WO2008094912A2 - Substituted gamma lactams as therapeutic agents - Google Patents

Substituted gamma lactams as therapeutic agents Download PDF

Info

Publication number
WO2008094912A2
WO2008094912A2 PCT/US2008/052318 US2008052318W WO2008094912A2 WO 2008094912 A2 WO2008094912 A2 WO 2008094912A2 US 2008052318 W US2008052318 W US 2008052318W WO 2008094912 A2 WO2008094912 A2 WO 2008094912A2
Authority
WO
WIPO (PCT)
Prior art keywords
another embodiment
phenyl
och
compound
pharmaceutically acceptable
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.)
Ceased
Application number
PCT/US2008/052318
Other languages
English (en)
French (fr)
Other versions
WO2008094912A3 (en
WO2008094912B1 (en
Inventor
Wha Bin Im
David W. Old
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.)
Allergan Inc
Original Assignee
Allergan 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 Allergan Inc filed Critical Allergan Inc
Priority to CA2676291A priority Critical patent/CA2676291C/en
Priority to NZ578698A priority patent/NZ578698A/en
Priority to BRPI0808377A priority patent/BRPI0808377B8/pt
Priority to CN200880003507.5A priority patent/CN101595106B/zh
Priority to EP08728470.9A priority patent/EP2121672B1/en
Priority to KR1020097017970A priority patent/KR101561706B1/ko
Priority to US12/524,803 priority patent/US7960381B2/en
Priority to JP2009548391A priority patent/JP5566692B2/ja
Priority to MX2009008039A priority patent/MX2009008039A/es
Priority to AU2008210559A priority patent/AU2008210559B2/en
Publication of WO2008094912A2 publication Critical patent/WO2008094912A2/en
Publication of WO2008094912A3 publication Critical patent/WO2008094912A3/en
Publication of WO2008094912B1 publication Critical patent/WO2008094912B1/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • 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
    • A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A61P17/14—Drugs for dermatological disorders for baldness or alopecia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00—Drugs for disorders of the senses
    • A61P27/02—Ophthalmic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00—Drugs for disorders of the senses
    • A61P27/02—Ophthalmic agents
    • A61P27/06—Antiglaucoma agents or miotics

Definitions

  • Ocular hypotensive agents are useful in the treatment of a number of various ocular hypertensive conditions, such as post-surgical and post-laser trabeculectomy ocular hypertensive episodes, glaucoma, and as presurgical adjuncts.
  • Glaucoma is a disease of the eye characterized by increased intraocular pressure. On the basis of its etiology, glaucoma has been classified as primary or secondary. For example, primary glaucoma in adults (congenital glaucoma) may be either open-angle or acute or chronic angle-closure. Secondary glaucoma results from pre-existing ocular diseases such as uveitis, intraocular tumor or an enlarged cataract.
  • the underlying causes of primary glaucoma are not yet known.
  • the increased intraocular tension is due to the obstruction of aqueous humor outflow.
  • chronic open-angle glaucoma the anterior chamber and its anatomic structures appear normal, but drainage of the aqueous humor is impeded.
  • acute or chronic angle-closure glaucoma the anterior chamber is shallow, the filtration angle is narrowed, and the iris may obstruct the trabecular meshwork at the entrance of the canal of Schlemm. Dilation of the pupil may push the root of the iris forward against the angle, and may produce pupilary block and thus precipitate an acute attack. Eyes with narrow anterior chamber angles are predisposed to acute angle-closure glaucoma attacks of various degrees of severity.
  • Secondary glaucoma is caused by any interference with the flow of aqueous humor from the posterior chamber into the anterior chamber and subsequently, into the canal of Schlemm.
  • Inflammatory disease of the anterior segment may prevent aqueous escape by causing complete posterior synechia in iris bombe, and may plug the drainage channel with exudates.
  • Other common causes are intraocular tumors, enlarged cataracts, central retinal vein occlusion, trauma to the eye, operative procedures and intraocular hemorrhage.
  • glaucoma occurs in about 2% of all persons over the age of 40 and may be asymptotic for years before progressing to rapid loss of vision.
  • topical ⁇ -adrenoreceptor antagonists have traditionally been the drugs of choice for treating glaucoma.
  • Certain eicosanoids and their derivatives are currently commercially available for use in glaucoma management. Eicosanoids and derivatives include numerous biologically important compounds such as prostaglandins and their derivatives. Prostaglandins can be described as derivatives of prostanoic acid which have the following structural formula:
  • prostaglandins are known, depending on the structure and substituents carried on the alicyclic ring of the prostanoic acid skeleton. Further classification is based on the number of unsaturated bonds in the side chain indicated by numerical subscripts after the generic type of prostaglandin [e.g. prostaglandin Ej (PGEj), prostaglandin E2 (PGE2)], and on the configuration of the substituents on the alicyclic ring indicated by ⁇ or ⁇ [e.g. prostaglandin F2 ⁇ (PGF2 ⁇ )].
  • PGEj prostaglandin Ej
  • PGE2 prostaglandin E2
  • PPF2 ⁇ prostaglandin F2 ⁇
  • a compound is disclosed herein comprising
  • Y is -CO 2 (CH 2 ) 2 OH or O .
  • A may be a group which is related to one of these three moieties in that any carbon is replaced with S or O.
  • A may be a moiety where S replaces one or two carbon atoms such as one of the following or the like.
  • A may be a moiety where O replaces one or two carbon atoms such as one of the following or the like.
  • A may have an O replacing one carbon atom and an S replacing another carbon atom, such as one of the following or the like.
  • Interarylene or heterointerarylene refers to an aryl ring or ring system or a heteroaryl ring or ring system which connects two other parts of a molecule, i.e. the two parts are bonded to the ring in two distinct ring positions.
  • Interarylene or heterointerarylene may be substituted or unsubstituted. Unsubstituted interarylene or heterointerarylene has no substituents other than the two parts of the molecule it connects. Substituted interarylene or heterointerarylene has substituents in addition to the two parts of the molecule it connects.
  • Ar is substituted or unsubstituted interphenylene, interthienylene, interfurylene, interpyridinylene, interoxazolylene, and interthiazolylene.
  • Ar is interphenylene (Ph).
  • A is ⁇ (CH 2 ) 2 -Ph-. While not intending to limit scope of the invention in any way, substituents may have 4 or less heavy atoms, wherein the heavy atoms are C, N, O, S, P, F, Cl, Br, and/or I in any stable combination. Any number of hydrogen atoms required for a particular substituent will also be included.
  • a substituent may also have a metal cation or any other stable cation having an atom not listed above if the substituent is acidic and the salt form is stable.
  • -OH may form an -(TNa + salt or CO 2 H may form a CO 2 K + salt. Any cation of the salt is not counted in the "4 or less heavy atoms.”
  • the substituent may be hydrocarbyl, i.e.
  • A is -(CH 2 ) m -Ph-(CH 2 ) 0 - wherein the sum of m and 0 is 1 , 2, or 3, and wherein one CH 2 may be replaced with S or O.
  • A is -CH 2 -Ar-OCH 2 -. In another embodiment A is -CH 2 -Ph-OCH 2 -. In another embodiment, Ph is attached at the 1 and 3 positions, otherwise known as m-interphenylene, such as when A has the structure shown below.
  • Ar is thienyl
  • A has one of the following structures
  • A is -CH 2 -Ph-OCH 2 -, wherein Ph is interphenylene,.
  • A is -CH 2 -mPh-OCH 2 -, wherein mPh is w-interphenylene.
  • A is -CH 2 -O-(CH2) 4 -. In another embodiment A is -CH 2 -O-CH 2 -Ar-, wherein Ar is 2,5-interthienylene.
  • A is -CH 2 -O-CH 2 -Ar-, wherein Ar is 2,5-interfurylene.
  • A is (3-methylphenoxy)methyl.
  • A is (4-but-2-ynyloxy)methyl.
  • A is 2-(2-ethylthio)thiazol-4-yl. In another embodiment A is 2-(3-propyl)thiazol-5-yl.
  • A is 3-(methoxymethyl)phenyl.
  • A is 3-(3-propylphenyl).
  • A is 3-methylphenethyl.
  • A is 4-(2-ethyl)phenyl. In another embodiment A is 4-phenethyl.
  • A is 4-methoxybutyl.
  • A is 5-(methoxymethyl)furan-2-yl .
  • A is 5-(methoxymethyl)thiophen-2-yl.
  • A is 5-(3-propyl)furan-2-yl. In another embodiment A is 5-(3-propyl)thiophen-2-yl.
  • A is 6-hexyl
  • A is (Z)-6-hex-4-enyl.
  • B is aryl or heteroaryl.
  • Aryl is an unsubstituted or substituted aromatic ring or ring system such as phenyl, naphthyl, biphenyl, and the like.
  • Heteroaryl is aryl having one or more N, O, or S atoms in the ring, i.e. a ring carbon is substituted by N, O, or S.
  • heteroaryl include unsubstituted or substituted thienyl, pyridinyl, furyl, benzothienyl, benzoruryl, imidizololyl, indolyl, and the like.
  • the substituents of aryl or heteroaryl may have up to 12 non-hydrogen atoms each and as many hydrogen atoms as necessary.
  • the substituents may be: hydrocarbyl. i.e.
  • a moiety consisting of only carbon and hydrogen such as alkyl, alkenyl, alkynyl, and the like, including linear, branched or cyclic hydrocarbyl, and combinations thereof; hydrocarbyloxy, meaning O-hydrocarbyl such as OCH 3 , OCH 2 CH 3 , O-cyclohexyl, etc, up to 11 carbon atoms; other ether substituents such as CH 2 OCH 3 , (CH 2 ) 2 OCH(CH 3 ) 2 , and the like; thioether substituents including S-hydrocarbyl and other thioether substituents; hvdroxyhvdrocarbyl.
  • hydrocarbyl-OH such as CH 2 OH, C(CH 3 ) 2 OH, etc, up to 11 carbon atoms; nitrogen substituents such as NO 2 , CN, and the like, including amino, such as NH 2 , NH(CH 2 CH 3 OH), NHCH 3 , and the like up to 1 1 carbon atoms; carbonyl substituents.
  • halogen such as chloro, fluoro, bromo, and the like fluorocarbyl, such as CF 3 , CF 2 CF 3 , etc.
  • phosphorous substituents such as PO 3 2* , and the like
  • sulfur substituents including S-hydrocarbyl, SH, SO 3 H, SO 2 -hydrocarbyl, SO 3 -hydrocarbyl, and the like.
  • the number of non-hydrogen atoms is 6 or less in a substituent. In other embodiments, the number of non-hydrogen atoms is 3 or less in a substituent. In other embodiments, the number of non-hydrogen atoms on a substituent is 1.
  • the substituents contain only hydrogen, carbon, oxygen, halogen, nitrogen, and sulfur. In other embodiments, the substituents contain only hydrogen, carbon, oxygen, and halogen.
  • references to aryl, heteroaryl, phenyl, thienyl, benzothienyl, and the like are intended to mean both the substituted and the unsubstituted moiety.
  • Substituted aryl or heteroaryl may have one or more substituents, up to as many as the ring or ring system will bear, and the substituents may be the same or different.
  • an aryl ring or a heteroaryl ring may be substituted with chloro and methyl; methyl, OH, and F; CN, NO 2 , and ethyl; and the like including any conceivable substituent or combination of substituent possible in light of this disclosure.
  • B is phenyl.
  • B is chlorophenyl, meaning phenyl with one or more chloro substituents.
  • D is 3,5-dichlorophenyl.
  • B is unsubstituted phenyl.
  • B is alkylphenyl.
  • B is t- butylphenyl.
  • B is not unsubstituted phenyl. In another embodiment B is not chlorophenyl. In another embodiment B is not fluorophenyl. In another embodiment B is not dimethylaminophenyl. In another embodiment B is not unsubstituted phenyl, chlorophenyl, fluorophenyl, or dimethylaminophenyl. In another embodiment B is hydroxyalkylphenyl, meaning phenyl with a hydroxyalkyl substitutuent such as Ph-CH(OH)C(CH 3 ) 3 .
  • B can also be any of the groups shown below, where the remainder of the molecule attaches to the phenyl ring. The names of these moieties are shown to the right of the structure. ( 1 -hydroxyhexy l)phenyl
  • One compound comprises
  • Another embodiment comprises
  • R 4 and R 5 are independently H or Ci -6 alkyl.
  • R 4 and R 5 may be two separate moieties.
  • R 4 and R 5 is methyl, and no bond is present where indicated by the dashed line.
  • R 4 and R 5 may form a ring.
  • a compound such as the one shown below is possible, wherein x is from 1 to 6.
  • a pharmaceutically acceptable salt, prodrug, or a metabolite thereof is also contemplated.
  • Another embodiment comprises
  • a pharmaceutically acceptable salt, prodrug, or a metabolite thereof is also contemplated.
  • Other useful compounds comprise
  • a pharmaceutically acceptable salt, prodrug, or a metabolite thereof is also contemplated.
  • Other useful examples of compounds comprise
  • R 6 is cycloalkyl comprising from 3 to 10 carbon atoms.
  • Other compounds comprise
  • R 7 is linear alkyl comprising from 3 to 7 carbon atoms.
  • Other compounds comprise
  • X 1 and X 2 are independently CH, O, or S; and R 7 is linear alkyl comprising from 3 to 7 carbon atoms.
  • Other compounds comprise
  • X 1 and X 2 are independently CH, O, or S.
  • Other compounds comprise or a pharmaceutically acceptable salt, prodrug, or a metabolite thereof.
  • Other compounds comprise
  • Another useful compound is
  • Another useful compound is
  • Another compound comprises
  • Another compound comprises
  • Another compound comprises
  • R is hydrocarbyl or hydroxyhydrocarbyl having from 1 to 12 carbon atoms
  • X is CH 2 , O, or S
  • G is 1 ,3-interaryl or interheteroaryl, or -(CH 2 ) 3 -.
  • A is -S(CH 2 ) 3 S(CH 2 ) 2 - and B is phenyl.
  • A is -(CH 2 ) 4 OCH 2 - and B is phenyl.
  • A is -(CH 2 ) 2 S(CH 2 ) 3 - and B is phenyl.
  • A is -CH 2 -Ph-OCH 2 -, wherein Ph is interphenylene, and B is phenyl.
  • A is -CH 2 -mPh-OCH 2 -, wherein mPh is /w-interphenylene, and B is phenyl.
  • A is -CH 2 -O-(CH 2 ⁇ - and B is phenyl.
  • A is -CH 2 -O-CH 2 -Ar-, wherein Ar is 2,5-interthienylene, and B is phenyl.
  • A is -CH 2 -O-CH 2 -Ar-, wherein Ar is 2,5-interfurylene, and B is phenyl.
  • phenyl in the above embodiments means substituted or unsubstituted phenyl unless indicated otherwise.
  • A is -S(CH 2 ) 3 S(CH 2 ) 2 - and B is (l-hydroxyhexyl)phenyl.
  • A is -(CH 2 ) 4 OCH 2 - and B is ( l-hydroxyhexyl)phenyl.
  • A is -CH 2 CH ⁇ CH-CH 2 OCH 2 - and B is (l-hydroxyhexyl)phenyl.
  • A is -(CH 2 ) 2 S(CH 2 ) 3 - and B is (l-hydroxyhexyl)phenyl.
  • A is -CH 2 -Ph-OCH 2 -, wherein Ph is interphenylene, and B is ( 1 - hydroxyhexyl)phenyl.
  • A is -CH 2 -mPh-OCH 2 -, wherein mPh is m-interphenylene, and B is ( 1 -hydroxyhexyl)phenyl.
  • A is -CH 2 -O-(CH 2 ) 4 - and B is (l-hydroxyhexyl)phenyl.
  • A is -CH 2 -O-CH 2 -Ar-, wherein Ar is 2,5-interthienylene, and B is (1- hydroxyhexyl)phenyl.
  • A is -CH 2 -O-CH 2 -Ar-, wherein Ar is 2,5-interfurylene, and B is (1- hydroxyhexyl)phenyl.
  • A is -S(CH 2 ) 3 S(CH 2 ) 2 - and B is (l-hydroxy-2,2- dimethylpropyl)phenyl.
  • A is -(CH?) 4 OCH 2 - and B is (l-hydroxy-2,2-dimethylpropyl)phenyl.
  • A is -CH 2 CH ⁇ CH-CH 2 OCH 2 - and B is (l-hydroxy-2,2- dimethylpropyOphenyl.
  • A is -(CH 2 ) 2 S(CH 2 ) 3 - and B is (l-hydroxy-2,2-dimethylpropyl)phenyl.
  • A is -CH 2 -Ph-OCH 2 -, wherein Ph is interphenylene, and B is (1- hydroxy-2,2-dimethylpropyl)phenyl.
  • A is -CH 2 -mPh-OCH 2 -, wherein mPh is w-interphenylene, and B is ( 1 -hydroxy-2,2-dimethylpropyl)phenyl.
  • A is -CH 2 -O-(CH 2 ) 4 - and B is (l-hydroxy-2,2-dimethylpropyl)phenyl.
  • A is -CH 2 -O-CH 2 -Ar-, wherein Ar is 2,5-interthienylene, and B is (1- hydroxy-2,2-dimethylpropyl)phenyl.
  • A is -CH 2 -O-CH 2 -Ar-, wherein Ar is 2,5-interfurylene, and B is (1- hydroxy-2,2-dimethylpropyl)phenyl.
  • A is -S(CH 2 ) 3 S(CH 2 ) 2 - and B is (l-hydroxy-2-methylpropyl)phenyl.
  • A is -(CH 2 ) 4 OCH 2 - and B is (l-hydroxy-2-methylpropyI)phenyl.
  • A is -(CH 2 ) 2 S(CH 2 ) 3 - and B is (l-hydroxy-2-methylpropyl)phenyl.
  • A is -CH 2 -Ph-OCH 2 -, wherein Ph is interphenylene, and B is (1- hydroxy-2-methylpropyl)phenyl.
  • A is -CH 2 -mPh-OCH 2 -, wherein mPh is m-interphenylene, and B is ( 1 -hydroxy-2-methylpropyl)phenyl.
  • A is -CH 2 -O-(CHi) 4 - and B is (l-hydroxy-2-methylpropyl)phenyl.
  • A is -CH 2 -O-CH 2 -Ar-, wherein Ar is 2,5-interthienylene, and B is (1- hydroxy-2 -methy lpropy l)pheny 1.
  • A is -CH 2 -O-CH 2 -Ar-, wherein Ar is 2,5-interfurylene, and B is (1- hydroxy-2-methylpropyl)phenyl.
  • A is -S(CH 2 ) 3 S(CH 2 ) 2 - and B is (hydroxymethyl)phenyl.
  • A is -(CH 2 ) 4 OCH 2 - and B is (hydroxymethyl)phenyl.
  • A is -CH 2 CH ⁇ CH-CH 2 OCH 2 - and B is (hydroxymethyl)phenyl.
  • A is -(CH 2 ) 2 S(CH?) 3 - and B is (hydroxymethyl) ⁇ henyl.
  • A is -CH 2 -Ph-OCH 2 -, wherein Ph is interphenylene, and B is (hydroxymethyl)phenyl.
  • A is -CH 2 -ITiPh-OCH 2 -, wherein mPh is w-interphenylene, and B is (hydroxymethyl)phenyl.
  • A is -CH 2 -O-(CH 2 ) 4 - and B is (hydroxymethyl)phenyl.
  • A is -CH 2 -O-CH 2 -Ar-, wherein Ar is 2,5-interthienylene, and B is (hydroxymethyl)phenyl.
  • A is -CH 2 -O-CH 2 -Ar-, wherein Ar is 2,5-interfurylene, and B is (hydroxymethyl)phenyl.
  • A is -S(CH 2 ) 3 S(CH 2 ) 2 - and B is [(I - propylcyclobutyl)hydroxymethyl]phenyl.
  • A is -(CH 2 ) 4 OCH 2 - and B is [(I - propylcyclobutyl)hydroxymethyl]phenyl.
  • A is -(CH 2 ) 2 S(CH 2 ) 3 - and B is [(I - propylcyclobutyl)hydroxymethyl]phenyl.
  • A is -CH 2 -Ph-OCH 2 -, wherein Ph is interphenylene, and B is [(I - propylcyclobutyl)hydroxymethyl]phenyl.
  • A is -CH 2 -ITiPh-OCH 2 -, wherein mPh is m-interphenylene, and B is [( 1 -propylcyclobutyOhydroxymethy l]pheny 1.
  • A is -CH 2 -O-(CH 2 ),,- and B is [( 1 - propylcyclobutyl)hydroxymethyl]phenyl.
  • A is -CH 2 -O-CH 2 -Ar-, wherein Ar is 2,5-interthienylene, and B is [( 1- propylcyclobutyl)hydroxymethyl]phenyl.
  • A is -CH 2 -O-CH 2 -Ar-, wherein Ar is 2,5-interf ⁇ irylene, and B is [(I - propylcyclobutyl)hydroxymethyl]phenyl.
  • A is -S(CH 2 ) 3 S(CH 2 ) 2 - and B is t-butylphenyl.
  • A is -(CH 2 ) 4 OCH 2 - and B is t-butylphenyl.
  • A is -(CH 2 ) 2 S(CH 2 ) 3 - and B is t-butylphenyl.
  • A is -CH 2 -Ph-OCH 2 -, wherein Ph is interphenylene, and B is t- butylphenyl.
  • A is -CH 2 -mPh-OCH 2 -, wherein mPh is /n-interphenylene, and B is t- butylphenyl.
  • A is -CH 2 -O-(CH 2 ) 4 - and B is t-butylphenyl.
  • A is -CH 2 -O-CH 2 -Ar-, wherein Ar is 2,5-interthienylene, and B is t- butylphenyl.
  • A is -CH 2 -O-CH 2 -Ar-, wherein Ar is 2,5-interfurylene, and B is t- butylphenyl.
  • A is -S(CH 2 ) 3 S(CH 2 ) 2 - and B is (cyclohexylhydroxymethyl)phenyl.
  • A is -(CH 2 ) 4 OCH 2 - and B is (cyclohexylhydroxymethyl)phenyl.
  • A is -(CH 2 ) 2 S(CH 2 ) 3 - and B is (cyclohexylhydroxymethy ⁇ phenyl.
  • A is -CH 2 -Ph-OCH 2 -, wherein Ph is interphenylene, and B is (cyclohexylhydroxymethyOphenyl.
  • A is -CH 2 -mPh-OCH 2 -, wherein mPh is /w-interphenylene, and B is (cyclohexylhydroxymethyl)phenyl.
  • A is -CH 2 -O-(CH 2 ) 4 - and B is (cyclohexylhydroxymethyl)phenyl.
  • A is -CH 2 -O-CH 2 -Ar-, wherein Ar is 2,5-interthienylene, and B is (cyclohexylhydroxymethy l)phenyl.
  • A is -CH 2 -O-CH 2 -Ar-, wherein Ar is 2,5-interfurylene, and B is (cyclohexylhydroxymethyl)phenyl.
  • A is -S(CH 2 ) 3 S(CH 2 ) 2 - and B is (cyclohexylmethyl)phenyl.
  • A is -(CH 2 ) 4 OCH 2 - and B is (cyclohexylmethyl)phenyl.
  • A is -CH 2 CH ⁇ CH-CH 2 OCH 2 - and B is (cyclohexylmethyl)phenyl.
  • A is -(CH 2 ) 2 S(CH 2 ) 3 - and B is (cyclohexylmethyl)phenyl.
  • A is -CH 2 -Ph-OCH 2 -, wherein Ph is interphenylene, and B is (cyclohexylmethyOphenyl.
  • A is -CH 2 -mPh-OCH 2 -, wherein mPh is w-interphenylene, and B is (cyclohexylmethyl)phenyl.
  • A is -CH 2 -O-(CH 2 ) 4 - and B is (cyclohexylmethyl)phenyl.
  • A is -CH 2 -O-CH 2 -Ar-, wherein Ar is 2,5-interthienylene, and B is (cyclohexylmethyl)phenyl.
  • A is -CH 2 -O-CH 2 -Ar-, wherein Ar is 2,5-interfurylene, and B is (cyclohexylmethyl)phenyl.
  • A is -S(CH 2 ) 3 S(CH 2 ) 2 - and B is indanyl.
  • A is -(CH 2 ) 4 OCH 2 - and B is indanyl.
  • A is -(CH 2 ) 2 S(CH 2 ) 3 - and B is indanyl.
  • A is -CH 2 -Ph-OCH 2 -, wherein Ph is interphenylene, and B is indanyl.
  • A is -CH 2 -mPh-OCH 2 -, wherein mPh is m-interphenylene, and B is indanyl.
  • A is -CH 2 -O-(CH 2 ) 4 - and B is indanyl.
  • A is -CH 2 -O-CH 2 -Ar-, wherein Ar is 2,5-interthienylene, and B is indanyl.
  • A is -CH 2 -O-CH 2 -Ar-, wherein Ar is 2,5-interfurylene, and B is indanyl.
  • A is -S(CH 2 ) 3 S(CH 2 ) 2 - and B is indanolyl.
  • A is -(CH 2 ) 4 OCH 2 - and B is indanolyl.
  • A is -CH 2 -Ph-OCH 2 -, wherein Ph is interphenylene, and B is indanolyl.
  • A is -CH 2 -mPh-OCH 2 -, wherein mPh is m-interphenylene, and B is indanolyl.
  • A is -CH 2 -O-(CH 2 ) 4 - and B is indanolyl.
  • A is -CH 2 -O-CH 2 -Ar-, wherein Ar is 2,5-interthienylene, and B is indanolyl.
  • A is -CH 2 -O-CH 2 -Ar-, wherein Ar is 2,5-interfurylene, and B is indanolyl.
  • A is -S(CH 2 ) 3 S(CH 2 ) 2 - and B is indanonyl.
  • A is -(CH 2 ) 4 OCH 2 - and B is indanonyl.
  • A is -CH 2 -Ph-OCH 2 -, wherein Ph is interphenylene, and B is indanonyl.
  • A is -CH 2 -mPh-OCH 2 -, wherein mPh is m-interphenylene, and B is indanonyl.
  • A is -CH 2 -O-(CH 2 ) 4 - and B is indanonyl.
  • A is -CH 2 -O-CH 2 -Ar-, wherein Ar is 2,5-interthienylene, and B is indanonyl.
  • A is -CH 2 -O-CH 2 -Ar-, wherein Ar is 2,5-interfurylene, and B is indanonyl.
  • A is -S(CH?) 3 S(CH 2 ) 2 - and B is (l-hydroxycyclobutyl)phenyl.
  • A is -(CH 2 ) 4 OCH 2 - and B is (l-hydroxycyclobutyl)phenyl.
  • A is -CH 2 CH ⁇ CH-CH 2 OCH 2 - and B is ( l-hydroxycyclobutyl)phenyl.
  • A is -(CH 2 ) 2 S(CH 2 ) 3 - and B is (l-hydroxycyclobutyl)phenyl.
  • A is -CH 2 -Ph-OCH 2 -, wherein Ph is interphenylene, and B is ( 1 - hydroxycyclobutyOphenyl.
  • A is -CH 2 -mPh-OCH 2 -, wherein mPh is /n-interphenylene, and B is ( 1 -hydroxycyclobutyOphenyl.
  • A is -CH 2 -O-(CH 2 V and B is (1 -hydroxycyclobutyOphenyl.
  • A is -CH 2 -O-CH 2 -Ar-, wherein Ar is 2,5-interthienylene, and B is (1- hy droxy cy c lobuty l)pheny 1.
  • A is -CH 2 -O-CH 2 -Ar-, wherein Ar is 2,5-interfurylene, and B is (1- hy droxy eye lobuty l)pheny 1.
  • A is -S(CH 2 ) 3 S(CH 2 ) 2 - and B is (2-methyl-3-hydroxypropyl)phenyl.
  • A is -(CH 2 ) 4 OCH 2 - and B is (2-methyl-3-hydroxypropyl)phenyl.
  • A is -CH 2 CH ⁇ CH-CH 2 OCH 2 - and B is (2-methyl-3- hydroxypropyl)phenyl.
  • A is -(CH 2 ) 2 S(CH 2 ) 3 - and B is (2-methyl-3-hydroxypropyl)phenyl.
  • A is -CH 2 -Ph-OCH 2 -, wherein Ph is interphenylene, and B is (2- methyl-3 -hydroxypropyl)phenyl.
  • A is -CH 2 -InPh-OCH 2 -, wherein mPh is /n-interphenylene, and B is (2-methyl-3-hydroxypropyl)phenyl.
  • A is -CH 2 -O-(CH 2 J 4 - and B is (2-methyl-3-hydroxypropyl)phenyl.
  • A is -CH 2 -O-CH 2 -Ar-, wherein Ar is 2,5-interthienylene, and B is (2- methyl-3 -hydroxypropyl)pheny 1.
  • A is -CH 2 -O-CH 2 -Ar-, wherein Ar is 2,5-interfurylene, and B is (2- methyl-3 -hydroxypropyl)pheny 1.
  • A is -S(CH 2 ) 3 S(CH 2 ) 2 - and B is (l-hydroxy-2-phenylethyl)phenyl.
  • A is -(CH 2 ) 4 OCH 2 - and B is (l-hydroxy-2-phenylethyl)phenyl.
  • A is -CH 2 CH ⁇ CH-CH 2 OCH 2 - and B is ( l-hydroxy-2- phenylethyl)phenyl.
  • A is -(CH 2 ) 2 S(CH 2 ) 3 - and B is (l-hydroxy-2-phenylethyl)phenyl.
  • A is -CH 2 -Ph-OCH 2 -, wherein Ph is interphenylene, and B is (1- hydroxy-2 -pheny lethy l)pheny 1.
  • A is -CH 2 -mPh-OCH 2 -, wherein mPh is /w-interphenylene, and B is ( 1 -hydroxy-2-phenylethyl)phenyl.
  • B is ( 1 -hydroxy-2-phenylethyl)phenyl.
  • A is -CH 2 -O-(CH 2 ) 4 - and B is (l-hydroxy-2-phenylethyl)phenyl.
  • A is -CH 2 -O-CH 2 -Ar-, wherein Ar is 2,5-interthienylene, and B is (1- hydroxy-2-phenylethyl)phenyl.
  • A is -CH 2 -O-CH 2 -Ar-, wherein Ar is 2,5-interfurylene, and B is (1- hydroxy-2-phenylethyl)phenyl.
  • the compounds of disclosed herein are useful for the prevention or treatment of glaucoma or ocular hypertension in mammals, or for the manufacture of a medicament for the treatment of glaucoma or ocular hypertension.
  • a "pharmaceutically acceptable salt” is any salt that retains the activity of the parent compound and does not impart any additional deleterious or untoward effects on the subject to which it is administered and in the context in which it is administered compared to the parent compound.
  • a pharmaceutically acceptable salt also refers to any salt which may form in vivo as a result of administration of an acid, another salt, or a prodrug which is converted into an acid or salt.
  • These compounds are also useful for growing hair, including one or more of: increasing the number of individual hairs, increasing the length of individual hairs, and increasing the width or thickness of individual hairs. These compounds are also useful for improving the appearance of hair, including increasing its gloss, shine, or other properties related to the reflection or dispersion of light, as well as changing the color of hair, including changing hair from grey or white to the color the hair was before it turned grey or white, such as red, brown, or black.
  • Pharmaceutically acceptable salts of acidic functional groups may be derived from organic or inorganic bases.
  • the salt may comprise a mono or polyvalent ion.
  • the inorganic ions lithium, sodium, potassium, calcium, and magnesium.
  • Organic salts may be made with amines, particularly ammonium salts such as mono-, di- and trialkyl amines or ethanol amines. Salts may also be formed with caffeine, tromethamine and similar molecules.
  • Hydrochloric acid or some other pharmaceutically acceptable acid may form a salt with a compound that includes a basic group, such as an amine or a pyridine ring.
  • "treat,” “treating,” or “treatment” refer to the use of a compound, composition, therapeutically active agent, or drug in the diagnosis, cure, mitigation, treatment, prevention of disease or other undesirable condition.
  • esterification method exemplified below is useful for a range of carboxylic acids.
  • any carboxylic acid prepared as described in United States Patent Application Serial No. 10/599046, filed on September 18, 2006, incorporated by reference herein, may be used.
  • Triethylamine (17.5 ⁇ L, 0.13 mmol) and ethyl chloroformate (6 ⁇ L, 0.063 mmol) were added sequentially to a solution 5-(3- ⁇ (S)-H4-(l-hydroxyhexyl)-phenyl]-5-oxo-pyrrolidin-2-yl ⁇ -propyl)- thiophene-2-carboxylic acid (derived from the faster eluting [HPLC] ester diastereomer, see US 10/599,046 or United States Provisional Patent Application No. 60/777,506, filed on February 28, 2006, incorporated by reference herein, 18 mg, 0.042 mmol) in CH 2 Cl 2 (0.6 mL) at 0 0 C.
  • Triethylamine (17.5 ⁇ L, 0.13 mmol) and ethyl chloroformate (6 ⁇ L, 0.063 mmol) were added sequentially to a solution of 5-(3- ⁇ (S)-l-[4-(l-hydroxyhexyl)-phenyl]-5-oxo-pyrrolidin-2-yl ⁇ -propyl)- thiophene-2-carboxylic acid (derived from the faster eluting [HPLC] ester diastereomer, see US 10/599046 or US 60/777,506, 18 mg, 0.042 mmol) in CH 2 Cl 2 (0.6 mL) at 0 0 C. The mixture was allowed to warm to room temperature.
  • Triethylamine (60 ⁇ L, 0.43 mmol) and ethyl chloroformate (21 ⁇ L, 0.22 mmol) were added sequentially to a solution of 9 (60 mg, 0.145 mmol) in CH 2 Cl 2 (2 mL) at 0 0 C.
  • the mixture was allowed to warm to rt. After 30 min at rt, ethylene glycol (81 ⁇ L, 1.45 mmol) was added. After stirring 3 days at room temperature, the reaction mixture was concentrated under a stream of nitrogen. The residue was diluted with EtOAc (50 mL) and washed with H 2 O (2x25 mL) and brine (25 mL).
  • Compound 1 was also tested in normotensive dogs at 0.001%, dosing once daily for 5 days.
  • the maximum intraocular pressure (IOP) decrease from baseline was 3.75 mmHg (23%) at 76 h; the maximum ocular surface hyperemia (OSH) score was 1.1 at 74 h.
  • Compound 1 was also tested in laser-induced hypertensive monkeys, using one single day dose. At 0.001%, the maximum IOP decrease from baseline was 12.7 mmHg (31%) at 24 h.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (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)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Ophthalmology & Optometry (AREA)
  • Dermatology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Hydrogenated Pyridines (AREA)
PCT/US2008/052318 2007-01-31 2008-01-29 Substituted gamma lactams as therapeutic agents Ceased WO2008094912A2 (en)

Priority Applications (10)

Application Number Priority Date Filing Date Title
CA2676291A CA2676291C (en) 2007-01-31 2008-01-29 Substituted gamma lactams as therapeutic agents
NZ578698A NZ578698A (en) 2007-01-31 2008-01-29 Substituted gamma lactams as therapeutic agents
BRPI0808377A BRPI0808377B8 (pt) 2007-01-31 2008-01-29 composto, composição e uso de um composto
CN200880003507.5A CN101595106B (zh) 2007-01-31 2008-01-29 作为治疗药物的取代的γ内酰胺
EP08728470.9A EP2121672B1 (en) 2007-01-31 2008-01-29 Substituted gamma lactams as therapeutic agents
KR1020097017970A KR101561706B1 (ko) 2007-01-31 2008-01-29 치료제로서의 치환된 감마 락탐
US12/524,803 US7960381B2 (en) 2007-01-31 2008-01-29 Substituted gamma lactams as therapeutic agents
JP2009548391A JP5566692B2 (ja) 2007-01-31 2008-01-29 治療薬としての置換ガンマラクタム類
MX2009008039A MX2009008039A (es) 2007-01-31 2008-01-29 Gamma lactamas substituidas como agentes terapeuticos.
AU2008210559A AU2008210559B2 (en) 2007-01-31 2008-01-29 Substituted gamma lactams as therapeutic agents

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US88741507P 2007-01-31 2007-01-31
US60/887,415 2007-01-31

Publications (3)

Publication Number Publication Date
WO2008094912A2 true WO2008094912A2 (en) 2008-08-07
WO2008094912A3 WO2008094912A3 (en) 2008-10-09
WO2008094912B1 WO2008094912B1 (en) 2008-11-20

Family

ID=39639429

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2008/052318 Ceased WO2008094912A2 (en) 2007-01-31 2008-01-29 Substituted gamma lactams as therapeutic agents

Country Status (11)

Country Link
US (1) US7960381B2 (enExample)
EP (1) EP2121672B1 (enExample)
JP (1) JP5566692B2 (enExample)
KR (1) KR101561706B1 (enExample)
CN (1) CN101595106B (enExample)
AU (1) AU2008210559B2 (enExample)
BR (1) BRPI0808377B8 (enExample)
CA (1) CA2676291C (enExample)
MX (1) MX2009008039A (enExample)
NZ (1) NZ578698A (enExample)
WO (1) WO2008094912A2 (enExample)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2009097223A1 (en) * 2008-01-29 2009-08-06 Allergan, Inc. Substituted gamma lactams as therapeutic agents
WO2009132097A1 (en) * 2008-04-24 2009-10-29 Allergan, Inc. Substituted gamma lactams as therapeutic agents
WO2009132085A1 (en) * 2008-04-24 2009-10-29 Allergan, Inc. Substituted arylcyclopentenes as prostaglandin ep2 agonists
US8124648B2 (en) * 2008-05-20 2012-02-28 Allergan, Inc. Therapeutic lactams

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102076681A (zh) * 2008-04-24 2011-05-25 阿勒根公司 作为治疗剂的取代γ-内酰胺
RU2010149494A (ru) * 2008-05-09 2012-06-20 Аллерган, Инк. (Us) Терапевтические замещенные тиазолидиноны, оксазолидиноны и родственные соединения

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20040015364A (ko) * 2001-07-16 2004-02-18 에프. 호프만-라 로슈 아게 Ｅｐ4 수용체 작용물질로서의 프로스타글란딘 유사체
CN1617868A (zh) * 2001-11-05 2005-05-18 阿勒根公司 作为EP2－受体激动剂的ω－环烷基17－杂芳基前列腺素E2 类似物
NZ535024A (en) * 2002-03-05 2006-10-27 Ono Pharmaceutical Co 8-azaprostaglandin derivative compound and agent comprising the compound as active ingredient
US6573294B1 (en) * 2002-05-14 2003-06-03 Allergan, Inc. 8-azaprostaglandin analogs as agents for lowering intraocular pressure
EP1556347A4 (en) * 2002-06-10 2006-08-09 Applied Research Systems GAMMA LACTAME AS PROSTAGLAND INAGONISTS AND THEIR USE
US7091231B2 (en) * 2004-12-10 2006-08-15 Allergan, Inc. 12-Aryl prostaglandin analogs
BRPI0609021A2 (pt) * 2005-03-10 2010-01-12 Allergan Inc gama lactamas substituìdas, composição e uso das mesmas
EP1996546B1 (en) * 2006-03-20 2014-11-26 Allergan, Inc. Substituted gamma lactams as prostaglandin ep2 agonists

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
None

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2009209330B2 (en) * 2007-01-31 2014-05-01 Allergan, Inc. Substituted gamma lactams as therapeutic agents
WO2009097223A1 (en) * 2008-01-29 2009-08-06 Allergan, Inc. Substituted gamma lactams as therapeutic agents
US8377984B2 (en) 2008-01-29 2013-02-19 Allergan, Inc. Substituted gamma lactams as therapeutic agents
WO2009132097A1 (en) * 2008-04-24 2009-10-29 Allergan, Inc. Substituted gamma lactams as therapeutic agents
WO2009132085A1 (en) * 2008-04-24 2009-10-29 Allergan, Inc. Substituted arylcyclopentenes as prostaglandin ep2 agonists
US7713968B2 (en) 2008-04-24 2010-05-11 Allergan, Inc. Substituted arylcyclopentenes as therapeutic agents
US8124648B2 (en) * 2008-05-20 2012-02-28 Allergan, Inc. Therapeutic lactams

Also Published As

Publication number Publication date
EP2121672A2 (en) 2009-11-25
NZ578698A (en) 2012-04-27
BRPI0808377B8 (pt) 2021-05-25
EP2121672B1 (en) 2014-12-10
CN101595106B (zh) 2014-05-07
KR101561706B1 (ko) 2015-10-19
JP2010516817A (ja) 2010-05-20
CA2676291C (en) 2017-11-28
US20100093729A1 (en) 2010-04-15
MX2009008039A (es) 2009-08-18
JP5566692B2 (ja) 2014-08-06
KR20090104905A (ko) 2009-10-06
US7960381B2 (en) 2011-06-14
WO2008094912A3 (en) 2008-10-09
AU2008210559A1 (en) 2008-08-07
WO2008094912B1 (en) 2008-11-20
CN101595106A (zh) 2009-12-02
BRPI0808377A2 (pt) 2014-07-08
CA2676291A1 (en) 2008-08-07
AU2008210559B2 (en) 2014-03-06
BRPI0808377B1 (pt) 2020-01-21

Similar Documents

Publication Publication Date Title
EP2121672B1 (en) Substituted gamma lactams as therapeutic agents
AU2007249443B2 (en) Isothiazolidines useful in the treatment of ocular hypertensive conditions
WO2008028032A2 (en) Therapeutic substituted hydantoins and related compounds
CA2653223C (en) Therapeutic pyrrolidine compounds
US8440819B2 (en) Therapeutic substituted beta-lactams
AU2009244325B2 (en) Therapeutic substituted thiazolidinones, oxazolidinones, and related compounds
AU2008216499B2 (en) Gamma-lactams for the treatment of glaucoma or elevated intraocular pressure
WO2009114744A1 (en) Therapeutic compounds
WO2009137343A1 (en) Therapeutic substituted hydantoins, and related compounds
WO2009105438A1 (en) Therapeutic substituted lactams
WO2009137339A2 (en) Therapeutic n-aryl or n-heteroaryl pyrazolidine and pyrazolidinone derivatives
EP2257548A1 (en) Therapeutic compounds

Legal Events

Date Code Title Description
WWE Wipo information: entry into national phase

Ref document number: 200880003507.5

Country of ref document: CN

WWE Wipo information: entry into national phase

Ref document number: 2676291

Country of ref document: CA

WWE Wipo information: entry into national phase

Ref document number: 4840/DELNP/2009

Country of ref document: IN

WWE Wipo information: entry into national phase

Ref document number: 2008210559

Country of ref document: AU

WWE Wipo information: entry into national phase

Ref document number: 12524803

Country of ref document: US

Ref document number: MX/A/2009/008039

Country of ref document: MX

WWE Wipo information: entry into national phase

Ref document number: 578698

Country of ref document: NZ

ENP Entry into the national phase

Ref document number: 2009548391

Country of ref document: JP

Kind code of ref document: A

NENP Non-entry into the national phase

Ref country code: DE

WWE Wipo information: entry into national phase

Ref document number: 2008728470

Country of ref document: EP

ENP Entry into the national phase

Ref document number: 2008210559

Country of ref document: AU

Date of ref document: 20080129

Kind code of ref document: A

WWE Wipo information: entry into national phase

Ref document number: 1020097017970

Country of ref document: KR

121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 08728470

Country of ref document: EP

Kind code of ref document: A2

ENP Entry into the national phase

Ref document number: PI0808377

Country of ref document: BR

Kind code of ref document: A2

Effective date: 20090729