WO2014125408A3 - Substituted 1h-pyrrolopyridinone derivatives as kinase inhibitors - Google Patents
Substituted 1h-pyrrolopyridinone derivatives as kinase inhibitors Download PDFInfo
- Publication number
- WO2014125408A3 WO2014125408A3 PCT/IB2014/058881 IB2014058881W WO2014125408A3 WO 2014125408 A3 WO2014125408 A3 WO 2014125408A3 IB 2014058881 W IB2014058881 W IB 2014058881W WO 2014125408 A3 WO2014125408 A3 WO 2014125408A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- present
- kinase inhibitors
- substituted
- disorder
- diseases
- Prior art date
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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
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
Abstract
The present invention provides novel substituted 1H-Pyrrolopyridinone derivatives of formula (1) as protein kinase inhibitors, in which R1, R2, R3, R4, R5, R6 and 'p' have the meanings given in the specification, and pharmaceutically acceptable salts thereof that are useful in the treatment and prevention in diseases or disorder, in particular their use in diseases or disorder where there is an advantage in inhibiting kinase enzyme, more particularly BTK enzyme. The present invention also provides methods for synthesizing and administering the kinase inhibitor compounds. The present invention also provides pharmaceutical formulations comprising at least one of the kinase inhibitor compounds together with a pharmaceutically acceptable carrier, diluent or excipient therefor.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IN598CH2013 | 2013-02-12 | ||
IN598/CHE/2013 | 2013-02-12 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2014125408A2 WO2014125408A2 (en) | 2014-08-21 |
WO2014125408A3 true WO2014125408A3 (en) | 2014-12-18 |
Family
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/IB2014/058881 WO2014125408A2 (en) | 2013-02-12 | 2014-02-10 | Substituted 1h-pyrrolopyridinone derivatives as kinase inhibitors |
Country Status (1)
Country | Link |
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WO (1) | WO2014125408A2 (en) |
Families Citing this family (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
MX2016012808A (en) * | 2014-04-02 | 2017-01-05 | Intermune Inc | Anti-fibrotic pyridinones. |
MA40943A (en) * | 2014-11-10 | 2017-09-19 | Constellation Pharmaceuticals Inc | SUBSTITUTED PYRROLOPYRIDINES USED AS BROMODOMA INHIBITORS |
EP3218376B1 (en) | 2014-11-10 | 2019-12-25 | Genentech, Inc. | Bromodomain inhibitors and uses thereof |
MA40940A (en) * | 2014-11-10 | 2017-09-19 | Constellation Pharmaceuticals Inc | SUBSTITUTED PYRROLOPYRIDINES USED AS BROMODOMA INHIBITORS |
WO2016123391A1 (en) | 2015-01-29 | 2016-08-04 | Genentech, Inc. | Therapeutic compounds and uses thereof |
SG11201808003RA (en) * | 2016-04-15 | 2018-10-30 | Abbvie Inc | Bromodomain inhibitors |
CN110167939B (en) * | 2017-01-11 | 2021-12-31 | 江苏豪森药业集团有限公司 | Pyrrolo [2,3-c ] pyridine derivatives, preparation method and medical application thereof |
MA47409A (en) * | 2017-02-06 | 2019-12-11 | Idorsia Pharmaceuticals Ltd | NEW PROCESS FOR THE SYNTHESIS OF 1-ARYL-1-TRIFLUOROMETHYLCYCLOPROPANES |
WO2020007322A1 (en) * | 2018-07-04 | 2020-01-09 | 清华大学 | Compound targeted to degrade bet protein and application thereof |
WO2020132004A1 (en) * | 2018-12-20 | 2020-06-25 | Saint Louis University | Bet inhibitors for modulating dux4 expression in fshd |
CA3133131A1 (en) * | 2019-03-17 | 2020-09-24 | Shanghai Ringene Biopharma Co., Ltd. | Pyrrole amidopyridone compound, preparation method therefor and use thereof |
GB201905721D0 (en) * | 2019-04-24 | 2019-06-05 | Univ Dundee | Compounds |
CN112625036A (en) * | 2019-10-08 | 2021-04-09 | 上海海和药物研究开发股份有限公司 | Compound with BRD4 inhibitory activity, preparation method and application thereof |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2007068728A2 (en) * | 2005-12-16 | 2007-06-21 | Pfizer Italia Srl | N-substituted pyrrolopyridinones active as kinase inhibitors |
EP2003129A1 (en) * | 2007-06-11 | 2008-12-17 | Nerviano Medical Sciences S.r.l. | 1H-Pyrido[3,4-B]indol-1-one and 2,3,4,9-Tetrahydro-1H-Beta-Carbolin-1-one Derivatives |
US20100056556A1 (en) * | 2007-02-27 | 2010-03-04 | Nerviano Medical Sciences S.R.L. | Isoquinolinopyrrolopyridinones active as kinase inhibitors |
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2014
- 2014-02-10 WO PCT/IB2014/058881 patent/WO2014125408A2/en active Application Filing
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2007068728A2 (en) * | 2005-12-16 | 2007-06-21 | Pfizer Italia Srl | N-substituted pyrrolopyridinones active as kinase inhibitors |
US20100056556A1 (en) * | 2007-02-27 | 2010-03-04 | Nerviano Medical Sciences S.R.L. | Isoquinolinopyrrolopyridinones active as kinase inhibitors |
EP2003129A1 (en) * | 2007-06-11 | 2008-12-17 | Nerviano Medical Sciences S.r.l. | 1H-Pyrido[3,4-B]indol-1-one and 2,3,4,9-Tetrahydro-1H-Beta-Carbolin-1-one Derivatives |
Also Published As
Publication number | Publication date |
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WO2014125408A2 (en) | 2014-08-21 |
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