US20190298705A1 - Chemical Compounds - Google Patents

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Publication number
US20190298705A1
US20190298705A1 US16/307,507 US201716307507A US2019298705A1 US 20190298705 A1 US20190298705 A1 US 20190298705A1 US 201716307507 A US201716307507 A US 201716307507A US 2019298705 A1 US2019298705 A1 US 2019298705A1
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United States
Prior art keywords
chlorophenoxy
acetamide
piperidin
disease
cancer
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
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US16/307,507
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English (en)
Inventor
Jeffrey Michael Axten
Mui Cheung
Michael P. DeMartino
Hilary Schenck Eidam
Raghava Reddy Kethiri
Biswajit KALITA
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.)
GlaxoSmithKline Intellectual Property Development Ltd
Original Assignee
GlaxoSmithKline Intellectual Property Development Ltd
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 GlaxoSmithKline Intellectual Property Development Ltd filed Critical GlaxoSmithKline Intellectual Property Development Ltd
Assigned to GLAXOSMITHKLINE INTELLECTUAL PROPERTY DEVELOPMENT LIMITED reassignment GLAXOSMITHKLINE INTELLECTUAL PROPERTY DEVELOPMENT LIMITED ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: CHEUNG, MUI, Kalita, Biswajit, KETHIRI, RAGHAVA REDDY, AXTEN, JEFFREY MICHAEL, DEMARTINO, MICHAEL P., EIDAM, HILARY SCHENCK
Publication of US20190298705A1 publication Critical patent/US20190298705A1/en
Priority to US18/075,664 priority Critical patent/US20230165848A1/en
Abandoned legal-status Critical Current

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no 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
    • C07D211/60—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C—CHEMISTRY; METALLURGY
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    • C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/08—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms
    • C07D211/18—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D211/26—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by nitrogen atoms
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    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/438—The ring being spiro-condensed with carbocyclic or heterocyclic ring systems
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    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
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    • A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
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    • C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
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    • C07—ORGANIC CHEMISTRY
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    • C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
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    • C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
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    • C07D211/32—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by doubly bound oxygen or sulfur atoms or by two oxygen or sulfur atoms singly bound to the same carbon atom by oxygen atoms
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    • C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no 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
    • C07D211/56—Nitrogen atoms
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    • C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no 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
    • C07D211/60—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D211/62—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals attached in position 4
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    • C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no 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
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    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
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    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D451/00—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof
    • C07D451/02—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof
    • C07D451/04—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof with hetero atoms directly attached in position 3 of the 8-azabicyclo [3.2.1] octane or in position 7 of the 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring system
    • 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
    • C07D471/08—Bridged systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D498/10—Spiro-condensed systems

Definitions

  • the present invention relates to substituted piperidine derivatives that are inhibitors of the ATF4 pathway.
  • the present invention also relates to pharmaceutical compositions comprising such compounds and methods of using such compounds in the treatment of diseases/injuries associated with activated unfolded protein response pathways, such as cancer, pre-cancerous syndromes, Alzheimer's disease, spinal cord injury, traumatic brain injury, ischemic stroke, stroke, diabetes, Parkinson disease, Huntington's disease, Creutzfeldt-Jakob Disease, and related prion diseases, progressive supranuclear palsy, amyotrophic lateral sclerosis, myocardial infarction, cardiovascular disease, inflammation, fibrosis, chronic and acute diseases of the liver, chronic and acute diseases of the lung, chronic and acute diseases of the kidney, chronic traumatic encephalopathy (CTE), neurodegeneration, dementia, cognitive impairment, atherosclerosis, ocular diseases, arrhythmias, in organ transplantation and in the transportation of organs for transplantation.
  • eIF2 ⁇ kinases in mammalian cells: PERK, which responds to an accumulation of unfolded proteins in the endoplasmic reticulum (ER), GCN2 to amino acid starvation and UV light, PKR to viral infection, and HRI to heme deficiency.
  • ISR integrated stress response
  • eIF2 (which is comprised of three subunits, ⁇ , ⁇ , and ⁇ ) binds GTP and the initiator Met-tRNA to form the ternary complex (eIF2-GTP-Met-tRNAi), which, in turn, associates with the 40S ribosomal subunit scanning the 5′UTR ofmRNAs to select the initiating AUG codon.
  • eIF2 Upon phosphorylation of its a-subunit, eIF2 becomes a competitive inhibitor of its GTP-exchange factor (GEF), eIF2B (2).
  • GEF GTP-exchange factor
  • eIF2B GTP-exchange factor
  • mRNAs that contain upstream open reading frames (uORFs) in their 5′UTR are translationally up-regulated (4,5).
  • uORFs upstream open reading frames
  • ATF4 a cAMP element binding (CREB) transcription factor
  • CHOP a pro-apoptotic transcription factor
  • ATF4 regulates the expression of many genes involved in metabolism and nutrient uptake and additional transcription factors, such as CHOP, which is under both translational and transcriptional control (9). Phosphorylation of eIF2 ⁇ thus leads to preferential translation of key regulatory molecules and directs diverse changes in the transcriptome of cells upon cellular stress.
  • UPR unfolded protein response
  • the UPR is activated by unfolded or misfolded proteins that accumulate in the ER lumen because of an imbalance between protein folding load and protein folding capacity, a condition known as “ER stress”.
  • the UPR is comprised of three signaling branches mediated by ER-localized transmembrane sensors, PERK, IRE1, and ATF6.
  • PERK and IRE1 are homologous and likely activated in analogous ways by direct binding to unfolded peptides (12). This binding event leads to oligomerization and trans-autophosphorylation of their cytosolic kinase domains, and, for PERK, phosphorylation of its only known substrate, eIF2 ⁇ . In this way, PERK activation results in a quick reduction in the load of newly synthesized proteins that are translocated into the ER-lumen (13).
  • both the transcription factor XBP1s produced as the consequence of a non-conventional mRNA splicing reaction initiated by IRE1
  • the transcription factor ATF6 produced by proteolysis and release from the ER membrane
  • ATF4 Upon ER stress, both the transcription factor XBP1s, produced as the consequence of a non-conventional mRNA splicing reaction initiated by IRE1, and the transcription factor ATF6, produced by proteolysis and release from the ER membrane, collaborate with ATF4 to induce the vast UPR transcriptional response.
  • Transcriptional targets of the UPR include the ER protein folding machinery, the ER-associated degradation machinery, and many other components functioning in the secretory pathway (14).
  • Small-molecule therapeutics that inhibit the UPR and/or the Integrated Stress Response could be used in cancer as a single agent or in combination with other chemotherapeutics (17,18,19), for enhancement of long-term memory (24,25), in neurodegenerative and prion associated diseases (20), in white matter disease (VWM) (23) and in biotechnology applications that would benefit from increased protein translation.
  • compositions that comprise a pharmaceutically acceptable excipient and compounds of Formula (III).
  • neurodegenerative diseases, cancer, and other diseases/injuries associated with activated unfolded protein response pathways such as: Alzheimer's disease, spinal cord injury
  • the invention is directed to substituted piperidine derivatives. Specifically, the invention is directed to compounds according to Formula III:
  • A, B, X, Y, L 1 , L 2 , L 3 , R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 9 , z 2 , z 4 , z 5 , and z 6 are as defined below; or a salt thereof including a pharmaceutically acceptable salt thereof.
  • the present invention also relates to the discovery that the compounds of Formula (III) are active as inhibitors of the ATF4 pathway.
  • the present invention also relates to the discovery that the compounds of Formula (III) prevent the translation of ATF4.
  • This invention also relates to a method of treating Alzheimer's disease, which comprises administering to a subject in need thereof an effective amount of a compound of Formula (III) or a pharmaceutically acceptable salt thereof.
  • This invention also relates to a method of treating Parkinson's disease, which comprises administering to a subject in need thereof an effective amount of a compound of Formula (III) or a pharmaceutically acceptable salt thereof.
  • This invention also relates to a method of treating amyotrophic lateral sclerosis, which comprises administering to a subject in need thereof an effective amount of a compound of Formula (III) or a pharmaceutically acceptable salt thereof.
  • This invention also relates to a method of treating Huntington's disease, which comprises administering to a subject in need thereof an effective amount of a compound of Formula (III) or a pharmaceutically acceptable salt thereof.
  • This invention also relates to a method of treating Creutzfeldt-Jakob Disease, which comprises administering to a subject in need thereof an effective amount of a compound of Formula (III) or a pharmaceutically acceptable salt thereof.
  • This invention also relates to a method of treating progressive supranuclear palsy (PSP), which comprises administering to a subject in need thereof an effective amount of a compound of Formula (III) or a pharmaceutically acceptable salt thereof.
  • PSP progressive supranuclear palsy
  • This invention also relates to a method of treating dementia, which comprises administering to a subject in need thereof an effective amount of a compound of Formula (III) or a pharmaceutically acceptable salt thereof.
  • This invention also relates to a method of treating spinal cord injury, which comprises administering to a subject in need thereof an effective amount of a compound of Formula (III) or a pharmaceutically acceptable salt thereof.
  • This invention also relates to a method of treating traumatic brain injury, which comprises administering to a subject in need thereof an effective amount of a compound of Formula (III) or a pharmaceutically acceptable salt thereof.
  • This invention also relates to a method of treating ischemic stroke, which comprises administering to a subject in need thereof an effective amount of a compound of Formula (III) or a pharmaceutically acceptable salt thereof.
  • This invention also relates to a method of treating diabetes, which comprises administering to a subject in need thereof an effective amount of a compound of Formula (III) or a pharmaceutically acceptable salt thereof.
  • This invention also relates to a method of treating a disease state selected from myocardial infarction, cardiovascular disease, atherosclerosis, ocular diseases, and arrhythmias, which comprises administering to a subject in need thereof an effective amount of a compound of Formula (III) or a pharmaceutically acceptable salt thereof.
  • This invention also relates to a method of treating an integrated stress response-associated disease in a patient in need of such treatment, the method including administering a therapeutically effective amount of a compound of Formula (III) or a pharmaceutically acceptable salt thereof, to the patient.
  • This invention also relates to a method of treating a disease associated with phosphorylation of eIF2 ⁇ in a patient in need of such treatment, the method including administering a therapeutically effective amount of a compound of Formula (III), or a pharmaceutically acceptable salt thereof, to the patient.
  • This invention also relates to a method of treating a disease in a patient in need of such treatment, the method including administering a therapeutically effective amount of a compound of Formula (III) or a pharmaceutically acceptable salt thereof, to the patient, wherein the disease is selected from the group consisting of cancer, a neurodegenerative disease, vanishing white matter disease, childhood ataxia with CNS hypomyelination, and an intellectual disability syndrome.
  • This invention also relates to a method of improving long-term memory in a patient, the method including administering a therapeutically effective amount of a compound of Formula (III) or a pharmaceutically acceptable salt thereof, to the patient.
  • This invention also relates to a method of increasing protein expression of a cell or in vitro expression system, the method including administering an effective amount of a compound of Formula (III) or a pharmaceutically acceptable salt thereof, to the cell or expression system.
  • This invention also relates to a method of treating an inflammatory disease in a patient in need of such treatment, the method including administering a therapeutically effective amount of a compound of Formula (III), or a pharmaceutically acceptable salt thereof, to the patient.
  • This invention also relates to a method of using the compounds of Formula (III) in organ transplantation and in the transportation of organs for transplantation.
  • Also included in the present invention are methods of co-administering the presently invented compounds with further active ingredients.
  • Included in the present invention is a method for treating neurodegenerative diseases, cancer, and other diseases/injuries associated with activated unfolded protein response pathways such as: Alzheimer's disease, spinal cord injury, traumatic brain injury, ischemic stroke, stroke, diabetes, Parkinson disease, Huntington's disease, Creutzfeldt-Jakob Disease, and related prion diseases, amyotrophic lateral sclerosis, progressive supranuclear palsy, myocardial infarction, cardiovascular disease, inflammation, fibrosis, chronic and acute diseases of the liver, chronic and acute diseases of the lung, chronic and acute diseases of the kidney, chronic traumatic encephalopathy (CTE), neurodegeneration, dementias, atherosclerosis, ocular diseases, arrhythmias, in organ transplantation and in the transportation of organs for transplantation that comprises administering the compounds of Formula (III).
  • Alzheimer's disease spinal cord injury, traumatic brain injury, ischemic stroke, stroke, diabetes, Parkinson disease, Huntington's disease, Creutzfeldt-Jakob Disease
  • the invention also relates to a compound of Formula (III) or a pharmaceutically acceptable salt thereof for use in therapy.
  • the invention also relates to a compound of Formula (III) or a pharmaceutically acceptable salt thereof for use in the treatment of Alzheimer's disease.
  • the invention also relates to a compound of Formula (III) or a pharmaceutically acceptable salt thereof for use in the treatment of Parkinson's disease syndromes.
  • the invention also relates to a compound of Formula (III) or a pharmaceutically acceptable salt thereof for use in the treatment of amyotrophic lateral sclerosis.
  • the invention also relates to a compound of Formula (III) or a pharmaceutically acceptable salt thereof for use in the treatment of Huntington's disease.
  • the invention also relates to a compound of Formula (III) or a pharmaceutically acceptable salt thereof for use in the treatment of Creutzfeldt-Jakob Disease.
  • the invention also relates to a compound of Formula (III) or a pharmaceutically acceptable salt thereof for use in the treatment of progressive supranuclear palsy (PSP).
  • PSP progressive supranuclear palsy
  • the invention also relates to a compound of Formula (III) or a pharmaceutically acceptable salt thereof for use in the treatment of dementia.
  • the invention also relates to a compound of Formula (III) or a pharmaceutically acceptable salt thereof for use in the treatment of spinal cord injury.
  • the invention also relates to a compound of Formula (III) or a pharmaceutically acceptable salt thereof for use in the treatment of traumatic brain injury.
  • the invention also relates to a compound of Formula (III) or a pharmaceutically acceptable salt thereof for use in the treatment of ischemic stroke.
  • the invention also relates to a compound of Formula (III) or a pharmaceutically acceptable salt thereof for use in the treatment of diabetes.
  • the invention also relates to a compound of Formula (III) or a pharmaceutically acceptable salt thereof for use in the treatment of a disease state selected from: myocardial infarction, cardiovascular disease, atherosclerosis, ocular diseases, and arrhythmias.
  • a disease state selected from: myocardial infarction, cardiovascular disease, atherosclerosis, ocular diseases, and arrhythmias.
  • the invention also relates to the use of a compound of Formula (III) or a pharmaceutically acceptable salt thereof in the manufacture of a medicament for the treatment of an integrated stress response-associated disease.
  • the invention also relates to the use of a compound of Formula (III) or a pharmaceutically acceptable salt thereof in the manufacture of a medicament for the treatment of a disease associated with phosphorylation of eIF2 ⁇ .
  • the invention also relates to the use of a compound of Formula (III) or a pharmaceutically acceptable salt thereof in the manufacture of a medicament for the treatment of a disease selected from the group consisting of: cancer, a neurodegenerative disease, vanishing white matter disease, childhood ataxia with CNS hypomyelination, and an intellectual disability syndrome.
  • a disease selected from the group consisting of: cancer, a neurodegenerative disease, vanishing white matter disease, childhood ataxia with CNS hypomyelination, and an intellectual disability syndrome.
  • the invention also relates to the use of a compound of Formula (III) or a pharmaceutically acceptable salt thereof in the manufacture of a medicament for improving long-term memory.
  • the invention also relates to the use of a compound of Formula (III) or a pharmaceutically acceptable salt thereof in the manufacture of a medicament for increasing protein expression of a cell or in vitro expression system.
  • the invention also relates to the use of a compound of Formula (III) or a pharmaceutically acceptable salt thereof in the manufacture of a medicament for the treatment of inflammatory disease.
  • the invention also relates to the use of a compound of Formula (III) or a pharmaceutically acceptable salt thereof in the manufacture of a medicament in organ transplantation and in the transportation of organs for transplantation.
  • the invention also relates to the use of a compound of Formula (III) or a pharmaceutically acceptable salt thereof in the manufacture of a medicament for the treatment of a disease state selected from: neurodegenerative diseases, cancer, and other diseases/injuries associated with activated unfolded protein response pathways such as: Alzheimer's disease, spinal cord injury, traumatic brain injury, ischemic stroke, stroke, diabetes, Parkinson disease, Huntington's disease, Creutzfeldt-Jakob Disease, and related prion diseases, amyotrophic lateral sclerosis, progressive supranuclear palsy, myocardial infarction, cardiovascular disease, inflammation, fibrosis, chronic and acute diseases of the liver, chronic and acute diseases of the lung, chronic and acute diseases of the kidney, chronic traumatic encephalopathy (CTE), neurodegeneration, dementias, atherosclerosis, ocular diseases, arrhythmias, in organ transplantation and in the transportation of organs for transplantation.
  • a disease state selected from: neurodegenerative diseases, cancer, and other diseases/inju
  • compositions that comprise a pharmaceutical excipient and a compound of Formula (III) or a pharmaceutically acceptable salt thereof.
  • the invention also relates to a pharmaceutical composition as defined above for use in therapy.
  • the invention also relates to a combination for use in therapy which comprises a therapeutically effective amount of (i) a compound of Formula (III) or a pharmaceutically acceptable salt thereof; and (ii) further active ingredients.
  • This invention also relates to pharmaceutically acceptable salts of the compounds of Formula (I).
  • This invention also relates to pharmaceutically acceptable salts of the compounds of Formula (II).
  • This invention also relates to pharmaceutically acceptable salts of the compounds of Formula (III).
  • This invention also relates to pharmaceutically acceptable salts of the compounds of Formula (IV).
  • This invention also relates to pharmaceutically acceptable salts of the compounds of Formula (V).
  • L 1 may be a bond or substituted or unsubstituted C 1 -C 6 alkylene alkylene.
  • L 1 may be substituted or unsubstituted C 1 -C 5 alkylene.
  • L 1 may be substituted or unsubstituted C 1 -C 3 alkylene.
  • L 1 may be substituted or unsubstituted methylene.
  • L 1 may be a bond.
  • L 1 may be an unsubstituted alkylene.
  • L 1 may be an unsubstituted methylene.
  • L 1 may be an unsubstituted ethylene.
  • L 1 may be a methylene substituted with an unsubstituted alkyl.
  • L 1 may be a methylene substituted with an unsubstituted C 1 -C 4 alkyl.
  • L 1 may be a methylene substituted with an unsubstituted C 1 -C 3 alkyl.
  • R 3 is hydrogen.
  • R 3 is —CH 2 CCH.
  • R 3 is substituted or unsubstituted C 1-6 alkylene, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl.
  • R 3 is substituted or unsubstituted C 1-6 alkylene.
  • R 3 is substituted or unsubstituted C 1 -C 5 alkyl.
  • R 3 is substituted or unsubstituted C 1 -C 4 alkyl.
  • R 3 is substituted or unsubstituted C 1 -C 3 alkyl.
  • R 3 is unsubstituted C 1-6 alkylene.
  • R 3 is unsubstituted C 1 -C 5 alkyl.
  • R 3 is unsubstituted C 1 -C 4 alkyl.
  • R 3 is unsubstituted C 1 -C 3 alkyl.
  • R 3 is substituted or unsubstituted heteroalkyl.
  • R 3 is substituted or unsubstituted 2 to 8 membered heteroalkyl.
  • R 3 is unsubstituted 2 to 8 membered heteroalkyl.
  • R 5 is independently hydrogen, fluoro, chloro, bromo, iodo, —OCH 3 , —OCH 2 Ph, —C(O)Ph, —CH 3 , —CF 3 , —CN, —S(O)CH 3 , —OH, —NH 2 , —COOH, —CONH 2 , —NO 2 , —C(O)CH 3 , —CH(CH 3 ) 2 , —CCH, —CH 2 CCH, —SO 3 H, —SO 2 NH 2 , —NHC(O)NH 2 , —NHC(O)H, —NHOH, —OCH 3 , —OCF 3 , —OCHF 2 , substituted or unsubstituted C 1-6 alkylene, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycl
  • R 5 is independently hydrogen, fluoro, chloro, bromo, iodo, —OCH 3 , —OCH 2 Ph, —CH 3 , —OH, —CF 3 , —CN, —S(O)CH 3 , —NO 2 , —C(O)CH 3 , —C(O)Ph, —CH(CH 3 ) 2 , or —CCH.
  • R 5 is —F.
  • R 5 is —Cl.
  • R 5 is —Br.
  • R 5 is —I.
  • R 5 is substituted or unsubstituted C 1-6 alkylene, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl.
  • R 5 is unsubstituted C 1-6 alkylene, unsubstituted heteroalkyl, unsubstituted cycloalkyl, unsubstituted heterocycloalkyl, unsubstituted aryl, or unsubstituted heteroaryl.
  • R 5 is —OCH 3 .
  • R 5 is —OCH 2 Ph. In embodiments, R 5 is —CH 3 . In embodiments, R 5 is —OH. In embodiments, R 5 is —CF 3 . In embodiments, R 5 is —CN. In embodiments, R 5 is —S(O)CH 3 . In embodiments, R 5 is —NO 2 . In embodiments, R 5 is —C(O)CH 3 . In embodiments, R 5 is —C(O)Ph. In embodiments, R 5 is —CH(CH 3 ) 2 . In embodiments, R 5 is —CCH. In embodiments, R 5 is —CH 2 CCH. In embodiments, R 5 is —SO 3 H.
  • R 5 is —SO 2 NH 2 . In embodiments, R 5 is —NHC(O)NH 2 . In embodiments, R 5 is —NHC(O)H. In embodiments, R 5 is —NHOH. In embodiments, R 5 is-OCH 3 . In embodiments, R is —OCF 3 . In embodiments, R 5 is —OCHF 2 .
  • R 6 is independently hydrogen, fluoro, chloro, bromo, iodo, —OCH 3 , —OCH 2 Ph, —C(O)Ph, —CH 3 , —CF 3 , —CN, —S(O)CH 3 , —OH, —NH 2 , —COOH, —CONH 2 , —NO 2 , —C(O)CH 3 , —CH(CH 3 ) 2 , —CCH, —CH 2 CCH, —SO 3 H, —SO 2 NH 2 , —NHC(O)NH 2 , —NHC(O)H, —NHOH, —OCH 3 , —OCF 3 , —OCHF 2 , substituted or unsubstituted C 1-6 alkylene, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycl
  • R 6 is independently hydrogen, fluoro, chloro, bromo, iodo, —OCH 3 , —OCH 2 Ph, —CH 3 , —OH, —CF 3 , —CN, —S(O)CH 3 , —NO 2 , —C(O)CH 3 , —C(O)Ph, —CH(CH 3 ) 2 , or —CCH.
  • R 6 is —F.
  • R 6 is —Cl.
  • R 6 is —Br. In embodiments, R 6 is —I. In embodiments, R 6 is substituted or unsubstituted C 1-6 alkylene, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl.
  • R 6 is unsubstituted C 1-6 alkylene, unsubstituted heteroalkyl, unsubstituted cycloalkyl, unsubstituted heterocycloalkyl, unsubstituted aryl, or unsubstituted heteroaryl.
  • R 6 is —OCH 3 .
  • R 6 is —OCH 2 Ph.
  • R 6 is —CH 3 .
  • R 6 is —OH.
  • R 6 is —CF 3 .
  • R 6 is —CN.
  • R 6 is —S(O)CH 3 .
  • R 6 is —NO 2 .
  • R 6 is —C(O)CH 3 . In embodiments, R 6 is —C(O)Ph. In embodiments, R 6 is —CH(CH 3 ) 2 . In embodiments, R 6 is —CCH. In embodiments, R 6 is —CH 2 CCH. In embodiments, R 6 is —SO 3 H. In embodiments, R 6 is —SO 2 NH 2 . In embodiments, R 6 is —NHC(O)NH 2 . In embodiments, R 6 is —NHC(O)H. In embodiments, R 6 is —NHOH. In embodiments, R 6 is —OCH 3 . In embodiments, R 6 is —OCF 3 . In embodiments, R 6 is —OCHF 2 .
  • R 2 is NR 8 .
  • R 2 is NH.
  • R 2 is O.
  • R 2 is S.
  • R 4 is NR 8 .
  • R 4 is NH.
  • R 4 is O.
  • R 4 is S.
  • R 2 and R 4 are NH.
  • R 2 and R 4 are O.
  • R 2 and R 4 are S.
  • R 2 and R 4 are NR 8 .
  • L 2 is a bond. In embodiments, L 2 is a substituted or unsubstituted C 1-6 alkylene. In embodiments, L 2 is a substituted or unsubstituted C 1-6 heteroalkylene. In embodiments, L 2 is L 2A -L 2B -L 2C and L 2A is bonded to the substituted or unsubstituted phenyl, which may be substituted with R 5 .
  • L 2A is a bond, —O—, —S—, —NH—, —S(O)—, or —S(O) 2 —.
  • L 2B is a bond or substituted or unsubstituted C 1-6 alkylene.
  • L 2C is a bond, —O—, or —NH—.
  • L 2A is a bond.
  • L 2A is —O—.
  • L 2A is —S—.
  • L 2A is —NH—.
  • L 2A is —S(O)—.
  • L 2A is —S(O) 2 —.
  • L 2B is a bond.
  • L 2B is a substituted or unsubstituted C 1-6 alkylene.
  • L 2B is an unsubstituted C 1-6 alkylene.
  • L 2B is a substituted or unsubstituted C 1 -C 5 alkylene. In embodiments, L 2B is an unsubstituted C 1 -C 5 alkylene. In embodiments, L 2B is a substituted or unsubstituted C 1 -C 4 alkylene. In embodiments, L 2B is an unsubstituted C 1 -C 4 alkylene. In embodiments, L 2B is a substituted or unsubstituted C 1 -C 3 alkylene. In embodiments, L 2B is an unsubstituted C 1 -C 3 alkylene. In embodiments, L 2B is a substituted C 1 -C 5 alkylene.
  • L 2B is a substituted C 1 -C 6 alkylene. In embodiments, L 2B is a substituted C 1 -C 5 alkylene. In embodiments, L 2B is a substituted C 1 -C 4 alkylene. In embodiments, L 2B is a C 1 -C 6 alkylene substituted with —CF 3 . In embodiments, L 2C is a bond. In embodiments, L 2C is —O—. In embodiments, L 2C is —NH—. In embodiments, L 2A is a bond; L 2B is unsubstituted methylene; and L 2C is —O—.
  • L 3 is a bond. In embodiments, L 3 is a substituted or unsubstituted C 1-6 alkylene. In embodiments, L 3 is a substituted or unsubstituted C 1-6 heteroalkylene. In embodiments, L 3 is L 3A -L 3B -L 3C and L 3A is bonded to the substituted or unsubstituted phenyl, which may be substituted with R 5 .
  • L 3A is a bond, —O—, —S—, —NH—, —S(O)—, or —S(O) 2 —.
  • L 3B is a bond or substituted or unsubstituted C 1-6 alkylene.
  • L 3c is a bond, —O—, or —NH—.
  • L 3A is a bond.
  • L 3A is —O—.
  • L 3A is —S—.
  • L 3A is —NH—.
  • L 3A is —S(O)—.
  • L 3A is —S(O) 2 —.
  • L 3B is a bond.
  • L 3B is a substituted or unsubstituted C 1-6 alkylene.
  • L 3B is an unsubstituted C 1-6 alkylene.
  • L 3B is a substituted or unsubstituted C 1 -C 5 alkylene. In embodiments, L 3B is an unsubstituted C 1 -C 5 alkylene. In embodiments, L 3B is a substituted or unsubstituted C 1 -C 4 alkylene. In embodiments, L 3B is an unsubstituted C 1 -C 4 alkylene. In embodiments, L 3B is a substituted or unsubstituted C 1 -C 3 alkylene. In embodiments, L 3B is an unsubstituted C 1 -C 3 alkylene. In embodiments, L 3B is a substituted C 1 -C 5 alkylene.
  • L 3B is a substituted C 1 -C 6 alkylene. In embodiments, L 3B is a substituted C 1 -C 5 alkylene. In embodiments, L 3B is a substituted C 1 -C 4 alkylene. In embodiments, L 3B is a C 1 -C 6 alkylene substituted with —CF 3 . In embodiments, L 3c is a bond. In embodiments, L 3c is —O—. In embodiments, L 3c is —NH—. In embodiments, L 3A is a bond; L 3B is unsubstituted methylene; and L 3c is —O—.
  • the symbol z 2 is O. In embodiments, the symbol z 2 is 1. In embodiments, the symbol z 4 is O. In embodiments, the symbol z 4 is 1. In embodiments, the symbols z 2 and z 4 are O. In embodiments, the symbols z 2 and z 4 are 1. In embodiments, the symbol z 5 is O. In embodiments, the symbol z 5 is 1. In embodiments, the symbol z 5 is 2. In embodiments, the symbol z 5 is 3. In embodiments, the symbol z 5 is 4. In embodiments, the symbol z 6 is O. In embodiments, the symbol z 6 is 1. In embodiments, the symbol z 6 is 2. In embodiments, the symbol z 6 is 3. In embodiments, the symbol z 6 is 4.
  • salts, including pharmaceutically acceptable salts, of the compounds according to Formula (III) may be prepared. Indeed, in certain embodiments of the invention, salts including pharmaceutically-acceptable salts of the compounds according to Formula (III) may be preferred over the respective free or unsalted compound. Accordingly, the invention is further directed to salts, including pharmaceutically-acceptable salts, of the compounds according to Formula (III).
  • salts including pharmaceutically acceptable salts, of the compounds of the invention are readily prepared by those of skill in the art.
  • the salts of the present invention are pharmaceutically acceptable salts.
  • Salts encompassed within the term “pharmaceutically acceptable salts” refer to non-toxic salts of the compounds of this invention.
  • Representative pharmaceutically acceptable acid addition salts include, but are not limited to, 4-acetamidobenzoate, acetate, adipate, alginate, ascorbate, aspartate, benzenesulfonate (besylate), benzoate, bisulfate, bitartrate, butyrate, calcium edetate, camphorate, camphorsulfonate (camsylate), caprate (decanoate), caproate (hexanoate), caprylate (octanoate), cinnamate, citrate, cyclamate, digluconate, 2,5-dihydroxybenzoate, disuccinate, dodecylsulfate (estolate), edetate (ethylenediaminetetraacetate), estolate (lauryl sulfate), ethane-1,2-disulfonate (edisylate), ethanesulfonate (esylate), formate, fumarate, galactarate (
  • Representative pharmaceutically acceptable base addition salts include, but are not limited to, aluminium, 2-amino-2-(hydroxymethyl)-1,3-propanediol (TRIS, tromethamine), arginine, benethamine (N-benzylphenethylamine), benzathine (N,N′-dibenzylethylenediamine), bis-(2-hydroxyethyl)amine, bismuth, calcium, chloroprocaine, choline, clemizole (1-p chlorobenzyl-2-pyrrolildine-1′-ylmethylbenzimidazole), cyclohexylamine, dibenzylethylenediamine, diethylamine, diethyltriamine, dimethylamine, dimethylethanolamine, dopamine, ethanolamine, ethylenediamine, L-histidine, iron, isoquinoline, lepidine, lithium, lysine, magnesium, meglumine (N-methylglucamine), piperazine, piperidine, potassium,
  • the compounds according to Formula (III) may contain one or more asymmetric centers (also referred to as a chiral center) and may, therefore, exist as individual enantiomers, diastereomers, or other stereoisomeric forms, or as mixtures thereof.
  • Chiral centers such as chiral carbon atoms, may be present in a substituent such as an alkyl group.
  • compounds according to Formula (III) containing one or more chiral centers may be used as racemic mixtures, enantiomerically or diastereomerically enriched mixtures, or as enantiomerically or diastereomerically pure individual stereoisomers.
  • the compounds according to Formula (III) and pharmaceutically acceptable salts thereof may contain isotopically-labelled compounds, which are identical to those recited in Formula (III) and following, but for the fact that one or more atoms are replaced by an atom having an atomic mass or mass number different from the atomic mass or mass number usually found in nature.
  • isotopes include isotopes of hydrogen, carbon, nitrogen, oxygen, phosphorous, sulphur, fluorine, iodine, and chlorine, such as 2H, 3H, 11C, 13C, 14C, 15N, 17O, 18O, 31P, 32P, 35S, 18F, 36Cl, 123I and 125I.
  • Isotopically-labelled compounds for example those into which radioactive isotopes such as 3H or 14C are incorporated, are useful in drug and/or substrate tissue distribution assays. Tritiated, i.e., 3H, and carbon-14, i.e., 14C, isotopes are particularly preferred for their ease of preparation and detectability. 11C and 18F isotopes are particularly useful in PET (positron emission tomography), and 125I isotopes are particularly useful in SPECT (single photon emission computerized tomography), both are useful in brain imaging.
  • Isotopically labelled compounds can generally be prepared by substituting a readily available isotopically labelled reagent for a non-isotopically labelled reagent.
  • the compounds according to Formula (III) may also contain double bonds or other centers of geometric asymmetry. Where the stereochemistry of a center of geometric asymmetry present in Formula (III), or in any chemical structure illustrated herein, is not specified, the structure is intended to encompass the trans (E) geometric isomer, the cis (Z) geometric isomer, and all mixtures thereof. Likewise, all tautomeric forms are also included in Formula (III) whether such tautomers exist in equilibrium or predominately in one form.
  • the compounds of Formula (III) or salts, including pharmaceutically acceptable salts, thereof may exist in solid or liquid form.
  • the compounds of the invention may exist in crystalline or noncrystalline form, or as a mixture thereof.
  • pharmaceutically acceptable solvates may be formed wherein solvent molecules are incorporated into the crystalline lattice during crystallization.
  • Solvates wherein water is the solvent that is incorporated into the crystalline lattice are typically referred to as “hydrates.” Hydrates include stoichiometric hydrates as well as compositions containing vaiable amounts of water.
  • Polymorphs may have different physical properties such as shape, density, hardness, deformability, stability, and dissolution properties. Polymorphs typically exhibit different melting points, IR spectra, and X-ray powder diffraction patterns, which may be used for identification. The skilled artisan will appreciate that different polymorphs may be produced, for example, by changing or adjusting the reaction conditions or reagents, used in making the compound. For example, changes in temperature, pressure, or solvent may result in polymorphs. In addition, one polymorph may spontaneously convert to another polymorph under certain conditions.
  • Alkyl and “alkylene”, and derivatives thereof, refer to a hydrocarbon chain having the specified number of “member atoms”. Alkyl being monovalent and alkylene being bivalent. For example, C 1 -C 6 alkyl refers to an alkyl group having from 1 to 6 member atoms. Alkyl groups may be saturated, unsaturated, straight or branched. Representative branched alkyl groups have one, two, or three branches.
  • Alkyl and alkylene includes methyl, ethyl, ethylene, propyl (n-propyl and isopropyl), butene, butyl (n-butyl, isobutyl, and t-butyl), pentyl, methylcyclopropane, and hexyl.
  • alkyl and “alkylene” further includes cycloalkyl in the carbon chain, for example —CH 3 cyclopropane-.
  • Alkoxy refers to an —O-alkyl group wherein “alkyl” is as defined herein.
  • C 1 -C 4 alkoxy refers to an alkoxy group having from 1 to 4 member atoms.
  • Representative branched alkoxy groups have one, two, or three branches. Examples of such groups include methoxy, ethoxy, propoxy, and butoxy.
  • Aryl refers to an aromatic hydrocarbon ring.
  • Aryl groups are monocyclic, bicyclic, and tricyclic ring systems having a total of five to fourteen ring member atoms, wherein at least one ring system is aromatic and wherein each ring in the system contains 3 to 7 member atoms, such as phenyl, naphthalene, tetrahydronaphthalene and biphenyl.
  • aryl is phenyl.
  • Cycloalkyl refers to a saturated or unsaturated non aromatic hydrocarbon ring having from three to seven carbon atoms. Cycloalkyl groups are monocyclic ring systems. For example, C 3 -C 7 cycloalkyl refers to a cycloalkyl group having from 3 to 7 member atoms. Examples of cycloalkyl as used herein include: cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cyclobutenyl, cyclopentenyl, cyclohexenyl and cycloheptyl.
  • Halo refers to the halogen radicals fluoro, chloro, bromo, and iodo.
  • Heteroaryl refers to a monocyclic aromatic 4 to 8 member ring containing 1 to 7 carbon atoms and 1 to 4 heteroatoms, provided that when the number of carbon atoms is 3, the aromatic ring contains at least two heteroatoms, or to such aromatic ring fused to one or more rings, such as heteroaryl rings, aryl rings, heterocyclic rings, cycloalkyl rings. Heteroaryl groups containing more than one heteroatom may contain different heteroatoms.
  • Heteroaryl includes but is not limited to: benzoimidazolyl, benzothiazolyl, benzothiophenyl, benzopyrazinyl, benzotriazolyl, benzotriazinyl, benzo[1,4]dioxanyl, benzofuranyl, 9H-a-carbolinyl, cinnolinyl, furanyl, pyrazolyl, imidazolyl, indolizinyl, naphthyridinyl, oxazolyl, oxothiadiazolyl, oxadiazolyl, phthalazinyl, pyridyl, pyrrolyl, purinyl, pteridinyl, phenazinyl, pyrazolopyrimidinyl, pyrazolopyridinyl, pyrrolizinyl, pyrimidyl, isothiazolyl, furazanyl, pyrimidinyl, tetrazin
  • heteroaryl is selected from: pyrazolyl, imidazolyl, oxazolyl and thienyl.
  • heteroaryl is a pyridyl group or an imidazolyl group.
  • heteroaryl is a pyridyl.
  • Heterocycloalkyl refers to a saturated or unsaturated non-aromatic ring containing 4 to 12 member atoms, of which 1 to 11 are carbon atoms and from 1 to 6 are heteroatoms. Heterocycloalkyl groups containing more than one heteroatom may contain different heteroatoms. Heterocycloalkyl groups are monocyclic ring systems or a monocyclic ring fused with an aryl ring or to a heteroaryl ring having from 3 to 6 member atoms.
  • Heterocycloalkyl includes: pyrrolidinyl, tetrahydrofuranyl, dihydrofuranyl, pyranyl, tetrahydropyranyl, dihydropyranyl, tetrahydrothienyl, pyrazolidinyl, oxazolidinyl, oxetanyl, thiazolidinyl, piperidinyl, homopiperidinyl, piperazinyl, morpholinyl, thiamorpholinyl, 1,3-dioxolanyl, 1,3-dioxanyl, 1,4-dioxanyl, 1,3-oxathiolanyl, 1,3-oxathianyl, 1,3-dithianyl, 1,3oxazolidin-2-one, hexahydro-1H-azepin, 4,5,6,7,tetrahydro-1H-benzimidazol, piperidinyl, 1,2,3,6-te
  • Heteroatom refers to a nitrogen, sulphur or oxygen atom.
  • Heteroalkyl and “heteroalkylene” by itself or in combination with another term, means, unless otherwise stated, a non-cyclic stable straight or branched chain, or combinations thereof, including at least one carbon atom and at least one heteroatom selected from the group consisting of O, N, P, Si, and S, and wherein the nitrogen and sulfur atoms may optionally be oxidized, and the nitrogen heteroatom may optionally be quaternized. Heteroalkyl being monovalent and heteroalkylene being bivalent. The heteroalkyl and heteroalkylene groups may be taken together with another substituent to form a heterocycloalkyl group.
  • the heteroatom(s) 0, N, P, S, and Si may be placed at any interior position of the heteroalkyl or heteroalkylene group or at the position at which the alkyl group is attached to the remainder of the molecule.
  • Examples include, but are not limited to: —CH 2 —CH 2 —O—CH 3 , —CH 2 —CH 2 —NH—CH 3 , —CH 2 —CH 2 —N(CH 3 ) 2 , —CH 2 —S—CH 2 —CH 3 , —CH 2 —CH 3 , —S(O)—CH 3 , —CH 2 —CH 2 —S(O) 2 —CH 3 , —CH ⁇ CH—O—CH 3 , —Si(CH 3 ) 3 , —CH 2 —CH ⁇ N—OCH 3 , —CH ⁇ CHN(CH 3 ) 2 , —O—CH 3 , —O—CH 2 —CH 3 , and —CN.
  • Examples include, but are not limited to: —CH 3 , —CH 2 —, —CH 2 —CH 2 —O—CH 2 —, CH 2 —CH 2 —NH—CH 2 —, —CH 2 —CH 2 —N(CH 3 )CH 2 —, —CH 2 —S—CH 2 —CH 2 —, —CH 2 —CH 2 —, —S(O)—CH 2 —, —CH 2 —CH 2 —S(O) 2 —CH 2 —, —CH ⁇ CH—O—CH 2 —, —Si(CH 3 ) 2 CH 2 —, —N(CH 3 )CH 2 —; —O—CH 2 —CH 2 —CH 2 —.
  • Up to two or three heteroatoms may be consecutive, such as, for example, —CH 2 —NH—OCH 3 and —CH 2 —O—Si(CH 3 ) 3 .
  • substituted means the subject chemical moiety has from one to four substituents selected from the group consisting of:
  • DCE (1,2-dichloroethane); DCM (dichloromethane); DDQ (2,3-Dichloro-5,6-dicyano-1,4-benzoquinone); ATP (adenosine triphosphate); Bis-pinacolatodiboron (4,4,4′,4′,5,5,5′,5′-Octamethyl-2,2′-bi-1,3,2-dioxaborolane); BSA (bovine serum albumin); C18 (refers to 18-carbon alkyl groups on silicon in HPLC stationary phase); CH 3 CN (acetonitrile); Cy (cyclohexyl); DCM (dichloromethane); DIPEA (Hünig's base, N-ethyl-N-(1-methylethyl)-2-propanamine); Dioxane (1,4-dioxane); DMAP (4-dimethylaminopyridine); DME (1,2-dimethoxyethane); DMED
  • DMSO dimethylsulfoxide
  • DPPA diphenyl phosphoryl azide
  • EDC N-(3-dimethylaminopropyl)-N′ethylcarbodiimide
  • EDTA ethylenediaminetetraacetic acid
  • EtOAc ethyl acetate
  • EtOH ethanol
  • Et 2 O diethyl ether
  • HEPES 4-(2-hydroxyethyl)-1-piperazine ethane sulfonic acid
  • HATU O-(7-Azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate
  • HOAt (1-hydroxy-7-azabenzotriazole
  • HOBt (1-hydroxybenzotriazole
  • HOAc acetic acid
  • HPLC high pressure liquid chromatography
  • HMDS hexamethyldisilazide
  • Hunig's Base N,N-Diisopropylethylamine
  • IPA isopropyl alcohol
  • KHMDS potassium hexamethyldisilazide
  • LAH lithium aluminum hydride
  • LDA lithium diisopropylamide
  • LHMDS lithium hexamethyldisilazide
  • MeOH methanol
  • MTBE methyl tert-butyl ether
  • mCPBA m-chloroperbezoic acid
  • NaHMDS sodium hexamethyldisilazide
  • NBS N-bromosuccinimide
  • PE petroleum ether
  • Pd 2 (dba) 3 Tris(dibenzylideneacetone)dipalladium(0)
  • Pd(dppf)Cl 2 .DCM Complex [1,1′-Bis(diphenylphosphino)ferrocene]dichloropalladium(II).dichloromethane complex
  • PyBOP benzotriazol-1-yl-oxytripyrrolidinophosphonium hexafluorophosphate
  • PyBrOP bromotripyrrolidinophosphonium hexafluorophosphate
  • RPHPLC reverse phase high pressure liquid chromatography
  • RT room temperature
  • the compounds according to Formula (III) and pharmaceutically acceptable salts thereof are inhibitors of the ATF4 pathway.
  • Compounds which are inhibitors of the ATF4 pathway are readily identified by exhibiting activity in the ATF4 Cell Based Assay below. These compounds are potentially useful in the treatment of conditions wherein the underlying pathology is attributable to (but not limited to) modulation of the eIF2alpha pathway, for example, neurodegenerative disorders, cancer, cardiovascular and metabolic diseases. Accordingly, in another aspect the invention is directed to methods of treating such conditions.
  • the Integrated Stress Response is a collection of cellular stress response pathways that converge in phosphorylation of the translation initiation factor eIF2 ⁇ resulting in a reduction in overall translation in cells.
  • Mammalian cells have four eIF2 ⁇ kinases that phosphorylate this initiation factor in the same residue (serine 51); PERK is activated by the accumulation of unfolded proteins in the endoplasmic reticulum (ER), GCN2 is activated by amino acid starvation, PKR by viral infection and HRI by heme deficiency. Activation of these kinases decreases bulk protein synthesis but it also culminates in increased expression of specific mRNAs that contain uORFs.
  • An integrated stress response-associated disease is a disease characterized by increased activity in the integrated stress response (e.g. increased phosphorylation of eIF2 ⁇ by an eIF2 ⁇ kinase compared to a control such as a subject without the disease).
  • a disease associated with phosphorylation of eIF2 ⁇ is disease characterized by an increase in phosphorylation of eIF2 ⁇ relative to a control, such as a subject without the disease.
  • PERK Activation of PERK occurs upon ER stress and hypoxic conditions and its activation and effect on translation has been shown to be cytoprotective for tumor cells [17]. Adaptation to hypoxia in the tumor microenvironment is critical for survival and metastatic potential. PERK has also been shown to promote cancer proliferation by limiting oxidative DNA damage and death [18, 19]. Moreover, a newly identified PERK inhibitor has been shown to have antitumor activity in a human pancreatic tumor xenograft model [20]. Compounds disclosed herein decrease the viability of cells that are subjected to ER-stress. Thus, pharmacological and acute inhibition of the PERK branch with the compounds disclosed herein results in reduced cellular fitness. During tumor growth, compounds disclosed herein, that block the cytoprotective effects of eIF2 ⁇ phosphorylation upon stress may prove to be potent anti-proliferative agents.
  • Prolonged ER stress leads to the accumulation of CHOP, a pro-apoptotic molecule.
  • CHOP a pro-apoptotic molecule.
  • overexpression of the phosphatase of eIF2 ⁇ increased survival of prion-infected mice whereas sustained eIF2 ⁇ phosphorylation decreased survival [22].
  • the restoration of protein translation rates during prion disease was shown to rescue synaptic deficits and neuronal loss.
  • the compounds disclosed herein that make cells insensitive to eIF2 ⁇ phosphorylation sustain protein translation. Compounds disclosed herein could prove potent inhibitors of neuronal cell death in prion disease by blocking the deleterious effects of prolonged eIF2 ⁇ phosphorylation.
  • tissue-specific pathology that is linked to heightened eIF2 ⁇ phosphorylation is the fatal brain disorder, vanishing white matter disease (VWM) or childhood ataxia with CNS hypo-myelination (CACH).
  • VWM vanishing white matter disease
  • CACH CNS hypo-myelination
  • eIF2 ⁇ phosphorylation inhibits the activity of eIF2B and mutations in this exchange factor that reduce its exchange activity exacerbate the effects of eIF2 ⁇ phosphorylation.
  • the severe consequences of the CACH mutations point to the dangers of UPR hyper-activation, especially as it pertains to the myelin-producing oligodendrocyte.
  • Small molecules, such as compounds disclosed herein, that block signaling through eIF2 ⁇ phosphorylation may reduce the deleterious effects of its hyper-activation in VWM.
  • a method of improving long-term memory in a patient including administering a therapeutically effective amount of a compound of Formula (III) to the patient.
  • the patient is human.
  • the patient is a mammal.
  • the compounds set forth herein are provided as pharmaceutical compositions including the compound and a pharmaceutically acceptable excipient.
  • the compound, or a pharmaceutically acceptable salt thereof is co-adminstered with a second agent (e.g. therapeutic agent).
  • the compound, or a pharmaceutically acceptable salt thereof is co-adminstered with a second agent (e.g. therapeutic agent), which is administered in a therapeutically effective amount.
  • the second agent is an agent for improving memory.
  • Regulators of translation could serve as therapeutic agents that improve memory in human disorders associated with memory loss such as Alzheimer's disease and in other neurological disorders that activate the UPR in neurons and thus could have negative effects on memory consolidation such as Parkinson's disease, Amyotrophic lateral sclerosis and prion diseases.
  • eIF2 ⁇ that disrupts complex integrity linked intellectual disability (intellectual disability syndrome or ID) to impaired translation initiation in humans [27].
  • ID and VWM two diseases with impaired eIF2 function, display distinct phenotypes but both affect mainly the brain and impair learning.
  • the compounds of Formula (III) are also useful in applications where increasing protein production output is desirable, such as in vitro cell free systems for protein production.
  • In vitro systems have basal levels of eIF2 ⁇ phosphorylation that reduce translational output [28, 29].
  • production of antibodies by hybridomas may also be improved by addition of compounds disclosed herein.
  • a method of increasing protein expression of a cell or in vitro expression system including administering an effective amount of a compound of Formula (III) to the cell or expression system.
  • the method is a method of increasing protein expression by a cell and includes administering an effective amount of a compound of Formula (III) to the cell.
  • the method is a method of increasing protein expression by an in vitro protein expression system and includes administering an effective amount of a compound of Formula (III) to the in vitro (e.g. cell free) protein expression system.
  • the compounds set forth herein are provided as pharmaceutical compositions including the compound and a pharmaceutically acceptable excipient.
  • the compound, or a pharmaceutically acceptable salt thereof is co-adminstered with a second agent.
  • the compound, or a pharmaceutically acceptable salt thereof is co-adminstered with a second agent, which is administered in a therapeutically effective amount.
  • the second agent is an agent for improving protein expression.
  • the present invention relates to a method for treating or lessening the severity of breast cancer, including inflammatory breast cancer, ductal carcinoma, and lobular carcinoma.
  • the present invention relates to a method for treating or lessening the severity of colon cancer.
  • the present invention relates to a method for treating or lessening the severity of pancreatic cancer, including insulinomas, adenocarcinoma, ductal adenocarcinoma, adenosquamous carcinoma, acinar cell carcinoma, and glucagonoma.
  • the present invention relates to a method for treating or lessening the severity of skin cancer, including melanoma, including metastatic melanoma.
  • the present invention relates to a method for treating or lessening the severity of lung cancer including small cell lung cancer, non-small cell lung cancer, squamous cell carcinoma, adenocarcinoma, and large cell carcinoma.
  • the present invention relates to a method for treating or lessening the severity of cancers selected from the group consisting of brain (gliomas), glioblastomas, astrocytomas, glioblastoma multiforme, Bannayan-Zonana syndrome, Cowden disease, Lhermitte-Duclos disease, Wilm's tumor, Ewing's sarcoma, Rhabdomyosarcoma, ependymoma, medulloblastoma, head and neck, kidney, liver, melanoma, ovarian, pancreatic, adenocarcinoma, ductal adenocarcinoma, adenosquamous carcinoma, acinar cell carcinoma, glucagonoma, insulinoma, prostate, sarcoma, osteosarcoma, giant cell tumor of bone, thyroid, lymphoblastic T cell leukemia, chronic myelogenous leukemia, chronic lymphocytic leukemia,
  • the present invention relates to a method for treating or lessening the severity of pre-cancerous syndromes in a mammal, including a human, wherein the pre-cancerous syndrome is selected from: cervical intraepithelial neoplasia, monoclonal gammapathy of unknown significance (MGUS), myelodysplastic syndrome, aplastic anemia, cervical lesions, skin nevi (pre-melanoma), prostatic intraepithleial (intraductal) neoplasia (PIN), Ductal Carcinoma in situ (DCIS), colon polyps and severe hepatitis or cirrhosis.
  • MGUS monoclonal gammapathy of unknown significance
  • MUS monoclonal gammapathy of unknown significance
  • myelodysplastic syndrome aplastic anemia
  • cervical lesions aplastic anemia
  • cervical lesions skin nevi (pre-melanoma)
  • PIN prostatic intraepithleial (intr
  • the present invention relates to a method for treating or lessening the severity of neurodegenerative diseases/injury, such as Alzheimer's disease, spinal cord injury, traumatic brain injury, ischemic stroke, stroke, diabetes, Parkinson disease, Huntington's disease, Creutzfeldt-Jakob Disease, and related prion diseases, progressive supranuclear palsy, amyotrophic lateral sclerosis, myocardial infarction, cardiovascular disease, inflammation, fibrosis, chronic and acute diseases of the liver, chronic and acute diseases of the lung, chronic and acute diseases of the kidney, chronic traumatic encephalopathy (CTE), neurodegeneration, dementia, cognitive impairment, atherosclerosis, ocular diseases, arrhythmias, in organ transplantation and in the transportation of organs for transplantation.
  • neurodegenerative diseases/injury such as Alzheimer's disease, spinal cord injury, traumatic brain injury, ischemic stroke, stroke, diabetes, Parkinson disease, Huntington's disease, Creutzfeldt-Jakob Disease, and related prion diseases
  • the present invention relates to a method for preventing organ damage during and after organ transplantation and in the transportation of organs for transplantation.
  • the method of preventing organ damage during and after organ transplantation will comprise the in vivo administration of a compound of Formula (III).
  • the method of preventing organ damage during the transportation of organs for transplantation will comprise adding a compound of Formula (III) to the solution housing the organ during transportation.
  • the present invention relates to a method for treating or lessening the severity of ocular diseases/angiogenesis.
  • the method of treating or lessening the severity of ocular diseases/angiogenesis will comprise the in vivo administration of a compound of Formula (III).
  • the disorder of ocular diseases can be: edema or neovascularization for any occlusive or inflammatory retinal vascular disease, such as rubeosis irides, neovascular glaucoma, pterygium, vascularized glaucoma filtering blebs, conjunctival papilloma; choroidal neovascularization, such as neovascular age-related macular degeneration (AMD), myopia, prior uveitis, trauma, or idiopathic; macular edema, such as post surgical macular edema, macular edema secondary to uveitis including retinal and/or choroidal inflammation, macular edema secondary to diabetes, and macular edema secondary to retinovascular occlusive disease (i.e.
  • retinal vascular disease such as rubeosis irides, neovascular glaucoma, pterygium,
  • retinal neovascularization due to diabetes such as retinal vein occlusion, uveitis, ocular ischemic syndrome from carotid artery disease, ophthalmic or retinal artery occlusion, sickle cell retinopathy, other ischemic or occlusive neovascular retinopathies, retinopathy of prematurity, or Eale's Disease; and genetic disorders, such as VonHippel-Lindau syndrome.
  • the neovascular age-related macular degeneration is wet age-related macular degeneration. In other embodiments, the neovascular age-related macular degeneration is dry age-related macular degeneration and the patient is characterized as being at increased risk of developing wet age-related macular degeneration.
  • the methods of treatment of the invention comprise administering an effective amount of a compound according to Formula (III) or a pharmaceutically acceptable salt, thereof to a patient in need thereof.
  • the invention also provides a compound according to Formula (III) or a pharmaceutically-acceptable salt thereof for use in medical therapy, and particularly in therapy for: cancer, pre-cancerous syndromes, Alzheimer's disease, spinal cord injury, traumatic brain injury, ischemic stroke, stroke, diabetes, Parkinson disease, Huntington's disease, Creutzfeldt-Jakob Disease, and related prion diseases, progressive supranuclear palsy, amyotrophic lateral sclerosis, myocardial infarction, cardiovascular disease, inflammation, fibrosis, chronic and acute diseases of the liver, chronic and acute diseases of the lung, chronic and acute diseases of the kidney, chronic traumatic encephalopathy (CTE), neurodegeneration, dementia, cognitive impairment, atherosclerosis, ocular diseases, in organ transplantation and arrhythmias.
  • cancer pre-cancerous syndromes
  • Alzheimer's disease spinal cord injury
  • traumatic brain injury ischemic stroke
  • stroke stroke
  • diabetes diabetes
  • Parkinson disease Huntington's disease
  • the invention also provides a compound according to Formula (II) or a pharmaceutically-acceptable salt thereof for use in preventing organ damage during the transportation of organs for transplantation.
  • the invention is directed to the use of a compound according to Formula (III) or a pharmaceutically acceptable salt thereof in the preparation of a medicament for the treatment of a disorder characterized by activation of the UPR, such as cancer.
  • the methods of treatment of the invention comprise administering a safe and effective amount of a compound of Formula (III), or a pharmaceutically acceptable salt thereof to a mammal, suitably a human, in need thereof.
  • treating in reference to a condition means: (1) to ameliorate or prevent the condition or one or more of the biological manifestations of the condition, (2) to interfere with (a) one or more points in the biological cascade that leads to or is responsible for the condition or (b) one or more of the biological manifestations of the condition, (3) to alleviate one or more of the symptoms or effects associated with the condition, or (4) to slow the progression of the condition or one or more of the biological manifestations of the condition.
  • treating and derivatives thereof refers to therapeutic therapy.
  • Therapeutic therapy is appropriate to alleviate symptions or to treat at early signs of disease or its progression.
  • Prophylactic therapy is appropriate when a subject has, for example, a strong family history of neurodegenerative diseases.
  • Prophylactic therapy is appropriate when a subject has, for example, a strong family history of cancer or is otherwise considered at high risk for developing cancer, or when a subject has been exposed to a carcinogen.
  • prevention is not an absolute term. In medicine, “prevention” is understood to refer to the prophylactic administration of a drug to substantially diminish the likelihood or severity of a condition or biological manifestation thereof, or to delay the onset of such condition or biological manifestation thereof.
  • safe and effective amount in reference to a compound of Formula (III), or a pharmaceutically acceptable salt thereof, means an amount of the compound sufficient to treat the patient's condition but low enough to avoid serious side effects (at a reasonable benefit/risk ratio) within the scope of sound medical judgment.
  • a safe and effective amount of the compound will vary with the particular route of administration chosen; the condition being treated; the severity of the condition being treated; the age, size, weight, and physical condition of the patient being treated; the medical history of the patient to be treated; the duration of the treatment; the nature of concurrent therapy; the desired therapeutic effect; and like factors, but can nevertheless be routinely determined by the skilled artisan.
  • patient refers to a human or other mammal, suitably a human.
  • the compounds of Formula (III) or pharmaceutically acceptable salts thereof may be administered by any suitable route of administration, including systemic administration.
  • Systemic administration includes oral administration, and parenteral administration.
  • Parenteral administration refers to routes of administration other than enteral, transdermal, or by inhalation, and is typically by injection or infusion.
  • Parenteral administration includes intravenous, intramuscular, and subcutaneous injection or infusion.
  • the compounds of Formula (III) or pharmaceutically acceptable salts thereof may be administered once or according to a dosing regimen wherein a number of doses are administered at varying intervals of time for a given period of time. For example, doses may be administered one, two, three, or four times per day. Doses may be administered until the desired therapeutic effect is achieved or indefinitely to maintain the desired therapeutic effect. Suitable dosing regimens for a compound of the invention depend on the pharmacokinetic properties of that compound, such as absorption, distribution, and half-life, which can be determined by the skilled artisan.
  • suitable dosing regimens including the duration such regimens are administered, for a compound of the invention depend on the condition being treated, the severity of the condition being treated, the age and physical condition of the patient being treated, the medical history of the patient to be treated, the nature of concurrent therapy, the desired therapeutic effect, and like factors within the knowledge and expertise of the skilled artisan. It will be further understood by such skilled artisans that suitable dosing regimens may require adjustment given an individual patient's response to the dosing regimen or over time as individual patient needs change.
  • a “prodrug” of a compound of the invention is a functional derivative of the compound which, upon administration to a patient, eventually liberates the compound of the invention in vivo.
  • Administration of a compound of the invention as a prodrug may enable the skilled artisan to do one or more of the following: (a) modify the onset of the compound in vivo; (b) modify the duration of action of the compound in vivo; (c) modify the transportation or distribution of the compound in vivo; (d) modify the solubility of the compound in vivo; and (e) overcome a side effect or other difficulty encountered with the compound.
  • esters can be employed, for example methyl, ethyl, and the like for —COOH, and acetate maleate and the like for —OH, and those esters known in the art for modifying solubility or hydrolysis characteristics.
  • the compounds of Formula (III) and pharmaceutically acceptable salts thereof may be co-administered with at least one other active agent known to be useful in the treatment of cancer or pre-cancerous syndromes.
  • co-administration is meant either simultaneous administration or any manner of separate sequential administration of an ATF4 pathway inhibiting compound, as described herein, and a further active agent or agents, known to be useful in the treatment of cancer, including chemotherapy and radiation treatment.
  • further active agent or agents includes any compound or therapeutic agent known to or that demonstrates advantageous properties when administered to a patient in need of treatment for cancer.
  • the compounds are administered in a close time proximity to each other.
  • the compounds are administered in the same dosage form, e.g. one compound may be administered by injection and another compound may be administered orally.
  • any anti-neoplastic agent that has activity versus a susceptible tumor being treated may be co-administered in the treatment of cancer in the present invention.
  • examples of such agents can be found in Cancer Principles and Practice of Oncology by V. T. Devita and S. Hellman (editors), 6 th edition (Feb. 15, 2001), Lippincott Williams & Wilkins Publishers.
  • a person of ordinary skill in the art would be able to discern which combinations of agents would be useful based on the particular characteristics of the drugs and the cancer involved.
  • Typical anti-neoplastic agents useful in the present invention include, but are not limited to, anti-microtubule agents such as diterpenoids and vinca alkaloids; platinum coordination complexes; alkylating agents such as nitrogen mustards, oxazaphosphorines, alkylsulfonates, nitrosoureas, and triazenes; antibiotic agents such as anthracyclins, actinomycins and bleomycins; topoisomerase II inhibitors such as epipodophyllotoxins; antimetabolites such as purine and pyrimidine analogues and anti-folate compounds; topoisomerase I inhibitors such as camptothecins; hormones and hormonal analogues; signal transduction pathway inhibitors; non-receptor tyrosine kinase angiogenesis inhibitors; immunotherapeutic agents; proapoptotic agents; cell cycle signaling inhibitors; proteasome inhibitors; and inhibitors of cancer metabolism.
  • anti-microtubule agents such as
  • Examples of a further active ingredient or ingredients (anti-neoplastic agent) for use in combination or co-administered with the presently invented ATF4 pathway inhibiting compounds are chemotherapeutic agents.
  • the pharmaceutically active compounds of the invention are used in combination with a VEGFR inhibitor, suitably 5-[[4-[(2,3-dimethyl-2H-indazol-6-yl)methylamino]-2-pyrimidinyl]amino]-2-methylbenzenesulfonamide, or a pharmaceutically acceptable salt, suitably the monohydrochloride salt thereof, which is disclosed and claimed in in International Application No. PCT/US01/49367, having an International filing date of Dec. 19, 2001, International Publication Number WO02/059110 and an International Publication date of Aug. 1, 2002, the entire disclosure of which is hereby incorporated by reference, and which is the compound of Example 69.
  • a VEGFR inhibitor suitably 5-[[4-[(2,3-dimethyl-2H-indazol-6-yl)methylamino]-2-pyrimidinyl]amino]-2-methylbenzenesulfonamide, or a pharmaceutically acceptable salt, suitably the monohydrochloride salt thereof
  • the cancer treatment method of the claimed invention includes the co-administration a compound of Formula (III) and/or a pharmaceutically acceptable salt thereof and at least one anti-neoplastic agent, such as one selected from the group consisting of anti-microtubule agents, platinum coordination complexes, alkylating agents, antibiotic agents, topoisomerase II inhibitors, antimetabolites, topoisomerase I inhibitors, hormones and hormonal analogues, signal transduction pathway inhibitors, non-receptor tyrosine kinase angiogenesis inhibitors, immunotherapeutic agents, proapoptotic agents, cell cycle signaling inhibitors; proteasome inhibitors; and inhibitors of cancer metabolism.
  • anti-neoplastic agent such as one selected from the group consisting of anti-microtubule agents, platinum coordination complexes, alkylating agents, antibiotic agents, topoisomerase II inhibitors, antimetabolites, topoisomerase I inhibitors, hormones and hormonal analogues, signal transduction pathway inhibitors, non-receptor t
  • “Chemotherapeutic” or “chemotherapeutic agent” is used in accordance with its plain ordinary meaning and refers to a chemical composition or compound having antineoplastic properties or the ability to inhibit the growth or proliferation of cells.
  • the compounds described herein can be co-administered with conventional immunotherapeutic agents including, but not limited to, immunostimulants (e.g., Bacillus Calmette-Guerin (BCG), levamisole, interleukin-2, alpha-interferon, etc.), monoclonal antibodies (e.g., anti-CD20, anti-HER2, anti-CD52, anti-HLA-DR, and anti-VEGF monoclonal antibodies), immunotoxins (e.g., anti-CD33 monoclonal antibody-calicheamicin conjugate, anti-CD22 monoclonal antibody-pseudomonas exotoxin conjugate, etc.), and radioimmunotherapy (e.g., anti-CD20 monoclonal antibody conjugated to 111 In, 90 Y, or 131 I, etc.).
  • immunostimulants e.g., Bacillus Calmette-Guerin (BCG), levamisole, interleukin-2, alpha-interferon, etc
  • the compounds described herein can be co-administered with conventional radiotherapeutic agents including, but not limited to, radionuclides such as 47 Sc, 64 C 67 C, 89 Sr, 86 Y, 87 Y, and 212 Bi, optionally conjugated to antibodies directed against tumor antigens.
  • conventional radiotherapeutic agents including, but not limited to, radionuclides such as 47 Sc, 64 C 67 C, 89 Sr, 86 Y, 87 Y, and 212 Bi, optionally conjugated to antibodies directed against tumor antigens.
  • anti-neoplastic agent for use in combination or co-administered with the presently invented ATF4 pathway inhibiting compounds are anti-PD-L1 agents.
  • Anti-PD-L1 antibodies and methods of making the same are known in the art.
  • Such antibodies to PD-L1 may be polyclonal or monoclonal, and/or recombinant, and/or humanized.
  • Exemplary PD-L1 antibodies are disclosed in:
  • PD-L1 also referred to as CD274 or B7-H1
  • methods for use are disclosed in U.S. Pat. No. 7,943,743; US20130034559, WO2014055897, U.S. Pat. Nos. 8,168,179; and 7,595,048.
  • PD-L1 antibodies are in development as immuno-modulatory agents for the treatment of cancer.
  • the antibody to PD-L1 is an antibody disclosed in U.S. Pat. No. 8,217,149.
  • the anti-PD-L1 antibody comprises the CDRs of an antibody disclosed in U.S. Pat. No. 8,217,149.
  • the antibody to PD-L1 is an antibody disclosed in U.S. application Ser. No. 13/511,538.
  • the anti-PD-L1 antibody comprises the CDRs of an antibody disclosed in U.S. application Ser. No. 13/511,538.
  • the antibody to PD-L1 is an antibody disclosed in application Ser. No. 13/478,511.
  • the anti-PD-L1 antibody comprises the CDRs of an antibody disclosed in U.S. application Ser. No. 13/478,511.
  • the anti-PD-L1 antibody is BMS-936559 (MDX-1105). In another embodiment, the anti-PD-L1 antibody is MPDL3280A (RG7446). In another embodiment, the anti-PD-L1 antibody is MED14736.
  • a further active ingredient or ingredients for use in combination or co-administered with the presently invented ATF4 pathway inhibiting compounds are PD-1 antagonist.
  • PD-1 antagonist means any chemical compound or biological molecule that blocks binding of PD-L1 expressed on a cancer cell to PD-1 expressed on an immune cell (T cell, B cell or NKT cell) and preferably also blocks binding of PD-L2 expressed on a cancer cell to the immune-cell expressed PD-1.
  • Alternative names or synonyms for PD-1 and its ligands include: PDCD1, PD1, CD279 and SLEB2 for PD-1; PDCD1L1, PDL1, B7H1, B7-4, CD274 and B7-H for PD-L1; and PDCD1L2, PDL2, B7-DC, Btdc and CD273 for PD-L2.
  • the PD-1 antagonist blocks binding of human PD-L1 to human PD-1, and preferably blocks binding of both human PD-L1 and PD-L2 to human PD-1.
  • Human PD-1 amino acid sequences can be found in NCBI Locus No.: NP 005009.
  • Human PD-L1 and PD-L2 amino acid sequences can be found in NCBI Locus No.: NP_054862 and NP_079515, respectively.
  • PD-1 antagonists useful in the any of the aspects of the present invention include a monoclonal antibody (mAb), or antigen binding fragment thereof, which specifically binds to PD-1 or PD-L1, and preferably specifically binds to human PD-1 or human PD-L1.
  • the mAb may be a human antibody, a humanized antibody or a chimeric antibody, and may include a human constant region.
  • the human constant region is selected from the group consisting of IgG1, IgG2, IgG3 and IgG4 constant regions, and in preferred embodiments, the human constant region is an IgG1 or IgG4 constant region.
  • the antigen binding fragment is selected from the group consisting of Fab, Fab′-SH, F(ab′) 2 , scFv and Fv fragments.
  • Specific anti-human PD-1 mAbs useful as the PD-1 antagonist in any of the aspects and embodiments of the present invention include: MK-3475, a humanized IgG4 mAb with the structure described in WHO Drug Information, Vol. 27, No. 2, pages 161-162 (2013) and which comprises the heavy and light chain amino acid sequences shown in FIG. 6; nivolumab, a human IgG4 mAb with the structure described in WHO Drug Information, Vol. 27, No. 1, pages 68-69 (2013) and which comprises the heavy and light chain amino acid sequences shown in FIG. 7; the humanized antibodies h409A11, h409A16 and h409A17, which are described in WO2008/156712, and AMP-514, which is being developed by Medimmune.
  • PD-1 antagonists useful in the any of the aspects and embodiments of the present invention include an immunoadhesin that specifically binds to PD-1, and preferably specifically binds to human PD-1, e.g., a fusion protein containing the extracellular or PD-1 binding portion of PD-L1 or PD-L2 fused to a constant region such as an Fc region of an immunoglobulin molecule.
  • immunoadhesion molecules that specifically bind to PD-1 are described in WO2010/027827 and WO2011/066342.
  • Specific fusion proteins useful as the PD-1 antagonist in the treatment method, medicaments and uses of the present invention include AMP-224 (also known as B7-DCIg), which is a PD-L2-FC fusion protein and binds to human PD-1.
  • mAbs that bind to human PD-L1 are described in WO2013/019906, WO2010/077634 A1 and U.S. Pat. No. 8,383,796.
  • Specific anti-human PD-L1 mAbs useful as the PD-1 antagonist in the treatment method, medicaments and uses of the present invention include MPDL3280A, BMS-936559, MED14736, MSB0010718C.
  • KEYTRUDA/pembrolizumab is an anti-PD-1 antibody marketed for the treatment of lung cancer by Merck.
  • the amino acid sequence of pembrolizumab and methods of using are disclosed in U.S. Pat. No. 8,168,757.
  • Opdivo/nivolumab is a fully human monoclonal antibody marketed by Bristol Myers Squibb directed against the negative immunoregulatory human cell surface receptor PD-1 (programmed death-1 or programmed cell death-1/PCD-1) with immunopotentiation activity.
  • Nivolumab binds to and blocks the activation of PD-1, an Ig superfamily transmembrane protein, by its ligands PD-L1 and PD-L2, resulting in the activation of T-cells and cell-mediated immune responses against tumor cells or pathogens.
  • Activated PD-1 negatively regulates T-cell activation and effector function through the suppression of P13k/Akt pathway activation.
  • nivolumab Other names for nivolumab include: BMS-936558, MDX-1106, and ONO-4538.
  • the amino acid sequence for nivolumab and methods of using and making are disclosed in U.S. Pat. No. 8,008,449.
  • Additional examples of a further active ingredient or ingredients (anti-neoplastic agent) for use in combination or co-administered with the presently invented ATF4 pathway inhibiting compounds are immuno-modulators.
  • immuno-modulators refer to any substance including monoclonal antibodies that affects the immune system.
  • the ICOS binding proteins of the present invention can be considered immune-modulators.
  • Immuno-modulators can be used as anti-neoplastic agents for the treatment of cancer.
  • immune-modulators include, but are not limited to, anti-CTLA-4 antibodies such as ipilimumab (YERVOY) and anti-PD-1 antibodies (Opdivo/nivolumab and Keytruda/pembrolizumab).
  • Other immuno-modulators include, but are not limited to, OX-40 antibodies, PD-L1 antibodies, LAG3 antibodies, TIM-3 antibodies, 41BB antibodies and GITR antibodies.
  • Yervoy is a fully human CTLA-4 antibody marketed by Bristol Myers Squibb.
  • the protein structure of ipilimumab and methods are using are described in U.S. Pat. Nos. 6,984,720 and 7,605,238.
  • the compounds of the invention are combined with an inhibitor of the activity of the protein kinase R (PKR)-like ER kinase, PERK.
  • PPKR protein kinase R
  • the compounds of Formula (III) and pharmaceutically acceptable salts thereof may be co-administered with at least one other active agent known to be useful in the treatment of neurodegenerative diseases/injury.
  • the compounds of Formula (III) and pharmaceutically acceptable salts thereof may be co-administered with at least one other active agent known to be useful in the treatment of diabetes.
  • the compounds of Formula (III) and pharmaceutically acceptable salts thereof may be co-administered with at least one other active agent known to be useful in the treatment of cardiovascular disease.
  • the compounds of Formula (III) and pharmaceutically acceptable salts thereof may be co-administered with at least one other active agent known to be useful in the treatment of ocular diseases.
  • the compounds described herein can be used in combination with one another, with other active agents known to be useful in treating cancer (e.g. pancreatic cancer, breast cancer, multiple myeloma, or cancers of secretory cells), neurodegenerative diseases, vanishing white matter disease, childhood ataxia with CNS hypo-myelination, and/or intellectual disability syndromes (e.g. associated with impaired function of eIF2 or components in a signal transduction pathway including eIF2), or with adjunctive agents that may not be effective alone, but may contribute to the efficacy of the active agent.
  • cancer e.g. pancreatic cancer, breast cancer, multiple myeloma, or cancers of secretory cells
  • neurodegenerative diseases e.g. pancreatic cancer, breast cancer, multiple myeloma, or cancers of secretory cells
  • neurodegenerative diseases e.g. pancreatic cancer, breast cancer, multiple myeloma, or cancers of secretory cells
  • neurodegenerative diseases vanishing
  • the compounds set forth herein are provided as pharmaceutical compositions including the compound and a pharmaceutically acceptable excipient.
  • the compound, or a pharmaceutically acceptable salt thereof is co-adminstered with a second agent (e.g. therapeutic agent).
  • the compound, or a pharmaceutically acceptable salt thereof is co-adminstered with a second agent (e.g. therapeutic agent), which is administered in a therapeutically effective amount.
  • the second agent is an agent for treating cancer (e.g.
  • the second agent is an anti-cancer agent.
  • the second agent is a chemotherapeutic.
  • the second agent is an agent for improving memory.
  • the second agent is an agent for treating a neurodegenerative disease.
  • the second agent is an agent for treating vanishing white matter disease.
  • the second agent is an agent for treating childhood ataxia with CNS hypo-myelination. In embodiments, the second agent is an agent for treating an intellectual disability syndrome. In embodiments, the second agent is an agent for treating pancreatic cancer. In embodiments, the second agent is an agent for treating breast cancer. In embodiments, the second agent is an agent for treating multiple myeloma. In embodiments, the second agent is an agent for treating myeloma. In embodiments, the second agent is an agent for treating a cancer of a secretory cell. In embodiments, the second agent is an agent for reducing eIF2 ⁇ phosphorylation. In embodiments, the second agent is an agent for inhibiting a pathway activated by eIF2 ⁇ phosphorylation. In embodiments, the second agent is an agent for inhibiting the integrated stress response. In embodiments, the second agent is an anti-inflammatory agent.
  • eIF2alpha refers to the protein “Eukaryotic translation initiation factor 2A”.
  • eIF2alpha refers to the human protein. Included in the term “eIF2alpha” or “eIF2 ⁇ ” are the wildtype and mutant forms of the protein.
  • eIF2alpha refers to the protein associated with Entrez Gene 83939, OMIM 609234, UniProt Q9BY44, and/or RefSeq (protein) NP 114414.
  • the present invention relates to a method for treating an integrated stress response associated disease in a patient in need of such treatment, the method including administering a therapeutically effective amount of a compound of Formula (III), or a pharmaceutically acceptable salt thereof, to the patient.
  • the integrated stress response-associated disease is cancer.
  • the integrated stress response-associated disease is a neurodegenerative disease.
  • the integrated stress response-associated disease is vanishing white matter disease.
  • the integrated stress response-associated disease is childhood ataxia with CNS hypo-myelination.
  • the integrated stress response-associated disease is an intellectual disability syndrome.
  • the present invention relates to a method for treating a disease associated with phosphorylation of eIF2 ⁇ in a patient in need of such treatment, the method including administering a therapeutically effective amount of a compound of Formula (III), or a pharmaceutically acceptable salt thereof, to the patient.
  • the disease associated with phosphorylation of eIF2 ⁇ is cancer.
  • the disease associated with phosphorylation of eIF2 ⁇ is a neurodegenerative disease.
  • the disease associated with phosphorylation of eIF2 ⁇ is vanishing white matter disease.
  • the disease associated with phosphorylation of eIF2 ⁇ is childhood ataxia with CNS hypo-myelination.
  • the disease associated with phosphorylation of eIF2 ⁇ is an intellectual disability syndrome.
  • the present invention relates to a method for treating a disease selected from the group consisting of cancer, a neurodegenerative disease, vanishing white matter disease, childhood ataxia with CNS hypomyelination, and an intellectual disability syndrome.
  • the present invention relates to a method for treating an inflammatory disease in a patient in need of such treatment, the method including administering a therapeutically effective amount of a compound of Formula (III), or a pharmaceutically acceptable salt thereof, to the patient.
  • the inflammatory disease is associated with neurological inflammation.
  • the inflammatory disease is postoperative cognitive dysfunction.
  • the inflammatory disease is traumatic brain injury or chronic traumatic encephalopathy (CTE).
  • the disease is selected from the group consisting of cancer, a neurodegenerative disease, vanishing white matter disease, childhood ataxia with CNS hypo-myelination, and an intellectual disability syndrome.
  • the disease is cancer.
  • the disease is a neurodegenerative disease. In embodiments of the method of treating a disease, the disease is vanishing white matter disease. In embodiments of the method of treating a disease, the disease is childhood ataxia with CNS hypo-myelination. In embodiments of the method of treating a disease, the disease is an intellectual disability syndrome. In embodiments of the method of treating a disease, the disease is associated with phosphorylation of eIF2 ⁇ . In embodiments of the method of treating a disease, the disease is associated with an eIF2 ⁇ signaling pathway. In embodiments of the method of treating a disease, the disease is a cancer of a secretory cell type.
  • the disease is pancreatic cancer. In embodiments of the method of treating a disease, the disease is breast cancer. In embodiments of the method of treating a disease, the disease is multiple myeloma. In embodiments of the method of treating a disease, the disease is lymphoma. In embodiments of the method of treating a disease, the disease is leukemia. In embodiments of the method of treating a disease, the disease is a hematopoietic cell cancer.
  • the disease is Alzheimer's disease. In embodiments of the method of treating a disease, the disease is Amyotrophic lateral sclerosis. In embodiments of the method of treating a disease, the disease is Creutzfeldt-Jakob disease. In embodiments of the method of treating a disease, the disease is frontotemporal dementia. In embodiments of the method of treating a disease, the disease is Gerstmann-Straussler-Scheinker syndrome. In embodiments of the method of treating a disease, the disease is Huntington's disease. In embodiments of the method of treating a disease, the disease is HIV-associated dementia. In embodiments of the method of treating a disease, the disease is kuru.
  • the disease is Lewy body dementia. In embodiments of the method of treating a disease, the disease is Multiple sclerosis. In embodiments of the method of treating a disease, the disease is Parkinson's disease. In embodiments of the method of treating a disease, the disease is a Prion disease.
  • the disease is an inflammatory disease.
  • the inflammatory disease is postoperative cognitive dysfunction.
  • the inflammatory disease is traumatic brain injury.
  • the inflammatory disease is arthritis.
  • the inflammatory disease is rheumatoid arthritis.
  • the inflammatory disease is psoriatic arthritis.
  • the inflammatory disease is juvenile idiopathic arthritis.
  • the inflammatory disease is multiple sclerosis.
  • the inflammatory disease is systemic lupus erythematosus (SLE).
  • the inflammatory disease is myasthenia gravis.
  • the inflammatory disease is juvenile onset diabetes.
  • the inflammatory disease is diabetes mellitus type 1. In embodiments, the inflammatory disease is Guillain-Barre syndrome. In embodiments, the inflammatory disease is Hashimoto's encephalitis. In embodiments, the inflammatory disease is Hashimoto's thyroiditis. In embodiments, the inflammatory disease is ankylosing spondylitis. In embodiments, the inflammatory disease is psoriasis. In embodiments, the inflammatory disease is Sjogren's syndrome. In embodiments, the inflammatory disease is vasculitis. In embodiments, the inflammatory disease is glomerulonephritis. In embodiments, the inflammatory disease is auto-immune thyroiditis. In embodiments, the inflammatory disease is Behcet's disease.
  • the inflammatory disease is Crohn's disease. In embodiments, the inflammatory disease is ulcerative colitis. In embodiments, the inflammatory disease is bullous pemphigoid. In embodiments, the inflammatory disease is sarcoidosis. In embodiments, the inflammatory disease is ichthyosis. In embodiments, the inflammatory disease is Graves ophthalmopathy. In embodiments, the inflammatory disease is inflammatory bowel disease. In embodiments, the inflammatory disease is Addison's disease. In embodiments, the inflammatory disease is Vitiligo. In embodiments, the inflammatory disease is asthma. In embodiments, the inflammatory disease is allergic asthma. In embodiments, the inflammatory disease is acne vulgaris.
  • the inflammatory disease is celiac disease. In embodiments, the inflammatory disease is chronic prostatitis. In embodiments, the inflammatory disease is inflammatory bowel disease. In embodiments, the inflammatory disease is pelvic inflammatory disease. In embodiments, the inflammatory disease is reperfusion injury. In embodiments, the inflammatory disease is sarcoidosis. In embodiments, the inflammatory disease is transplant rejection. In embodiments, the inflammatory disease is interstitial cystitis. In embodiments, the inflammatory disease is atherosclerosis. In embodiments, the inflammatory disease is atopic dermatitis.
  • the method of treatment is a method of prevention.
  • a method of treating postsurgical cognitive dysfunction may include preventing postsurgical cognitive dysfunction or a symptom of postsurgical cognitive dysfunction or reducing the severity of a symptom of postsurgical cognitive dysfunction by administering a compound described herein prior to surgery.
  • this invention provides a compound of Formula (III), or a pharmaceutically acceptable salt thereof, for use in the treatment of a disease selected from the group consisting of cancer, a neurodegenerative disease, vanishing white matter disease, childhood ataxia with CNS hypomyelination, and an intellectual disability syndrome.
  • a disease selected from the group consisting of cancer, a neurodegenerative disease, vanishing white matter disease, childhood ataxia with CNS hypomyelination, and an intellectual disability syndrome.
  • this invention provides a compound of Formula (III), or a pharmaceutically acceptable salt thereof, for use in the treatment of an integrated stress response associated disease.
  • this invention provides a compound of Formula (III), or a pharmaceutically acceptable salt thereof, for use in the treatment of a disease associated with phosphorylation of eIF2 ⁇ .
  • this invention provides for the use of a compound of Formula (III), or a pharmaceutically acceptable salt thereof, in the manufacture of a medicament for the treatment of a disease selected from the group consisting of cancer, a neurodegenerative disease, vanishing white matter disease, childhood ataxia with CNS hypomyelination, and an intellectual disability syndrome.
  • a disease selected from the group consisting of cancer, a neurodegenerative disease, vanishing white matter disease, childhood ataxia with CNS hypomyelination, and an intellectual disability syndrome.
  • this invention provides for the use of a compound of Formula (III), or a pharmaceutically acceptable salt thereof, in the manufacture of a medicament for the treatment an integrated stress response associated disease.
  • this invention provides for the use of a compound of Formula (III), or a pharmaceutically acceptable salt thereof, in the manufacture of a medicament for the treatment of a disease associated with phosphorylation of eIF2 ⁇ .
  • the pharmaceutically active compounds within the scope of this invention are useful as ATF4 pathway inhibitors in mammals, particularly humans, in need thereof.
  • the present invention therefore provides a method of treating cancer, neurodegeneration and other conditions requiring ATF4 pathway inhibition, which comprises administering an effective amount of a compound of Formula (III) or a pharmaceutically acceptable salt thereof.
  • the compounds of Formula (III) also provide for a method of treating the above indicated disease states because of their demonstrated ability to act as ATF4 pathway inhibitors.
  • the drug may be administered to a patient in need thereof by any conventional route of administration, including, but not limited to, intravenous, intramuscular, oral, topical, subcutaneous, intradermal, intraocular and parenteral.
  • a ATF4 pathway inhibitor may be delivered directly to the brain by intrathecal or intraventricular route, or implanted at an appropriate anatomical location within a device or pump that continuously releases the ATF4 pathway inhibiting drug.
  • Solid or liquid pharmaceutical carriers are employed.
  • Solid carriers include, starch, lactose, calcium sulfate dihydrate, terra alba, sucrose, talc, gelatin, agar, pectin, acacia, magnesium stearate, and stearic acid.
  • Liquid carriers include syrup, peanut oil, olive oil, saline, and water.
  • the carrier or diluent may include any prolonged release material, such as glyceryl monostearate or glyceryl distearate, alone or with a wax.
  • the amount of solid carrier varies widely but, preferably, will be from about 25 mg to about 1 g per dosage unit.
  • the preparation will be in the form of a syrup, elixir, emulsion, soft gelatin capsule, sterile injectable liquid such as an ampoule, or an aqueous or nonaqueous liquid suspension.
  • compositions are made following conventional techniques of a pharmaceutical chemist involving mixing, granulating, and compressing, when necessary, for tablet forms, or mixing, filling and dissolving the ingredients, as appropriate, to give the desired oral or parenteral products.
  • Doses of the presently invented pharmaceutically active compounds in a pharmaceutical dosage unit as described above will be an efficacious, nontoxic quantity preferably selected from the range of 0.001-100 mg/kg of active compound, preferably 0.001-50 mg/kg.
  • the selected dose is administered preferably from 1-6 times daily, orally or parenterally.
  • Preferred forms of parenteral administration include topically, rectally, transdermally, by injection and continuously by infusion.
  • Oral dosage units for human administration preferably contain from 0.05 to 3500 mg of active compound.
  • Oral administration which uses lower dosages, is preferred. Parenteral administration, at high dosages, however, also can be used when safe and convenient for the patient.
  • Optimal dosages to be administered may be readily determined by those skilled in the art, and will vary with the particular ATF4 pathway inhibitor in use, the strength of the preparation, the mode of administration, and the advancement of the disease condition. Additional factors depending on the particular patient being treated will result in a need to adjust dosages, including patient age, weight, diet, and time of administration.
  • a compound of Formula (III) When administered to prevent organ damage in the transportation of organs for transplantation, a compound of Formula (III) is added to the solution housing the organ during transportation, suitably in a buffered solution.
  • the method of this invention of inducing ATF4 pathway inhibitory activity in mammals, including humans, comprises administering to a subject in need of such activity an effective ATF4 pathway inhibiting amount of a pharmaceutically active compound of the present invention.
  • the invention also provides for the use of a compound of Formula (III) or a pharmaceutically acceptable salt thereof in the manufacture of a medicament for use as a ATF4 pathway inhibitor.
  • the invention also provides for the use of a compound of Formula (III) or a pharmaceutically acceptable salt thereof in the manufacture of a medicament for use in therapy.
  • the invention also provides for the use of a compound of Formula (III) or a pharmaceutically acceptable salt thereof in the manufacture of a medicament for use in treating cancer, pre-cancerous syndromes, Alzheimer's disease, spinal cord injury, traumatic brain injury, ischemic stroke, stroke, diabetes, Parkinson disease, Huntington's disease, Creutzfeldt-Jakob Disease, and related prion diseases, progressive supranuclear palsy, amyotrophic lateral sclerosis, myocardial infarction, cardiovascular disease, inflammation, fibrosis, chronic and acute diseases of the liver, chronic and acute diseases of the lung, chronic and acute diseases of the kidney, chronic traumatic encephalopathy (CTE), neurodegeneration, dementia, cognitive impairment, atherosclerosis, ocular diseases, arrhythmias, in organ transplantation and in the transportation of organs for transplantation.
  • CTE chronic traumatic encephalopathy
  • the invention also provides for the use of a compound of Formula (III) or a pharmaceutically acceptable salt thereof in the manufacture of a medicament for use in preventing organ damage during the transportation of organs for transplantation.
  • the invention also provides for a pharmaceutical composition for use as a ATF4 pathway inhibitor which comprises a compound of Formula (III) or a pharmaceutically acceptable salt thereof and a pharmaceutically acceptable carrier.
  • the invention also provides for a pharmaceutical composition for use in the treatment of cancer which comprises a compound of Formula (III) or a pharmaceutically acceptable salt thereof and a pharmaceutically acceptable carrier.
  • the pharmaceutically active compounds of the present invention can be co-administered with further active ingredients, such as other compounds known to treat cancer, or compounds known to have utility when used in combination with a ATF4 pathway inhibitor.
  • the invention also provides novel processes and novel intermedites useful in preparing the presently invented compounds.
  • the invention also provides a pharmaceutical composition
  • a pharmaceutical composition comprising from 0.5 to 1,000 mg of a compound of Formula (I) or pharmaceutically acceptable salt thereof and from 0.5 to 1,000 mg of a pharmaceutically acceptable excipient.
  • the combined organic extract was washed with a saturated brine solution (10 mL), dried over anhydrous sodium sulphate, filtered and concentrated under reduced pressure to give the crude product.
  • the crude product was purified by flash column chromatography using a silica gel column and mixture of ethyl acetate in hexane as eluent. The product was eluted at 58-62% ethylacetate in hexane. Fractions containing product were concentrated under reduced pressure to give tert-butyl (1-(3-(4-chlorophenoxy)propyl)piperidin-4-yl)carbamate (0.510 g, 55.43% yield) as color less liquid.
  • Example 10 The Compounds of Example 10 was prepared generally according to the procedures described above for Example 9.
  • reaction mixture was concentrated under reduced pressure and the crude product was purified by silica-gel column chromatography by using 4% MeOH:DCM as an eluent to get the product and the position of the hydroxyl group was confirmed by 13NMR, COSY, HSQC and HMBC NMR. Yield: 0.9 g (60.8%) as a white solid.
  • reaction mixture was quenched with DCM 5 mL, and diluted with water 50 mL and extracted with DCM 50 mL ⁇ 2, the combined organic layer was washed with sodium bicarbonate solution and dried over anhydrous Na 2 SO 4 , filtered and concentrated under reduced pressure and the crude product was purified by prep. TLC by using 50% EA: Hex as an eluent to get the product. Yield: 0.0119 g (11.9%) as a white solid.
  • reaction mixture was quenched with ice and extracted with ethyl acetate 100 mL, the organic layer was separated and dried over anhydrous sodium sulphate, filtered and concentrated under reduced pressure to get the crude product.
  • the crude product was purified by silica gel column chromatography by using 9% EA; Hex. Yield: 1.3 g (82.80%) as colorless liquid.
  • reaction mixture was diluted with 50 mL of water and extracted with DCM (50 mL ⁇ 2), the combined organic layer was dried over anhydrous sodium sulphate, filtered and concentrated to get the crude product and the crude product was purified by prep TLC by using 5% MeOH:DCM as an eluent to get the pure product. Yield: 0.021 g (9.5%), as white solid.
  • reaction mixture was diluted with water (50 mL), the product was extracted with ethyl acetate (3 ⁇ 50 mL). The combined organic layers were washed with cold water (25 mL), brine (20 mL), dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to get the crude product.
  • reaction mixture was filtered through celite pad, washed the celite pad with ethyl acetate (20 mL). The filtrate was washed with water (20 mL), brine (20 mL), dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to get the crude product.
  • the crude product was purified by silicagel column chromatography using 6% methanol in dichloromethane as eluent to obtain the title compound 2-(4-chlorophenoxy)-N-(1-(3-((5-chloropyridin-2-yl)oxy)propyl)piperidin-4-yl)acetamide (0.02 g, 10% yield), as white solid.
  • Example 21 was prepared generally according to the procedure described above for Example 20.
  • reaction mixture was diluted with water (100 mL), the product was extracted with ethyl acetate (3 ⁇ 100 mL). The combined organic layers were washed with cold water (50 mL), brine (50 mL), dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to get the crude product.
  • the crude product was purified by silicagel column chromatography using 20% ethyl acetate in hexane as eluent to obtain the title compound 1-chloro-4-(2,2-dimethoxyethoxy)benzene (3.2 g, 38% yield) as colourless oil.
  • reaction mixture was allowed to warm to 25° C. and stirred for 6 h. The progress of the reaction was monitored by TLC. After completion of reaction, the reaction mixture was diluted with dichloromethane (70 mL), washed with water (2 ⁇ 30 mL), brine (30 mL), derid over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to get the crude product.
  • reaction mixture was quenched with water (50 mL) and extracted with ethyl acetate (3 ⁇ 30 mL), the combined organics were washed with water (30 mL), brine (20 mL), dried over anhydrous sodium sulphate, filtered and concentrated under reduced pressure to get the crude product.
  • the crude product was purified by silica gel column chromatography (Combiflash) using 50% ethyl acetate in hexane as eluent.
  • the obtained solid was dissolved with dichloromethane (10 mL) and 2M hydrochloric acid (20 mL) and stirred for 30 minutes at 27° C.
  • the organic phases were separated out and the aqueous layer was extracted with dichloromethane (20 mL).
  • the combined organics were dried over anhydrous sodium sulphate, filtered and concentrated under reduced pressure to give the crude intermediate.
  • the crude intermediate was dissolved with acetonitrile (10 mL) and water (0.5 mL) and the mixture was heated to 70° C. and stirred for 1 h.
  • reaction mixture was allowed to warm to 27° C., stirred for 16 h. The progress of the reaction was monitored by TLC. After completion of reaction, the reaction mixture was diluted with dichloromethane (30 mL), washed with water (30 mL), brine (25 mL), dried over anhydrous sodium sulphate, filtered and concentrated under reduced pressure to give the crude product.
  • reaction mixture was diluted with ethyl acetate (100 mL), washed with water (2 ⁇ 30 mL), brine (30 mL), dried over anhydrous sodium sulphate, filtered and concentrated under reduced pressure to give the crude product.
  • the crude product was purified by flash column chromatography (Combiflash) using a silica gel column and the product was eluted at 5% methanol in dichloromethane as eluent to obtain the title compound ethyl 4-(4-chlorophenoxy)-2-(4-(2-(3,4-dichlorophenoxy)acetamido)piperidin-1-yl)butanoate (0.07 g) as pale brown gum.
  • reaction mixture was quenched with water (50 mL) and extracted with ethyl acetate (3 ⁇ 50 mL), the combined organics were washed with water (30 mL), brine (20 mL), dried over anhydrous sodium sulphate, filtered and concentrated under reduced pressure to give the crude product.
  • reaction mixture was diluted with DCM (100 mL), washed with ice cold water (2 ⁇ 50 mL), saturated ammonium chloride solution (50 mL) and water (50 mL). The combined organic layer was dried over anhydrous sodium sulphate, filtered and concentrated under reduced pressure. Crude was purified by flash column chromatography using 6% methanol in dichloromethane to give 2-chloro-N-(1-(3-(4-chlorophenoxy)propyl)piperidin-4-yl)acetamide (0.15 g, 26.5% yield) as off white solid.
  • LCMS (ES) m/z 345.1 [M+H] + .
  • Example 56 was prepared generally according to the procedure described above for Example 55.
  • Methyl 4-(2-(4-chlorophenoxy)acetamido)-1-(3-(4-chlorophenoxy)propyl)piperidine-2-carboxylate was purified by prep HPLC (Analytical conditions: Column: Inertsil ODS 3V (250 mm ⁇ 4.6 mm ⁇ 5 mic), Mobile phase (A): 0.1% Ammonia in water, Mobile phase (B): Acetonitrile, Flow rate: 1.0 mL/min, compound RT (pair-1): 14.108 minutes, compound RT (pair ⁇ 2): 17.987 minutes) to get Z14 (pair-1) and Z15 (pair ⁇ 2). Z15 is used to next step (Methyl ester hydrolysis).
  • the ATF4 reporter assay measures the effect of Thapsigargin induced cellular stress on ATF4 expression.
  • a stable cell line was created by transfecting SH-SY5Y cells with a plasmid containing the NanoLuc® luciferase gene fused to the 5′-UTR of ATF4, under the control of the CMV promoter.
  • the ATF4 5′-UTR contains two open reading frames which mediate the cellular stress-dependent translation of the reporter gene.
  • Clones stably expressing the reporter construct were isolated and selected based on the luminescence response to thapsigargin and inhibition of this signal by test compounds. Briefly, SH-SY5Y-ATF4-NanoLuc cells were challenged with Thapsigargin for 14-18 hours to determine the stress effect with or without test compounds.
  • Cells were propagated in growth media consisting of 90% DMEM F12 (InVitrogen #11320-033), 10% Fetal Bovine Serum (Gibco #10438-026), 5 mM Glutamax (Gibco #35050-061), 5 mM Hepes, (Gibco #15630-080), and 0.5 mg/ml Geneticin (Gibco #10131-027).
  • Cells were prepared for the assay by removing all media from cells, washing the plated cells with phosphate buffered saline, and detached by adding a solution comprised of 10% Tryple express solution (InVitrogen12604-021) and 90% enzyme-free cell dissociation buffer HANKS base (Gibco 13150-016).
  • the trypsin was deactivated by adding assay media comprised of 90% phenol-red free DMEM F12 (InVitrogen, 11039), 10% Fetal Bovine Serum (Gibco #10438-026), (5 mM Glutamax (Gibco #35050-061), 5 mM Hepes, (Gibco #15630-080), and 0.5 mg/ml Geneticin (Gibco #10131-027). Suspended cells were spun down at 300 g for 5 min, the supernatant was removed and the cell pellet was suspended in warm media (30-37° C.) comprised as above at (1e6 cell/ml).
  • assay media comprised of 90% phenol-red free DMEM F12 (InVitrogen, 11039), 10% Fetal Bovine Serum (Gibco #10438-026), (5 mM Glutamax (Gibco #35050-061), 5 mM Hepes, (Gibco #15630-080), and 0.5
  • Assay plates were prepared by adding 250 nL of compound stock solution in 100% DMSO to each well, followed by dispensing 20 microliters/well cell suspension to deliver 15-20k cell/well. Cells were incubated for 1 hour at 37° C. Then, 5 ⁇ L of 1.5 ⁇ M or 1 ⁇ M of Thapsigargin (final concentration: 200-300 nM) was added to each well of cells. Assay plates containing cells were incubated for 14-18 hours at 37° C.
  • luciferase produced by the ATF4 constructs was measured as follows. Aliquots of the Nano-Glo reagent (Nano-Glo® Luciferase Assay Substrate, Promega, N113, Nano-Glo® Luciferase Assay Buffer, Promega, N112 (parts of Nano-Glo® Luciferase Assay System, N1150) were brought to room temperature, the substrate and buffer were mixed according to manufacturer's instructions. The cell plates were equilibrated to room temperature. 25 microliters/well of the mixed Nano-Glo reagent were dispensed into assay wells and pulse spun to settle contents and the plate was sealed with film. The plates were incubated at room temperature for 1 hour before detecting luminescence on an Envision plate reader.
  • An oral dosage form for administering the present invention is produced by filing a standard two piece hard gelatin capsule with the ingredients in the proportions shown in Table 2, below.
  • An injectable form for administering the present invention is produced by stirring 1.7% by weight of 2-(4-chlorophenoxy)-N-(1-(3-(4-chlorophenoxy)propyl)piperidin-4-yl)acetamide (Compound of Example 2) in 10% by volume propylene glycol in water.
  • sucrose, calcium sulfate dihydrate and a PERK inhibitor as shown in Table 4 below are mixed and granulated in the proportions shown with a 10% gelatin solution.
  • the wet granules are screened, dried, mixed with the starch, talc and stearic acid, screened and compressed into a tablet.
  • Examples 1 and 3 to 8 were tested generally according to the above ATF4 cell based assay and in a set of two or more experimental runs exhibited an average ATF4 pathway inhibitory activity (IC 50 ) ⁇ 300 nM.
  • Example 1 The compound of Example 1 was tested generally according to the above ATF4 cell based assay and in a set of two or more experimental runs exhibited an average ATF4 pathway inhibitory activity (IC 50 ) of 75.86 nM.
  • Example 2 The compound of Example 2 was tested generally according to the above ATF4 cell based assay and in a set of two or more experimental runs exhibited an average ATF4 pathway inhibitory activity (IC 50 ) ⁇ 4000 nM.
  • Examples 27, 29, 39, 40, 49, and 56 were tested generally according to the above ATF4 cell based assay and in a set of two or more experimental runs exhibited an average ATF4 pathway inhibitory activity (IC 50 )>1,000 nM.
  • Example 11 The compound of Example 11 was tested generally according to the above ATF4 cell based assay and in a set of two or more experimental runs exhibited an average ATF4 pathway inhibitory activity (IC 50 ) of 32 nM.
  • Example 17 The compound of Example 17 was tested generally according to the above ATF4 cell based assay and in a set of two or more experimental runs exhibited an average ATF4 pathway inhibitory activity (IC 50 ) of 76.8 nM.
  • Example 24 The compound of Example 24 was tested generally according to the above ATF4 cell based assay and in a set of two or more experimental runs exhibited an average ATF4 pathway inhibitory activity (IC 50 ) of 200.6 nM.
  • Example 30 The compound of Example 30 was tested generally according to the above ATF4 cell based assay and in a set of two or more experimental runs exhibited an average ATF4 pathway inhibitory activity (IC 50 ) of 110.5 nM.
  • Example 37 The compound of Example 37 was tested generally according to the above ATF4 cell based assay and in a set of two or more experimental runs exhibited an average ATF4 pathway inhibitory activity (IC 50 ) of 98.7 nM.
  • Example 43 The compound of Example 43 was tested generally according to the above ATF4 cell based assay and in a set of two or more experimental runs exhibited an average ATF4 pathway inhibitory activity (IC 50 ) of 58.4 nM.
  • Example 50 The compound of Example 50 was tested generally according to the above ATF4 cell based assay and in a set of two or more experimental runs exhibited an average ATF4 pathway inhibitory activity (IC 50 ) of 93.9 nM.
  • Example 57 The compound of Example 57 was tested generally according to the above ATF4 cell based assay and in a set of two or more experimental runs exhibited an average ATF4 pathway inhibitory activity (IC 50 ) of 61.2 nM.
  • Example 59 The compound of Example 59 was tested generally according to the above ATF4 cell based assay and in a set of two or more experimental runs exhibited an average ATF4 pathway inhibitory activity (IC 50 ) of 172.5 nM.

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EP3468960A1 (en) 2019-04-17
CN109563071A (zh) 2019-04-02
WO2017212425A1 (en) 2017-12-14
US11547704B2 (en) 2023-01-10
AU2017279029A1 (en) 2018-12-20
CA3026982A1 (en) 2017-12-14
CN109563071B (zh) 2021-08-03
BR112018075598A2 (pt) 2019-03-26
US20200297710A1 (en) 2020-09-24
EP3468960B1 (en) 2022-03-23
US20230165848A1 (en) 2023-06-01
RU2018145734A (ru) 2020-07-14

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