CA2869541A1 - N-alkyltriazole compounds as lpar antagonists - Google Patents
N-alkyltriazole compounds as lpar antagonists Download PDFInfo
- Publication number
- CA2869541A1 CA2869541A1 CA2869541A CA2869541A CA2869541A1 CA 2869541 A1 CA2869541 A1 CA 2869541A1 CA 2869541 A CA2869541 A CA 2869541A CA 2869541 A CA2869541 A CA 2869541A CA 2869541 A1 CA2869541 A1 CA 2869541A1
- Authority
- CA
- Canada
- Prior art keywords
- phenyl
- methyl
- triazol
- substituted
- biphenyl
- 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
Links
- 150000001875 compounds Chemical class 0.000 title claims abstract description 94
- 239000005557 antagonist Substances 0.000 title description 7
- 150000003839 salts Chemical class 0.000 claims abstract description 27
- 238000011282 treatment Methods 0.000 claims abstract description 17
- 208000005069 pulmonary fibrosis Diseases 0.000 claims abstract description 12
- 239000008194 pharmaceutical composition Substances 0.000 claims abstract description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 66
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 59
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Natural products CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 50
- 229910052739 hydrogen Inorganic materials 0.000 claims description 40
- 229910052736 halogen Chemical group 0.000 claims description 28
- 150000002367 halogens Chemical group 0.000 claims description 28
- 238000002360 preparation method Methods 0.000 claims description 28
- 239000001257 hydrogen Substances 0.000 claims description 27
- -1 cycloalkyl acetic acid Chemical group 0.000 claims description 26
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 25
- 238000000034 method Methods 0.000 claims description 17
- YMGUBTXCNDTFJI-UHFFFAOYSA-N cyclopropanecarboxylic acid Chemical compound OC(=O)C1CC1 YMGUBTXCNDTFJI-UHFFFAOYSA-N 0.000 claims description 16
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 16
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 10
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 10
- 238000011321 prophylaxis Methods 0.000 claims description 10
- 239000003814 drug Substances 0.000 claims description 9
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 7
- 229910052731 fluorine Chemical group 0.000 claims description 7
- 239000011737 fluorine Chemical group 0.000 claims description 7
- 239000013543 active substance Substances 0.000 claims description 6
- 229910052794 bromium Inorganic materials 0.000 claims description 6
- PKAHQJNJPDVTDP-UHFFFAOYSA-N methyl cyclopropanecarboxylate Chemical compound COC(=O)C1CC1 PKAHQJNJPDVTDP-UHFFFAOYSA-N 0.000 claims description 6
- MYFYYMWMWSGKDE-UHFFFAOYSA-N n-methylsulfonylcyclopropanecarboxamide Chemical compound CS(=O)(=O)NC(=O)C1CC1 MYFYYMWMWSGKDE-UHFFFAOYSA-N 0.000 claims description 6
- JOMBXHCJYIMCPC-UHFFFAOYSA-N 5-cyclopropyl-2h-tetrazole Chemical compound C1CC1C1=NNN=N1 JOMBXHCJYIMCPC-UHFFFAOYSA-N 0.000 claims description 5
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 5
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical group FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 4
- RCVHTKMAMPDRAT-GOSISDBHSA-N 1-[3-[4-[1-methyl-5-[[(1r)-1-phenylethoxy]carbonylamino]triazol-4-yl]phenyl]phenyl]cyclopropane-1-carboxylic acid Chemical compound O([C@H](C)C=1C=CC=CC=1)C(=O)NC(N(N=N1)C)=C1C(C=C1)=CC=C1C(C=1)=CC=CC=1C1(C(O)=O)CC1 RCVHTKMAMPDRAT-GOSISDBHSA-N 0.000 claims description 2
- 125000001246 bromo group Chemical group Br* 0.000 claims description 2
- IPBJLADFKWCTMI-QGZVFWFLSA-N 1-[4-[3-fluoro-4-[1-methyl-5-[[(1r)-1-phenylethoxy]carbonylamino]triazol-4-yl]phenyl]phenyl]cyclopropane-1-carboxylic acid Chemical compound O([C@H](C)C=1C=CC=CC=1)C(=O)NC(N(N=N1)C)=C1C(C(=C1)F)=CC=C1C(C=C1)=CC=C1C1(C(O)=O)CC1 IPBJLADFKWCTMI-QGZVFWFLSA-N 0.000 claims 1
- HKSCEHNRNXWQAZ-UHFFFAOYSA-N 1-[4-[4-[1-methyl-5-[1-[3-(trifluoromethyl)phenyl]ethoxycarbonylamino]triazol-4-yl]phenyl]phenyl]cyclopropane-1-carboxylic acid Chemical compound C=1C=CC(C(F)(F)F)=CC=1C(C)OC(=O)NC(N(N=N1)C)=C1C(C=C1)=CC=C1C(C=C1)=CC=C1C1(C(O)=O)CC1 HKSCEHNRNXWQAZ-UHFFFAOYSA-N 0.000 claims 1
- HKSCEHNRNXWQAZ-QGZVFWFLSA-N 1-[4-[4-[1-methyl-5-[[(1r)-1-[3-(trifluoromethyl)phenyl]ethoxy]carbonylamino]triazol-4-yl]phenyl]phenyl]cyclopropane-1-carboxylic acid Chemical compound O([C@H](C)C=1C=C(C=CC=1)C(F)(F)F)C(=O)NC(N(N=N1)C)=C1C(C=C1)=CC=C1C(C=C1)=CC=C1C1(C(O)=O)CC1 HKSCEHNRNXWQAZ-QGZVFWFLSA-N 0.000 claims 1
- QTUMYGXPEACCGE-GOSISDBHSA-N 1-[4-[4-[1-methyl-5-[[(1r)-1-phenylethoxy]carbonylamino]triazol-4-yl]phenyl]phenyl]cyclopropane-1-carboxylic acid Chemical compound O([C@H](C)C=1C=CC=CC=1)C(=O)NC(N(N=N1)C)=C1C(C=C1)=CC=C1C(C=C1)=CC=C1C1(C(O)=O)CC1 QTUMYGXPEACCGE-GOSISDBHSA-N 0.000 claims 1
- HKSCEHNRNXWQAZ-KRWDZBQOSA-N 1-[4-[4-[1-methyl-5-[[(1s)-1-[3-(trifluoromethyl)phenyl]ethoxy]carbonylamino]triazol-4-yl]phenyl]phenyl]cyclopropane-1-carboxylic acid Chemical compound O([C@@H](C)C=1C=C(C=CC=1)C(F)(F)F)C(=O)NC(N(N=N1)C)=C1C(C=C1)=CC=C1C(C=C1)=CC=C1C1(C(O)=O)CC1 HKSCEHNRNXWQAZ-KRWDZBQOSA-N 0.000 claims 1
- GTLJBSMYSBXGGC-MRXNPFEDSA-N 1-[4-[4-[1-methyl-5-[[(2r)-3-methylbutan-2-yl]oxycarbonylamino]triazol-4-yl]phenyl]phenyl]cyclopropane-1-carboxylic acid Chemical compound N1=NN(C)C(NC(=O)O[C@H](C)C(C)C)=C1C1=CC=C(C=2C=CC(=CC=2)C2(CC2)C(O)=O)C=C1 GTLJBSMYSBXGGC-MRXNPFEDSA-N 0.000 claims 1
- VXALZEHUUVEFBN-GOSISDBHSA-N 1-[4-[4-[3-methyl-5-[[(1r)-1-phenylethoxy]carbonylamino]triazol-4-yl]phenyl]phenyl]cyclopropane-1-carboxylic acid Chemical compound O([C@H](C)C=1C=CC=CC=1)C(=O)NC=1N=NN(C)C=1C(C=C1)=CC=C1C(C=C1)=CC=C1C1(C(O)=O)CC1 VXALZEHUUVEFBN-GOSISDBHSA-N 0.000 claims 1
- QVGKIYDRQMXFEP-PGYGNJIDSA-N 2-[4-[4-[1-methyl-5-[[(1r)-1-phenylethoxy]carbonylamino]triazol-4-yl]phenyl]cyclohexyl]acetic acid Chemical compound O([C@H](C)C=1C=CC=CC=1)C(=O)NC(N(N=N1)C)=C1C(C=C1)=CC=C1C1CCC(CC(O)=O)CC1 QVGKIYDRQMXFEP-PGYGNJIDSA-N 0.000 claims 1
- CTNSCPPHPORJPG-QGZVFWFLSA-N 2-[4-[4-[1-methyl-5-[[(1r)-1-phenylethoxy]carbonylamino]triazol-4-yl]phenyl]phenyl]acetic acid Chemical compound O([C@H](C)C=1C=CC=CC=1)C(=O)NC(N(N=N1)C)=C1C(C=C1)=CC=C1C1=CC=C(CC(O)=O)C=C1 CTNSCPPHPORJPG-QGZVFWFLSA-N 0.000 claims 1
- IKJZZCLSUSZHFO-GOSISDBHSA-N [(1r)-1-[3-(trifluoromethyl)phenyl]ethyl] n-[3-methyl-5-[4-[4-[1-(methylsulfonylcarbamoyl)cyclopropyl]phenyl]phenyl]triazol-4-yl]carbamate Chemical compound O([C@H](C)C=1C=C(C=CC=1)C(F)(F)F)C(=O)NC(N(N=N1)C)=C1C(C=C1)=CC=C1C(C=C1)=CC=C1C1(C(=O)NS(C)(=O)=O)CC1 IKJZZCLSUSZHFO-GOSISDBHSA-N 0.000 claims 1
- UNLCLTXWXXTYTO-LJQANCHMSA-N [(1r)-1-phenylethyl] n-[3-methyl-5-[4-[4-[1-(methylsulfonylcarbamoyl)cyclopropyl]phenyl]phenyl]triazol-4-yl]carbamate Chemical compound O([C@H](C)C=1C=CC=CC=1)C(=O)NC(N(N=N1)C)=C1C(C=C1)=CC=C1C(C=C1)=CC=C1C1(C(=O)NS(C)(=O)=O)CC1 UNLCLTXWXXTYTO-LJQANCHMSA-N 0.000 claims 1
- XRJSXUZNJJHOSM-GFCCVEGCSA-N [(1r)-1-phenylethyl] n-[5-(4-bromophenyl)-3-methyltriazol-4-yl]carbamate Chemical compound O([C@H](C)C=1C=CC=CC=1)C(=O)NC(N(N=N1)C)=C1C1=CC=C(Br)C=C1 XRJSXUZNJJHOSM-GFCCVEGCSA-N 0.000 claims 1
- XUKSHLCUXSONSG-GOSISDBHSA-N methyl 1-[4-[3-fluoro-4-[1-methyl-5-[[(1r)-1-phenylethoxy]carbonylamino]triazol-4-yl]phenyl]phenyl]cyclopropane-1-carboxylate Chemical compound C=1C=C(C=2C=C(F)C(C3=C(N(C)N=N3)NC(=O)O[C@H](C)C=3C=CC=CC=3)=CC=2)C=CC=1C1(C(=O)OC)CC1 XUKSHLCUXSONSG-GOSISDBHSA-N 0.000 claims 1
- 208000027866 inflammatory disease Diseases 0.000 abstract description 5
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- WLJNZVDCPSBLRP-UHFFFAOYSA-N pamoic acid Chemical compound C1=CC=C2C(CC=3C4=CC=CC=C4C=C(C=3O)C(=O)O)=C(O)C(C(O)=O)=CC2=C1 WLJNZVDCPSBLRP-UHFFFAOYSA-N 0.000 description 1
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- 125000003386 piperidinyl group Chemical group 0.000 description 1
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- 125000004309 pyranyl group Chemical group O1C(C=CC=C1)* 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 125000000719 pyrrolidinyl group Chemical group 0.000 description 1
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- 229960004017 salmeterol Drugs 0.000 description 1
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- 239000008159 sesame oil Substances 0.000 description 1
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- 230000011664 signaling Effects 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000020183 skimmed milk Nutrition 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
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- 238000003756 stirring Methods 0.000 description 1
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- 229960001967 tacrolimus Drugs 0.000 description 1
- QJJXYPPXXYFBGM-SHYZHZOCSA-N tacrolimus Natural products CO[C@H]1C[C@H](CC[C@@H]1O)C=C(C)[C@H]2OC(=O)[C@H]3CCCCN3C(=O)C(=O)[C@@]4(O)O[C@@H]([C@H](C[C@H]4C)OC)[C@@H](C[C@H](C)CC(=C[C@@H](CC=C)C(=O)C[C@H](O)[C@H]2C)C)OC QJJXYPPXXYFBGM-SHYZHZOCSA-N 0.000 description 1
- 230000008685 targeting Effects 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/04—1,2,3-Triazoles; Hydrogenated 1,2,3-triazoles
- C07D249/06—1,2,3-Triazoles; Hydrogenated 1,2,3-triazoles with aryl radicals directly attached to ring atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/04—1,2,3-Triazoles; Hydrogenated 1,2,3-triazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4192—1,2,3-Triazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- 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
- A61P37/00—Drugs for immunological or allergic disorders
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Pulmonology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201261661961P | 2012-06-20 | 2012-06-20 | |
| US61/661,961 | 2012-06-20 | ||
| PCT/EP2013/062461 WO2013189864A1 (en) | 2012-06-20 | 2013-06-17 | N-alkyltriazole compounds as lpar antagonists |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2869541A1 true CA2869541A1 (en) | 2013-12-27 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA2869541A Abandoned CA2869541A1 (en) | 2012-06-20 | 2013-06-17 | N-alkyltriazole compounds as lpar antagonists |
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| EP (1) | EP2864300A1 (enExample) |
| JP (1) | JP2015520202A (enExample) |
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| BR (1) | BR112014030685A2 (enExample) |
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| IL (1) | IL236088A0 (enExample) |
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| MX (1) | MX2014014710A (enExample) |
| PE (1) | PE20142448A1 (enExample) |
| PH (1) | PH12014502789A1 (enExample) |
| SG (1) | SG11201407220YA (enExample) |
| UA (1) | UA109868C2 (enExample) |
| WO (1) | WO2013189864A1 (enExample) |
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| WO2013025733A1 (en) | 2011-08-15 | 2013-02-21 | Intermune, Inc. | Lysophosphatidic acid receptor antagonists |
| PE20142305A1 (es) * | 2012-06-20 | 2015-01-16 | Hoffmann La Roche | Compuestos de n-ariltriazol como antagonistas de lpar |
| SG11201507459YA (en) | 2013-03-15 | 2015-10-29 | Epigen Biosciences Inc | Heterocyclic compounds useful in the treatment of disease |
| MX370408B (es) | 2014-06-27 | 2019-12-11 | Ube Industries | Sal de compuesto heterociclico sustituido con halogeno. |
| AR108838A1 (es) * | 2016-06-21 | 2018-10-03 | Bristol Myers Squibb Co | Ácidos de carbamoiloximetil triazol ciclohexilo como antagonistas de lpa |
| EP3728240B1 (en) * | 2017-12-19 | 2022-06-29 | Bristol-Myers Squibb Company | Isoxazole o-linked carbamoyl cyclohexyl acids as lpa antagonists |
| ES2924704T3 (es) | 2017-12-19 | 2022-10-10 | Bristol Myers Squibb Co | Pirazol azoles del ácido ciclohexílico como antagonistas de LPA |
| KR102702231B1 (ko) | 2017-12-19 | 2024-09-02 | 브리스톨-마이어스 스큅 컴퍼니 | Lpa 길항제로서의 피라졸 o-연결된 카르바모일 시클로헥실 산 |
| US11319309B2 (en) | 2017-12-19 | 2022-05-03 | Bristol-Myers Squibb Company | Cyclohexyl acid isoxazole azines as LPA antagonists |
| WO2019126090A1 (en) * | 2017-12-19 | 2019-06-27 | Bristol-Myers Squibb Company | Triazole n-linked carbamoyl cyclohexyl acids as lpa antagonists |
| JP7256807B2 (ja) * | 2017-12-19 | 2023-04-12 | ブリストル－マイヤーズ スクイブ カンパニー | Ｌｐａアンタゴニストとしてのシクロヘキシル酸イソキサゾールアゾール |
| US11312706B2 (en) | 2017-12-19 | 2022-04-26 | Bristol-Myers Squibb Company | Cyclohexyl acid pyrazole azines as LPA antagonists |
| KR102777148B1 (ko) * | 2017-12-19 | 2025-03-05 | 브리스톨-마이어스 스큅 컴퍼니 | Lpa 길항제로서의 시클로헥실 산 트리아졸 아진 |
| WO2019126099A1 (en) | 2017-12-19 | 2019-06-27 | Bristol-Myers Squibb Company | Isoxazole n-linked carbamoyl cyclohexyl acids as lpa antagonists |
| WO2019126085A1 (en) | 2017-12-19 | 2019-06-27 | Bristol-Myers Squibb Company | Pyrazole n-linked carbamoyl cyclohexyl acids as lpa antagonists |
| CA3085938A1 (en) * | 2017-12-19 | 2019-06-27 | Bristol-Myers Squibb Company | Cyclohexyl acid triazole azoles as lpa antagonists |
| KR20200112860A (ko) * | 2017-12-29 | 2020-10-05 | 바이오마린 파머수티컬 인크. | 질환의 치료를 위한 글리콜레이트 산화효소 억제제 |
| KR20210061383A (ko) | 2018-09-18 | 2021-05-27 | 브리스톨-마이어스 스큅 컴퍼니 | Lpa 길항제로서의 시클로펜틸 산 |
| JP7412424B2 (ja) * | 2018-09-18 | 2024-01-12 | ブリストル－マイヤーズ スクイブ カンパニー | Ｌｐａアンタゴニストとしてのオキサビシクロ酸 |
| US20220041572A1 (en) * | 2018-09-18 | 2022-02-10 | Bristol-Myers Squibb Company | Cycloheptyl acids as lpa antagonists |
| CA3158743A1 (en) * | 2019-11-15 | 2021-05-20 | Gilead Sciences, Inc. | Triazole carbamate pyridyl sulfonamides as lpa receptor antagonists and uses thereof |
| TWI843503B (zh) | 2020-06-03 | 2024-05-21 | 美商基利科學股份有限公司 | Lpa受體拮抗劑及其用途 |
| CA3185689A1 (en) | 2020-06-03 | 2021-12-09 | Gilead Sciences, Inc. | Lpa receptor antagonists and uses thereof |
| CA3218917A1 (en) | 2021-05-11 | 2022-11-17 | Gilead Sciences, Inc. | Lpa receptor antagonists and uses thereof |
| KR20240007233A (ko) * | 2021-05-13 | 2024-01-16 | 길리애드 사이언시즈, 인코포레이티드 | Lpa 수용체 길항제 및 이의 용도 |
| AU2022405082B2 (en) | 2021-12-08 | 2025-09-25 | Gilead Sciences, Inc. | Lpa receptor antagonists and uses thereof |
| AR128613A1 (es) | 2022-02-25 | 2024-05-29 | Lhotse Bio Inc | Compuestos y composiciones para el tratamiento de afecciones asociadas con la actividad del receptor de lpa |
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| TW200827346A (en) | 2006-11-03 | 2008-07-01 | Astrazeneca Ab | Chemical compounds |
| GB2466121B (en) * | 2008-12-15 | 2010-12-08 | Amira Pharmaceuticals Inc | Antagonists of lysophosphatidic acid receptors |
| GB2470833B (en) * | 2009-06-03 | 2011-06-01 | Amira Pharmaceuticals Inc | Polycyclic antagonists of lysophosphatidic acid receptors |
| US20110065695A1 (en) | 2009-09-11 | 2011-03-17 | Jeremy Beauchamp | Use of aminodihydrothiazines for the treatment or prevention of diabetes |
| GB2474748B (en) * | 2009-10-01 | 2011-10-12 | Amira Pharmaceuticals Inc | Polycyclic compounds as lysophosphatidic acid receptor antagonists |
| WO2011159550A2 (en) * | 2010-06-14 | 2011-12-22 | Amidra Pharmaceuticals, Inc. | Lysophosphatidic acid receptor antagonist and uses thereof |
| WO2011159633A1 (en) | 2010-06-15 | 2011-12-22 | Amira Pharmaceuticals, Inc. | Inhalable formulations of lysophosphatdic acid receptor antagonists |
| BR112013014019A2 (pt) | 2010-12-07 | 2016-09-13 | Amira Pharmaceuticals Inc | antagonistas do receptor do ácido lisofosfatídico e seus usos |
| WO2012138648A1 (en) | 2011-04-06 | 2012-10-11 | Irm Llc | Compositions and methods for modulating lpa receptors |
| WO2013025733A1 (en) | 2011-08-15 | 2013-02-21 | Intermune, Inc. | Lysophosphatidic acid receptor antagonists |
-
2013
- 2013-06-17 EP EP13729330.4A patent/EP2864300A1/en not_active Withdrawn
- 2013-06-17 UA UAA201500428A patent/UA109868C2/ru unknown
- 2013-06-17 PE PE2014002232A patent/PE20142448A1/es not_active Application Discontinuation
- 2013-06-17 CN CN201380032285.0A patent/CN104411692A/zh active Pending
- 2013-06-17 IN IN9348DEN2014 patent/IN2014DN09348A/en unknown
- 2013-06-17 BR BR112014030685A patent/BR112014030685A2/pt not_active Application Discontinuation
- 2013-06-17 CA CA2869541A patent/CA2869541A1/en not_active Abandoned
- 2013-06-17 HK HK15106927.8A patent/HK1206342A1/xx unknown
- 2013-06-17 EA EA201492285A patent/EA201492285A1/ru unknown
- 2013-06-17 AU AU2013279512A patent/AU2013279512A1/en not_active Abandoned
- 2013-06-17 WO PCT/EP2013/062461 patent/WO2013189864A1/en not_active Ceased
- 2013-06-17 MX MX2014014710A patent/MX2014014710A/es unknown
- 2013-06-17 JP JP2015517704A patent/JP2015520202A/ja not_active Ceased
- 2013-06-17 KR KR1020147035768A patent/KR20150021057A/ko not_active Ceased
- 2013-06-17 US US14/401,009 patent/US9321738B2/en not_active Expired - Fee Related
- 2013-06-17 MA MA37764A patent/MA37764A1/fr unknown
- 2013-06-17 SG SG11201407220YA patent/SG11201407220YA/en unknown
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2014
- 2014-11-17 CR CR20140525A patent/CR20140525A/es unknown
- 2014-11-21 CO CO14256136A patent/CO7131358A2/es unknown
- 2014-11-28 CL CL2014003243A patent/CL2014003243A1/es unknown
- 2014-12-04 IL IL236088A patent/IL236088A0/en unknown
- 2014-12-15 PH PH12014502789A patent/PH12014502789A1/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| EA201492285A1 (ru) | 2015-04-30 |
| PH12014502789A1 (en) | 2015-02-09 |
| HK1206342A1 (en) | 2016-01-08 |
| AU2013279512A1 (en) | 2014-10-16 |
| CO7131358A2 (es) | 2014-12-01 |
| CL2014003243A1 (es) | 2015-03-20 |
| JP2015520202A (ja) | 2015-07-16 |
| PE20142448A1 (es) | 2015-01-28 |
| EP2864300A1 (en) | 2015-04-29 |
| SG11201407220YA (en) | 2014-12-30 |
| CR20140525A (es) | 2015-01-12 |
| MA37764A1 (fr) | 2016-01-29 |
| WO2013189864A1 (en) | 2013-12-27 |
| CN104411692A (zh) | 2015-03-11 |
| IN2014DN09348A (enExample) | 2015-07-17 |
| US20150133511A1 (en) | 2015-05-14 |
| KR20150021057A (ko) | 2015-02-27 |
| IL236088A0 (en) | 2015-02-01 |
| MX2014014710A (es) | 2015-03-04 |
| US9321738B2 (en) | 2016-04-26 |
| UA109868C2 (ru) | 2015-10-12 |
| BR112014030685A2 (pt) | 2017-06-27 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EEER | Examination request |
Effective date: 20141003 |
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| FZDE | Discontinued |
Effective date: 20170809 |