JP2014511891A5 - - Google Patents

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Publication number
JP2014511891A5
JP2014511891A5 JP2014505610A JP2014505610A JP2014511891A5 JP 2014511891 A5 JP2014511891 A5 JP 2014511891A5 JP 2014505610 A JP2014505610 A JP 2014505610A JP 2014505610 A JP2014505610 A JP 2014505610A JP 2014511891 A5 JP2014511891 A5 JP 2014511891A5
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JP
Japan
Prior art keywords
compound
salt
methyl
pharmaceutically acceptable
acetyl
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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
JP2014505610A
Other languages
English (en)
Japanese (ja)
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JP5840763B2 (ja
JP2014511891A (ja
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Publication date
Priority claimed from GB201106743A external-priority patent/GB201106743D0/en
Application filed filed Critical
Publication of JP2014511891A publication Critical patent/JP2014511891A/ja
Publication of JP2014511891A5 publication Critical patent/JP2014511891A5/ja
Application granted granted Critical
Publication of JP5840763B2 publication Critical patent/JP5840763B2/ja
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

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JP2014505610A 2011-04-21 2012-04-19 ブロモドメイン阻害剤として有用なテトラヒドロキノリン誘導体 Expired - Fee Related JP5840763B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GB201106743A GB201106743D0 (en) 2011-04-21 2011-04-21 Novel compounds
GB1106743.6 2011-04-21
PCT/EP2012/057111 WO2012143413A1 (en) 2011-04-21 2012-04-19 Tetrahydroquinoline derivatives useful as bromodomain inhibitors

Publications (3)

Publication Number Publication Date
JP2014511891A JP2014511891A (ja) 2014-05-19
JP2014511891A5 true JP2014511891A5 (cg-RX-API-DMAC10.html) 2015-04-30
JP5840763B2 JP5840763B2 (ja) 2016-01-06

Family

ID=44147335

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2014505610A Expired - Fee Related JP5840763B2 (ja) 2011-04-21 2012-04-19 ブロモドメイン阻害剤として有用なテトラヒドロキノリン誘導体

Country Status (16)

Country Link
US (1) US9029395B2 (cg-RX-API-DMAC10.html)
EP (1) EP2699550B1 (cg-RX-API-DMAC10.html)
JP (1) JP5840763B2 (cg-RX-API-DMAC10.html)
KR (1) KR101896599B1 (cg-RX-API-DMAC10.html)
CN (1) CN103619820B (cg-RX-API-DMAC10.html)
AU (1) AU2012244759B2 (cg-RX-API-DMAC10.html)
BR (1) BR112013026834A2 (cg-RX-API-DMAC10.html)
CA (1) CA2832763C (cg-RX-API-DMAC10.html)
EA (1) EA022341B1 (cg-RX-API-DMAC10.html)
ES (1) ES2544302T3 (cg-RX-API-DMAC10.html)
GB (1) GB201106743D0 (cg-RX-API-DMAC10.html)
IL (1) IL228707A (cg-RX-API-DMAC10.html)
MX (1) MX338515B (cg-RX-API-DMAC10.html)
SG (1) SG194469A1 (cg-RX-API-DMAC10.html)
WO (1) WO2012143413A1 (cg-RX-API-DMAC10.html)
ZA (1) ZA201307645B (cg-RX-API-DMAC10.html)

Families Citing this family (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB201107325D0 (en) 2011-05-04 2011-06-15 Glaxosmithkline Llc Novel compounds
US9765039B2 (en) 2012-11-21 2017-09-19 Zenith Epigenetics Ltd. Biaryl derivatives as bromodomain inhibitors
US9073878B2 (en) 2012-11-21 2015-07-07 Zenith Epigenetics Corp. Cyclic amines as bromodomain inhibitors
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
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.
US9636328B2 (en) 2013-06-21 2017-05-02 Zenith Epigenetics Ltd. Substituted bicyclic compounds as bromodomain inhibitors
CA2915838C (en) 2013-06-21 2023-04-18 Zenith Epigenetics Corp. Bicyclic 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
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
US9315501B2 (en) 2013-11-26 2016-04-19 Incyte Corporation Bicyclic heterocycles as BET protein inhibitors
US9309246B2 (en) 2013-12-19 2016-04-12 Incyte Corporation Tricyclic heterocycles as BET protein inhibitors
WO2015120393A1 (en) 2014-02-10 2015-08-13 Concert Pharmaceuticals, Inc. Substituted triazolobenzodiazepines
EA034972B1 (ru) 2014-04-23 2020-04-13 Инсайт Корпорейшн 1h-пирроло[2,3-c]пиридин-7(6h)-оны в качестве ингибиторов белков bet
ES2896400T3 (es) * 2014-08-01 2022-02-24 Nuevolution As Compuestos activos frente a bromdominios
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
AU2015326910B2 (en) * 2014-10-02 2018-03-01 Glaxosmithkline Intellectual Property (No.2) Limited Compound
EP3227280B1 (en) 2014-12-01 2019-04-24 Zenith Epigenetics Ltd. Substituted pyridines as bromodomain inhibitors
EP3227281A4 (en) 2014-12-01 2018-05-30 Zenith Epigenetics Ltd. Substituted pyridinones 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
US11833155B2 (en) 2020-06-03 2023-12-05 Incyte Corporation Combination therapy for treatment of myeloproliferative neoplasms

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GB9004781D0 (en) 1990-03-02 1990-04-25 Glaxo Group Ltd Device
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
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
EP2415764A4 (en) * 2009-03-31 2012-08-08 Kowa Co PROPHYLACTIC AND / OR THERAPEUTIC AGENT AGAINST ANEMIA WITH A TETRAHYDROCHINOLINE COMPOUND AS AN ACTIVE SUBSTANCE
GB0919431D0 (en) * 2009-11-05 2009-12-23 Glaxosmithkline Llc Novel compounds
US9360482B2 (en) * 2009-11-05 2016-06-07 Glaxosmithkline Llc Process for the identification of a compound which inhibits the binding of the second bromodomain of each of human BRD-2, BRD-3, and BRD-4
GB0919432D0 (en) * 2009-11-05 2009-12-23 Glaxosmithkline Llc Use
GB0919434D0 (en) * 2009-11-05 2009-12-23 Glaxosmithkline Llc Novel compounds
GB201106750D0 (en) * 2011-04-21 2011-06-01 Glaxosmithkline Llc Novel compounds
GB201107325D0 (en) * 2011-05-04 2011-06-15 Glaxosmithkline Llc Novel compounds
WO2013033268A2 (en) * 2011-08-29 2013-03-07 Coferon, Inc. Bivalent bromodomain ligands, and methods of using same

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