SG11202005704RA - 6-azaindole compounds - Google Patents
6-azaindole compoundsInfo
- Publication number
- SG11202005704RA SG11202005704RA SG11202005704RA SG11202005704RA SG11202005704RA SG 11202005704R A SG11202005704R A SG 11202005704RA SG 11202005704R A SG11202005704R A SG 11202005704RA SG 11202005704R A SG11202005704R A SG 11202005704RA SG 11202005704R A SG11202005704R A SG 11202005704RA
- Authority
- SG
- Singapore
- Prior art keywords
- azaindole compounds
- azaindole
- compounds
- Prior art date
Links
Classifications
-
- 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
-
- 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
- A61K31/4353—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 ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- 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
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201762607507P | 2017-12-19 | 2017-12-19 | |
PCT/US2018/066107 WO2019126082A1 (en) | 2017-12-19 | 2018-12-18 | 6-azaindole compounds |
Publications (1)
Publication Number | Publication Date |
---|---|
SG11202005704RA true SG11202005704RA (en) | 2020-07-29 |
Family
ID=65003572
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SG11202005704RA SG11202005704RA (en) | 2017-12-19 | 2018-12-18 | 6-azaindole compounds |
Country Status (13)
Country | Link |
---|---|
US (2) | US11427580B2 (en) |
EP (1) | EP3728253B1 (en) |
JP (1) | JP7304352B2 (en) |
KR (1) | KR20200101956A (en) |
CN (1) | CN111699185B (en) |
AU (1) | AU2018390543A1 (en) |
BR (1) | BR112020011788A2 (en) |
CA (1) | CA3085761A1 (en) |
EA (1) | EA202091508A1 (en) |
IL (1) | IL275365A (en) |
MX (1) | MX2020005873A (en) |
SG (1) | SG11202005704RA (en) |
WO (1) | WO2019126082A1 (en) |
Families Citing this family (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US10071079B2 (en) | 2016-06-29 | 2018-09-11 | Bristol-Myers Squibb Company | [1,2,4]triazolo[1,5-a]pyridinyl substituted indole compounds |
EA202091479A1 (en) * | 2017-12-20 | 2020-11-24 | Бристол-Маерс Сквибб Компани | ARYL- AND HETEROARYL-SUBSTITUTED INDOL COMPOUNDS |
CN111491929B (en) * | 2017-12-20 | 2023-11-28 | 百时美施贵宝公司 | Aminoindole compounds useful as TLR inhibitors |
SG11202005733QA (en) * | 2017-12-20 | 2020-07-29 | Bristol Myers Squibb Co | Diazaindole compounds |
WO2019155042A1 (en) | 2018-02-12 | 2019-08-15 | F. Hoffmann-La Roche Ag | Novel sulfone compounds and derivatives for the treatment and prophylaxis of virus infection |
WO2019238616A1 (en) | 2018-06-12 | 2019-12-19 | F. Hoffmann-La Roche Ag | Novel heteroaryl heterocyclyl compounds for the treatment of autoimmune disease |
CN112584903A (en) | 2018-07-23 | 2021-03-30 | 豪夫迈·罗氏有限公司 | Novel piperazine compounds for the treatment of autoimmune diseases |
CN112638908A (en) | 2018-09-04 | 2021-04-09 | 豪夫迈·罗氏有限公司 | Benzothiazoles for treatment of autoimmune diseases |
JP2022502353A (en) | 2018-09-06 | 2022-01-11 | エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft | A novel cyclic amidine compound for the treatment of autoimmune disorders |
GB201913752D0 (en) | 2019-09-24 | 2019-11-06 | Syngenta Crop Protection Ag | Herbicidal compounds |
GB201914277D0 (en) | 2019-10-03 | 2019-11-20 | Syngenta Crop Protection Ag | Herbicidal compounds |
GB201917898D0 (en) | 2019-12-06 | 2020-01-22 | Syngenta Crop Protection Ag | Herbicidal compounds |
WO2022035294A1 (en) | 2020-08-13 | 2022-02-17 | 주식회사 엘지에너지솔루션 | Battery module having improved electrode lead connection structure, and battery pack and vehicle including same |
AU2021328577A1 (en) * | 2020-08-19 | 2023-03-23 | Bristol-Myers Squibb Company | 1H-pyrrolo[3,2-c]pyridine and 1H-pyrrolo[2,3-c]pyridine derivatives as TLR9 inhibitors for the treatment of fibrosis |
BR112023002662A2 (en) * | 2020-08-19 | 2023-03-14 | Bristol Myers Squibb Co | SUBSTITUTED HETEROARYL COMPOUNDS USEFUL AS TLR9 INHIBITORS |
US11767321B2 (en) | 2020-10-05 | 2023-09-26 | Enliven Inc. | 5- and 6-azaindole compounds for inhibition of BCR-ABL tyrosine kinases |
US11661431B2 (en) | 2021-04-16 | 2023-05-30 | Gilead Sciences, Inc. | Thienopyrrole compounds |
CN114591339B (en) * | 2022-05-10 | 2022-08-02 | 上海维申医药有限公司 | Toll-like receptor inhibitor and preparation and application thereof |
Family Cites Families (41)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6187777B1 (en) | 1998-02-06 | 2001-02-13 | Amgen Inc. | Compounds and methods which modulate feeding behavior and related diseases |
US6867200B1 (en) | 1998-12-18 | 2005-03-15 | Axys Pharmaceuticals, Inc. | (Hetero)aryl-bicyclic heteroaryl derivatives, their preparation and their use as protease inhibitors |
CA2348740A1 (en) * | 1998-12-23 | 2000-07-06 | Ruth R. Wexler | Thrombin or factor xa inhibitors |
IL148891A0 (en) | 1999-10-19 | 2002-09-12 | Merck & Co Inc | Tyrosine kinase inhibitors |
MXPA04006614A (en) | 2002-01-07 | 2004-10-04 | Eisai Co Ltd | Deazapurines and uses thereof. |
BRPI0411514A (en) | 2003-06-20 | 2006-08-01 | Coley Pharm Gmbh | small molecule toll-like receptor antagonists |
WO2006113458A1 (en) * | 2005-04-15 | 2006-10-26 | Bristol-Myers Squibb Company | Heterocyclic inhibitors of protein arginine methyl transferases |
CA2648652A1 (en) | 2006-04-04 | 2007-10-11 | Myriad Genetics, Inc. | Compounds for diseases and disorders |
DE102006033109A1 (en) | 2006-07-18 | 2008-01-31 | Grünenthal GmbH | Substituted heteroaryl derivatives |
US8027888B2 (en) | 2006-08-31 | 2011-09-27 | Experian Interactive Innovation Center, Llc | Online credit card prescreen systems and methods |
ATE495743T1 (en) | 2006-12-01 | 2011-02-15 | Galapagos Nv | TRIAZOLOPYRIDINE COMPOUNDS FOR THE TREATMENT OF DEGENERATIONAL AND INFLAMMATORY DISEASES |
WO2008152471A1 (en) | 2007-06-12 | 2008-12-18 | Coley Pharmaceutical Group, Inc. | Quinazoline derivative useful as toll-like receptor antagonist |
WO2009030996A1 (en) | 2007-09-05 | 2009-03-12 | Coley Pharmaceutical Group, Inc. | Triazole compounds as toll-like receptor (tlr) agonists |
WO2009042092A1 (en) | 2007-09-25 | 2009-04-02 | Merck & Co., Inc. | 2-aryl or heteroaryl indole derivatives |
FR2930249B1 (en) | 2008-04-21 | 2010-05-14 | Sanofi Aventis | NOVEL 3-AMINOALKYL-1,3-DIHYDRO-2H-INDOL-2-ONE DERIVATIVES, THEIR PREPARATION AND THERAPEUTIC USE THEREOF |
EP2350032B1 (en) | 2008-09-26 | 2016-05-25 | Eisai R&D Management Co., Ltd. | Benzoxazole compounds and methods of use |
WO2010042337A1 (en) | 2008-10-07 | 2010-04-15 | Merck Sharp & Dohme Corp. | Novel 6-azaindole aminopyrimidine derivatives having nik inhibitory activity |
EP2340243B1 (en) | 2008-10-17 | 2014-10-08 | Boehringer Ingelheim International GmbH | Heteroaryl substituted indole compounds useful as mmp-13 inhibitors |
TWI462920B (en) | 2009-06-26 | 2014-12-01 | 葛萊伯格有限公司 | Novel compound useful for the treatment of degenerative and inflammatory diseases |
AU2010273253B2 (en) | 2009-07-16 | 2015-03-12 | Mallinckrodt Llc | (+) - morphinans as antagonists of Toll-like receptor 9 and therapeutic uses thereof |
WO2011036130A1 (en) | 2009-09-24 | 2011-03-31 | F. Hoffmann-La Roche Ag | Indole derivatives as crac modulators |
WO2011050325A1 (en) | 2009-10-22 | 2011-04-28 | Vertex Pharmaceuticals Incorporated | Compositions for treatment of cystic fibrosis and other chronic diseases |
US9241991B2 (en) | 2010-10-21 | 2016-01-26 | The Brigham And Women's Hospital, Inc. | Agents, compositions, and methods for treating pruritus and related skin conditions |
US20140088085A1 (en) | 2011-01-12 | 2014-03-27 | Array Biopharma, Inc | Substituted Benzoazepines As Toll-Like Receptor Modulators |
HUE032036T2 (en) | 2011-01-12 | 2017-08-28 | Ventirx Pharmaceuticals Inc | Substituted benzoazepines as toll-like receptor modulators |
WO2012167046A1 (en) | 2011-06-01 | 2012-12-06 | Janus Biotherapeutics, Inc. | Novel immune system modulators |
AU2012262021B2 (en) | 2011-06-01 | 2016-07-28 | Janus Biotherapeutics, Inc. | Novel immune system modulators |
AU2012267556B9 (en) | 2011-06-09 | 2017-05-11 | Rhizen Pharmaceuticals Sa | Novel compounds as modulators of GPR-119 |
IN2014MN00258A (en) | 2011-07-15 | 2015-09-25 | Janssen Pharmaceuticals Inc | |
DE102011111400A1 (en) * | 2011-08-23 | 2013-02-28 | Merck Patent Gmbh | Bicyclic heteroaromatic compounds |
CA2850932A1 (en) | 2011-10-04 | 2013-04-11 | Janus Biotherapeutics, Inc. | Novel imidazole quinoline-based immune system modulators |
CN104302628B (en) | 2012-05-18 | 2017-06-23 | 大日本住友制药株式会社 | Carboxylic acid compound |
JO3407B1 (en) | 2012-05-31 | 2019-10-20 | Eisai R&D Man Co Ltd | Tetrahydropyrazolopyrimidine Compounds |
EP2738172A1 (en) * | 2012-11-28 | 2014-06-04 | Almirall, S.A. | New bicyclic compounds as crac channel modulators |
WO2015057659A1 (en) | 2013-10-14 | 2015-04-23 | Eisai R&D Management Co., Ltd. | Selectively substituted quinoline compounds |
CA2933466A1 (en) | 2013-12-13 | 2015-06-18 | Takeda Pharmaceutical Company Limited | Pyrrolo[3,2-c]pyridine derivatives as tlr inhibitors |
UA117634C2 (en) | 2014-08-15 | 2018-08-27 | Чиа Тай Тяньцін Фармасьютикал Ґруп Ко., Лтд. | Pyrrolopyrimidine compounds used as tlr7 agonist |
US20170275287A1 (en) | 2014-08-22 | 2017-09-28 | Janus Biotherapeutics, Inc. | Novel n2, n4, n7, 6-tetrasubstituted pteridine-2,4,7-triamine and 2, 4, 6, 7-tetrasubstituted pteridine compounds and methods of synthesis and use thereof |
US10071079B2 (en) | 2016-06-29 | 2018-09-11 | Bristol-Myers Squibb Company | [1,2,4]triazolo[1,5-a]pyridinyl substituted indole compounds |
US11180474B2 (en) | 2016-07-30 | 2021-11-23 | Bristol-Myers Squibb Company | Dimethoxyphenyl substituted indole compounds as TLR7, TLR8 or TLR9 inhibitors |
ES2902504T3 (en) | 2016-09-09 | 2022-03-28 | Bristol Myers Squibb Co | Pyridyl Substituted Indole Compounds |
-
2018
- 2018-12-18 EP EP18830673.2A patent/EP3728253B1/en active Active
- 2018-12-18 CN CN201880089130.3A patent/CN111699185B/en active Active
- 2018-12-18 BR BR112020011788-9A patent/BR112020011788A2/en not_active Application Discontinuation
- 2018-12-18 WO PCT/US2018/066107 patent/WO2019126082A1/en unknown
- 2018-12-18 CA CA3085761A patent/CA3085761A1/en active Pending
- 2018-12-18 MX MX2020005873A patent/MX2020005873A/en unknown
- 2018-12-18 SG SG11202005704RA patent/SG11202005704RA/en unknown
- 2018-12-18 JP JP2020534474A patent/JP7304352B2/en active Active
- 2018-12-18 US US16/955,089 patent/US11427580B2/en active Active
- 2018-12-18 EA EA202091508A patent/EA202091508A1/en unknown
- 2018-12-18 AU AU2018390543A patent/AU2018390543A1/en not_active Abandoned
- 2018-12-18 KR KR1020207020877A patent/KR20200101956A/en not_active Application Discontinuation
-
2020
- 2020-06-14 IL IL275365A patent/IL275365A/en unknown
-
2022
- 2022-06-30 US US17/854,089 patent/US11912703B2/en active Active
Also Published As
Publication number | Publication date |
---|---|
EA202091508A1 (en) | 2020-09-14 |
AU2018390543A1 (en) | 2020-08-06 |
EP3728253B1 (en) | 2024-03-27 |
WO2019126082A1 (en) | 2019-06-27 |
US20200385382A1 (en) | 2020-12-10 |
IL275365A (en) | 2020-07-30 |
CA3085761A1 (en) | 2019-06-27 |
BR112020011788A2 (en) | 2020-11-24 |
JP7304352B2 (en) | 2023-07-06 |
MX2020005873A (en) | 2020-08-13 |
KR20200101956A (en) | 2020-08-28 |
CN111699185B (en) | 2023-06-27 |
CN111699185A (en) | 2020-09-22 |
EP3728253A1 (en) | 2020-10-28 |
US20220348576A1 (en) | 2022-11-03 |
US11912703B2 (en) | 2024-02-27 |
JP2021507912A (en) | 2021-02-25 |
US11427580B2 (en) | 2022-08-30 |
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