6 are each H or methyl.
  • R 7 is hydrogen, optionally substituted C 1 -C 6 alkyl, optionally substituted C 2 -C 6 alkenyl, optionally substituted C 2 -C 6 alkynyl, optionally substituted carbocyclyl, optionally substituted heterocyclyl, optionally substituted aryl, or optionally substituted heteroaryl.
  • R 7 is hydrogen, optionally substituted C 1 -C 3 alkyl, optionally substituted C 2 -C 3 alkenyl, optionally substituted C 2 -C 3 alkynyl, optionally substituted carbocyclyl, optionally substituted heterocyclyl, optionally substituted aryl, or optionally substituted heteroaryl.
  • R 7 is hydrogen, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, carbocyclyl, heterocyclyl, aryl, or heteroaryl.
  • R 7 is hydrogen, C 1 -C 3 alkyl, C 2 -C 3 alkenyl, C 2 -C 3 alkynyl, carbocyclyl, heterocyclyl, aryl, or heteroaryl. In some embodiments, R 7 is hydrogen, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, or C 2 -C 6 alkynyl. In some embodiments, R 7 is hydrogen, C 1 -C 3 alkyl, C 2 -C 3 alkenyl, or C 2 -C 3 alkynyl. In some embodiments, R 7 is hydrogen or C 1 -C 6 alkyl. In some embodiments, R 7 is hydrogen or C 1 -C 4 alkyl. In some embodiments of the compounds of formula (I)-(VI) and (A)-(H-I), R 7 is hydrogen or C 1 -C 3 alkyl.
  • R 8a and R 9a are each independently hydrogen, halogen, optionally substituted C 1 -C 6 alkyl, optionally substituted C 2 -C 6 alkenyl, optionally substituted C 2 -C 6 alkynyl, optionally substituted C 1 -C 6 alkoxy, —NR 13 R 14 , optionally substituted —(C 1 -C 6 alkyl)-NR 13 R 14 , —NR 14 COR 16 , optionally substituted —(C 1 -C 6 alkyl)-NR 14 COR 16 , —CONR 14 R 15 , optionally substituted —(C 1 -C 6 alkyl)-CONR 14 R 15 , optionally substituted carbocyclyl, optionally substituted heterocyclyl, optionally substituted aryl, or optionally substituted heteroaryl, or R 8a and R 9a taken together form an optionally substituted carbocycl
  • R 8a and R 8b are each independently hydrogen, —OH, halogen, C 1 -C 3 alkyl, C 2 -C 3 alkenyl, C 2 -C 3 alkynyl, C 1 -C 3 alkoxy, —NR 13 R 14 , —(C 1 -C 3 alkyl)-NR 13 R 14 , —NR 14 COR 16 , —(C 1 -C 3 alkyl)-NR 14 COR 16 , —CONR 14 R 15 , or —(C 1 -C 3 alkyl)-CONR 14 R 15 ; or R 8a and R 8b taken together form an optionally substituted 3- to 6-membered carbocyclyl or heterocyclyl.
  • R 8a and R 9a are each independently hydrogen, halogen, C 1 -C 3 alkyl, C 2 -C 3 alkenyl, C 2 -C 3 alkynyl, C 1 -C 3 alkoxy, —NR 13 R 14 , —(C 1 -C 3 alkyl)-NR 13 R 14 , —NR 14 COR 16 , —(C 1 -C 3 alkyl)-NR 14 COR 16 , —CONR 14 R 15 , or —(C 1 -C 3 alkyl)-CONR 14 R 15 .
  • R 8a and R 9a are not —OH. In one embodiment, R 8a and R 9a are not —OH.
  • R 7 and R 8a taken together form an optionally substituted heterocyclyl. In one embodiment, R 7 and R 8a taken together form an optionally substituted 3- to 7-membered heterocycle.
  • R 8 and R 9 are each independently hydrogen, halogen, or C 1 -C 3 alkyl.
  • R 10 is hydrogen, optionally substituted C 1 -C 6 alkyl, optionally substituted C 2 -C 6 alkenyl, optionally substituted C 2 -C 6 alkynyl, optionally substituted carbocyclyl, optionally substituted heterocyclyl, optionally substituted aryl, or optionally substituted heteroaryl.
  • R 10 is hydrogen, optionally substituted C 1 -C 3 alkyl, optionally substituted C 2 -C 3 alkenyl, optionally substituted C 2 -C 3 alkynyl, optionally substituted carbocyclyl, optionally substituted heterocyclyl, optionally substituted aryl, or optionally substituted heteroaryl.
  • R 10 is hydrogen, C 1 -C 3 alkyl, C 2 -C 3 alkenyl, C 2 -C 3 alkynyl, carbocyclyl, heterocyclyl, aryl, or heteroaryl.
  • R 10 is hydrogen, C 1 -C 3 alkyl, C 2 -C 3 alkenyl, C 2 -C 3 alkynyl.
  • R 10 is hydrogen or C 1 -C 3 alkyl.
  • R 11 and R 12 are each independently hydrogen, optionally substituted C 1 -C 6 alkyl, optionally substituted C 2 -C 6 alkenyl, optionally substituted C 2 -C 6 alkynyl, optionally substituted carbocyclyl, optionally substituted heterocyclyl, optionally substituted aryl, or optionally substituted heteroaryl.
  • R 11 and R 12 are each independently hydrogen, optionally substituted C 1 -C 6 alkyl, optionally substituted C 2 -C 6 alkenyl, or optionally substituted C 2 -C 6 alkynyl. In some embodiments.
  • R 11 and R 12 are each independently hydrogen, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, or C 2 -C 6 alkynyl. In some embodiments. R 11 and R 12 are each independently hydrogen or C 1 -C 3 alkyl.
  • R 11 and R 12 taken together form an optionally substituted heterocyclyl. In one embodiment, R 11 and R 12 taken together form an optionally substituted 3- to 7-membered heterocyclyl. In other embodiments, R 11 and R 12 taken together form 3- to 7-membered heterocyclyl.
  • R 13 and R 14 are each independently hydrogen, optionally substituted C 1 -C 6 alkyl, optionally substituted C 2 -C 6 alkenyl, optionally substituted C 2 -C 6 alkynyl, optionally substituted carbocyclyl, optionally substituted heterocyclyl, optionally substituted aryl, or optionally substituted heteroaryl.
  • R 13 and R 14 are each independently hydrogen, optionally substituted C 1 -C 6 alkyl, optionally substituted C 2 -C 6 alkenyl, or optionally substituted C 2 -C 6 alkynyl.
  • R 13 and R 14 are each independently hydrogen, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, or C 2 -C 6 alkynyl. In some embodiments R 13 and R 14 are each independently hydrogen or C 1 -C 3 alkyl.
  • R 15 is hydrogen, optionally substituted C 1 -C 6 alkyl, optionally substituted C 2 -C 6 alkenyl, optionally substituted C 2 -C 6 alkynyl, optionally substituted carbocyclyl, optionally substituted heterocyclyl, optionally substituted aryl, or optionally substituted heteroaryl. In one embodiment, R 15 is hydrogen, optionally substituted C 1 -C 6 alkyl, optionally substituted C 2 -C 6 alkenyl, or optionally substituted C 2 -C 6 alkynyl.
  • R 15 is hydrogen, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, or C 2 -C 6 alkynyl. In some embodiments, R 15 is hydrogen or C 1 -C 3 alkyl.
  • R 14 and R 15 taken together form an optionally substituted heterocyclyl. In one embodiment, R 14 and R 15 taken together form an optionally substituted 3- to 7-membered heterocyclyl. In other embodiments, R 14 and R 15 taken together form 3- to 7-membered heterocyclyl.
  • R 16 is hydrogen, optionally substituted C 1 -C 6 alkyl, optionally substituted C 2 -C 6 alkenyl, optionally substituted C 2 -C 6 alkynyl, optionally substituted carbocyclyl, optionally substituted heterocyclyl, optionally substituted aryl, or optionally substituted heteroaryl.
  • R 16 is hydrogen, optionally substituted C 1 -C 3 alkyl, optionally substituted C 2 -C 3 alkenyl, optionally substituted C 2 -C 3 alkynyl, optionally substituted carbocyclyl, optionally substituted heterocyclyl, optionally substituted aryl, or optionally substituted heteroaryl. In some embodiments, R 16 is hydrogen, C 1 -C 3 alkyl, C 2 -C 3 alkenyl, C 2 -C 3 alkynyl, carbocyclyl, heterocyclyl, aryl, or heteroaryl.
  • R 16 is hydrogen, C 1 -C 3 alkyl, C 2 -C 3 alkenyl, or C 2 -C 3 alkynyl. In some embodiments, R 16 is hydrogen or C 1 -C 3 alkyl.
  • m is 1 or 2.
  • t is 1 or 2. In one embodiment of the compounds of formula (I)-(VI) and (A)-(H-I), t is 1.
  • optional substituent is selected from halogen, —CN, —CF 3 , —OH, —S(C 1 -C 3 alkyl), C 1 -C 3 alkyl, C 2 -C 3 alkenyl, C 2 -C 3 alkynyl, C 1 -C 3 alkoxy, —(C 1 -C 3 alkyl)-(C 1 -C 3 alkoxy), —(C 1 -C 3 alkyl)-OH, —NR 13 R 14 , —(C 1 -C 3 alkyl)-NR 13 R 14 , —NR 14 SO 2 R 16 , —(C 1 -C 3 alkyl)NR 14 SO 2 R 16 , —NR 14 COR 16 , —(C 1 -C 6 alkyl)-NR 14 COR 16 , —CONR 14 R 15 , —(C 1 -C 3 alkyl), —(C 1 -C 3 alkyl), —CONR 14 R 15
  • the optional substituent is selected from halogen, —CN, —CF 3 , —OH, C 1 -C 3 alkyl, C 1 -C 3 alkoxy, —NH 2 , —SCH 3 , —SO 2 CH 3 , —NHSO 2 CH 3 , —CH 2 NHSO 2 CH 3 , —SO 2 NH 2 , —CONH 2 , or —NHCOCH 3 .
  • a and B are each monocyclic ring.
  • B is phenyl, pyridyl, or pyrimidyl.
  • Z and V are not both a bond.
  • C is a 4- to 10-membered ring.
  • X is a bond, —CH 2 —, —C(CH 3 )H—, —C(CH 3 ) 2 —, or —CH 2 CH 2 —. In one embodiment, X is —CH 2 —, —C(CH 3 )H—, or —C(CH 3 ) 2 —. In some embodiments, X is —C(CH 3 ) 2 —.
  • X is —NR 7 —.
  • X is —NH—, —N(CH 3 )—, —N(CH 2 CH 3 )—, —N(iPr)—, or —N(tBu)-.
  • Y is —O—. In one embodiment of the compounds of formula (D)-(H-I), Z is —O—. In one embodiment of the compounds of formula (D)-(H-I), Y and Z are both —O—.
  • —V-L is CH 2 CH 2 C 1 , —CH 2 CH 2 CH 2 C 1 , or —CH 3 . In some embodiments, —V-L is CH 2 CH 2 Cl or —CH 2 CH 2 CH 2 Cl.
  • n1 is 0.
  • n2 is 0, 1, or 2. In some embodiments, n2 is 2. In some embodiments, n2 is 2 and R 2 are each ortho to Z. In other embodiments, n2 is 2 and R 2 are each ortho to Z, wherein R 2 is halogen or —CN.
  • the compound in one embodiment of the compound of formula (I)-(VI) and (A)-(H-I), can be a stereoisomer.
  • the carbon attached to R 5 and R 6 can be in an S configuration or an R configuration.
  • a hydrogen atom can be replaced with a deuterium atom.
  • the compound of formula (I)-(VA), (A), (A-I), or (D)-(H-I) is selected from Table A below, or a pharmaceutically acceptable salt, tautomer, stereoisomer or prodrug thereof.
  • the compound is selected from Compounds A3, A5, A7, A13, A17, A18, A22, A23, A24, A25, A28, A30, A31, A32, A34, A35, A38, A40, A41, A42, A45, A49, A52, A53, A54, A56, A57, A58, A62, A63, A64, A65, A68, A73, A74, A75, or A76, or a pharmaceutically acceptable salt, tautomer, stereoisomer or prodrug thereof.
  • the compound is selected from Compounds A1, A2, A4, A6, A8, A9, A10, A11, A12, A14, A15, A16, A19, A20, A21, A26, A27, A29, A33, A36, A37, A39, A43, A44, A46, A47, A48, A50, A51, A55, A59, A60, A61, A66, A67, A69, A70, A71, A72, A77, A78, A79, A80, A81, A82, A83, A84, A85, A86, A87, A88, A89, A90, A91, A92, A93, A94, A95, A96, or A97, or a pharmaceutically acceptable salt, tautomer, stereoisomer or prodrug thereof.
  • the compound is selected from Compounds A98-A186, or a pharmaceutically acceptable salt, tautomer, stereoisomer or prodrug thereof.
  • the compound is selected from Compounds A187-A211, or a pharmaceutically acceptable salt, tautomer, stereoisomer or prodrug thereof.
  • the compound is selected from Compounds A1-A211, or a pharmaceutically acceptable salt, tautomer, stereoisomer or prodrug thereof.
  • the compound is selected from Compounds A212-A234, or a pharmaceutically acceptable salt, tautomer, stereoisomer or prodrug thereof.
  • the compound is selected from Compounds A1-A234, or a pharmaceutically acceptable salt, tautomer, stereoisomer or prodrug thereof.
  • the compound is selected from Compounds A1-A96, A98-A116, A118-A159, A161-A175, and A177-A234, or a pharmaceutically acceptable salt, tautomer, stereoisomer or prodrug thereof.
  • the compound is selected from A13, A57, A74, A93, A109, A112, A122, A126, A131, A134, A136, A137, A164, A168, A169, A170, A171, A172, A184, A185, A195, and/or A204, or a pharmaceutically acceptable salt, tautomer, stereoisomer or prodrug thereof.
  • the compound in one embodiment of the compound of formula (I)-(IV), (VI), (B) or (C), the compound is selected from Table B below, or a pharmaceutically acceptable salt, tautomer, stereoisomer or prodrug thereof. In one embodiment of the compound of formula (I)-(IV), (VI), (B) or (C), the compound is selected from Compounds B1, B2, B3, or B6 or a pharmaceutically acceptable salt, tautomer, stereoisomer or prodrug thereof.
  • the compound is selected from Compounds B4, B5, B7, B8, B9, B10, or B11 or a pharmaceutically acceptable salt, tautomer, stereoisomer or prodrug thereof.
  • the compound is selected from Compounds B1-B11 or a pharmaceutically acceptable salt, tautomer, stereoisomer or prodrug thereof.
  • the present disclosure provides a pharmaceutical composition
  • a pharmaceutical composition comprising a pharmaceutically acceptable carrier or a pharmaceutically acceptable excipient and a compound of any one of formula (I), (IA), (IB), (IC), (II), (IIA), (IIIA), (IIB), (III), (IV), (IVA), (V), (VA), (VI), (A), (A-I), (B)-(D), (E), (E-I)-(E-VII), (F), (G), (G-I), (G-II), (H), and (H-I) (“formula (I)-(VI) and (A)-(H-I)”) or compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer, stereoisomer or prodrug thereof.
  • the present disclosure provides a pharmaceutical composition
  • a pharmaceutical composition comprising a pharmaceutically acceptable carrier or a pharmaceutically acceptable excipient and a compound selected from Compounds A3, A5, A7, A13, A17, A18, A22, A23, A24, A25, A28, A30, A31, A32, A34, A35, A38, A40, A41, A42, A45, A49, A52, A53, A54, A56, A57, A58, A62, A63, A64, A65, A68, A73, A74, A75, A76, B1, B2, B3, or B6 or a pharmaceutically acceptable salt, tautomer, stereoisomer or prodrug thereof.
  • the present disclosure provides a pharmaceutical composition
  • a pharmaceutical composition comprising a pharmaceutically acceptable carrier or a pharmaceutically acceptable excipient and a compound selected from Compounds A1, A2, A4, A6, A8, A9, A10, A11, A12, A14, A15, A16, A19, A20, A21, A26, A27, A29, A33, A36, A37, A39, A43, A44, A46, A47, A48, A50, A51, A55, A59, A60, A61, A66, A67, A69, A70, A71, A72, A77, A78, A79, A80, A81, A82, A83, A84, A85, A86, A87, A88, A89, A90, A91, A92, A93, A94, A95, A96, A97, B4, B5, B7, B8, B9, B10, or B11, or a pharmaceutically acceptable salt, tautomer, stereoisomer or prod
  • the present disclosure provides a pharmaceutical composition comprising a pharmaceutically acceptable carrier or a pharmaceutically acceptable excipient and a compound selected from Compounds A98-A186, or a pharmaceutically acceptable salt, tautomer, stereoisomer or prodrug thereof.
  • the present disclosure provides a pharmaceutical composition comprising a pharmaceutically acceptable carrier or a pharmaceutically acceptable excipient and a compound selected from Compounds A187-A211, or a pharmaceutically acceptable salt, tautomer, stereoisomer or prodrug thereof.
  • the present disclosure provides a pharmaceutical composition comprising a pharmaceutically acceptable carrier or a pharmaceutically acceptable excipient and a compound selected from Compounds A212-A234, or a pharmaceutically acceptable salt, tautomer, stereoisomer or prodrug thereof.
  • the present disclosure provides a pharmaceutical composition comprising a pharmaceutically acceptable carrier or a pharmaceutically acceptable excipient and a compound selected from Compounds A1-A96, A98-A116, A118-A159, A161-A175, and A177-A234, or a pharmaceutically acceptable salt, tautomer, stereoisomer or prodrug thereof.
  • the present disclosure provides a pharmaceutical composition
  • a pharmaceutical composition comprising a pharmaceutically acceptable carrier or a pharmaceutically acceptable excipient and a compound selected from Compounds A13, A57, A74, A93, A109, A112, A122, A126, A131, A134, A136, A137, A164, A168, A169, A170, A171, A172, A184, A185, A195, and/or A204, or a pharmaceutically acceptable salt, tautomer, stereoisomer or prodrug thereof.
  • the present disclosure provides a pharmaceutical composition comprising a pharmaceutically acceptable carrier or a pharmaceutically acceptable excipient and a compound selected from Compounds A1-A211 or B1-B11, or a pharmaceutically acceptable salt, tautomer, stereoisomer or prodrug thereof.
  • the present disclosure provides a pharmaceutical composition comprising a pharmaceutically acceptable carrier or a pharmaceutically acceptable excipient and a compound selected from Compounds A1-A234 or B1-B11, or a pharmaceutically acceptable salt, tautomer, stereoisomer or prodrug thereof.
  • the present disclosure provides a pharmaceutical composition
  • a pharmaceutical composition comprising a pharmaceutically acceptable carrier or a pharmaceutically acceptable excipient and a compound of any one of formula (D)-(H-I), or a pharmaceutically acceptable salt, tautomer, stereoisomer or prodrug thereof.
  • the present compounds find use in any number of methods.
  • the compounds are useful in methods for modulating androgen receptor (AR).
  • the present disclosure provides the use of any one of the foregoing compounds of formula (I)-(VI) and (A)-(H-I), or a pharmaceutically acceptable salt, tautomer, stereoisomer or prodrug thereof, for modulating androgen receptor (AR) activity.
  • modulating androgen receptor (AR) activity is in a mammalian cell.
  • Modulating androgen receptor (AR) can be in a subject in need thereof (e.g., a mammalian subject) and for treatment of any of the described conditions or diseases.
  • the modulating AR is binding to AR. In other embodiments, the modulating AR is inhibiting AR.
  • the modulating AR is modulating AR N-terminal domain (NTD). In one embodiment, the modulating AR is binding to AR NTD. In other embodiments, the modulating AR is inhibiting AR NTD. In one embodiment, the modulating AR is modulating AR N-terminal domain (NTD). In some embodiments, modulating the AR is inhibiting transactivation of androgen receptor N-terminal domain (NTD).
  • modulating androgen receptor (AR) activity is for treatment of at least one indication selected from the group consisting of: prostate cancer, breast cancer, ovarian cancer, bladder cancer, pancreatic cancer, hepatocellular cancer, endometrial cancer, salivary gland carcinoma, hair loss, acne, hirsutism, ovarian cysts, polycystic ovary disease, precocious puberty, spinal and bulbar muscular atrophy, age related macular degeneration, and combinations thereof.
  • the indication is prostate cancer.
  • the prostate cancer is primary/localized prostate cancer, locally advanced prostate cancer, recurrent prostate cancer, non-metastatic castration-resistant prostate cancer, metastatic prostate cancer, advanced prostate cancer, or metastatic castration-resistant prostate cancer (CRPC), or hormone-sensitive prostate cancer. While in other embodiments, the prostate cancer is androgen dependent prostate cancer. In other embodiments, the spinal and bulbar muscular atrophy is Kennedy's disease. In other embodiments, the prostate cancer is primary/localized prostate cancer, locally advanced prostate cancer, recurrent prostate cancer, metastatic prostate cancer, advanced prostate cancer, or metastatic castration-resistant prostate cancer (CRPC), or hormone-sensitive prostate cancer. While in other embodiments, the prostate cancer is androgen dependent prostate cancer. In other embodiments, the spinal and bulbar muscular atrophy is Kennedy's disease.
  • a method of treating a condition associated with cell proliferation in a patient in need thereof comprising administering a compounds of formula (I)-(VI) and (A)-(H-I), or a pharmaceutically acceptable salt, tautomer, stereoisomer or prodrug thereof, to a subject in need thereof.
  • the present invention provides a method of treating cancer or tumors.
  • the present invention provides a method of treating prostate cancer or breast cancer.
  • a method of reducing, inhibiting, or ameliorating proliferation comprising administering a therapeutically effective amount of a compound of formula (I)-(VI) and (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof is provided.
  • the reducing, inhibiting, or ameliorating in the method disclosed herein is in vivo.
  • the reducing, inhibiting, or ameliorating is in vitro.
  • the cells in the method disclosed herein are a cancer cells.
  • the cancer cells are a prostate cancer cells.
  • the prostate cancer cells are cells of primary/localized prostate cancer (newly diagnosed or early stage), locally advanced prostate cancer, recurrent prostate cancer (e.g., prostate cancer which was not responsive to primary therapy), metastatic prostate cancer, non-metastatic castration-resistant prostate cancer, advanced prostate cancer (e.g., after castration for recurrent prostate cancer), metastatic castration-resistant prostate cancer (CRPC), or hormone-sensitive prostate cancer.
  • the prostate cancer cells are cells of primary/localized prostate cancer (newly diagnosed or early stage), locally advanced prostate cancer, recurrent prostate cancer (e.g., prostate cancer which was not responsive to primary therapy), metastatic prostate cancer, advanced prostate cancer (e.g., after castration for recurrent prostate cancer), metastatic castration-resistant prostate cancer (CRPC), or hormone-sensitive prostate cancer.
  • the prostate cancer cells are cells of a metastatic castration-resistant prostate cancer.
  • the prostate cancer cells are an androgen-dependent prostate cancer cells or an androgen-independent prostate cancer cells.
  • the cancer cells are breast cancer cells.
  • the condition or disease associated with cell proliferation is cancer.
  • the cancer is selected from the group consisting of: prostate cancer, breast cancer, ovarian cancer, endometrial cancer, salivary gland carcinoma, hair loss, acne, hirsutism, ovarian cysts, polycystic ovary disease, precocious puberty, spinal and bulbar muscular atrophy, and age-related macular degeneration.
  • the condition or disease is prostate cancer.
  • prostate cancer is selected from primary/localized prostate cancer, locally advanced prostate cancer, recurrent prostate cancer, metastatic prostate cancer, non-metastatic castration-resistant prostate cancer, advanced prostate cancer, metastatic castration-resistant prostate cancer (CRPC), or hormone-sensitive prostate cancer.
  • prostate cancer is selected from primary/localized prostate cancer, locally advanced prostate cancer, recurrent prostate cancer, metastatic prostate cancer, advanced prostate cancer, metastatic castration-resistant prostate cancer (CRPC), or hormone-sensitive prostate cancer.
  • the prostate cancer is a metastatic castration-resistant prostate cancer.
  • the prostate cancer is an androgen-dependent prostate cancer cells or an androgen-independent prostate cancer.
  • the condition or disease is breast cancer.
  • a method for reducing or preventing tumor growth comprising contacting tumor cells with a therapeutically effective amount of a compound of (I)-(VI) and (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof is provided.
  • reducing or preventing tumor growth includes reduction in tumor volume. In one embodiment, reducing or preventing tumor growth includes complete elimination of tumors. In one embodiment, reducing or preventing tumor growth includes stopping or halting the existing tumor to grow. In one embodiment, reducing or preventing tumor growth includes reduction in the rate of tumor growth. In one embodiment, reducing or preventing tumor growth includes reduction in the rate of tumor growth such that the rate of tumor growth before treating a patient with the methods disclosed herein (r1) is faster than the rate of tumor growth after said treatment (r2) such that r1>r2.
  • the reducing or preventing in the method disclosed herein is in vivo. In another embodiment, the treating is in vitro.
  • the tumor cell in the method disclosed herein is selected from prostate cancer, breast cancer, ovarian cancer, endometrial cancer, or salivary gland carcinoma.
  • the tumor cells are prostate cancer tumor cells.
  • the prostate cancer tumor cells are tumor cells of primary/localized prostate cancer, locally advanced prostate cancer, recurrent prostate cancer, metastatic prostate cancer, non-metastatic castration-resistant prostate cancer, advanced prostate cancer, metastatic castration-resistant prostate cancer (CRPC), or hormone-sensitive prostate cancer.
  • the prostate cancer tumor cells are tumor cells of primary/localized prostate cancer, locally advanced prostate cancer, recurrent prostate cancer, metastatic prostate cancer, advanced prostate cancer, metastatic castration-resistant prostate cancer (CRPC), or hormone-sensitive prostate cancer.
  • the prostate cancer is a metastatic castration-resistant prostate cancer.
  • the prostate cancer is androgen-dependent prostate cancer or androgen-independent prostate cancer.
  • the tumor cells are is breast cancer tumor cells.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds provide metabolic stability.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro metabolic clearance in human liver microsomes (HLMs) of less than about 500 ⁇ L/min/mg protein, less than about 450 ⁇ L/min/mg protein, less than about 400 ⁇ L/min/mg protein, less than about 350 ⁇ L/min/mg protein, less than about 300 ⁇ L/min/mg protein, less than about 250 ⁇ L/min/mg protein, less than about 225 ⁇ L/min/mg protein, or less than about 200 ⁇ L/min/mg protein.
  • HLMs human liver microsomes
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro metabolic clearance in HLMs of less than about 200 ⁇ L/min/mg protein, less than about 190 ⁇ L/min/mg protein, less than about 180 ⁇ L/min/mg protein, less than about 170 ⁇ L/min/mg protein, less than about 160 ⁇ L/min/mg protein, less than about 150 ⁇ L/min/mg protein, less than about 140 ⁇ L/min/mg protein, less than about 130 ⁇ L/min/mg protein, less than about 120 ⁇ L/min/mg protein, less than about 110 ⁇ L/min/mg protein, less than about 100 ⁇ L/min/mg
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro metabolic clearance in HLMs of less than about 50 ⁇ L/min/mg protein, less than about 48 ⁇ L/min/mg protein, less than about 45 ⁇ L/min/mg protein, less than about 40 ⁇ L/min/mg protein, less than about 35 ⁇ L/min/mg protein, less than about 30 ⁇ L/min/mg protein, less than about 25 ⁇ L/min/mg protein, less than about 20 ⁇ L/min/mg protein, or less than about 15 ⁇ L/min/mg protein.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro metabolic clearance in HLMs of less than about 15 ⁇ L/min/mg protein, less than about 14 ⁇ L/min/mg protein, less than about 13 ⁇ L/min/mg protein, less than about 12 ⁇ L/min/mg protein, less than about 11 ⁇ L/min/mg protein, or less than about 10 ⁇ L/min/mg protein.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro metabolic clearance in HLMs of less than 12 ⁇ L/min/mg protein.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro metabolic clearance in HLMs in the range of about 0.1 ⁇ L/min/mg protein to about 12 ⁇ L/min/mg protein.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro metabolic clearance in HLMs of less than 48 ⁇ L/min/mg protein.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro metabolic clearance in HLMs in the range of about 12 ⁇ L/min/mg protein to about 48 ⁇ L/min/mg protein.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro metabolic clearance in HLMs in the range of about 0.1 ⁇ L/min/mg protein to about 48 ⁇ L/min/mg protein.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an HLM in vitro metabolic clearance of less than about 20 ⁇ L/min/mg protein.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an HLM in vitro metabolic clearance of less than about 15 ⁇ L/min/mg protein.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an HLM in vitro metabolic clearance of less than about 12 ⁇ L/min/mg protein.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an HLM in vitro metabolic clearance of less than about 11.55 ⁇ L/min/mg protein.
  • the compounds of the present disclosure are any compound of Tables A or B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an HLM in vitro metabolic clearance of less than about 20 ⁇ L/min/mg protein.
  • the compounds of the present disclosure are any compound of Tables A or B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an HLM in vitro metabolic clearance of less than about 15 ⁇ L/min/mg protein.
  • the compounds of the present disclosure are any compound of Tables A or B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an HLM in vitro metabolic clearance of less than about 12 ⁇ L/min/mg protein.
  • the compounds of the present disclosure are any compound of Tables A or B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an HLM in vitro metabolic clearance of less than about 11.55 ⁇ L/min/mg protein.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro metabolic clearance in mouse liver microsomes (MLMs) of less than about 500 ⁇ L/min/mg protein, less than about 450 ⁇ L/min/mg protein, less than about 400 ⁇ L/min/mg protein, less than about 350 ⁇ L/min/mg protein, less than about 300 ⁇ L/min/mg protein, less than about 250 ⁇ L/min/mg protein, less than about 225 ⁇ L/min/mg protein, or less than about 200 ⁇ L/min/mg protein.
  • MLMs mouse liver microsomes
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro metabolic clearance in MLMs of less than about 200 ⁇ L/min/mg protein, less than about 190 ⁇ L/min/mg protein, less than about 180 ⁇ L/min/mg protein, less than about 170 ⁇ L/min/mg protein, less than about 160 ⁇ L/min/mg protein, less than about 150 ⁇ L/min/mg protein, less than about 140 ⁇ L/min/mg protein, less than about 130 ⁇ L/min/mg protein, less than about 120 ⁇ L/min/mg protein, less than about 110 ⁇ L/min/mg protein, less than about 100 ⁇ L/min/mg
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro metabolic clearance in MLMs of less than about 50 ⁇ L/min/mg protein, less than about 48 ⁇ L/min/mg protein, less than about 45 ⁇ L/min/mg protein, less than about 40 ⁇ L/min/mg protein, less than about 35 ⁇ L/min/mg protein, less than about 30 ⁇ L/min/mg protein, less than about 25 ⁇ L/min/mg protein, less than about 20 ⁇ L/min/mg protein, or less than about 15 ⁇ L/min/mg protein.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro metabolic clearance in MLMs of less than about 15 ⁇ L/min/mg protein, less than about 14 ⁇ L/min/mg protein, less than about 13 ⁇ L/min/mg protein, less than about 12 ⁇ L/min/mg protein, less than about 11 ⁇ L/min/mg protein, or less than about 10 ⁇ L/min/mg protein.
  • the compounds of the present disclosure are any compound of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, and wherein the compounds have an in vitro metabolic clearance in MLMs of less than 12 ⁇ L/min/mg protein.
  • the compounds of the present disclosure are any compound of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, and wherein the compounds have an in vitro metabolic clearance in MLMs in the range of about 0.1 ⁇ L/min/mg protein to about 12 ⁇ L/min/mg protein.
  • the compounds of the present disclosure are any compound of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, and wherein the compounds have an in vitro metabolic clearance in MLMs of less than 48 ⁇ L/min/mg protein.
  • the compounds of the present disclosure are any compound of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, and wherein the compounds have an in vitro metabolic clearance in MLMs in the range of about 12 ⁇ L/min/mg protein to about 48 ⁇ L/min/mg protein.
  • the compounds of the present disclosure are any compound of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, and wherein the compounds have an in vitro metabolic clearance in MLMs in the range of about 0.1 ⁇ L/min/mg protein to about 48 ⁇ L/min/mg protein.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an MLM in vitro metabolic clearance of less than about 20 ⁇ L/min/mg protein.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an MLM in vitro metabolic clearance of less than about 15 ⁇ L/min/mg protein.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an MLM in vitro metabolic clearance of less than about 12 ⁇ L/min/mg protein.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an MLM in vitro metabolic clearance of less than about 11.55 ⁇ L/min/mg protein.
  • the compounds of the present disclosure are any compound of Tables A or B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an MLM in vitro metabolic clearance of less than about 20 ⁇ L/min/mg protein.
  • the compounds of the present disclosure are any compound of Tables A or B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an MLM in vitro metabolic clearance of less than about 15 ⁇ L/min/mg protein.
  • the compounds of the present disclosure are any compound of Tables A or B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an MLM in vitro metabolic clearance of less than about 12 ⁇ L/min/mg protein.
  • the compounds of the present disclosure are any compound of Tables A or B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an MLM in vitro metabolic clearance of less than about 11.55 ⁇ L/min/mg protein.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro metabolic clearance in human hepatocytes (HHs) of less than about 500 ⁇ L/min/million cells, less than about 450 ⁇ L/min/million cells, less than about 400 ⁇ L/min/million cells, less than about 350 ⁇ L/min/million cells, less than about 300 ⁇ L/min/million cells, less than about 250 ⁇ L/min/million cells, less than about 225 ⁇ L/min/million cells, or less than about 200 ⁇ L/min/million cells.
  • HHs human hepatocytes
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro metabolic clearance in HHs of less than about 200 ⁇ L/min/million cells, less than about 190 ⁇ L/min/million cells, less than about 180 ⁇ L/min/million cells, less than about 170 ⁇ L/min/million cells, less than about 160 ⁇ L/min/million cells, less than about 150 ⁇ L/min/million cells, less than about 140 ⁇ L/min/million cells, less than about 130 ⁇ L/min/million cells, less than about 120 ⁇ L/min/million cells, less than about 110 ⁇ L/min/million cells, less than about 100 ⁇ L/min/million cells, less than about 90 ⁇ L/min
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro metabolic clearance in HHs of less than about 50 ⁇ L/min/million cells, less than about 48 ⁇ L/min/million cells, less than about 45 ⁇ L/min/million cells, less than about 40 ⁇ L/min/million cells, less than about 35 ⁇ L/min/million cells, less than about 30 ⁇ L/min/million cells, less than about 25 ⁇ L/min/million cells, less than about 20 ⁇ L/min/million cells, or less than about 15 ⁇ L/min/million cells.
  • the compounds of the present disclosure have an in vitro metabolic clearance in HHs of less than about 15 ⁇ L/min/million cells, less than about 14 ⁇ L/min/million cells, less than about 13 ⁇ L/min/million cells, less than about 12 ⁇ L/min/million cells, less than about 11 ⁇ L/min/million cells, less than about 10 ⁇ L/min/million cells, less than about 9 ⁇ L/min/million cells, less than about 8 ⁇ L/min/million cells, less than about 8 ⁇ L/min/million cells, less than about 6 ⁇ L/min/million cells, or less than about 5 ⁇ L/min/million cells.
  • the compounds of the present disclosure are any compound of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, and wherein the compounds have an in vitro metabolic clearance in HHs of less than 4 ⁇ L/min/million cells.
  • the compounds of the present disclosure are any compound of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, and wherein the compounds have an in vitro metabolic clearance in HHs in the range of about 0.1 ⁇ L/min/million cells to about 4 ⁇ L/min/million cells.
  • the compounds of the present disclosure are any compound of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, and wherein the compounds have an in vitro metabolic clearance in HHs of less than 18 ⁇ L/min/million cells.
  • the compounds of the present disclosure are any compound of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, and wherein the compounds have an in vitro metabolic clearance in HHs in the range of about 4 ⁇ L/min/million cells to about 18 ⁇ L/min/million cells.
  • the compounds of the present disclosure are any compound of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, and wherein the compounds have an in vitro metabolic clearance in HHs in the range of about 0.1 ⁇ L/min/million cells to about 18 ⁇ L/min/million cells.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro metabolic clearance in HHs of less than about 20 ⁇ L/min/million cells.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro metabolic clearance in HHs of less than about 10 ⁇ L/min/million cells.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro metabolic clearance in HHs of less than about 5 ⁇ L/min/million cells.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro metabolic clearance in HHs of less than about 3.85 ⁇ L/min/million cells.
  • the compounds of the present disclosure are any compound of Tables A or B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro metabolic clearance in HHs of less than about 20 ⁇ L/min/million cells.
  • the compounds of the present disclosure are any compound of Tables A or B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro metabolic clearance in HHs of less than about 10 ⁇ L/min/million cells.
  • the compounds of the present disclosure are any compound of Tables A or B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro metabolic clearance in HHs of less than about 5 ⁇ L/min/million cells.
  • the compounds of the present disclosure are any compound of Tables A or B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro metabolic clearance in human hepatocytes of less than about 3.85 ⁇ L/min/million cells.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro metabolic clearance in mouse hepatocytes (MHs) of less than about 500 ⁇ L/min/million cells, less than about 450 ⁇ L/min/million cells, less than about 400 ⁇ L/min/million cells, less than about 350 ⁇ L/min/million cells, less than about 300 ⁇ L/min/million cells, less than about 250 ⁇ L/min/million cells, less than about 225 ⁇ L/min/million cells, or less than about 200 ⁇ L/min/million cells.
  • MHs mouse hepatocytes
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro metabolic clearance in MHs of less than about 200 ⁇ L/min/million cells, less than about 190 ⁇ L/min/million cells, less than about 180 ⁇ L/min/million cells, less than about 170 ⁇ L/min/million cells, less than about 160 ⁇ L/min/million cells, less than about 150 ⁇ L/min/million cells, less than about 140 ⁇ L/min/million cells, less than about 130 ⁇ L/min/million cells, less than about 120 ⁇ L/min/million cells, less than about 110 ⁇ L/min/million cells, less than about 100 ⁇ L/min/million cells, less than about 90 ⁇ L/min
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro metabolic clearance in MHs of less than about 50 ⁇ L/min/million cells, less than about 48 ⁇ L/min/million cells, less than about 45 ⁇ L/min/million cells, less than about 40 ⁇ L/min/million cells, less than about 35 ⁇ L/min/million cells, less than about 30 ⁇ L/min/million cells, less than about 25 ⁇ L/min/million cells, less than about 20 ⁇ L/min/million cells, or less than about 15 ⁇ L/min/million cells.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro metabolic clearance in MHs of less than about 15 ⁇ L/min/million cells, less than about 14 ⁇ L/min/million cells, less than about 13 ⁇ L/min/million cells, less than about 12 ⁇ L/min/million cells, less than about 11 ⁇ L/min/million cells, less than about 10 ⁇ L/min/million cells, less than about 9 ⁇ L/min/million cells, less than about 8 ⁇ L/min/million cells, less than about 8 ⁇ L/min/million cells, less than about 6 ⁇ L/min/million cells, or less than about 5 ⁇ L/min/million cells.
  • the compounds of the present disclosure are any compound of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, and wherein the compounds have an in vitro metabolic clearance in MHs of less than 4 ⁇ L/min/million cells.
  • the compounds of the present disclosure are any compound of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, and wherein the compounds have an in vitro metabolic clearance in MHs in the range of about 0.1 ⁇ L/min/million cells to about 4 ⁇ L/min/million cells.
  • the compounds of the present disclosure are any compound of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, and wherein the compounds have an in vitro metabolic clearance in MHs of less than 18 ⁇ L/min/million cells.
  • the compounds of the present disclosure are any compound of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, and wherein the compounds have an in vitro metabolic clearance in MHs in the range of about 4 ⁇ L/min/million cells to about 18 ⁇ L/min/million cells.
  • the compounds of the present disclosure are any compound of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, and wherein the compounds have an in vitro metabolic clearance in MHs in the range of about 0.1 ⁇ L/min/million cells to about 18 ⁇ L/min/million cells.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro metabolic clearance in MHs of less than about 20 ⁇ L/min/million cells.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro metabolic clearance in MHs of less than about 17 ⁇ L/min/million cells.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro metabolic clearance in MHs of less than about 7 ⁇ L/min/million cells.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro metabolic clearance in MHs of less than about 3.85 ⁇ L/min/million cells.
  • the compounds of the present disclosure are any compound of Tables A or B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro metabolic clearance in MHs of less than about 20 ⁇ L/min/million cells.
  • the compounds of the present disclosure are any compound of Tables A or B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro metabolic clearance in MHs of less than about 17 ⁇ L/min/million cells.
  • the compounds of the present disclosure are any compound of Tables A or B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro metabolic clearance in MHs of less than about 7 ⁇ L/min/million cells.
  • the compounds of the present disclosure are any compound of Tables A or B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro metabolic clearance in MHs of less than about 3.85 ⁇ L/min/million cells.
  • the compounds of the present disclosure are any compounds with a combination of in vitro metabolic clearance in HLM, MLM, HHs, and MHs as described herein.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an HLM and MLM in vitro metabolic clearance of less than about 20 ⁇ L/min/mg protein.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an HLM and MLM in vitro metabolic clearance of less than about 15 ⁇ L/min/mg protein.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an HLM and MLM in vitro metabolic clearance of less than about 12 ⁇ L/min/mg protein.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an HLM and MLM in vitro metabolic clearance of less than about 11.55 ⁇ L/min/mg protein.
  • the compounds of the present disclosure are any compound of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, and wherein the compounds have an HLM and MLM in vitro metabolic clearance of less than about 20 ⁇ L/min/mg protein.
  • the compounds of the present disclosure are any compound of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, and wherein the compounds have an HLM and MLM in vitro metabolic clearance of less than about 15 ⁇ L/min/mg protein.
  • the compounds of the present disclosure are any compound of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, and wherein the compounds have an HLM and MLM in vitro metabolic clearance of less than about 12 ⁇ L/min/mg protein.
  • the compounds of the present disclosure are any compound of Tables A and B or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, and wherein the compounds have an HLM and MLM in vitro metabolic clearance of less than about 11.55 ⁇ L/min/mg protein.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro metabolic clearance in human and mouse hepatocytes of less than about 20 ⁇ L/min/million cells.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro metabolic clearance in mouse hepatocytes of less than about 17 ⁇ L/min/million cells and a an in vitro metabolic clearance in human hepatocytes of less than about 10 ⁇ L/min/million cells.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro metabolic clearance in mouse hepatocytes of less than about 7 ⁇ L/min/million cells, and an in vitro metabolic clearance in human hepatocytes of less than about 5 ⁇ L/min/million cells.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro metabolic clearance in human and mouse hepatocytes of less than about 3.85 ⁇ L/min/million cells.
  • the compounds of the present disclosure are any compound of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, and wherein the compounds have an in vitro metabolic clearance in human and mouse hepatocytes of less than about 20 ⁇ L/min/million cells.
  • the compounds of the present disclosure are any compound of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, and wherein the compounds have an in vitro metabolic clearance in mouse hepatocytes of less than about 17 ⁇ L/min/million cells and a an in vitro metabolic clearance in human hepatocytes of less than about 10 ⁇ L/min/million cells.
  • the compounds of the present disclosure are any compound of Tables A and B or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, and wherein the compounds have an in vitro metabolic clearance in mouse hepatocytes of less than about 7 ⁇ L/min/million cells, and an in vitro metabolic clearance in human hepatocytes of less than about 5 ⁇ L/min/million cells.
  • the compounds of the present disclosure are any compound of Tables A and B or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, and wherein the compounds have an in vitro metabolic clearance in human and mouse hepatocytes of less than about 3.85 ⁇ L/min/million cells.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an HLM and MLM in vitro metabolic clearance of less than about 20 ⁇ L/min/mg protein and an in vitro metabolic clearance in human and mouse hepatocytes of less than about 20 ⁇ L/min/million cells.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an HLM and MLM in vitro metabolic clearance of less than about 15 ⁇ L/min/mg protein, an in vitro metabolic clearance in human and mouse hepatocytes of less than about 17 ⁇ L/min/million cells.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an HLM and MLM in vitro metabolic clearance of less than about 12 ⁇ L/min/mg protein, an in vitro metabolic clearance in human and mouse hepatocytes of less than about 7 ⁇ L/min/million cells.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds s have an HLM and MLM in vitro metabolic clearance of less than about 11.55 ⁇ L/min/mg protein, an in vitro metabolic clearance in human and mouse hepatocytes of less than about 3.85 ⁇ L/min/million cells.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an a) HLM or MLM in vitro metabolic clearance of less than about 12 ⁇ L/min/mg protein and b) an in vitro metabolic clearance in human or mouse hepatocytes of less than about 4 ⁇ L/min/million cells.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an a) HLM or MLM in vitro metabolic clearance of less than 12 ⁇ L/min/mg protein and b) an in vitro metabolic clearance in human or mouse hepatocytes of less than 4 ⁇ L/min/million cells.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an a) HLM and MLM in vitro metabolic clearance of less than about 12 ⁇ L/min/mg protein and b) an in vitro metabolic clearance in human or mouse hepatocytes of less than about 4 ⁇ L/min/million cells.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an a) HLM or MLM in vitro metabolic clearance of less than about 12 ⁇ L/min/mg protein and b) an in vitro metabolic clearance in human and mouse hepatocytes of less than about 4 ⁇ L/min/million cells.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an a) HLM and MLM in vitro metabolic clearance of less than about 12 ⁇ L/min/mg protein and b) an in vitro metabolic clearance in human and mouse hepatocytes of less than about 4 ⁇ L/min/million cells.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an a) HLM and MLM in vitro metabolic clearance of less than 12 ⁇ L/min/mg protein and b) an in vitro metabolic clearance in human and mouse hepatocytes of less than 4 ⁇ L/min/million cells.
  • the compounds of the present disclosure are any compound of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an a) HLM and MLM in vitro metabolic clearance of less than 12 ⁇ L/min/mg protein and b) an in vitro metabolic clearance in human and mouse hepatocytes of less than 4 ⁇ L/min/million cells.
  • the compounds of the present disclosure are any compound of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, and wherein the compounds have an HLM and MLM in vitro metabolic clearance of less than about 20 ⁇ L/min/mg protein and an in vitro metabolic clearance in human and mouse hepatocytes of less than about 20 ⁇ L/min/million cells.
  • the compounds of the present disclosure are any compound of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, and wherein the compounds have an HLM and MLM in vitro metabolic clearance of less than about 15 ⁇ L/min/mg protein, an in vitro metabolic clearance in human and mouse hepatocytes of less than about 17 ⁇ L/min/million cells.
  • the compounds of the present are any compound of Tables A and B or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, and wherein the compounds have an HLM and MLM in vitro metabolic clearance of less than about 12 ⁇ L/min/mg protein, an in vitro metabolic clearance in human and mouse hepatocytes of less than about 7 ⁇ L/min/million cells.
  • the compounds of the present disclosure are any compound of Tables A and B or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, and wherein the compounds have an HLM and MLM in vitro metabolic clearance of less than about 11.55 ⁇ L/min/mg protein, an in vitro metabolic clearance in human and mouse hepatocytes of less than about 3.85 ⁇ L/min/million cells.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in human, mouse, rat, monkey or dog microsome greater than about 120 minutes.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in human, mouse, rat, monkey or dog microsome greater than about 110 minutes.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in human, mouse, rat, monkey or dog microsome greater than about 100 minutes.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in human, mouse, rat, monkey or dog microsome greater than about 90 minutes.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in human, mouse, rat, monkey or dog microsome greater than about 80 minutes.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in human, mouse, rat, monkey or dog microsome greater than about 70 minutes.
  • the compounds of the present disclosure are any compound of Tables A and B or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in human microsomes greater than about 120 min.
  • the compounds of the present disclosure are any compound of Tables A and B or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in mouse microsomes greater than about 120 min.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in rat microsome greater than about 120 minutes.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in rat microsome greater than about 110 minutes.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in rat microsome greater than about 100 minutes.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in rat microsome greater than about 90 minutes.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in rat microsome greater than about 80 minutes.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in rat microsome greater than about 70 minutes.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in rat microsome greater than about 60 minutes.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in rat microsome greater than about 50 minutes.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in rat microsome greater than about 40 minutes.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in rat microsome greater than about 30 minutes.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in rat microsome greater than about 20 minutes.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in rat microsome greater than about 10 minutes.
  • the compound is selected from any of the compound of Tables A and B or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in human hepatocytes greater than about 360 minutes.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in human hepatocytes greater than about 350 minutes.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in human hepatocytes greater than about 325 minutes.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in human hepatocytes greater than about 310 minutes.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in human hepatocytes greater than about 300 minutes.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in human hepatocytes greater than about 290 minutes.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in human hepatocytes greater than about 250 minutes.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in human hepatocytes greater than about 200 minutes.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in human hepatocytes greater than about 150 minutes.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in human hepatocytes greater than about 100 minutes.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in human hepatocytes greater than about 80 minutes.
  • the compound is selected from any of the compound of Tables A and B or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in mouse hepatocytes greater than about 360 minutes.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in mouse hepatocytes greater than about 350 minutes.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in mouse hepatocytes greater than about 325 minutes.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in mouse hepatocytes greater than about 300 minutes.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in mouse hepatocytes greater than about 250 minutes.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in mouse hepatocytes greater than about 225 minutes.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in mouse hepatocytes greater than about 200 minutes.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in mouse hepatocytes greater than about 150 minutes.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in mouse hepatocytes greater than about 100 minutes.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in mouse hepatocytes greater than about 50 minutes.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in mouse hepatocytes greater than about 30 minutes.
  • the compound is selected from any of the compound of Tables A and B or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in rat hepatocytes greater than about 360 minutes.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in rat hepatocytes greater than about 350 minutes.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in rat hepatocytes greater than about 325 minutes.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in rat hepatocytes greater than about 300 minutes.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in rat hepatocytes greater than about 250 minutes.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in rat hepatocytes greater than about 225 minutes.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in rat hepatocytes greater than about 200 minutes.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in rat hepatocytes greater than about 150 minutes.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in rat hepatocytes greater than about 100 minutes.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in rat hepatocytes greater than about 50 minutes. In one embodiment, the compounds have an in vitro half-life in rat hepatocytes greater than about 30 minutes. In one embodiment, the compound is selected from any of the compound of Tables A and B or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life stability in mammal microsome of greater than 80 minutes.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life stability in mammal microsome of greater than 90 minutes.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life stability in mammal microsome of greater than 100 minutes.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life stability in mammal microsome of greater than 110 minutes.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life stability in mammal microsome of greater than 115 minutes.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life stability in mammal microsome of greater than 120 minutes.
  • the compound is selected from any of the compound of Tables A and B or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof.
  • the mammal microsome is human or mouse microsome.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life stability in mammal microsome in the range of about 50 min to about 200 min.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life stability in mammal microsome in the range of about 80 min to about 180 min.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life stability in mammal microsome in the range of about 100 min to about 160 min.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life stability in mammal microsome in the range of about 110 min to about 150 min.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life stability in mammal microsome in the range of about 110 min to about 140 min.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life stability in mammal microsome in the range of about 110 min to about 130 min.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life stability in mammal microsome in the range of about 115 min to about 130 min.
  • the compounds of the present disclosure are any compound of Tables A and B or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, having an in vitro half-life stability in mammal microsome in the range of about 115 min to about 130 min.
  • the mammal microsome is human or mouse microsome.
  • the present disclosure provides compounds which demonstrate blocking androgen-induced PSA-luciferase activity (PSA-luciferase assay).
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro IC 50 in a PSA-luciferase assay of less than about 4500 nM.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro IC 50 in a PSA-luciferase assay of less than about 4000 nM.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro IC 50 in a PSA-luciferase assay of less than about 3500 nM.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro IC 50 in a PSA-luciferase assay of less than about 3000 nM.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro IC 50 in a PSA-luciferase assay of less than about 2500 nM.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro IC 50 in a PSA-luciferase assay of less than about 2000 nM.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro IC 50 in a PSA-luciferase assay of less than about 1500 nM.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro IC 50 in a PSA-luciferase assay of less than about 1000 nM.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro IC 50 in a PSA-luciferase assay of less than about 950 nm.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro IC 50 in a PSA-luciferase assay of less than about 900 nM.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro IC 50 in a PSA-luciferase assay of less than about 890 nM, less than about 880 nM, less than about 870 nM, less than about 860 nM, less than about 850 nM, less than about 840 nM, less than about 830 nM, less than about 820 nM, less than about 810 nM, or less than about 800 nM.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro IC 50 in a PSA-luciferase assay of less than about 790 nM, less than about 780 nM, less than about 770 nM, less than about 760 nM, less than about 750 nM, less than about 740 nM, less than about 730 nM, less than about 720 nM, less than about 710 nM, or less than about 700 nM.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro IC 50 in a PSA-luciferase assay of less than about 690 nM, less than about 680 nM, less than about 670 nM, less than about 660 nM, less than about 650 nM, less than about 640 nM, less than about 630 nM, less than about 620 nM, less than about 610 nM, or less than about 600 nM.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro IC 50 in a PSA-luciferase assay of less than about 590 nM, less than about 580 nM, less than about 570 nM, less than about 560 nM, less than about 550 nM, less than about 540 nM, less than about 530 nM, less than about 520 nM, less than about 510 nM, or less than about 500 nM.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro IC 50 in a PSA-luciferase assay of less than about 500 nM.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds having in vitro IC 50 in a PSA-luciferase assay of less than about 490 nM, less than about 480 nM, less than about 470 nM, less than about 460 nM, less than about 450 nM, less than about 440 nM, less than about 430 nM, less than about 420 nM, less than about 410 nM, or less than about 400 nM.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro IC 50 in a PSA-luciferase assay of less than about 390 nM, less than about 380 nM, less than about 370 nM, less than about 360 nM, less than about 350 nM, less than about 340 nM, less than about 330 nM, less than about 320 nM, less than about 310 nM, or less than about 300 nM.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro IC 50 in a PSA-luciferase assay of less than about 290 nM, less than about 280 nM, less than about 270 nM, less than about 260 nM, less than about 250 nM, less than about 240 nM, less than about 230 nM, less than about 220 nM, less than about 210 nM, or less than about 200 nM.
  • the compounds have an in vitro IC 50 in a PSA-luciferase assay of less than about 200 nM.
  • the compound is selected from any of the compound of Tables A and B or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in mammal microsome of greater than about 80 minutes and in vitro IC 50 in a PSA-luciferase assay of less than about 2000 nM.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in mammal microsome of greater than about 90 minutes and in vitro IC 50 in a PSA-luciferase assay of less than about 1500 nM.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in mammal microsome of greater than about 100 minutes and in vitro IC 50 in a PSA-luciferase assay of less than about 1000 nM.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in mammal microsome of greater than about 105 minutes and in vitro IC 50 in a PSA-luciferase assay of less than about 900 nM.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in mammal microsome of greater than about 110 minutes and in vitro IC 50 in a PSA-luciferase assay of less than about 850 nM.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in mammal microsome of greater than about 115 minutes and in vitro IC 50 in a PSA-luciferase assay of less than about 800 nM.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in mammal microsome of greater than about 115 minutes and in vitro IC 50 in a PSA-luciferase assay of less than about 750 nM.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in mammal microsome of greater than about 120 minutes and in vitro IC 50 in a PSA-luciferase assay of less than about 700 nM.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in mammal microsome of greater than about 120 minutes and in vitro IC 50 in a PSA-luciferase assay of less than about 650 nM.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in mammal microsome of greater than about 120 minutes and in vitro IC 50 in a PSA-luciferase assay of less than about 600 nM.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in mammal microsome of greater than about 120 minutes and in vitro IC 50 in a PSA-luciferase assay of less than about 550 nM.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro half-life in mammal microsome of greater than about 120 minutes and in vitro IC 50 in a PSA-luciferase assay of less than about 500 nM.
  • the compound is selected from any of the compound of Tables A and B or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof.
  • the mammal microsome is human or mouse microsome.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro IC 50 in a PSA-luciferase assay of less than about 1000 nM and a HLM or MLM in vitro metabolic clearance of less than 12 ⁇ L/min/mg protein.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro IC 50 in a PSA-luciferase assay of less than about 1000 nM and a HLM and MLM in vitro metabolic clearance of less than 12 ⁇ L/min/mg protein.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro IC 50 in a PSA-luciferase assay of less than about 1000 nM and an in vitro metabolic clearance in human or mouse hepatocytes of less than 4 ⁇ L/min/million cells.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro IC 50 in a PSA-luciferase assay of less than about 1000 nM and an in vitro metabolic clearance in human and mouse hepatocytes of less than 4 ⁇ L/min/million cells.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro IC 50 in a PSA-luciferase assay of less than about 1000 nM; a HLM or MLM in vitro metabolic clearance of less than 12 ⁇ L/min/mg protein; and an in vitro metabolic clearance in human or mouse hepatocytes of less than 4 ⁇ L/min/million cells.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro IC 50 in a PSA-luciferase assay of less than about 800 nM; a HLM or MLM in vitro metabolic clearance of less than 12 ⁇ L/min/mg protein; and an in vitro metabolic clearance in human or mouse hepatocytes of less than 4 ⁇ L/min/million cells.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, or the compounds of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro IC 50 in a PSA-luciferase assay of less than about 700 nM; a HLM or MLM in vitro metabolic clearance of less than 12 ⁇ L/min/mg protein; and an in vitro metabolic clearance in human or mouse hepatocytes of less than 4 ⁇ L/min/million cells.
  • the compound is selected from any of the compound of Tables A and B or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof.
  • the compounds of the present disclosure are any compound of Tables A and B, or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein the compounds have an in vitro IC 50 in a PSA-luciferase assay of less than about 1000 nM; a HLM or MLM in vitro metabolic clearance of less than 12 ⁇ L/min/mg protein; and an in vitro metabolic clearance in human or mouse hepatocytes of less than 4 ⁇ L/min/million cells.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, and wherein the compounds have an in vitro metabolic clearance in HHs of less than 4 ⁇ L/min/million cells.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, and wherein the compounds have an in vitro metabolic clearance in HHs of less than 4 ⁇ L/min/million cells and in vitro IC 50 in a PSA-luciferase assay of less than about 700 nM. In one embodiment, the compounds have an in vitro metabolic clearance in HHs of less than 4 ⁇ L/min/million cells and in vitro IC 50 in a PSA-luciferase assay of less than about 675 nM.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, and wherein the compounds have an in vitro half-life in HHs of less than about 350 minutes.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, and wherein the compounds have an in vitro half-life in HHs of greater than about 320 minutes and in vitro IC 50 in a PSA-luciferase assay of less than about 700 nM.
  • the compounds have an in vitro half-life in HHs of greater than about 350 minutes and in vitro IC 50 in a PSA-luciferase assay of less than about 700 nM.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, and wherein the compounds have an in vitro metabolic clearance in MLMs of less than 15 ⁇ L/min/mg protein.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, and wherein the compounds have an in vitro metabolic clearance in MLMs of less than 15 ⁇ L/min/mg protein and in vitro IC 50 in a PSA-luciferase assay of less than about 700 nM. In one embodiment, the compounds have an in vitro metabolic clearance in MLMs of less than 15 ⁇ L/min/mg protein and in vitro IC 50 in a PSA-luciferase assay of less than about 675 nM.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, and wherein the compounds have an in vitro metabolic clearance in MHs of less than 10 ⁇ L/min/million cells. In one embodiment, the compounds have an in vitro metabolic clearance in MHs of less than 8 ⁇ L/min/million cells.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, and wherein the compounds have an in vitro metabolic clearance in MHs of less than 10 ⁇ L/min/million cells and in vitro IC 50 in a PSA-luciferase assay of less than about 700 nM. In one embodiment, the compounds have an in vitro metabolic clearance in MHs of less than 8 ⁇ L/min/million cells and in vitro IC 50 in a PSA-luciferase assay of less than about 675 nM.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, and wherein the compounds have an in vitro half-life in MLMs of greater than about 100 minutes.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, and wherein the compounds have an in vitro half-life in MHs of greater than about 100 minutes. In one embodiment, the compounds have an in vitro half-life in MHs of greater than about 180 minutes.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, and wherein the compounds have an in vitro metabolic clearance in MHs in the range of 3 ⁇ L/min/million cells to about 20 ⁇ L/min/million cells. In one embodiment, the compounds have an in vitro metabolic clearance in MHs in the range of 3.2 ⁇ L/min/million cells to about 18 ⁇ L/min/million cells. In one embodiment, the compounds have an in vitro metabolic clearance in MHs in the range of 3.4 ⁇ L/min/million cells to about 17 ⁇ L/min/million cells.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, and wherein the compounds have an in vitro IC 50 in a PSA-luciferase assay of less than 650 nM. In one embodiment, the compounds have an in vitro IC 50 in a PSA-luciferase assay of less than about 640 nM. In one embodiment, the compounds have an in vitro IC 50 in a PSA-luciferase assay of less than about 635 nM.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, and wherein the compounds have an in vitro IC 50 in a PSA-luciferase assay in the range of 200 nM to about 700 nM. In one embodiment, the compounds have an in vitro IC 50 in a PSA-luciferase assay in the range of about 250 nM to about 700 nM. In one embodiment, the compounds have an in vitro IC 50 in a PSA-luciferase assay in the range of about 300 nM to about 700 nM. In one embodiment, the compounds have an in vitro IC 50 in a PSA-luciferase assay in the range of about 350 nM to about 675 nM.
  • the compounds of the present disclosure are compounds having the structure of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, and wherein the compounds have an in vitro IC 50 in a PSA-luciferase assay of less than 525 nM. In one embodiment, the compounds have an in vitro IC 50 in a PSA-luciferase assay of less than about 500 nM. In one embodiment, the compounds have an in vitro IC 50 in a PSA-luciferase assay of less than about 450 nM.
  • a pharmaceutical composition for modulating androgen receptor (AR) in a subject.
  • a pharmaceutical composition comprises one or more compounds of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt or solvate thereof.
  • a pharmaceutical composition comprises a therapeutically effective amounts of one or more compounds of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt or solvate thereof.
  • a pharmaceutical composition as described herein, comprises one or more compounds selected from Table A, or a pharmaceutically acceptable salt or solvate thereof. In one embodiment, a pharmaceutical composition as described herein comprise one or more compounds selected from Table B, or a pharmaceutically acceptable salt or solvate thereof.
  • a pharmaceutical composition comprises one or more compounds selected from Compounds A3, A5, A7, A13, A17, A18, A22, A23, A24, A25, A28, A30, A31, A32, A34, A35, A38, A40, A41, A42, A45, A49, A52, A53, A54, A56, A57, A58, A62, A63, A64, A65, A68, A73, A74, A75, A76, B1, B2, B3, or B6, or a pharmaceutically acceptable salt or solvate thereof.
  • a pharmaceutical composition comprises one or more compounds selected from Compounds A1, A2, A4, A6, A8, A9, A10, A11, A12, A14, A15, A16, A19, A20, A21, A26, A27, A29, A33, A36, A37, A39, A43, A44, A46, A47, A48, A50, A51, A55, A59, A60, A61, A66, A67, A69, A70, A71, A72, A77, A78, A79, A80, A81, A82, A83, A84, A85, A86, A87, A88, A89, A90, A91, A92, A93, A94, A95, A96, A97, B4, B5, B7, B8, B9, B10, or B11, or a pharmaceutically acceptable salt or solvate thereof.
  • a pharmaceutical composition comprises one or more compounds selected from Compounds A98-A186. In a specific embodiment, a pharmaceutical composition, as described herein, comprises one or more compounds selected from Compounds A187-A211. In a specific embodiment, a pharmaceutical composition, as described herein, comprises one or more compounds selected from Compounds A212-A234. In a specific embodiment, a pharmaceutical composition, as described herein, comprises one or more compounds selected from Compounds A1-A96, A98-A116, A118-A159, A161-A175, and A177-A234.
  • a pharmaceutical composition as described herein, comprises one or more compounds selected from Compounds A13, A57, A74, A93, A109, A112, A122, A126, A131, A134, A136, A137, A164, A168, A169, A170, A171, A172, A184, A185, A195, and/or A204, or a pharmaceutically acceptable salt, tautomer, stereoisomer or prodrug thereof.
  • a pharmaceutical composition as described herein, comprises one or more compounds selected from Compounds A1-A211 or B1-B11.
  • a pharmaceutical composition as described herein, comprises one or more compounds selected from Compounds A1-A234 or B1-B11.
  • a pharmaceutical composition as described herein, comprising one or more compounds of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt or solvate thereof, further comprises one or more additional therapeutically active agents.
  • one or more additional therapeutically active agents are selected from therapeutics useful for treating cancer, neurological disease, a disorder characterized by abnormal accumulation of ⁇ -synuclein, a disorder of an aging process, cardiovascular disease, bacterial infection, viral infection, mitochondrial related disease, mental retardation, deafness, blindness, diabetes, obesity, autoimmune disease, glaucoma, Leber's Hereditary Optic Neuropathy, and rheumatoid arthritis.
  • the one or more additional therapeutic agents is a poly (ADP-ribose) polymerase (PARP) inhibitor including but not limited to olaparib, niraparib, rucaparib, talazoparib; an androgen receptor ligand binding domain inhibitor including but not limited to enzalutamide, apalutamide, darolutamide, bicalutamide, nilutamide, flutamide, ODM-204, TAS3681; an inhibitor of CYP17 including but not limited to galeterone, abiraterone, abiraterone acetate; a microtubule inhibitor including but not limited to docetaxel, paclitaxel, cabazitaxel (XRP-6258); a modulator of PD-1 or PD-L1 including but not limited to pembrolizumab, durvalumab, nivolumab, atezolizumab; a gonadotropin releasing hormone agonist including
  • PARP
  • a pharmaceutical composition comprising one or more compounds of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt or solvate thereof, and a pharmaceutically acceptable excipient or adjuvant.
  • the pharmaceutically acceptable excipients and adjuvants are added to the composition or formulation for a variety of purposes.
  • a pharmaceutical composition comprising one or more compounds of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt or solvate thereof, further comprises a pharmaceutically acceptable carrier.
  • a pharmaceutically acceptable carrier includes a pharmaceutically acceptable excipient, binder, and/or diluent.
  • suitable pharmaceutically acceptable excipients include, but are not limited to, water, salt solutions, alcohol, polyethylene glycols, gelatin, lactose, amylase, magnesium stearate, talc, silicic acid, viscous paraffin, hydroxymethylcellulose and polyvinylpyrrolidone.
  • the pharmaceutical compositions of the present disclosure may additionally contain other adjunct components conventionally found in pharmaceutical compositions, at their art-established usage levels.
  • the pharmaceutical compositions may contain additional, compatible, pharmaceutically-active materials such as, for example, antipruritics, astringents, local anesthetics or anti-inflammatory agents, or may contain additional materials useful in physically formulating various dosage forms of the compositions of the present invention, such as dyes, flavoring agents, preservatives, antioxidants, opacifiers, thickening agents and stabilizers.
  • additional materials useful in physically formulating various dosage forms of the compositions of the present invention such as dyes, flavoring agents, preservatives, antioxidants, opacifiers, thickening agents and stabilizers.
  • such materials when added, should not unduly interfere with the biological activities of the components of the compositions of the present invention.
  • the formulations can be sterilized and, if desired, mixed with auxiliary agents, e.g., lubricants, preservatives, stabilizers, wetting agents, emulsifiers, salts for influencing osmotic pressure, buffers, colorings, flavorings and/or aromatic substances and the like which do not deleteriously interact with the oligonucleotide(s) of the formulation.
  • auxiliary agents e.g., lubricants, preservatives, stabilizers, wetting agents, emulsifiers, salts for influencing osmotic pressure, buffers, colorings, flavorings and/or aromatic substances and the like which do not deleteriously interact with the oligonucleotide(s) of the formulation.
  • the compounds of the present disclosure can be formulated for administration by a variety of means including orally, parenterally, by inhalation spray, topically, or rectally in formulations containing pharmaceutically acceptable carriers, adjuvants and vehicles.
  • parenteral as used here includes subcutaneous, intravenous, intramuscular, and intraarterial injections with a variety of infusion techniques.
  • Intraarterial and intravenous injection as used herein includes administration through catheters.
  • the compounds disclosed herein can be formulated in accordance with the routine procedures adapted for desired administration route. Accordingly, the compounds disclosed herein can take such forms as suspensions, solutions or emulsions in oily or aqueous vehicles, and can contain formulatory agents such as suspending, stabilizing and/or dispersing agents.
  • the compounds disclosed herein can also be formulated as a preparation for implantation or injection. Thus, for example, the compounds can be formulated with suitable polymeric or hydrophobic materials (e.g., as an emulsion in an acceptable oil) or ion exchange resins, or as sparingly soluble derivatives (e.g., as a sparingly soluble salt).
  • the active ingredient can be in powder form for constitution with a suitable vehicle, e.g., sterile pyrogen-free water, before use.
  • a suitable vehicle e.g., sterile pyrogen-free water
  • suitable formulations for each of these methods of administration can be found, for example, in Remington: The Science and Practice of Pharmacy, A. Gennaro, ed., 20th edition, Lippincott, Williams & Wilkins, Philadelphia, Pa.
  • a pharmaceutical composition of the present disclosure is prepared using known techniques, including, but not limited to mixing, dissolving, granulating, dragee-making, levigating, emulsifying, encapsulating, entrapping or tableting processes.
  • the present disclosure provides a pharmaceutical composition
  • a pharmaceutical composition comprising a compound of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt or solvate thereof, as disclosed herein, combined with a pharmaceutically acceptable carrier.
  • suitable pharmaceutically acceptable carriers include, but are not limited to, inert solid fillers or diluents and sterile aqueous or organic solutions.
  • Pharmaceutically acceptable carriers are well known to those skilled in the art and include, but are not limited to, from about 0.01 to about 0.1 M and preferably 0.05M phosphate buffer or 0.8% saline.
  • Such pharmaceutically acceptable carriers can be aqueous or non-aqueous solutions, suspensions and emulsions. Examples of non-aqueous solvents suitable for use in the present application include, but are not limited to, propylene glycol, polyethylene glycol, vegetable oils such as olive oil, and injectable organic esters such as ethyl oleate.
  • Aqueous carriers suitable for use in the present application include, but are not limited to, water, ethanol, alcoholic/aqueous solutions, glycerol, emulsions or suspensions, including saline and buffered media.
  • Oral carriers can be elixirs, syrups, capsules, tablets and the like.
  • Liquid carriers suitable for use in the present application can be used in preparing solutions, suspensions, emulsions, syrups, elixirs and pressurized compounds.
  • the active ingredient can be dissolved or suspended in a pharmaceutically acceptable liquid carrier such as water, an organic solvent, a mixture of both or pharmaceutically acceptable oils or fats.
  • the liquid carrier can contain other suitable pharmaceutical additives such as solubilizers, emulsifiers, buffers, preservatives, sweeteners, flavoring agents, suspending agents, thickening agents, colors, viscosity regulators, stabilizers or osmo-regulators.
  • Liquid carriers suitable for use in the present application include, but are not limited to, water (partially containing additives as above, e.g. cellulose derivatives, preferably sodium carboxymethyl cellulose solution), alcohols (including monohydric alcohols and polyhydric alcohols, e.g. glycols) and their derivatives, and oils (e.g. fractionated coconut oil and arachis oil).
  • the carrier can also include an oily ester such as ethyl oleate and isopropyl myristate.
  • Sterile liquid carriers are useful in sterile liquid form comprising compounds for parenteral administration.
  • the liquid carrier for pressurized compounds disclosed herein can be halogenated hydrocarbon or other pharmaceutically acceptable propellent.
  • Solid carriers suitable for use in the present application include, but are not limited to, inert substances such as lactose, starch, glucose, methyl-cellulose, magnesium stearate, dicalcium phosphate, mannitol and the like.
  • a solid carrier can further include one or more substances acting as flavoring agents, lubricants, solubilizers, suspending agents, fillers, glidants, compression aids, binders or tablet-disintegrating agents; it can also be an encapsulating material.
  • the carrier can be a finely divided solid which is in admixture with the finely divided active compound.
  • the active compound is mixed with a carrier having the necessary compression properties in suitable proportions and compacted in the shape and size desired.
  • the powders and tablets preferably contain up to 99% of the active compound.
  • suitable solid carriers include, for example, calcium phosphate, magnesium stearate, talc, sugars, lactose, dextrin, starch, gelatin, cellulose, polyvinylpyrrolidine, low melting waxes and ion exchange resins.
  • a tablet may be made by compression or molding, optionally with one or more accessory ingredients.
  • Compressed tablets may be prepared by compressing in a suitable machine the active ingredient in a free flowing form such as a powder or granules, optionally mixed with a binder (e.g., povidone, gelatin, hydroxypropylmethyl cellulose), lubricant, inert diluent, preservative, disintegrant (e.g., sodium starch glycolate, cross-linked povidone, cross-linked sodium carboxymethyl cellulose) surface active or dispersing agent.
  • Molded tablets may be made by molding in a suitable machine a mixture of the powdered compound moistened with an inert liquid diluent.
  • the tablets may optionally be coated or scored and may be formulated so as to provide slow or controlled release of the active ingredient therein using, for example, hydroxypropyl methylcellulose in varying proportions to provide the desired release profile. Tablets may optionally be provided with an enteric coating, to provide release in parts of the gut other than the stomach.
  • Parenteral carriers suitable for use in the present application include, but are not limited to, sodium chloride solution, Ringer's dextrose, dextrose and sodium chloride, lactated Ringer's and fixed oils.
  • Intravenous carriers include fluid and nutrient replenishers, electrolyte replenishers such as those based on Ringer's dextrose and the like.
  • Preservatives and other additives can also be present, such as, for example, antimicrobials, antioxidants, chelating agents, inert gases and the like.
  • Carriers suitable for use in the present application can be mixed as needed with disintegrants, diluents, granulating agents, lubricants, binders and the like using conventional techniques known in the art.
  • the carriers can also be sterilized using methods that do not deleteriously react with the compounds, as is generally known in the art.
  • Diluents may be added to the formulations of the present invention. Diluents increase the bulk of a solid pharmaceutical composition and/or combination, and may make a pharmaceutical dosage form containing the composition and/or combination easier for the patient and care giver to handle. Diluents for solid compositions and/or combinations include, for example, microcrystalline cellulose (e.g., AVICEL), microfine cellulose, lactose, starch, pregelatinized starch, calcium carbonate, calcium sulfate, sugar, dextrates, dextrin, dextrose, dibasic calcium phosphate dihydrate, tribasic calcium phosphate, kaolin, magnesium carbonate, magnesium oxide, maltodextrin, mannitol, polymethacrylates (e.g., EUDRAGIT(r)), potassium chloride, powdered cellulose, sodium chloride, sorbitol, and talc.
  • microcrystalline cellulose e.g., AVICEL
  • microfine cellulose lacto
  • a pharmaceutical composition of the present invention is a solid (e.g., a powder, tablet, a capsule, granulates, and/or aggregates).
  • a solid pharmaceutical composition comprising one or more ingredients known in the art, including, but not limited to, starches, sugars, diluents, granulating agents, lubricants, binders, and disintegrating agents.
  • Solid pharmaceutical compositions that are compacted into a dosage form, such as a tablet may include excipients whose functions include helping to bind the active ingredient and other excipients together after compression.
  • Binders for solid pharmaceutical compositions and/or combinations include acacia, alginic acid, carbomer (e.g., carbopol), carboxymethylcellulose sodium, dextrin, ethyl cellulose, gelatin, guar gum, gum tragacanth, hydrogenated vegetable oil, hydroxyethyl cellulose, hydroxypropyl cellulose (e.g., KLUCEL), hydroxypropyl methyl cellulose (e.g., METHOCEL), liquid glucose, magnesium aluminum silicate, maltodextrin, methylcellulose, polymethacrylates, povidone (e.g., KOLLIDON, PLASDONE), pregelatinized starch, sodium alginate, and starch.
  • carbomer e.g., carbopol
  • the dissolution rate of a compacted solid pharmaceutical composition in the patient's stomach may be increased by the addition of a disintegrant to the composition and/or combination.
  • Disintegrants include alginic acid, carboxymethylcellulose calcium, carboxymethylcellulose sodium (e.g., AC-DI-SOL and PRIMELLOSE), colloidal silicon dioxide, croscarmellose sodium, crospovidone (e.g., KOLLIDON and POLYPLASDONE), guar gum, magnesium aluminum silicate, methyl cellulose, microcrystalline cellulose, polacrilin potassium, powdered cellulose, pregelatinized starch, sodium alginate, sodium starch glycolate (e.g., EXPLOTAB), potato starch, and starch.
  • a disintegrant include alginic acid, carboxymethylcellulose calcium, carboxymethylcellulose sodium (e.g., AC-DI-SOL and PRIMELLOSE), colloidal silicon dioxide, croscarmellose sodium, crospovidone (e.
  • Glidants can be added to improve the flowability of a non-compacted solid composition and/or combination and to improve the accuracy of dosing.
  • Excipients that may function as glidants include colloidal silicon dioxide, magnesium trisilicate, powdered cellulose, starch, talc, and tribasic calcium phosphate.
  • a dosage form such as a tablet
  • the composition is subjected to pressure from a punch and dye.
  • Some excipients and active ingredients have a tendency to adhere to the surfaces of the punch and dye, which can cause the product to have pitting and other surface irregularities.
  • a lubricant can be added to the composition and/or combination to reduce adhesion and ease the release of the product from the dye.
  • Lubricants include magnesium stearate, calcium stearate, glyceryl monostearate, glyceryl palmitostearate, hydrogenated castor oil, hydrogenated vegetable oil, mineral oil, polyethylene glycol, sodium benzoate, sodium lauryl sulfate, sodium stearyl fumarate, stearic acid, talc, and zinc stearate.
  • Flavoring agents and flavor enhancers make the dosage form more palatable to the patient.
  • Common flavoring agents and flavor enhancers for pharmaceutical products that may be included in the composition and/or combination of the present invention include maltol, vanillin, ethyl vanillin, menthol, citric acid, fumaric acid, ethyl maltol, and tartaric acid.
  • Solid and liquid compositions may also be dyed using any pharmaceutically acceptable colorant to improve their appearance and/or facilitate patient identification of the product and unit dosage level.
  • a pharmaceutical composition of the present invention is a liquid (e.g., a suspension, elixir and/or solution).
  • a liquid pharmaceutical composition is prepared using ingredients known in the art, including, but not limited to, water, glycols, oils, alcohols, flavoring agents, preservatives, and coloring agents.
  • Liquid pharmaceutical compositions can be prepared using compounds of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt or solvate thereof, and any other solid excipients where the components are dissolved or suspended in a liquid carrier such as water, vegetable oil, alcohol, polyethylene glycol, propylene glycol, or glycerin.
  • a liquid carrier such as water, vegetable oil, alcohol, polyethylene glycol, propylene glycol, or glycerin.
  • formulations for parenteral administration can contain as common excipients sterile water or saline, polyalkylene glycols such as polyethylene glycol, oils of vegetable origin, hydrogenated naphthalenes and the like.
  • polyalkylene glycols such as polyethylene glycol, oils of vegetable origin, hydrogenated naphthalenes and the like.
  • biocompatible, biodegradable lactide polymer, lactide/glycolide copolymer, or polyoxyethylene-polyoxypropylene copolymers can be useful excipients to control the release of active compounds.
  • Other potentially useful parenteral delivery systems include ethylene-vinyl acetate copolymer particles, osmotic pumps, implantable infusion systems, and liposomes.
  • Formulations for inhalation administration contain as excipients, for example, lactose, or can be aqueous solutions containing, for example, polyoxyethylene-9-auryl ether, glycocholate and deoxycholate, or oily solutions for administration in the form of nasal drops, or as a gel to be applied intranasally.
  • Formulations for parenteral administration can also include glycocholate for buccal administration, methoxysalicylate for rectal administration, or citric acid for vaginal administration.
  • Liquid pharmaceutical compositions can contain emulsifying agents to disperse uniformly throughout the composition and/or combination an active ingredient or other excipient that is not soluble in the liquid carrier.
  • Emulsifying agents that may be useful in liquid compositions and/or combinations of the present invention include, for example, gelatin, egg yolk, casein, cholesterol, acacia, tragacanth, chondrus, pectin, methyl cellulose, carbomer, cetostearyl alcohol, and cetyl alcohol.
  • Liquid pharmaceutical compositions can also contain a viscosity enhancing agent to improve the mouth-feel of the product and/or coat the lining of the gastrointestinal tract.
  • a viscosity enhancing agent include acacia, alginic acid bentonite, carbomer, carboxymethylcellulose calcium or sodium, cetostearyl alcohol, methyl cellulose, ethylcellulose, gelatin guar gum, hydroxyethyl cellulose, hydroxypropyl cellulose, hydroxypropyl methyl cellulose, maltodextrin, polyvinyl alcohol, povidone, propylene carbonate, propylene glycol alginate, sodium alginate, sodium starch glycolate, starch tragacanth, and xanthan gum.
  • Sweetening agents such as aspartame, lactose, sorbitol, saccharin, sodium saccharin, sucrose, aspartame, fructose, mannitol, and invert sugar may be added to improve the taste.
  • Preservatives and chelating agents such as alcohol, sodium benzoate, butylated hydroxyl toluene, butylated hydroxyanisole, and ethylenediamine tetraacetic acid may be added at levels safe for ingestion to improve storage stability.
  • a liquid composition can also contain a buffer such as guconic acid, lactic acid, citric acid or acetic acid, sodium guconate, sodium lactate, sodium citrate, or sodium acetate. Selection of excipients and the amounts used may be readily determined by the formulation scientist based upon experience and consideration of standard procedures and reference works in the field.
  • a buffer such as guconic acid, lactic acid, citric acid or acetic acid, sodium guconate, sodium lactate, sodium citrate, or sodium acetate.
  • a pharmaceutical composition is prepared for administration by injection (e.g., intravenous, subcutaneous, intramuscular, etc.).
  • a pharmaceutical composition comprises a carrier and is formulated in aqueous solution, such as water or physiologically compatible buffers such as Hanks's solution, Ringer's solution, or physiological saline buffer.
  • other ingredients are included (e.g., ingredients that aid in solubility or serve as preservatives).
  • injectable suspensions are prepared using appropriate liquid carriers, suspending agents and the like.
  • compositions for injection are suspensions, solutions or emulsions in oily or aqueous vehicles, and may contain formulatory agents such as suspending, stabilizing and/or dispersing agents.
  • Certain solvents suitable for use in pharmaceutical compositions for injection include, but are not limited to, lipophilic solvents and fatty oils, such as sesame oil, synthetic fatty acid esters, such as ethyl oleate or triglycerides, and liposomes.
  • Aqueous injection suspensions may contain substances that increase the viscosity of the suspension, such as sodium carboxymethyl cellulose, sorbitol, or dextran.
  • such suspensions may also contain suitable stabilizers or agents that increase the solubility of the pharmaceutical agents to allow for the preparation of highly concentrated solutions.
  • the sterile injectable preparation may also be a sterile injectable solution or suspension in a non-toxic parenterally acceptable diluent or solvent, such as a solution in 1,3-butane-diol or prepared as a lyophilized powder.
  • a non-toxic parenterally acceptable diluent or solvent such as a solution in 1,3-butane-diol or prepared as a lyophilized powder.
  • sterile fixed oils may conventionally be employed as a solvent or suspending medium.
  • any bland fixed oil may be employed including synthetic mono- or diglycerides.
  • fatty acids such as oleic acid may likewise be used in the preparation of injectables.
  • Formulations for intravenous administration can comprise solutions in sterile isotonic aqueous buffer.
  • the formulations can also include a solubilizing agent and a local anesthetic to ease pain at the site of the injection.
  • the ingredients are supplied either separately or mixed together in unit dosage form, for example, as a dry lyophilized powder or water free concentrate in a hermetically sealed container such as an ampule or sachet indicating the quantity of active agent.
  • the compound can be dispensed in a formulation with an infusion bottle containing sterile pharmaceutical grade water, saline or dextrose/water.
  • an ampule of sterile water for injection or saline can be provided so that the ingredients can be mixed prior to administration.
  • Suitable formulations further include aqueous and non-aqueous sterile injection solutions that can contain antioxidants, buffers, bacteriostats, bactericidal antibiotics and solutes that render the formulation isotonic with the bodily fluids of the intended recipient; and aqueous and non-aqueous sterile suspensions, which can include suspending agents and thickening agents.
  • a pharmaceutical composition of the present invention is formulated as a depot preparation. Certain such depot preparations are typically longer acting than non-depot preparations. In certain embodiments, such preparations are administered by implantation (for example subcutaneously or intramuscularly) or by intramuscular injection. In certain embodiments, depot preparations are prepared using suitable polymeric or hydrophobic materials (for example an emulsion in an acceptable oil) or ion exchange resins, or as sparingly soluble derivatives, for example, as a sparingly soluble salt.
  • a pharmaceutical composition of the present invention comprises a delivery system.
  • delivery systems include, but are not limited to, liposomes and emulsions.
  • Certain delivery systems are useful for preparing certain pharmaceutical compositions including those comprising hydrophobic compounds.
  • certain organic solvents such as dimethylsulfoxide are used.
  • a pharmaceutical composition of the present invention comprises a co-solvent system.
  • co-solvent systems comprise, for example, benzyl alcohol, a nonpolar surfactant, a water-miscible organic polymer, and an aqueous phase.
  • co-solvent systems are used for hydrophobic compounds.
  • a non-limiting example of such a co-solvent system is the VPD co-solvent system, which is a solution of absolute ethanol comprising 3% w/v benzyl alcohol, 8% w/v of the nonpolar surfactant Polysorbate 80 and 65% w/v polyethylene glycol 300.
  • the proportions of such co-solvent systems may be varied considerably without significantly altering their solubility and toxicity characteristics.
  • co-solvent components may be varied: for example, other surfactants may be used instead of Polysorbate 80; the fraction size of polyethylene glycol may be varied; other biocompatible polymers may replace polyethylene glycol, e.g., polyvinyl pyrrolidone; and other sugars or polysaccharides may substitute for dextrose.
  • a pharmaceutical composition of the present invention comprises a sustained-release system.
  • a sustained-release system is a semi-permeable matrix of solid hydrophobic polymers.
  • sustained-release systems may, depending on their chemical nature, release pharmaceutical agents over a period of hours, days, weeks or months.
  • Appropriate pharmaceutical compositions of the present disclosure can be determined according to any clinically-acceptable route of administration of the composition to the subject.
  • the manner in which the composition is administered is dependent, in part, upon the cause and/or location.
  • One skilled in the art will recognize the advantages of certain routes of administration.
  • the method includes administering an effective amount of the agent or compound (or composition comprising the agent or compound) to achieve a desired biological response, e.g., an amount effective to alleviate, ameliorate, or prevent, in whole or in part, a symptom of a condition to be treated, e.g., oncology and neurology disorders.
  • the route of administration is systemic, e.g., oral or by injection.
  • agents or compounds, or pharmaceutically acceptable salts or derivatives thereof are administered orally, nasally, transdermally, pulmonary, inhalationally, buccally, sublingually, intraperintoneally, subcutaneously, intramuscularly, intravenously, rectally, intrapleurally, intrathecally, intraportally, and parenterally.
  • the route of administration is local, e.g., topical, intra-tumor and peri-tumor.
  • the compound is administered orally.
  • a pharmaceutical composition of the present disclosure is prepared for oral administration.
  • a pharmaceutical composition is formulated by combining one or more agents and pharmaceutically acceptable carriers. Certain of such carriers enable pharmaceutical compositions to be formulated as tablets, pills, dragees, capsules, liquids, gels, syrups, slurries, suspensions and the like, for oral ingestion by a subject.
  • Suitable excipients include, but are not limited to, fillers, such as sugars, including lactose, sucrose, mannitol, or sorbitol; cellulose preparations such as, for example, maize starch, wheat starch, rice starch, potato starch, gelatin, gum tragacanth, methyl cellulose, hydroxypropylmethyl-cellulose, sodium carboxymethylcellulose, and/or polyvinylpyrrolidone (PVP).
  • PVP polyvinylpyrrolidone
  • such a mixture is optionally ground and auxiliaries are optionally added.
  • pharmaceutical compositions are formed to obtain tablets or dragee cores.
  • disintegrating agents e.g., cross-linked polyvinyl pyrrolidone, agar, or alginic acid or a salt thereof, such as sodium alginate are added.
  • dragee cores are provided with coatings.
  • concentrated sugar solutions may be used, which may optionally contain gum arabic, talc, polyvinyl pyrrolidone, carbopol gel, polyethylene glycol, and/or titanium dioxide, lacquer solutions, and suitable organic solvents or solvent mixtures.
  • Dyestuffs or pigments may be added to tablets or dragee coatings.
  • compositions for oral administration are push-fit capsules made of gelatin.
  • Certain of such push-fit capsules comprise one or more pharmaceutical agents of the present invention in admixture with one or more filler such as lactose, binders such as starches, and/or lubricants such as talc or magnesium stearate and, optionally, stabilizers.
  • pharmaceutical compositions for oral administration are soft, sealed capsules made of gelatin and a plasticizer, such as glycerol or sorbitol.
  • one or more pharmaceutical agents of the present invention are be dissolved or suspended in suitable liquids, such as fatty oils, liquid paraffin, or liquid polyethylene glycols.
  • stabilizers may be added.
  • compositions are prepared for buccal administration. Certain of such pharmaceutical compositions are tablets or lozenges formulated in conventional manner.
  • a pharmaceutical composition is prepared for transmucosal administration.
  • penetrants appropriate to the barrier to be permeated are used in the formulation. Such penetrants are generally known in the art.
  • a pharmaceutical composition is prepared for administration by inhalation.
  • Certain of such pharmaceutical compositions for inhalation are prepared in the form of an aerosol spray in a pressurized pack or a nebulizer.
  • Certain of such pharmaceutical compositions comprise a propellant, e.g., dichlorodifluoromethane, trichlorofluoromethane, dichlorotetrafluoroethane, carbon dioxide or other suitable gas.
  • the dosage unit may be determined with a valve that delivers a metered amount.
  • capsules and cartridges for use in an inhaler or insufflator may be formulated.
  • Certain of such formulations comprise a powder mixture of a pharmaceutical agent of the invention and a suitable powder base such as lactose or starch.
  • the compound of the present disclosure are administered by the intravenous route.
  • the parenteral administration may be provided in a bolus or by infusion.
  • a pharmaceutical composition is prepared for rectal administration, such as a suppository or retention enema.
  • Certain of such pharmaceutical compositions comprise known ingredients, such as cocoa butter and/or other glycerides.
  • a pharmaceutical composition is prepared for topical administration.
  • Certain of such pharmaceutical compositions comprise bland moisturizing bases, such as ointments or creams.
  • ointments or creams include, but are not limited to, petrolatum, petrolatum plus volatile silicones, and lanolin and water in oil emulsions.
  • suitable cream bases include, but are not limited to, cold cream and hydrophilic ointment.
  • the therapeutically effective amount is sufficient to prevent, alleviate or ameliorate symptoms of a disease or to prolong the survival of the subject being treated. Determination of a therapeutically effective amount is well within the capability of those skilled in the art.
  • one or more compounds of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt or solvate thereof are formulated as a prodrug.
  • a prodrug upon in vivo administration, a prodrug is chemically converted to the biologically, pharmaceutically or therapeutically more active form.
  • prodrugs are useful because they are easier to administer than the corresponding active form.
  • a prodrug may be more bioavailable (e.g., through oral administration) than is the corresponding active form.
  • a prodrug may have improved solubility compared to the corresponding active form.
  • prodrugs are less water soluble than the corresponding active form.
  • a prodrug is an ester.
  • the ester is metabolically hydrolyzed to carboxylic acid upon administration.
  • the carboxylic acid containing compound is the corresponding active form.
  • a prodrug comprises a short peptide (polyaminoacid) bound to an acid group.
  • the peptide is cleaved upon administration to form the corresponding active form.
  • a prodrug is produced by modifying a pharmaceutically active compound such that the active compound will be regenerated upon in vivo administration.
  • the prodrug can be designed to alter the metabolic stability or the transport characteristics of a drug, to mask side effects or toxicity, to improve the flavor of a drug or to alter other characteristics or properties of a drug.
  • the amount of the compound of formula (I)-(VI) and/or (A)-(H-I), or a pharmaceutically acceptable salt or solvate thereof, or compounds disclosed in Tables A and B, or a pharmaceutically acceptable salt or solvate thereof can be administered at about 0.001 mg/kg to about 100 mg/kg body weight (e.g., about 0.01 mg/kg to about 10 mg/kg or about 0.1 mg/kg to about 5 mg/kg).
  • the concentration of a disclosed compound in a pharmaceutically acceptable mixture will vary depending on several factors, including the dosage of the compound to be administered, the pharmacokinetic characteristics of the compound(s) employed, and the route of administration.
  • the agent may be administered in a single dose or in repeat doses.
  • the dosage regimen utilizing the compounds of the present invention is selected in accordance with a variety of factors including type, species, age, weight, sex and medical condition of the patient; the severity of the condition to be treated; the route of administration; the renal and hepatic function of the patient; and the particular compound or salt thereof employed. Treatments may be administered daily or more frequently depending upon a number of factors, including the overall health of a patient, and the formulation and route of administration of the selected compound(s). An ordinarily skilled physician or veterinarian can readily determine and prescribe the effective amount of the drug required to prevent, counter or arrest the progress of the condition.
  • the compounds or pharmaceutical compositions of the present disclosure may be manufactured and/or administered in single or multiple unit dose forms.
  • novel compounds of the present invention can be prepared in a variety of ways known to one skilled in the art of organic synthesis.
  • the compounds of the present invention can be synthesized using the methods as hereinafter described below, together with synthetic methods known in the art of synthetic organic chemistry or variations thereon as appreciated by those skilled in the art.
  • Preparation of compounds can involve the protection and deprotection of various chemical groups.
  • the need for protection and deprotection, and the selection of appropriate protecting groups can be readily determined by one skilled in the art.
  • the chemistry of protecting groups can be found, for example, in Greene and Wuts, Protective Groups in Organic Synthesis, 44th. Ed., Wiley & Sons, 2006, as well as in Jerry March, Advanced Organic Chemistry, 4 th edition, John Wiley & Sons, publisher, New York, 1992 which are incorporated herein by reference in their entirety.
  • the groups and/or the substituents of the compounds of the present invention can be synthesized and attached to these scaffolds by the literature methods cited in the following text.
  • reaction conditions are given, and reaction products can be purified by general known methods including crystallization, silica gel chromatography using various organic solvents such as hexane, cyclohexane, ethyl acetate, methanol and the like, preparative high pressure liquid chromatography or preparative reverse phase high pressure liquid chromatography.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Epidemiology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Urology & Nephrology (AREA)
  • Engineering & Computer Science (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Pyrrole Compounds (AREA)
  • Pyridine Compounds (AREA)
US16/657,625 2018-10-18 2019-10-18 Androgen receptor modulators and methods for their use Abandoned US20200123117A1 (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
US16/657,625 US20200123117A1 (en) 2018-10-18 2019-10-18 Androgen receptor modulators and methods for their use
US16/852,810 US11059795B2 (en) 2018-10-18 2020-04-20 Androgen receptor modulators and methods for their use
US17/363,534 US20220380325A1 (en) 2018-10-18 2021-06-30 Androgen receptor modulators and methods for their use

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US201862747209P 2018-10-18 2018-10-18
US201962803516P 2019-02-10 2019-02-10
US201962857516P 2019-06-05 2019-06-05
US16/657,625 US20200123117A1 (en) 2018-10-18 2019-10-18 Androgen receptor modulators and methods for their use

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US16/852,810 Continuation US11059795B2 (en) 2018-10-18 2020-04-20 Androgen receptor modulators and methods for their use

Publications (1)

Publication Number Publication Date
US20200123117A1 true US20200123117A1 (en) 2020-04-23

Family

ID=70280422

Family Applications (3)

Application Number Title Priority Date Filing Date
US16/657,625 Abandoned US20200123117A1 (en) 2018-10-18 2019-10-18 Androgen receptor modulators and methods for their use
US16/852,810 Active US11059795B2 (en) 2018-10-18 2020-04-20 Androgen receptor modulators and methods for their use
US17/363,534 Abandoned US20220380325A1 (en) 2018-10-18 2021-06-30 Androgen receptor modulators and methods for their use

Family Applications After (2)

Application Number Title Priority Date Filing Date
US16/852,810 Active US11059795B2 (en) 2018-10-18 2020-04-20 Androgen receptor modulators and methods for their use
US17/363,534 Abandoned US20220380325A1 (en) 2018-10-18 2021-06-30 Androgen receptor modulators and methods for their use

Country Status (16)

Country Link
US (3) US20200123117A1 (https=)
EP (1) EP3867216A4 (https=)
JP (2) JP7581192B2 (https=)
KR (1) KR20210093886A (https=)
CN (2) CN118684633A (https=)
AU (1) AU2019362061B2 (https=)
CA (1) CA3115101A1 (https=)
CL (1) CL2021000977A1 (https=)
CO (1) CO2021006354A2 (https=)
IL (1) IL282257A (https=)
MX (2) MX2021004427A (https=)
PE (1) PE20211543A1 (https=)
PH (1) PH12021550800A1 (https=)
SG (1) SG11202103325WA (https=)
WO (1) WO2020081999A1 (https=)
ZA (1) ZA202102202B (https=)

Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11059795B2 (en) 2018-10-18 2021-07-13 Essa Pharma, Inc. Androgen receptor modulators and methods for their use
US11142508B2 (en) 2016-04-15 2021-10-12 The University Of British Columbia Bisphenol derivatives and their use as androgen receptor activity modulators
US11242324B2 (en) 2020-04-17 2022-02-08 Essa Pharma, Inc. Solid forms of an n-terminal domain androgen receptor inhibitor and uses thereof
WO2022051330A1 (en) 2020-09-02 2022-03-10 Propella Therapeutics, Inc. Abiraterone prodrugs
US11345670B2 (en) 2015-01-13 2022-05-31 The University Of British Columbia Heterocyclic compounds for cancer imaging and treatment and methods for their use
WO2022174134A1 (en) 2021-02-15 2022-08-18 Propella Therapeutics, Inc. Abiraterone prodrugs
US11485713B2 (en) 2018-05-25 2022-11-01 Essa Pharma, Inc. Androgen receptor modulators and methods for their use
WO2023034916A1 (en) * 2021-09-01 2023-03-09 Essa Pharma, Inc. Pharmaceutical compositions and combinations comprising inhibitors of the androgen receptor and uses thereof
WO2023038933A1 (en) 2021-09-08 2023-03-16 Propella Therapeutics, Inc. Oral abiraterone formulations
WO2023056423A1 (en) * 2021-09-30 2023-04-06 Essa Pharma, Inc. Androgen receptor modulators and methods for use as bifunctional degraders
WO2023167783A1 (en) 2022-03-01 2023-09-07 Propella Therapeutics, Inc. Abiraterone decanoate prodrugs and use in therapy
US11779550B2 (en) 2015-03-12 2023-10-10 The University Of British Columbia Bisphenol ether derivatives and methods for using the same
WO2024107928A1 (en) 2022-11-16 2024-05-23 Propella Therapeutics, Inc. Abiraterone decanoate composition and use in therapy
US12109179B2 (en) 2019-03-28 2024-10-08 Essa Pharma Inc. Pharmaceutical compositions and combinations comprising inhibitors of the androgen receptor and uses thereof
US12441707B2 (en) 2019-12-30 2025-10-14 Tyra Biosciences, Inc. Indazole compounds

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114502539A (zh) * 2019-03-28 2022-05-13 埃萨制药股份有限公司 包含雄激素受体的抑制剂的药物组合物和组合及其用途
AU2020348675B2 (en) 2019-09-16 2025-11-20 Takeda Pharmaceutical Company Limited Azole-fused pyridazin-3(2H)-one derivatives
JP2021050161A (ja) 2019-09-25 2021-04-01 武田薬品工業株式会社 複素環化合物及びその用途
JP2021080177A (ja) 2019-11-14 2021-05-27 武田薬品工業株式会社 複素環化合物及びその用途
WO2022060969A1 (en) * 2020-09-16 2022-03-24 Essa Pharma, Inc. Pharmaceutical compositions and combinations comprising inhibitors of the androgen receptor and uses thereof
CN115368244B (zh) * 2021-05-17 2025-08-08 北京鼎材科技有限公司 2-芳基-2-（4-胺基苯基）丙烷的合成方法
CN113603695B (zh) * 2021-08-05 2022-06-14 青岛恒宁生物科技有限公司 一种取代的嘧啶胺类化合物或其作为农药可接受的盐、组合物及其用途
WO2023031371A1 (en) 2021-09-01 2023-03-09 Janssen Pharmaceutica Nv Combination therapies for metastatic castration-resistant prostate cancer
WO2023110473A1 (en) 2021-12-14 2023-06-22 Basf Se Heterocyclic compounds for the control of invertebrate pests
EP4198033A1 (en) 2021-12-14 2023-06-21 Basf Se Heterocyclic compounds for the control of invertebrate pests
WO2024006207A1 (en) * 2022-06-26 2024-01-04 Essa Pharma Inc. An n-terminal domain androgen receptor inhibitor and uses thereof

Family Cites Families (87)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2571217A (en) 1951-10-16 Horace s
US2890189A (en) 1954-06-14 1959-06-09 Johnson & Son Inc S C Alkali soluble resins and compositions containing the same
US3074974A (en) 1957-12-06 1963-01-22 Monsanto Chemicals Method for the preparation of diglycidyl ether of tetrachlorobisphenol-a
US3162615A (en) 1961-01-03 1964-12-22 Dow Chemical Co Polyesters from cyclic polyhaloalkane polyols and unsaturated dicarboxylic acids
FR1389005A (fr) 1963-01-09 1965-02-12 Bayer Ag Procédé perfectionné pour durcir des polyépoxydes
SU638596A1 (ru) 1975-09-01 1978-12-25 Государственный Научно-Исследовательский И Проектный Институт Полимерных Клеев Им. Э.Л.Тер-Газаряна Хлоргидриднное производное диаллилизоциануровой кислоты в качестве пластификатора поливинилацетатной эмульсии
US4284574A (en) 1979-06-15 1981-08-18 Ciba-Geigy Corporation Diglycidyl ethers of di-secondary alcohols, their preparation, and curable compositions containing them
SU929630A1 (ru) 1980-02-06 1982-05-23 Научно-Исследовательский Институт Биологии При Иркутском Государственном Университете Им.А.А.Жданова Способ получени ди-или триоксидифенил-сульфонов
US4369298A (en) 1980-05-27 1983-01-18 Tokuyama Soda Kabushiki Kaisha Novel cured resin, process for production thereof, and lens composed of said resin from bis(alkyleneoxyphenyl)-diacrylate, bis(alkyleneoxyphenyl)diallyl ether, bis(alkyleneoxyphenyl)diallyl carbonate monomers
EP0056175B1 (en) 1981-01-13 1985-05-02 Teijin Limited Ion-permeable composite membrane and its use in selective separation
IN169231B (https=) 1984-03-15 1991-09-14 Ciba Geigy Ag
PL141793B1 (en) 1984-10-08 1987-08-31 Politechnika Warszawska Method of obtaining bisphenolic resins
US5753730A (en) 1986-12-15 1998-05-19 Mitsui Toatsu Chemicals, Inc. Plastic lenses having a high-refractive index, process for the preparation thereof and casting polymerization process for preparing sulfur-containing urethane resin lens and lens prepared thereby
JPH0832844B2 (ja) 1987-02-09 1996-03-29 パイロツトインキ株式会社 筆記板用不透明性インキ
DE3852839T2 (de) 1987-04-27 1995-06-22 Mitsubishi Gas Chemical Co Hitzehärtbare Harzzusammensetzung.
WO1988009782A1 (en) 1987-06-01 1988-12-15 The Dow Chemical Company Process for making propargyl ethers of hydroxyaromatic compounds
US5155196A (en) 1987-06-01 1992-10-13 The Dow Chemical Company Polymer resulting from the cure of a preformed chromene-containing mixture
JP2572020B2 (ja) 1987-06-19 1997-01-16 竹本油脂株式会社 熱硬化性樹脂用難燃剤
DE3821585A1 (de) 1987-09-13 1989-03-23 Hoechst Ag Positiv arbeitendes strahlungsempfindliches gemisch und daraus hergestelltes strahlungsempfindliches aufzeichnungsmaterial fuer hochenergetische strahlung
US4855184A (en) 1988-02-02 1989-08-08 Minnesota Mining And Manufacturing Company Radiation-curable protective coating composition
DE3939760A1 (de) 1989-12-01 1991-06-06 Bayer Ag Verfahren zur lackierung von kunststoffen, lackierte kunststoffe und die verwendung von hierzu geeigneten haftvermittlern
EP0515128A1 (en) 1991-05-23 1992-11-25 Konica Corporation Silver halide color photographic light-sensitive material
JPH0649473A (ja) 1992-08-04 1994-02-22 Asahi Chem Ind Co Ltd 冷媒組成物
DE4323512A1 (de) 1992-09-01 1994-04-28 Agfa Gevaert Ag Fotografisches Aufzeichnungsmaterial
DE4326393A1 (de) * 1993-08-06 1995-02-09 Merck Patent Gmbh Trifluorethoxypyri(mi)din-Derivate und flüssigkristallines Medium
JPH07117349A (ja) 1993-10-27 1995-05-09 Asahi Denka Kogyo Kk 感熱記録材料
CN1167437A (zh) 1994-11-29 1997-12-10 赫彻斯特马里恩鲁斯公司 用三芳基-乙烯衍生物治疗和预防骨质疏松的方法
DE19526146A1 (de) 1995-07-07 1997-01-09 Schering Ag Triphenylethylene, Verfahren zu deren Herstellung, diese Triphenylethylene enthaltene pharmazeutische Präparate sowie deren Verwendung zur Herstellung von Arzneimitteln
JPH09176240A (ja) 1995-12-27 1997-07-08 Mitsubishi Chem Corp 光重合性組成物
JPH10133427A (ja) 1996-11-05 1998-05-22 Fuji Xerox Co Ltd 静電潜像現像用キャリア、静電潜像現像剤及び画像形成方法
ZA98900B (en) 1997-02-07 1998-08-03 Shell Int Research Process for the manufacture of epoxy compounds
JPH10316803A (ja) 1997-05-16 1998-12-02 Teijin Chem Ltd 難燃性樹脂組成物
IL125840A (en) 1997-08-22 2002-12-01 Teijin Chemicals Ltd Bromine compound production method
JPH11166087A (ja) 1997-12-04 1999-06-22 Teijin Chem Ltd 難燃性樹脂組成物
AU4494399A (en) 1998-06-30 2000-01-24 University Of British Columbia, The Inhibitors of androgen-independent activation of androgen receptor
US6245117B1 (en) 1998-08-07 2001-06-12 Ipposha Oil Industries Co., Ltd. Modifier of cellulose fibers and modification method of cellulose fibers
US6218430B1 (en) 1998-08-24 2001-04-17 Ligand Pharmaceuticals Incorporated Vitamin D3 mimics
JP3795679B2 (ja) 1998-09-01 2006-07-12 帝人化成株式会社 臭素化合物の製造方法
AU775928B2 (en) 1999-10-14 2004-08-19 Bristol-Myers Squibb Company Crystallographic structure of the androgen receptor ligand binding domain
US6534621B2 (en) 2000-05-18 2003-03-18 Dow Global Technologies Inc. Process for manufacturing a hydroxyester derivative intermediate and epoxy resins prepared therefrom
US6472436B1 (en) 2000-07-17 2002-10-29 The Salk Institute For Biological Studies Methods for protecting cells from amyloid toxicity and for inhibiting amyloid protein production
US6756400B2 (en) 2000-08-31 2004-06-29 Theravance, Inc. Sodium channel modulators
DE10102322A1 (de) * 2001-01-19 2002-07-25 Merck Patent Gmbh Phenylderivate
US6646102B2 (en) 2001-07-05 2003-11-11 Dow Global Technologies Inc. Process for manufacturing an alpha-dihydroxy derivative and epoxy resins prepared therefrom
US20030092724A1 (en) 2001-09-18 2003-05-15 Huaihung Kao Combination sustained release-immediate release oral dosage forms with an opioid analgesic and a non-opioid analgesic
US7344700B2 (en) 2002-02-28 2008-03-18 University Of Tennessee Research Corporation Radiolabeled selective androgen receptor modulators and their use in prostate cancer imaging and therapy
GB0324551D0 (en) 2003-10-21 2003-11-26 Karobio Ab Novel compounds
US7595345B2 (en) 2003-11-20 2009-09-29 Eli Lilly And Company Vitamin D receptor modulators
CA2555597C (en) 2004-02-13 2016-06-14 The University Of British Columbia Radiolabeled compounds and compositions, their precursors and methods for their production
JP2005325301A (ja) 2004-05-17 2005-11-24 Fuji Photo Film Co Ltd セルロースアシレートドープ組成物、およびセルロースアシレートフィルム
EP1781280A2 (en) 2004-08-18 2007-05-09 Warner-Lambert Company LLC Androgen modulators
JP2006208607A (ja) 2005-01-26 2006-08-10 Fuji Photo Film Co Ltd パターン形成材料、並びにパターン形成装置及び永久パターン形成方法
JP4753601B2 (ja) 2005-03-23 2011-08-24 旭化成イーマテリアルズ株式会社 感光性組成物
EP1717235A3 (en) 2005-04-29 2007-02-28 Bioprojet Phenoxypropylpiperidines and -pyrrolidines and their use as histamine H3-receptor ligands
FR2885904B1 (fr) 2005-05-19 2007-07-06 Aventis Pharma Sa Nouveaux derives du fluorene, compositions les contenant et utilisation
EP1792622A1 (en) 2005-11-11 2007-06-06 GPC Biotech AG Anti-proliferative combination therapy comprising a platinum-based chemotherapeutic agent and EGFR inhibitors or pyrimidine analogues
WO2007079078A1 (en) * 2005-12-29 2007-07-12 Bayer Schering Pharma Aktiengesellschaft Diamine derivatives as inhibitors of leukotriene a4 hydrolase
JP2007290980A (ja) 2006-04-21 2007-11-08 Shin Etsu Chem Co Ltd 含フッ素（メタ）アクリル酸エステル
DE102006019044A1 (de) * 2006-04-25 2007-10-31 Merck Patent Gmbh Antioxidantien
TW200819421A (en) 2006-10-31 2008-05-01 Univ Nat Chunghsing The method of synthesizing biphenol A, BPA having di-alkoxyl group by using polycarbonate or its waste
US8198311B2 (en) * 2006-11-01 2012-06-12 Bristol-Myers Squibb Company Modulators of glucocorticoid receptor, AP-1, and/or NF-κB activity and use thereof
KR20090115797A (ko) 2007-02-20 2009-11-06 바스프 에스이 고굴절률 단량체, 이의 조성물 및 용도
RU2572596C2 (ru) 2008-07-02 2016-01-20 Бритиш Коламбиа Кэнсер Эйдженси Бранч Терапевтические средства на основе производных диглицилиловых простых эфиров и способы их применения
AU2009279936A1 (en) 2008-08-05 2010-02-11 Banyu Pharmaceutical Co., Ltd. Therapeutic compounds
AR079975A1 (es) 2010-01-06 2012-03-07 British Columbia Cancer Agency Agentes terapeuticos derivados de bisfenol u metodos para su uso, composiciones farmaceuticas y uso de los mismos
AR079846A1 (es) 2010-01-06 2012-02-22 British Columbia Cancer Agency Agentes terapeuticos derivados de bisfenol que contienen un grupo aquiral y su uso en el tratamiento del cancer
EP2693875A4 (en) 2011-04-08 2014-10-22 British Columbia Cancer Agency BISPHENOL COMPOUNDS AND METHOD FOR THEIR USE
WO2012145328A1 (en) 2011-04-18 2012-10-26 The University Of British Columbia Dibenzylphenyl compounds and methods for their use
WO2012145330A1 (en) 2011-04-18 2012-10-26 The University Of British Columbia Fluorene-9-bisphenol compounds and methods for their use
WO2013028572A1 (en) 2011-08-19 2013-02-28 British Columbia Cancer Agency Branch Fluorinated bisphenol ether compounds and methods for their use
WO2013028791A1 (en) 2011-08-22 2013-02-28 British Columbia Cancer Agency Branch 18f compounds for cancer imaging and methods for their use
WO2013131018A1 (en) * 2012-03-02 2013-09-06 Zalicus Pharmaceuticals Ltd. Biaryl inhibitors of the sodium channel
US9365510B2 (en) 2012-04-16 2016-06-14 British Columbia Cancer Agency Branch Aziridine bisphenol ethers and related compounds and methods for their use
CN105358522A (zh) * 2013-05-10 2016-02-24 不列颠哥伦比亚癌症局分支机构 雄激素受体调节剂的酯衍生物及其使用方法
CN103342892A (zh) 2013-06-06 2013-10-09 西安交通大学 一种双马来酰亚胺树脂的增韧改性剂及其制备方法
US20150010469A1 (en) 2013-07-03 2015-01-08 British Columbia Cancer Agency Branch Bisphenol ether compounds with novel bridging groups and methods for their use
SG11201601431VA (en) 2013-09-09 2016-03-30 British Columbia Cancer Agency Halogenated compounds for cancer imaging and treatment and methods for their use
WO2015042414A1 (en) * 2013-09-20 2015-03-26 Karyopharm Therapeutics Inc. Multicyclic compounds and methods of using same
WO2016058080A1 (en) 2014-10-14 2016-04-21 British Columbia Cancer Agency Branch Fluoro-chloro bisphenol ether compounds and methods for their use
WO2016058082A1 (en) 2014-10-14 2016-04-21 British Columbia Cancer Agency Branch 18f compounds for cancer imaging and methods for their use
JP6884100B2 (ja) * 2015-01-13 2021-06-09 ブリティッシュ コロンビア キャンサー エージェンシー ブランチ がんの画像化及び治療用のヘテロ環式化合物ならびにそれらの使用方法
US10471023B2 (en) 2015-03-12 2019-11-12 British Columbia Cancer Agency Branch Bisphenol ether derivatives and methods for using the same
CA2929345A1 (en) 2015-09-02 2017-03-02 British Columbia Cancer Agency Branch Co-targeting androgen receptor splice variants and mtor signaling pathway for the treatment of castration-resistant prostate cancer
US20170298033A1 (en) * 2016-04-15 2017-10-19 The University Of British Columbia Bisphenol derivatives and their use as androgen receptor activity modulators
WO2017210771A1 (en) 2016-06-06 2017-12-14 British Columbia Cancer Agency Branch Compounds and compositions for radiation therapy and methods of using the same
WO2018045450A1 (en) * 2016-09-09 2018-03-15 British Columbia Cancer Agency Branch Bisphenol a compounds and methods for treating drug-resistant androgen receptor mediated cancers
MX2021004427A (es) 2018-10-18 2021-11-12 Univ British Columbia Moduladores del receptor de andrógenos y métodos para su uso.

Cited By (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11345670B2 (en) 2015-01-13 2022-05-31 The University Of British Columbia Heterocyclic compounds for cancer imaging and treatment and methods for their use
US11779550B2 (en) 2015-03-12 2023-10-10 The University Of British Columbia Bisphenol ether derivatives and methods for using the same
US11142508B2 (en) 2016-04-15 2021-10-12 The University Of British Columbia Bisphenol derivatives and their use as androgen receptor activity modulators
US11919874B2 (en) 2016-04-15 2024-03-05 The University Of British Columbia Bisphenol derivatives and their use as androgen receptor activity modulators
US11485713B2 (en) 2018-05-25 2022-11-01 Essa Pharma, Inc. Androgen receptor modulators and methods for their use
US11059795B2 (en) 2018-10-18 2021-07-13 Essa Pharma, Inc. Androgen receptor modulators and methods for their use
US12109179B2 (en) 2019-03-28 2024-10-08 Essa Pharma Inc. Pharmaceutical compositions and combinations comprising inhibitors of the androgen receptor and uses thereof
US12441707B2 (en) 2019-12-30 2025-10-14 Tyra Biosciences, Inc. Indazole compounds
US11518747B2 (en) 2020-04-17 2022-12-06 Essa Pharma, Inc. Solid forms of an N-terminal domain androgen receptor inhibitor and uses thereof
US11814357B2 (en) 2020-04-17 2023-11-14 Essa Pharma Inc. Solid forms of an N-terminal domain androgen receptor inhibitor and uses thereof
US11358938B2 (en) 2020-04-17 2022-06-14 Essa Pharma, Inc. Solid forms of an N-terminal domain androgen receptor inhibitor and uses thereof
US11242324B2 (en) 2020-04-17 2022-02-08 Essa Pharma, Inc. Solid forms of an n-terminal domain androgen receptor inhibitor and uses thereof
WO2022051330A1 (en) 2020-09-02 2022-03-10 Propella Therapeutics, Inc. Abiraterone prodrugs
WO2022174134A1 (en) 2021-02-15 2022-08-18 Propella Therapeutics, Inc. Abiraterone prodrugs
WO2023034916A1 (en) * 2021-09-01 2023-03-09 Essa Pharma, Inc. Pharmaceutical compositions and combinations comprising inhibitors of the androgen receptor and uses thereof
WO2023038933A1 (en) 2021-09-08 2023-03-16 Propella Therapeutics, Inc. Oral abiraterone formulations
WO2023056423A1 (en) * 2021-09-30 2023-04-06 Essa Pharma, Inc. Androgen receptor modulators and methods for use as bifunctional degraders
WO2023167783A1 (en) 2022-03-01 2023-09-07 Propella Therapeutics, Inc. Abiraterone decanoate prodrugs and use in therapy
WO2024107928A1 (en) 2022-11-16 2024-05-23 Propella Therapeutics, Inc. Abiraterone decanoate composition and use in therapy

Also Published As

Publication number Publication date
BR112021007222A8 (pt) 2022-11-22
AU2019362061A1 (en) 2021-05-06
CN113195441B (zh) 2024-07-12
JP7581192B2 (ja) 2024-11-12
US20200247763A1 (en) 2020-08-06
MX2023010043A (es) 2023-09-05
US20220380325A1 (en) 2022-12-01
WO2020081999A1 (en) 2020-04-23
CA3115101A1 (en) 2020-04-23
EP3867216A1 (en) 2021-08-25
AU2019362061B2 (en) 2024-09-26
CN118684633A (zh) 2024-09-24
IL282257A (en) 2021-05-31
US11059795B2 (en) 2021-07-13
BR112021007222A2 (pt) 2021-08-10
EP3867216A4 (en) 2022-07-13
SG11202103325WA (en) 2021-05-28
NZ774611A (en) 2025-03-28
CL2021000977A1 (es) 2021-10-22
KR20210093886A (ko) 2021-07-28
CO2021006354A2 (es) 2021-05-31
MX2021004427A (es) 2021-11-12
JP2022504949A (ja) 2022-01-13
JP2024123097A (ja) 2024-09-10
ZA202102202B (en) 2024-06-26
PH12021550800A1 (en) 2021-10-04
PE20211543A1 (es) 2021-08-16
AU2019362061A8 (en) 2021-06-17
CN113195441A (zh) 2021-07-30

Similar Documents

Publication Publication Date Title
US11059795B2 (en) Androgen receptor modulators and methods for their use
US20220202780A1 (en) Pharmaceutical compositions and combinations comprising inhibitors of the androgen receptor and uses thereof
US12109179B2 (en) Pharmaceutical compositions and combinations comprising inhibitors of the androgen receptor and uses thereof
US11485713B2 (en) Androgen receptor modulators and methods for their use
US20230078913A1 (en) Androgen receptor modulators and methods for use as proteolysis targeting chimera ligands
US20220380378A1 (en) Androgen receptor modulators and methods for their use
JP6033835B2 (ja) カルシウム感知受容体モジュレーターとしてのベンゾ［ｂ］［１，４］オキサジン誘導体
US20050165074A1 (en) Amide derivatives as C-KIT modulators
US9446047B2 (en) Substituted 2,3-dihydro-1H-inden-1-one retinoic acid-related orphan nuclear receptor antagonists for treating multiple sclerosis
US20230373934A1 (en) Androgen receptor modulators and methods for their use
RU2797622C2 (ru) Модуляторы андрогенового рецептора и способы их применения
BR112021007222B1 (pt) Compostos moduladores de receptor de androgênio, seus usos, e composições farmacêuticas
JP2009507815A (ja) チアゾール化合物およびｐｇｄ２アンタゴニストとしてのその使用
CZ2022277A3 (cs) Triterpeny s inhibiční aktivitou na Hedgehog signální dráhu pro použití při léčbě nádorových onemocnění

Legal Events

Date Code Title Description
AS Assignment

Owner name: ESSA PHARMA, INC., CANADA

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:ZHOU, HAN-JIE;VIRSIK, PETER;REEL/FRAME:050890/0146

Effective date: 20191022

STPP Information on status: patent application and granting procedure in general

Free format text: RESPONSE TO NON-FINAL OFFICE ACTION ENTERED AND FORWARDED TO EXAMINER

STPP Information on status: patent application and granting procedure in general

Free format text: NOTICE OF ALLOWANCE MAILED -- APPLICATION RECEIVED IN OFFICE OF PUBLICATIONS

STPP Information on status: patent application and granting procedure in general

Free format text: DOCKETED NEW CASE - READY FOR EXAMINATION

STPP Information on status: patent application and granting procedure in general

Free format text: NOTICE OF ALLOWANCE MAILED -- APPLICATION RECEIVED IN OFFICE OF PUBLICATIONS

STPP Information on status: patent application and granting procedure in general

Free format text: AWAITING TC RESP., ISSUE FEE NOT PAID

STPP Information on status: patent application and granting procedure in general

Free format text: NOTICE OF ALLOWANCE MAILED -- APPLICATION RECEIVED IN OFFICE OF PUBLICATIONS

STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO PAY ISSUE FEE

STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO PAY ISSUE FEE