AU2015236428B2 - TrkA kinase inhibitors, compositions and methods thereof - Google Patents
TrkA kinase inhibitors, compositions and methods thereof Download PDFInfo
- Publication number
- AU2015236428B2 AU2015236428B2 AU2015236428A AU2015236428A AU2015236428B2 AU 2015236428 B2 AU2015236428 B2 AU 2015236428B2 AU 2015236428 A AU2015236428 A AU 2015236428A AU 2015236428 A AU2015236428 A AU 2015236428A AU 2015236428 B2 AU2015236428 B2 AU 2015236428B2
- Authority
- AU
- Australia
- Prior art keywords
- methyl
- trifluoromethyl
- benzamide
- pyrazol
- fluoro
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
Links
- 0 Cc1c(C)c(*)c(C(N)=O)c(*)c1* Chemical compound Cc1c(C)c(*)c(C(N)=O)c(*)c1* 0.000 description 4
- YRIWTSXETKLENH-UHFFFAOYSA-N CCOC(C(CC#N)c(cc1)nc(-c2ccccc2)c1N)=O Chemical compound CCOC(C(CC#N)c(cc1)nc(-c2ccccc2)c1N)=O YRIWTSXETKLENH-UHFFFAOYSA-N 0.000 description 2
- CTCBNTHODLJXLB-UHFFFAOYSA-N CCOC(Cc(cc1)nc(-c2ccccc2)c1[N+]([O-])=O)=O Chemical compound CCOC(Cc(cc1)nc(-c2ccccc2)c1[N+]([O-])=O)=O CTCBNTHODLJXLB-UHFFFAOYSA-N 0.000 description 2
- RBTMVLQVZKYOJG-UHFFFAOYSA-N CC(C)(C)OC(N(CCc1c2)Cc1nc(-c1ccccc1)c2N)=O Chemical compound CC(C)(C)OC(N(CCc1c2)Cc1nc(-c1ccccc1)c2N)=O RBTMVLQVZKYOJG-UHFFFAOYSA-N 0.000 description 1
- MUBNGYAVVSHDBE-UHFFFAOYSA-N CC(C)(C)OC(Nc1c(-c2ccccc2)nc(CCl)nc1)=O Chemical compound CC(C)(C)OC(Nc1c(-c2ccccc2)nc(CCl)nc1)=O MUBNGYAVVSHDBE-UHFFFAOYSA-N 0.000 description 1
- VDNIRHDGPHZDGQ-UHFFFAOYSA-N CC1(C)OB(c2c(C(F)(F)F)ccc(C(OC)=O)c2)OC1 Chemical compound CC1(C)OB(c2c(C(F)(F)F)ccc(C(OC)=O)c2)OC1 VDNIRHDGPHZDGQ-UHFFFAOYSA-N 0.000 description 1
- ZXYLTFBPBFXKBU-UHFFFAOYSA-N CCOC(C(C(OCC)=O)c(cc1)nc(-c2ccccc2)c1[N+]([O-])=O)=O Chemical compound CCOC(C(C(OCC)=O)c(cc1)nc(-c2ccccc2)c1[N+]([O-])=O)=O ZXYLTFBPBFXKBU-UHFFFAOYSA-N 0.000 description 1
- YPMBEQSBXQZRGR-UHFFFAOYSA-N CCOC(C(CC#N)c(cc1)nc(-c2ccccc2)c1[N+]([O-])=O)=O Chemical compound CCOC(C(CC#N)c(cc1)nc(-c2ccccc2)c1[N+]([O-])=O)=O YPMBEQSBXQZRGR-UHFFFAOYSA-N 0.000 description 1
- HUTURXUEGGHMAW-UHFFFAOYSA-N CCOC(C(Cc(nc1)nc(-c2ccccc2)c1NC(OC(C)(C)C)=O)C(OCC)=O)=O Chemical compound CCOC(C(Cc(nc1)nc(-c2ccccc2)c1NC(OC(C)(C)C)=O)C(OCC)=O)=O HUTURXUEGGHMAW-UHFFFAOYSA-N 0.000 description 1
- KRBIMWDSILHGKR-UHFFFAOYSA-N COC(c1ccc(C(F)(F)F)c(Br)c1)=O Chemical compound COC(c1ccc(C(F)(F)F)c(Br)c1)=O KRBIMWDSILHGKR-UHFFFAOYSA-N 0.000 description 1
- CMZSTOBUWAXOQQ-AWEZNQCLSA-N C[C@@H](C(NCc(nc1)nc(-c2ccccc2)c1NC(c1cc(-c2n[n](C)cc2)c(C(F)(F)F)cc1F)=O)=O)O Chemical compound C[C@@H](C(NCc(nc1)nc(-c2ccccc2)c1NC(c1cc(-c2n[n](C)cc2)c(C(F)(F)F)cc1F)=O)=O)O CMZSTOBUWAXOQQ-AWEZNQCLSA-N 0.000 description 1
- SRLWGYASZLTADR-UHFFFAOYSA-N C[n](cc1)nc1-c(c(C(F)(F)F)c1)cc(C(Nc(cnc(CC(N)=C)c2)c2-c2ccccc2)=O)c1F Chemical compound C[n](cc1)nc1-c(c(C(F)(F)F)c1)cc(C(Nc(cnc(CC(N)=C)c2)c2-c2ccccc2)=O)c1F SRLWGYASZLTADR-UHFFFAOYSA-N 0.000 description 1
- GNPUNNKJDPIRJO-UHFFFAOYSA-N C[n](cc1)nc1-c(c(C(F)(F)F)c1)cc(C(Nc2c(-c3ccccc3)nc(CCC(N)=O)nc2)=O)c1F Chemical compound C[n](cc1)nc1-c(c(C(F)(F)F)c1)cc(C(Nc2c(-c3ccccc3)nc(CCC(N)=O)nc2)=O)c1F GNPUNNKJDPIRJO-UHFFFAOYSA-N 0.000 description 1
- VKVPCGGCSYOSEG-UHFFFAOYSA-N C[n](cc1)nc1-c(c(C(F)(F)F)c1)cc(C(O)=O)c1F Chemical compound C[n](cc1)nc1-c(c(C(F)(F)F)c1)cc(C(O)=O)c1F VKVPCGGCSYOSEG-UHFFFAOYSA-N 0.000 description 1
- YEFMNLGGXARXIR-UHFFFAOYSA-N C[n](cc1)nc1-c(cc1C(Nc2c(-c3ccccc3)nc(C(CCN3)C3=O)nc2)=O)c(C(F)(F)F)cc1F Chemical compound C[n](cc1)nc1-c(cc1C(Nc2c(-c3ccccc3)nc(C(CCN3)C3=O)nc2)=O)c(C(F)(F)F)cc1F YEFMNLGGXARXIR-UHFFFAOYSA-N 0.000 description 1
- JVOAFOKZLQICPH-UHFFFAOYSA-N C[n](cc1)nc1-c(cc1C(Nc2cnc(CN)nc2-c2ccccc2)=O)c(C(F)(F)F)cc1F Chemical compound C[n](cc1)nc1-c(cc1C(Nc2cnc(CN)nc2-c2ccccc2)=O)c(C(F)(F)F)cc1F JVOAFOKZLQICPH-UHFFFAOYSA-N 0.000 description 1
- JLBSYBPJDMIGOD-UHFFFAOYSA-N NC(Cc(nc1)cc(-c2ccccc2)c1NC(c1cc(-c2ncccc2)c(C(F)(F)F)cc1F)=O)=O Chemical compound NC(Cc(nc1)cc(-c2ccccc2)c1NC(c1cc(-c2ncccc2)c(C(F)(F)F)cc1F)=O)=O JLBSYBPJDMIGOD-UHFFFAOYSA-N 0.000 description 1
- OTFCRUXLUASLQC-UHFFFAOYSA-N NC(Cc(nc1)nc(-c2ccccc2)c1NC(c1cc(-c2n[nH]cc2)c(C(F)(F)F)cc1F)=O)=O Chemical compound NC(Cc(nc1)nc(-c2ccccc2)c1NC(c1cc(-c2n[nH]cc2)c(C(F)(F)F)cc1F)=O)=O OTFCRUXLUASLQC-UHFFFAOYSA-N 0.000 description 1
- MOHDQGLXHCXEEG-UHFFFAOYSA-N Nc1c(-c2ccccc2)nc(CC(CC(N2)=O)C2=O)nc1 Chemical compound Nc1c(-c2ccccc2)nc(CC(CC(N2)=O)C2=O)nc1 MOHDQGLXHCXEEG-UHFFFAOYSA-N 0.000 description 1
- VVBTXZXYKASRRZ-UHFFFAOYSA-N Nc1c(-c2ccccc2)nc(CNCC2)c2c1 Chemical compound Nc1c(-c2ccccc2)nc(CNCC2)c2c1 VVBTXZXYKASRRZ-UHFFFAOYSA-N 0.000 description 1
- LJLKHQYPIKYWOG-UHFFFAOYSA-N Nc1cc(C(NCC2)=O)c2nc1-c1ncccc1 Chemical compound Nc1cc(C(NCC2)=O)c2nc1-c1ncccc1 LJLKHQYPIKYWOG-UHFFFAOYSA-N 0.000 description 1
- JBBYUKGSTCNWSA-UHFFFAOYSA-N Nc1cc(N2CCOCC2)cnc1-c1ccccc1 Chemical compound Nc1cc(N2CCOCC2)cnc1-c1ccccc1 JBBYUKGSTCNWSA-UHFFFAOYSA-N 0.000 description 1
- OCLDSIAHVMNJMC-UHFFFAOYSA-N O=C(c(ccc(C(F)(F)F)c1)c1Cl)Cl Chemical compound O=C(c(ccc(C(F)(F)F)c1)c1Cl)Cl OCLDSIAHVMNJMC-UHFFFAOYSA-N 0.000 description 1
- DHHOSTLGHAVLHW-UHFFFAOYSA-N O=C(c(ccc(C(F)(F)F)c1)c1Cl)Nc1cc(N2CCOCC2)cnc1-c1ccccc1 Chemical compound O=C(c(ccc(C(F)(F)F)c1)c1Cl)Nc1cc(N2CCOCC2)cnc1-c1ccccc1 DHHOSTLGHAVLHW-UHFFFAOYSA-N 0.000 description 1
- IGMJZXTVWRCLKZ-UHFFFAOYSA-N [O-][N+](c(cc1)c(-c2ccccc2)nc1Cl)=O Chemical compound [O-][N+](c(cc1)c(-c2ccccc2)nc1Cl)=O IGMJZXTVWRCLKZ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/10—Spiro-condensed systems
- C07D491/107—Spiro-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/64—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings
- C07C233/66—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by halogen atoms or by nitro or nitroso groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/72—Nitrogen atoms
- C07D213/75—Amino or imino radicals, acylated by carboxylic or carbonic acids, or by sulfur or nitrogen analogues thereof, e.g. carbamates
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/32—One oxygen, sulfur or nitrogen atom
- C07D239/42—One nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- 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
- C07D401/02—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 containing two hetero rings
- C07D401/04—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 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- 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
- C07D401/02—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 containing two hetero rings
- C07D401/06—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 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- 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
- C07D401/02—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 containing two hetero rings
- C07D401/12—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 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- 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
- C07D401/14—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 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Hematology (AREA)
- Diabetes (AREA)
- Dermatology (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pyridine Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PCT/CN2014/074145 WO2015143654A1 (en) | 2014-03-26 | 2014-03-26 | TrkA KINASE INHIBITORS,COMPOSITIONS AND METHODS THEREOF |
| AUPCT/CN2014/074145 | 2014-03-26 | ||
| PCT/US2015/021936 WO2015148344A2 (en) | 2014-03-26 | 2015-03-23 | Trka kinase inhibitors, compositions and methods thereof |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU2015236428A1 AU2015236428A1 (en) | 2016-09-29 |
| AU2015236428B2 true AU2015236428B2 (en) | 2018-11-08 |
Family
ID=54193895
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2015236428A Ceased AU2015236428B2 (en) | 2014-03-26 | 2015-03-23 | TrkA kinase inhibitors, compositions and methods thereof |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US9815846B2 (cg-RX-API-DMAC7.html) |
| EP (1) | EP3122346B1 (cg-RX-API-DMAC7.html) |
| JP (1) | JP2017512794A (cg-RX-API-DMAC7.html) |
| KR (1) | KR20160128420A (cg-RX-API-DMAC7.html) |
| CN (1) | CN106794161A (cg-RX-API-DMAC7.html) |
| AU (1) | AU2015236428B2 (cg-RX-API-DMAC7.html) |
| BR (1) | BR112016022069A2 (cg-RX-API-DMAC7.html) |
| CA (1) | CA2943858A1 (cg-RX-API-DMAC7.html) |
| MX (1) | MX2016012480A (cg-RX-API-DMAC7.html) |
| RU (1) | RU2672583C2 (cg-RX-API-DMAC7.html) |
| WO (2) | WO2015143654A1 (cg-RX-API-DMAC7.html) |
Families Citing this family (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3967312A1 (en) | 2014-09-12 | 2022-03-16 | UNION therapeutics A/S | Antibacterial use of halogenated salicylanilides |
| GB201509326D0 (en) | 2015-05-29 | 2015-07-15 | Antibio Tx Aps | Novel use |
| GB201604484D0 (en) | 2016-03-16 | 2016-04-27 | Antibiotx Aps And Københavns Uni University Of Copenhagen | Topical antibacterial compositions |
| JP6965083B2 (ja) * | 2017-10-04 | 2021-11-10 | 公益財団法人微生物化学研究会 | 化合物、及び発光化合物 |
| CN108794414B (zh) * | 2018-06-22 | 2021-01-01 | 浙江大学 | 芳酰胺基取代的均三嗪类化合物及制备和应用 |
| CN108997224B (zh) * | 2018-08-28 | 2023-04-28 | 韶远科技(上海)有限公司 | 一种2-氯-5-氰基含氮六元杂环化合物的制备方法 |
| CA3123227A1 (en) | 2018-12-20 | 2020-06-25 | Amgen Inc. | Heteroaryl amides useful as kif18a inhibitors |
| AU2019401495B2 (en) | 2018-12-20 | 2025-06-26 | Amgen Inc. | Heteroaryl amides useful as KIF18A inhibitors |
| US12459932B2 (en) | 2018-12-20 | 2025-11-04 | Amgen Inc. | KIF18A inhibitors |
| US11419834B2 (en) | 2019-02-25 | 2022-08-23 | Rhode Island Hospital | Methods for treating diseases or infections caused by or associated with H. pylori using a halogenated salicylanilide |
| CN114364798A (zh) | 2019-03-21 | 2022-04-15 | 欧恩科斯欧公司 | 用于治疗癌症的Dbait分子与激酶抑制剂的组合 |
| CN114401953A (zh) * | 2019-08-02 | 2022-04-26 | 美国安进公司 | Kif18a抑制剂 |
| US20220401436A1 (en) | 2019-11-08 | 2022-12-22 | INSERM (Institute National de la Santé et de la Recherche Médicale) | Methods for the treatment of cancers that have acquired resistance to kinase inhibitors |
| WO2021148581A1 (en) | 2020-01-22 | 2021-07-29 | Onxeo | Novel dbait molecule and its use |
| IL298363A (en) | 2020-05-20 | 2023-01-01 | Flagship Pioneering Innovations Vi Llc | Immunogenic compositions and uses thereof |
| TW202210467A (zh) * | 2020-05-28 | 2022-03-16 | 美商美國禮來大藥廠 | TrkA抑制劑 |
| WO2022090101A1 (en) | 2020-10-26 | 2022-05-05 | Boehringer Ingelheim International Gmbh | Process for synthesis of 2,4-dichloro-5-aminopyrimidine |
| IL311465A (en) * | 2021-09-14 | 2024-05-01 | Univ Vanderbilt | Phenyl core compounds as mglu5 negative allosteric modulators and methods of making and using the same |
| CN113880724A (zh) * | 2021-12-06 | 2022-01-04 | 南京桦冠生物技术有限公司 | 一种3-(2-氨基苯基)-2-丙烯酸酯的制备方法 |
| WO2023211256A1 (ko) * | 2022-04-29 | 2023-11-02 | 제일약품주식회사 | 신규한 pim 키나아제 억제 화합물 및 이의 용도 |
| WO2024233922A2 (en) * | 2023-05-10 | 2024-11-14 | Texas Tech University System | Pyridine-piperazine-based scaffolds as highly potent and selective neurolysin activators |
| WO2024244972A1 (zh) * | 2023-05-30 | 2024-12-05 | 浙江海正药业股份有限公司 | 芳香酰胺类衍生物及其制备方法和用途 |
| CN116751115A (zh) * | 2023-07-03 | 2023-09-15 | 苏州诚和医药化学有限公司 | 一种间甲氧基氯苄的制备方法 |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20020103203A1 (en) * | 2000-01-21 | 2002-08-01 | Bender Steven Lee | Amide compounds and pharmaceutical compositions for inhibiting protein kinases, and methods for their use |
| EP2151435A1 (en) * | 2007-04-24 | 2010-02-10 | Shionogi&Co., Ltd. | Pharmaceutical composition for treatment of alzheimer's disease |
| WO2013171641A1 (en) * | 2012-05-15 | 2013-11-21 | Novartis Ag | Compounds and compositions for inhibiting the activity of abl1, abl2 and bcr-abl1 |
Family Cites Families (54)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4638014A (en) * | 1985-08-26 | 1987-01-20 | Research Corporation | Anticonvulsant method and formulations |
| US6022884A (en) * | 1997-11-07 | 2000-02-08 | Amgen Inc. | Substituted pyridine compounds and methods of use |
| IT1306704B1 (it) | 1999-05-26 | 2001-10-02 | Sirs Societa Italiana Per La R | Anticorpi monoclonali e suoi derivati sintetici o biotecnologici ingrado di agire come molecole antagoniste per il ngf. |
| JP2003506387A (ja) * | 1999-08-04 | 2003-02-18 | アイカゲン インコーポレイテッド | カリウムチャンネルオープナーとしてのベンズアニリド |
| FR2807660A1 (fr) | 2000-04-13 | 2001-10-19 | Warner Lambert Co | Utilisation d'antagonistes du ngf pour la prevention ou le traitement de douleurs viscerales chroniques |
| EP1388341A1 (en) | 2002-08-07 | 2004-02-11 | Aventis Pharma Deutschland GmbH | Acylamino-substituted heteroaromatic compounds and their use as pharmaceuticals |
| UA80447C2 (en) | 2002-10-08 | 2007-09-25 | Methods for treating pain by administering nerve growth factor antagonist and opioid analgesic | |
| SI2263692T1 (sl) | 2002-12-24 | 2020-10-30 | Rinat Neuroscience Corp. | Anti-NGF protitelesa in postopki, v katerih se le-ta uporabljajo |
| PL1618092T3 (pl) | 2003-05-01 | 2011-02-28 | Bristol Myers Squibb Co | Związki amidopirazolowe z podstawnikami arylowymi jako inhibitory kinazy |
| CN102358903B (zh) | 2003-07-15 | 2017-04-26 | 安姆根有限公司 | 作为选择性ngf途径抑制剂的人抗ngf中和抗体 |
| WO2005030128A2 (en) | 2003-09-23 | 2005-04-07 | Merck & Co., Inc. | Pyrazole modulators of metabotropic glutamate receptors |
| US20050143384A1 (en) | 2003-10-30 | 2005-06-30 | Eric Sartori | Amide thiadiazole inhibitors of plasminogen activator inhibitor-1 |
| ITRM20030601A1 (it) | 2003-12-24 | 2005-06-25 | Lay Line Genomics Spa | Metodo per l'umanizzazione di anticorpi e anticorpi umanizzati con esso ottenuti. |
| CN101010315A (zh) | 2004-04-30 | 2007-08-01 | 拜耳制药公司 | 用于治疗癌症的取代的吡唑基脲衍生物 |
| PL1853602T3 (pl) | 2005-02-16 | 2010-11-30 | Astrazeneca Ab | Związki chemiczne |
| EP1853610A1 (en) * | 2005-03-03 | 2007-11-14 | Sirtris Pharmaceuticals, Inc. | N-phenyl benzamide derivatives as sirtuin modulators |
| EP1877057A1 (en) | 2005-04-27 | 2008-01-16 | AstraZeneca AB | Use of pyrazolyl-pyrimidine derivatives in the treatment of pain |
| JP2008540622A (ja) | 2005-05-16 | 2008-11-20 | アストラゼネカ アクチボラグ | 化合物 |
| ITRM20050290A1 (it) | 2005-06-07 | 2006-12-08 | Lay Line Genomics Spa | Uso di molecole in grado di inibire il legame tra ngf e il suo recettore trka come analgesici ad effetto prolungato. |
| ITRM20050332A1 (it) | 2005-06-24 | 2006-12-25 | Lay Line Genomics Spa | Uso di molecole in grado di bloccare l'attivita' di trka per potenziare gli effetti di analgesici oppiacei sul dolore. |
| JP2009502734A (ja) | 2005-07-29 | 2009-01-29 | アステラス製薬株式会社 | Lck阻害剤としての縮合複素環 |
| AU2006278397B2 (en) * | 2005-08-04 | 2013-01-17 | Sirtris Pharmaceuticals, Inc. | Oxazolopyridine derivatives as sirtuin modulators |
| DE102005042742A1 (de) | 2005-09-02 | 2007-03-08 | Schering Ag | Substituierte Imidazo[1,2b]pyridazine als Kinase-Inhibitoren, deren Herstellung und Verwendung als Arzneimittel |
| WO2007042321A2 (en) | 2005-10-13 | 2007-04-19 | Devgen N.V. | Kinase inhibitors |
| EP1959944A1 (en) | 2005-12-15 | 2008-08-27 | Shionogi Co., Ltd. | A pharmaceutical composition comprising an amide derivative |
| BRPI0712795A2 (pt) | 2006-07-07 | 2012-09-04 | Boehringer Ingelheim Int | derivados de heteroarila substituìdos com fenila e uso dos mesmos como agentes antitumorais |
| BRPI0718266A2 (pt) | 2006-10-30 | 2014-01-07 | Novartis Ag | Compostos heterocíclicos como agentes anti-inflamatórios. |
| KR101506750B1 (ko) | 2007-04-06 | 2015-03-27 | 뉴로크린 바이오사이언시즈 인코퍼레이티드 | 고나도트로핀-방출 호르몬 수용체 길항제 및 그와 관련된 방법 |
| CL2008001822A1 (es) * | 2007-06-20 | 2009-03-13 | Sirtris Pharmaceuticals Inc | Compuestos derivados de tiazolo[5,4-b]piridina; composicion farmaceutica que comprende a dichos compuestos; y uso del compuesto en el tratamiento de la resistencia a la insulina, sindrome metabolico, diabetes, entre otras. |
| PE20090837A1 (es) * | 2007-07-02 | 2009-07-24 | Boehringer Ingelheim Int | Nuevos compuestos quimicos |
| EP2176249A2 (en) | 2007-07-02 | 2010-04-21 | Boehringer Ingelheim International GmbH | New chemical compounds |
| PL2197849T3 (pl) | 2007-10-09 | 2013-05-31 | Merck Patent Gmbh | Pochodne n-(pirazolo-3-ylo)-benzamidowe jako aktywatory glukokinazowe |
| KR20100134693A (ko) * | 2008-04-23 | 2010-12-23 | 교와 핫꼬 기린 가부시키가이샤 | 2-아미노퀴나졸린 유도체 |
| EP2272832A4 (en) * | 2008-04-28 | 2011-09-07 | Asahi Kasei Pharma Corp | PHENYLPROPIONIC ACID DERIVATIVE AND USE THEREOF |
| CN102224153B (zh) | 2008-09-22 | 2014-04-30 | 阵列生物制药公司 | 作为trk激酶抑制剂的取代的咪唑并[1,2-b]哒嗪化合物 |
| AU2009300318A1 (en) * | 2008-10-01 | 2010-04-08 | Synta Pharmaceuticals Corp. | Compounds for inflammation and immune-related uses |
| US8703962B2 (en) | 2008-10-24 | 2014-04-22 | Purdue Pharma L.P. | Monocyclic compounds and their use as TRPV1 ligands |
| KR101805754B1 (ko) | 2008-12-08 | 2017-12-07 | 먼디파머 인터내셔널 코포레이션 리미티드 | 단백질 수용체 티로신 키나아제 억제제의 조성물 |
| US20120065247A1 (en) | 2009-03-27 | 2012-03-15 | Discoverybiomed, Inc. | Modulating ires-mediated translation |
| JP2013522192A (ja) * | 2010-03-11 | 2013-06-13 | ブリストル−マイヤーズ スクイブ カンパニー | C型肝炎の処置のための化合物 |
| CN102985553B (zh) * | 2010-04-15 | 2015-11-25 | 西特里斯药业公司 | 沉默调节蛋白活化剂和活化测定 |
| NZ604831A (en) | 2010-07-02 | 2014-12-24 | Gilead Sciences Inc | Apoptosis signal-regulating kinase inhibitors |
| BR112013005070B1 (pt) | 2010-09-01 | 2018-04-03 | Bayer Intellectual Property Gmbh | Compostos n-(tetrazol-5-il)- e n-(triazol-5-il) arilcarboxamidas, composição herbicida, seus usos como herbicidas e método para controlar plantas indesejadas |
| WO2012100223A1 (en) | 2011-01-21 | 2012-07-26 | John Irwin | Synthetic lethal targeting of glucose transport |
| MX2013009067A (es) * | 2011-02-09 | 2013-10-01 | Syngenta Participations Ag | Compuestos insecticidas. |
| AU2012238369A1 (en) * | 2011-04-05 | 2013-10-03 | Pfizer Limited | Pyrrolo (2, 3 -d) pyrimidine derivatives as inhibitors of tropomyosin- related kinases |
| BR112013029201B1 (pt) | 2011-05-13 | 2022-08-09 | Array Biopharma Inc | Compostos de pirrolidinil ureia e pirrolidinil tioureia, seu processo de preparação, seu uso e composições farmacêuticas |
| SG194107A1 (en) | 2011-05-23 | 2013-11-29 | Merck Patent Gmbh | Thiazole derivatives |
| CN102796103A (zh) | 2011-05-23 | 2012-11-28 | 南京英派药业有限公司 | 6-(芳基甲酰)咪唑并[1,2-a]嘧啶和6-(芳基甲酰)[1,2,4]三唑并[4,3-a]嘧啶作为Hedgehog抑制剂及其应用 |
| KR20130077390A (ko) * | 2011-12-29 | 2013-07-09 | 제이더블유중외제약 주식회사 | 단백질 키나아제 저해활성을 가지는 6-아미노-3-카복스아미도인다졸 유도체 |
| WO2013176970A1 (en) * | 2012-05-22 | 2013-11-28 | Merck Sharp & Dohme Corp. | TrkA KINASE INHIBITORS, COMPOSITIONS AND METHODS THEREOF |
| TW201406736A (zh) * | 2012-06-28 | 2014-02-16 | Fujifilm Corp | 新穎的醯胺衍生物或其鹽 |
| EP2689779A1 (en) * | 2012-07-27 | 2014-01-29 | Pierre Fabre Medicament | Derivatives of azaindazole or diazaindazole type for treating a cancer overexpressing trk |
| WO2014171464A1 (ja) * | 2013-04-15 | 2014-10-23 | 株式会社レナサイエンス | Pai-1阻害剤の新規用途 |
-
2014
- 2014-03-26 WO PCT/CN2014/074145 patent/WO2015143654A1/en not_active Ceased
-
2015
- 2015-03-23 MX MX2016012480A patent/MX2016012480A/es unknown
- 2015-03-23 AU AU2015236428A patent/AU2015236428B2/en not_active Ceased
- 2015-03-23 US US15/128,689 patent/US9815846B2/en active Active
- 2015-03-23 KR KR1020167029501A patent/KR20160128420A/ko not_active Withdrawn
- 2015-03-23 WO PCT/US2015/021936 patent/WO2015148344A2/en not_active Ceased
- 2015-03-23 BR BR112016022069A patent/BR112016022069A2/pt not_active Application Discontinuation
- 2015-03-23 EP EP15769367.2A patent/EP3122346B1/en not_active Not-in-force
- 2015-03-23 CA CA2943858A patent/CA2943858A1/en not_active Abandoned
- 2015-03-23 RU RU2016141646A patent/RU2672583C2/ru not_active IP Right Cessation
- 2015-03-23 CN CN201580029747.2A patent/CN106794161A/zh active Pending
- 2015-03-23 JP JP2016559249A patent/JP2017512794A/ja active Pending
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20020103203A1 (en) * | 2000-01-21 | 2002-08-01 | Bender Steven Lee | Amide compounds and pharmaceutical compositions for inhibiting protein kinases, and methods for their use |
| EP2151435A1 (en) * | 2007-04-24 | 2010-02-10 | Shionogi&Co., Ltd. | Pharmaceutical composition for treatment of alzheimer's disease |
| WO2013171641A1 (en) * | 2012-05-15 | 2013-11-21 | Novartis Ag | Compounds and compositions for inhibiting the activity of abl1, abl2 and bcr-abl1 |
Non-Patent Citations (3)
| Title |
|---|
| SAHU S K ET AL, "Synthesis and biological evaluation of 3-(phthalimidomethyl)-4-(5-substituted isoxazoline and pyrazoline) substituted benzanilides", JOURNAL OF THE INDIAN CHEMICAL SOCIETY,, (2007-10), vol. 84, no. 10, pages 1011 - 1015 * |
| SÖREN J WACKER ET AL, "The identification of novel, high affinity AQP9 inhibitors in an intracellular binding site", MOLECULAR MEMBRANE BIOLOGY,, (2013), vol. 30, no. 3, pages 246 - 260 * |
| WEISBERG ET AL, "Discovery and Characterization of Novel Mutant FLT3 Kinase Inhibitors", THERAPEUTIC DISCOVERY,, (2010-09), vol. 9, no. 9, pages 2468 - 2477 * |
Also Published As
| Publication number | Publication date |
|---|---|
| AU2015236428A1 (en) | 2016-09-29 |
| KR20160128420A (ko) | 2016-11-07 |
| EP3122346A4 (en) | 2017-08-23 |
| WO2015148344A2 (en) | 2015-10-01 |
| CN106794161A (zh) | 2017-05-31 |
| EP3122346A2 (en) | 2017-02-01 |
| BR112016022069A2 (pt) | 2017-08-15 |
| RU2016141646A3 (cg-RX-API-DMAC7.html) | 2018-06-26 |
| MX2016012480A (es) | 2016-12-20 |
| JP2017512794A (ja) | 2017-05-25 |
| RU2672583C2 (ru) | 2018-11-16 |
| WO2015143654A8 (en) | 2015-12-10 |
| EP3122346B1 (en) | 2020-07-15 |
| WO2015143654A1 (en) | 2015-10-01 |
| RU2016141646A (ru) | 2018-04-27 |
| US20170114071A1 (en) | 2017-04-27 |
| WO2015148344A3 (en) | 2015-11-26 |
| CA2943858A1 (en) | 2015-10-01 |
| US9815846B2 (en) | 2017-11-14 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| AU2015236428B2 (en) | TrkA kinase inhibitors, compositions and methods thereof | |
| EP3122344B1 (en) | Trka kinase inhibitors, compositions and methods thereof | |
| US9914736B2 (en) | TrKA kinase inhibitors, compositions and methods thereof | |
| CN104254533A (zh) | 用作激酶抑制剂的噻唑或噻二唑取代的吡啶基化合物 | |
| CN104169275A (zh) | 用作激酶抑制剂的三唑取代的吡啶化合物 | |
| CN104159896A (zh) | 用作激酶抑制剂的杂环取代的吡啶基化合物 | |
| CA2681516A1 (en) | Compounds useful as inhibitors of janus kinases | |
| JP2018506571A (ja) | Rho関連プロテインキナーゼの阻害及び疾患の治療のためのインダゾリルチアジアゾールアミン及び関連する化合物 | |
| IL285246B1 (en) | Substituted bicyclic compounds as farnesoid x receptor modulators | |
| WO2016054807A1 (en) | TrkA KINASE INHIBITORS, COMPOSITIONS AND METHODS THEREOF | |
| WO2016164286A2 (en) | TrkA KINASE INHIBITORS, COMPOSITIONS AND METHODS THEREOF | |
| US9102673B2 (en) | Substituted pyrrolo[3,2-c]pyridines as TrkA kinase inhibitors |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FGA | Letters patent sealed or granted (standard patent) | ||
| MK14 | Patent ceased section 143(a) (annual fees not paid) or expired |