JP2014513110A5 - - Google Patents

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Publication number
JP2014513110A5
JP2014513110A5 JP2014508771A JP2014508771A JP2014513110A5 JP 2014513110 A5 JP2014513110 A5 JP 2014513110A5 JP 2014508771 A JP2014508771 A JP 2014508771A JP 2014508771 A JP2014508771 A JP 2014508771A JP 2014513110 A5 JP2014513110 A5 JP 2014513110A5
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JP
Japan
Prior art keywords
compound
salt
methyl
methoxyethyl
amino
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.)
Granted
Application number
JP2014508771A
Other languages
English (en)
Japanese (ja)
Other versions
JP2014513110A (ja
JP5926793B2 (ja
Filing date
Publication date
Priority claimed from GBGB1107325.1A external-priority patent/GB201107325D0/en
Application filed filed Critical
Publication of JP2014513110A publication Critical patent/JP2014513110A/ja
Publication of JP2014513110A5 publication Critical patent/JP2014513110A5/ja
Application granted granted Critical
Publication of JP5926793B2 publication Critical patent/JP5926793B2/ja
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2014508771A 2011-05-04 2012-05-02 ブロモドメイン阻害剤としてのテトラヒドロキノリン誘導体 Expired - Fee Related JP5926793B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GBGB1107325.1A GB201107325D0 (en) 2011-05-04 2011-05-04 Novel compounds
GB1107325.1 2011-05-04
PCT/EP2012/057978 WO2012150234A1 (en) 2011-05-04 2012-05-02 Dihydroquinoline derivatives as bromodomain inhibitors

Publications (3)

Publication Number Publication Date
JP2014513110A JP2014513110A (ja) 2014-05-29
JP2014513110A5 true JP2014513110A5 (cg-RX-API-DMAC10.html) 2015-05-28
JP5926793B2 JP5926793B2 (ja) 2016-05-25

Family

ID=44203063

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2014508771A Expired - Fee Related JP5926793B2 (ja) 2011-05-04 2012-05-02 ブロモドメイン阻害剤としてのテトラヒドロキノリン誘導体

Country Status (6)

Country Link
US (1) US9315487B2 (cg-RX-API-DMAC10.html)
EP (1) EP2705032B1 (cg-RX-API-DMAC10.html)
JP (1) JP5926793B2 (cg-RX-API-DMAC10.html)
ES (1) ES2589801T3 (cg-RX-API-DMAC10.html)
GB (1) GB201107325D0 (cg-RX-API-DMAC10.html)
WO (1) WO2012150234A1 (cg-RX-API-DMAC10.html)

Families Citing this family (33)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB201106743D0 (en) * 2011-04-21 2011-06-01 Glaxosmithkline Llc Novel compounds
CN105073744B (zh) 2012-12-21 2019-11-08 齐尼思表观遗传学有限公司 作为溴结构域抑制剂的新型杂环化合物
TWI613182B (zh) * 2013-02-21 2018-02-01 必治妥美雅史谷比公司 雙環化合物
JP2016516701A (ja) 2013-03-11 2016-06-09 アッヴィ・インコーポレイテッド 縮合四環系ブロモドメイン阻害剤
JP2016512524A (ja) 2013-03-11 2016-04-28 アッヴィ・インコーポレイテッド ブロモドメイン阻害剤
HRP20182179T1 (hr) 2013-03-14 2019-02-22 Glaxosmithkline Intellectual Property (No. 2) Limited 2,3-disupstituirani 1-acil-4-amino-1,2,3,4-tetrahidrokonolin derivati i njihova uporaba kao inhibitora bromodomena
MX366703B (es) 2013-03-15 2019-07-22 Incyte Holdings Corp Heterociclos tricíclicos como inhibidores de la proteína bet.
EP2792355A1 (en) 2013-04-17 2014-10-22 Albert-Ludwigs-Universität Freiburg Compounds for use as bromodomain inhibitors
CA2915838C (en) 2013-06-21 2023-04-18 Zenith Epigenetics Corp. Bicyclic bromodomain inhibitors
US9636328B2 (en) 2013-06-21 2017-05-02 Zenith Epigenetics Ltd. Substituted bicyclic compounds as bromodomain inhibitors
US9290514B2 (en) 2013-07-08 2016-03-22 Incyte Holdings Corporation Tricyclic heterocycles as BET protein inhibitors
CN105593224B (zh) 2013-07-31 2021-05-25 恒元生物医药科技(苏州)有限公司 作为溴结构域抑制剂的新型喹唑啉酮类化合物
EP3640241B1 (en) 2013-10-18 2022-09-28 Celgene Quanticel Research, Inc. Bromodomain inhibitors
HUE053645T2 (hu) * 2013-11-18 2021-07-28 Forma Therapeutics Inc Tetrahidrokinolin kompozíciók mint BET bromodomén inhibitorok
WO2015074081A1 (en) 2013-11-18 2015-05-21 Bair Kenneth W Benzopiperazine compositions as bet bromodomain inhibitors
US9315501B2 (en) 2013-11-26 2016-04-19 Incyte Corporation Bicyclic heterocycles as BET protein inhibitors
US9399640B2 (en) 2013-11-26 2016-07-26 Incyte Corporation Substituted pyrrolo[2,3-c]pyridines and pyrazolo[3,4-c]pyridines as BET protein inhibitors
US9309246B2 (en) 2013-12-19 2016-04-12 Incyte Corporation Tricyclic heterocycles as BET protein inhibitors
PL3092227T3 (pl) * 2014-01-09 2018-12-31 Orion Corporation Bicykliczne pochodne heterocykliczne jako inhibitory bromodomeny
EA034972B1 (ru) 2014-04-23 2020-04-13 Инсайт Корпорейшн 1h-пирроло[2,3-c]пиридин-7(6h)-оны в качестве ингибиторов белков bet
SMT201900019T1 (it) 2014-09-12 2019-02-28 Glaxosmithkline Ip No 2 Ltd Derivati di tetraidrochinolina come inibitori di bromodominio
EP3194406B8 (en) 2014-09-15 2021-03-31 Incyte Corporation Tricyclic heterocycles for use as bet protein inhibitors
EP3227280B1 (en) 2014-12-01 2019-04-24 Zenith Epigenetics Ltd. Substituted pyridines as bromodomain inhibitors
US10292968B2 (en) 2014-12-11 2019-05-21 Zenith Epigenetics Ltd. Substituted heterocycles as bromodomain inhibitors
HK1245247A1 (zh) 2014-12-17 2018-08-24 恒翼生物医药科技(上海)有限公司 溴结构域的抑制剂
GB201504694D0 (en) 2015-03-19 2015-05-06 Glaxosmithkline Ip Dev Ltd Covalent conjugates
WO2016203335A1 (en) 2015-06-18 2016-12-22 Pfizer Inc. Novel pyrido[2,3-b]pyrazinones as bet-family bromodomain inhibitors
AR106520A1 (es) 2015-10-29 2018-01-24 Incyte Corp Forma sólida amorfa de un inhibidor de proteína bet
PT3472157T (pt) 2016-06-20 2023-05-30 Incyte Corp Formas sólidas cristalinas de um inibidor bet
ES2937307T3 (es) 2016-07-26 2023-03-27 Univ Southern California Inhibición selectiva del bromodominio del BDF1 fúngico
WO2018111805A1 (en) * 2016-12-13 2018-06-21 St. Jude Children's Research Hospital Tetrahydroquinoline-based bromodomain inhibitors
US11629152B2 (en) 2018-03-30 2023-04-18 Kyowa Kirin Co., Ltd. Compound with anticancer activity
US11833155B2 (en) 2020-06-03 2023-12-05 Incyte Corporation Combination therapy for treatment of myeloproliferative neoplasms

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9004781D0 (en) 1990-03-02 1990-04-25 Glaxo Group Ltd Device
EP1435356A1 (en) * 2003-01-06 2004-07-07 Warner-Lambert Company LLC Quinoline derivatives as CRTH2 antagonists
JP4641526B2 (ja) 2003-11-03 2011-03-02 グラクソ グループ リミテッド 流体分配デバイス
WO2006083692A2 (en) * 2005-01-28 2006-08-10 Mount Sinai Schoool Of Medicine Methods of identifying modulators of bromodomains
JP2008156311A (ja) 2006-12-26 2008-07-10 Institute Of Physical & Chemical Research Brd2ブロモドメイン結合剤
EP2239264A4 (en) 2007-12-28 2012-01-11 Mitsubishi Tanabe Pharma Corp ANTITUMORAL MEDIUM
GB0919431D0 (en) * 2009-11-05 2009-12-23 Glaxosmithkline Llc Novel compounds
GB0919434D0 (en) 2009-11-05 2009-12-23 Glaxosmithkline Llc Novel compounds
GB201106750D0 (en) 2011-04-21 2011-06-01 Glaxosmithkline Llc Novel compounds
GB201106743D0 (en) 2011-04-21 2011-06-01 Glaxosmithkline Llc Novel compounds

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