DK3681885T3 - Tetrahydro-imidazo-quinolinsammensætninger som cbp/p300-inhibitorer - Google Patents
Tetrahydro-imidazo-quinolinsammensætninger som cbp/p300-inhibitorer Download PDFInfo
- Publication number
- DK3681885T3 DK3681885T3 DK18833127.6T DK18833127T DK3681885T3 DK 3681885 T3 DK3681885 T3 DK 3681885T3 DK 18833127 T DK18833127 T DK 18833127T DK 3681885 T3 DK3681885 T3 DK 3681885T3
- Authority
- DK
- Denmark
- Prior art keywords
- cbp
- imidazo
- tetrahydro
- inhibitors
- quinoline compounds
- Prior art date
Links
- GCGNWZMOENODOJ-UHFFFAOYSA-N 2,3,3a,4-tetrahydro-1h-imidazo[4,5-h]quinoline Chemical class C1C=C2C=CC=NC2=C2C1NCN2 GCGNWZMOENODOJ-UHFFFAOYSA-N 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
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
-
- 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 (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201762559436P | 2017-09-15 | 2017-09-15 | |
US201862692593P | 2018-06-29 | 2018-06-29 | |
PCT/US2018/051235 WO2019055877A1 (en) | 2017-09-15 | 2018-09-14 | TETRAHYDROIMIDAZO QUINOLINE COMPOSITIONS AS INHIBITORS OF CBP / P300 |
Publications (1)
Publication Number | Publication Date |
---|---|
DK3681885T3 true DK3681885T3 (da) | 2024-04-15 |
Family
ID=63714164
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DK18833127.6T DK3681885T3 (da) | 2017-09-15 | 2018-09-14 | Tetrahydro-imidazo-quinolinsammensætninger som cbp/p300-inhibitorer |
Country Status (8)
Country | Link |
---|---|
US (3) | US11292791B2 (da) |
EP (1) | EP3681885B1 (da) |
AU (1) | AU2018334272B2 (da) |
CA (1) | CA3075880A1 (da) |
DK (1) | DK3681885T3 (da) |
MA (1) | MA50250A (da) |
TW (2) | TWI795440B (da) |
WO (2) | WO2019055869A1 (da) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2019055869A1 (en) | 2017-09-15 | 2019-03-21 | Forma Therapeutics, Inc. | TETRAHYDROIMIDAZO QUINOLINE COMPOSITIONS AS INHIBITORS OF CBP / P300 |
MX2020014303A (es) | 2018-06-29 | 2021-03-25 | Forma Therapeutics Inc | Inhibición de la proteína de union a creb (cbp). |
EP3587418B1 (en) * | 2018-06-29 | 2021-09-01 | Forma Therapeutics, Inc. | Inhibitors of creb binding protein (cbp) |
AU2020241709A1 (en) * | 2019-03-15 | 2021-09-23 | Forma Therapeutics, Inc. | Compositions and methods for treating androgen receptor positive forms of cancer |
WO2020190780A1 (en) * | 2019-03-15 | 2020-09-24 | Forma Therapeutics, Inc. | Inhibiting cyclic amp-responsive element-binding protein (creb) |
US11801243B2 (en) | 2020-09-23 | 2023-10-31 | Forma Therapeutics, Inc. | Bromodomain inhibitors for androgen receptor-driven cancers |
US11795168B2 (en) | 2020-09-23 | 2023-10-24 | Forma Therapeutics, Inc. | Inhibiting cyclic amp-responsive element-binding protein (CREB) binding protein (CBP) |
JPWO2022138944A1 (da) * | 2020-12-25 | 2022-06-30 |
Family Cites Families (64)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4404207A (en) | 1981-11-06 | 1983-09-13 | Riker Laboratories, Inc. | Antimicrobial 8-substituted benzo [IJ]quinolizines |
AU1868195A (en) | 1994-01-28 | 1995-08-15 | Cell Therapeutics, Inc. | Cell signaling inhibitors |
US6011029A (en) | 1996-02-26 | 2000-01-04 | Bristol-Myers Squibb Company | Inhibitors of farnesyl protein transferase |
US6455564B1 (en) | 1999-01-06 | 2002-09-24 | Pharmacia & Upjohn Company | Method of treating sexual disturbances |
US7101869B2 (en) | 1999-11-30 | 2006-09-05 | Pfizer Inc. | 2,4-diaminopyrimidine compounds useful as immunosuppressants |
US7345051B2 (en) | 2000-01-31 | 2008-03-18 | Genaera Corporation | Mucin synthesis inhibitors |
US7122227B2 (en) | 2000-11-20 | 2006-10-17 | Merck Patent Gesellschaft | Chiral photoisomerizable compounds |
CA2463136A1 (en) | 2001-10-17 | 2003-04-24 | Raymond Andersen | Ship 1 modulators |
WO2003045929A1 (fr) | 2001-11-26 | 2003-06-05 | Takeda Chemical Industries, Ltd. | Derive bicyclique, procede de production de ce derive et utilisation correspondante |
HUP0203976A3 (en) | 2002-11-15 | 2004-08-30 | Sanofi Aventis | Adenozine a3 receptors, process for their preparation and pharmaceutical compositions containing them |
TWI322012B (en) | 2002-12-20 | 2010-03-21 | Organon Nv | Tetrahydroquinoline derivatives |
IN2003CH00929A (da) | 2003-11-13 | 2008-10-06 | ||
WO2005066162A1 (en) | 2003-12-23 | 2005-07-21 | Human Biomolecular Research Institute | Synthetic compounds and derivatives as modulators of smoking or nicotine ingestion and lung cancer |
CA2562244A1 (en) | 2004-04-07 | 2005-10-27 | Takeda Pharmaceutical Company Limited | Cyclic compounds |
WO2005105814A1 (en) | 2004-04-28 | 2005-11-10 | Incyte Corporation | Tetracyclic inhibitors of janus kinases |
JP2009520038A (ja) | 2005-12-19 | 2009-05-21 | ジェネンテック・インコーポレーテッド | ピリミジンキナーゼインヒビター |
US20070203236A1 (en) | 2006-01-11 | 2007-08-30 | Smith Jeffrey W | Novel antagonists of the human fatty acid synthase thioesterase |
BRPI0713096A2 (pt) | 2006-05-09 | 2012-10-16 | Hemaquest Pharmaceuticals Inc | métodos para tratar distúrbios sangüìneos |
EP1878724A1 (en) | 2006-07-15 | 2008-01-16 | sanofi-aventis | A regioselective palladium catalyzed synthesis of benzimidazoles and azabenzimidazoles |
CA2574531C (en) | 2007-01-19 | 2016-10-25 | The University Of British Columbia | Hat acetylation promoters and uses of compositions thereof in promoting immunogenicity |
US8476458B2 (en) | 2007-06-21 | 2013-07-02 | The Wistar Institute | Methods and compositions for modulating P300/CBP activity |
KR20100023907A (ko) | 2007-06-26 | 2010-03-04 | 사노피-아벤티스 | 벤즈이미다졸 및 아자벤즈이미다졸의 위치선택적 구리 촉매화 합성 |
US8222417B2 (en) | 2007-06-27 | 2012-07-17 | Taisho Pharmaceutical Co., Ltd | Compound having 11β-HSD1 inhibitory activity |
TW200930369A (en) | 2007-11-15 | 2009-07-16 | Astrazeneca Ab | Bis-(sulfonylamino) derivatives in therapy |
AR072008A1 (es) | 2008-06-13 | 2010-07-28 | Merck & Co Inc | Compuestos heterobiciclicos como agentes de inhibicion de quinasa p38 |
KR20110022672A (ko) | 2008-06-16 | 2011-03-07 | 유니버시티 오브 테네시 리서치 파운데이션 | 암 치료용 화합물 |
JP5586585B2 (ja) | 2009-03-27 | 2014-09-10 | 興和株式会社 | 縮合ピペリジン化合物及びこれを含有する医薬 |
WO2010118208A1 (en) | 2009-04-09 | 2010-10-14 | Exelixis, Inc. | Benzoxazepin-4- (5h) -yl derivatives and their use to treat cancer |
BRPI1014574A2 (pt) | 2009-04-15 | 2015-08-25 | Jw Pharmaceutical Corp | Compostos inéditos de imitadores de ligação revesa, método para fabricar os mesmos e uso destes |
WO2010138490A1 (en) | 2009-05-26 | 2010-12-02 | Exelixis, Inc. | Benzoxazepines as inhibitors of mtor and methods of their use and manufacture |
NZ596552A (en) | 2009-05-26 | 2014-02-28 | Exelixis Inc | Benzoxazepines as inhibitors of pi3k/mtor and methods of their use and manufacture |
US9005670B2 (en) | 2010-01-05 | 2015-04-14 | The Johns Hopkins University | Use of histone acetyltransferase inhibitors as novel anti-cancer therapies |
CA2791738C (en) | 2010-03-01 | 2020-06-09 | Gtx, Inc. | Aryl imidazolyl compounds for the treatment of cancer |
CA2800618C (en) | 2010-05-26 | 2018-08-28 | Sunovion Pharmaceuticals Inc. | Heteroaryl compounds and methods of use thereof |
WO2012019093A1 (en) | 2010-08-05 | 2012-02-09 | Human Biomolecular Research Institute | Synthetic compounds and methods to decrease nicotine self-administration |
JP5937102B2 (ja) | 2010-12-14 | 2016-06-22 | エレクトロフォレティクス リミテッド | カゼインキナーゼ1デルタ(ck1デルタ)阻害剤 |
US8765978B2 (en) | 2010-12-16 | 2014-07-01 | Transitions Optical, Inc. | Method of making indeno-fused naphthol materials |
CA2827392A1 (en) | 2011-02-24 | 2012-08-30 | Emory University | Noggin blocking compositions for ossification and methods related thereto |
TW201837023A (zh) | 2011-07-01 | 2018-10-16 | 美商基利科學股份有限公司 | 作為離子通道調節劑之稠合雜環化合物 |
GB201111705D0 (en) | 2011-07-07 | 2011-08-24 | Takeda Pharmaceutical | Compounds and their use |
WO2013148114A1 (en) | 2012-03-30 | 2013-10-03 | University Of Florida Research Foundation, Inc. | P300/cbp inhibitors and methods of use |
US9211333B2 (en) | 2012-06-05 | 2015-12-15 | Hong Kong Baptist University | Anti-cancer agents synthesized based on miliusane compounds |
US9593115B2 (en) | 2012-09-21 | 2017-03-14 | Advinus Therapeutics Ltd. | Substituted fused tricyclic compounds, compositions, and medicinal applications thereof |
RU2543485C2 (ru) | 2013-02-26 | 2015-03-10 | Андрей Александрович Иващенко | Гетероциклические агонисты рецепторов желчных кислот tgr5, фармацевтическая композиция, способы их получения и применения |
TWI527811B (zh) | 2013-05-09 | 2016-04-01 | 吉李德科學股份有限公司 | 作爲溴結構域抑制劑的苯並咪唑衍生物 |
EP3010918B1 (en) | 2013-06-21 | 2018-08-15 | Zenith Epigenetics Ltd. | Novel substituted bicyclic compounds as bromodomain inhibitors |
EP3674300B1 (en) | 2013-06-21 | 2022-10-12 | Zenith Epigenetics Ltd. | Novel bicyclic bromodomain inhibitors |
RU2016105108A (ru) | 2013-07-25 | 2017-08-30 | Дана-Фарбер Кэнсер Инститьют, Инк. | Ингибиторы факторов транскрипции и их применение |
DE102013215912B3 (de) | 2013-08-12 | 2015-02-26 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Farbneutral beschichteter kupferhaltiger Gegenstand, Verfahren zu dessen Herstellung sowie Verwendung einer entsprechenden farbneutralen Beschichtung |
TW201605859A (zh) | 2013-11-14 | 2016-02-16 | 必治妥美雅史谷比公司 | 作為酪蛋白激酶1δ/ε抑制劑之新穎經取代之吡唑并-哌 |
WO2015074081A1 (en) | 2013-11-18 | 2015-05-21 | Bair Kenneth W | Benzopiperazine compositions as bet bromodomain inhibitors |
CN110627770A (zh) | 2013-11-18 | 2019-12-31 | 福马疗法公司 | 作为bet溴域抑制剂的四氢喹啉组成物 |
EP3193866A1 (en) | 2014-09-19 | 2017-07-26 | Genentech, Inc. | Use of cbp/ep300 and bet inhibitors for treatment of cancer |
CN107531690B (zh) * | 2014-11-27 | 2020-11-06 | 基因泰克公司 | 用作CBP和/或EP300抑制剂的4,5,6,7-四氢-1H-吡唑并[4,3-c]吡啶-3-胺化合物 |
WO2016110821A1 (en) | 2015-01-08 | 2016-07-14 | Advinus Therapeutics Limited | Bicyclic compounds, compositions and medicinal applications thereof |
WO2016128908A1 (en) | 2015-02-12 | 2016-08-18 | Advinus Therapeutics Limited | Bicyclic compounds, compositions and medicinal applications thereof |
GB201506660D0 (en) | 2015-04-20 | 2015-06-03 | Cellcentric Ltd | Pharmaceutical compounds |
GB201506658D0 (en) | 2015-04-20 | 2015-06-03 | Cellcentric Ltd | Pharmaceutical compounds |
WO2017197056A1 (en) | 2016-05-10 | 2017-11-16 | C4 Therapeutics, Inc. | Bromodomain targeting degronimers for target protein degradation |
US11883381B2 (en) | 2016-05-12 | 2024-01-30 | The Regents Of The University Of Michigan | ASH1L inhibitors and methods of treatment therewith |
JP7160688B2 (ja) | 2016-05-24 | 2022-10-25 | ジェネンテック, インコーポレイテッド | Cbp/ep300の複素環式インヒビターおよびがんの処置におけるそれらの使用 |
GB201617630D0 (en) | 2016-10-18 | 2016-11-30 | Cellcentric Ltd | Pharmaceutical compounds |
GB201617627D0 (en) | 2016-10-18 | 2016-11-30 | Cellcentric Ltd | Pharmaceutical compounds |
WO2019055869A1 (en) | 2017-09-15 | 2019-03-21 | Forma Therapeutics, Inc. | TETRAHYDROIMIDAZO QUINOLINE COMPOSITIONS AS INHIBITORS OF CBP / P300 |
-
2018
- 2018-09-14 WO PCT/US2018/051214 patent/WO2019055869A1/en active Application Filing
- 2018-09-14 US US16/647,478 patent/US11292791B2/en active Active
- 2018-09-14 EP EP18833127.6A patent/EP3681885B1/en active Active
- 2018-09-14 AU AU2018334272A patent/AU2018334272B2/en active Active
- 2018-09-14 MA MA050250A patent/MA50250A/fr unknown
- 2018-09-14 TW TW107132421A patent/TWI795440B/zh active
- 2018-09-14 CA CA3075880A patent/CA3075880A1/en active Pending
- 2018-09-14 TW TW112106967A patent/TW202340191A/zh unknown
- 2018-09-14 DK DK18833127.6T patent/DK3681885T3/da active
- 2018-09-14 WO PCT/US2018/051235 patent/WO2019055877A1/en active Search and Examination
-
2022
- 2022-02-10 US US17/669,135 patent/US11787803B2/en active Active
-
2023
- 2023-09-08 US US18/463,587 patent/US20240150349A1/en active Pending
Also Published As
Publication number | Publication date |
---|---|
AU2018334272B2 (en) | 2023-06-15 |
CA3075880A1 (en) | 2019-03-21 |
AU2018334272A1 (en) | 2020-04-16 |
MA50250A (fr) | 2020-07-22 |
US20240150349A1 (en) | 2024-05-09 |
EP3681885A1 (en) | 2020-07-22 |
US20200216445A1 (en) | 2020-07-09 |
WO2019055869A1 (en) | 2019-03-21 |
EP3681885B1 (en) | 2024-02-28 |
TW201920169A (zh) | 2019-06-01 |
US11292791B2 (en) | 2022-04-05 |
US11787803B2 (en) | 2023-10-17 |
TW202340191A (zh) | 2023-10-16 |
US20220169647A1 (en) | 2022-06-02 |
TWI795440B (zh) | 2023-03-11 |
WO2019055877A1 (en) | 2019-03-21 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DK3442980T3 (da) | Heterocykliske forbindelser som ret-kinase-hæmmere | |
DK3873903T3 (da) | Substituerede 6-azabenzimidazolforbindelser som hpk1-hæmmere | |
DK3788040T3 (da) | Pyridazinoner som parp7-inhibitorer | |
DK3697785T3 (da) | Imidazo-pyridine forbindelser som pad-inhibitorer | |
DK3656769T3 (da) | Aryl-phosphor-oxygen-forbindelse som egfr-kinase-inhibitor | |
DK3277677T3 (da) | 1-cyano-pyrrolidinforbindelser som usp30-hæmmere | |
DK3436461T3 (da) | Pyrrolotriazinforbindelser som tam-inhibitorer | |
DK3371190T3 (da) | Heterocykliske forbindelser som pi3k-gamma-inhibitorer | |
DK3472167T3 (da) | Heterocykliske forbindelser som immunomodulatorer | |
DK3377488T3 (da) | Heterocykliske forbindelser som immunomodulatorer | |
DK3442947T3 (da) | Aminsubstituerede aryl- eller heteroarylforbindelser som ehmt1- og ehmt2-hæmmere | |
DK3728252T3 (da) | 4-azaindolforbindelser | |
DK3298002T3 (da) | Heterocykliske amider som kinasehæmmere | |
DK3303348T3 (da) | Naphthyridinforbindelser som JAK-kinaseinhibitorer | |
DK3390395T3 (da) | Forbindelser, der kan anvendes som kinase-inhibitorer | |
DK3681885T3 (da) | Tetrahydro-imidazo-quinolinsammensætninger som cbp/p300-inhibitorer | |
DK3324977T3 (da) | Benzodiazepinderivater som rsv-inhibitorer | |
DK3461821T3 (da) | Indolcarboxamidforbindelser, der er brugbar som kinasehæmmere | |
DK3190113T3 (da) | Pyrrolopyrimidinforbindelser anvendt som tlr7-agonist | |
DK3582780T3 (da) | Aminopyrimidinforbindelser, der er anvendelige som SSAO-inhibitorer | |
DK3294713T5 (da) | Substituerede tetrahydroquinolinonforbindelser som ror-gamma-modulatorer | |
DK3580220T3 (da) | Aminotriazolpyridiner som kinasehæmmere | |
DK3768674T3 (da) | Aminopyrimidinderivater som ctps1-hæmmere | |
DK3762368T3 (da) | Aminopyrazindiolforbindelser som pi3k-y-inhibitorer | |
DK3235819T3 (da) | Pyrrolopyrimidinforbindelser, der er anvendelige som JAK-inhibitorer |