JP2016531108A5 - - Google Patents

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Publication number
JP2016531108A5
JP2016531108A5 JP2016528587A JP2016528587A JP2016531108A5 JP 2016531108 A5 JP2016531108 A5 JP 2016531108A5 JP 2016528587 A JP2016528587 A JP 2016528587A JP 2016528587 A JP2016528587 A JP 2016528587A JP 2016531108 A5 JP2016531108 A5 JP 2016531108A5
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JP
Japan
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group
branched
linear
alkyl
compound
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JP2016528587A
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English (en)
Japanese (ja)
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JP2016531108A (ja
JP6458028B2 (ja
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Priority claimed from FR1357277A external-priority patent/FR3008978A1/fr
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Publication of JP2016531108A publication Critical patent/JP2016531108A/ja
Publication of JP2016531108A5 publication Critical patent/JP2016531108A5/ja
Application granted granted Critical
Publication of JP6458028B2 publication Critical patent/JP6458028B2/ja
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

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JP2016528587A 2013-07-23 2014-07-22 インドール及びピロールの新規な誘導体、その製造方法及びそれを含む医薬組成物 Expired - Fee Related JP6458028B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
FR13/57277 2013-07-23
FR1357277A FR3008978A1 (fr) 2013-07-23 2013-07-23 "nouveaux derives d'indole et de pyrrole, leur procede de preparation et les compositions pharmaceutiques qui les contiennent"
PCT/FR2014/051884 WO2015011396A1 (fr) 2013-07-23 2014-07-22 Nouveaux derives d'indole et de pyrrole, leur procede de preparation et les compositions pharmaceutiques qui les contiennent

Publications (3)

Publication Number Publication Date
JP2016531108A JP2016531108A (ja) 2016-10-06
JP2016531108A5 true JP2016531108A5 (https=) 2017-08-24
JP6458028B2 JP6458028B2 (ja) 2019-01-23

Family

ID=49911607

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2016528587A Expired - Fee Related JP6458028B2 (ja) 2013-07-23 2014-07-22 インドール及びピロールの新規な誘導体、その製造方法及びそれを含む医薬組成物

Country Status (31)

Country Link
US (2) US9765056B2 (https=)
EP (2) EP3027602B1 (https=)
JP (1) JP6458028B2 (https=)
KR (1) KR102337149B1 (https=)
CN (1) CN105408321B (https=)
AR (1) AR099914A1 (https=)
AU (1) AU2014294866B2 (https=)
BR (1) BR112016001333B1 (https=)
CA (1) CA2917965C (https=)
CY (1) CY1120475T1 (https=)
DK (1) DK3027602T3 (https=)
EA (1) EA028609B1 (https=)
ES (1) ES2687475T3 (https=)
FR (1) FR3008978A1 (https=)
HK (1) HK1218753A1 (https=)
HR (1) HRP20181333T1 (https=)
HU (1) HUE039507T2 (https=)
LT (1) LT3027602T (https=)
MX (1) MX364479B (https=)
NZ (1) NZ715847A (https=)
PL (1) PL3027602T3 (https=)
PT (1) PT3027602T (https=)
RS (1) RS57545B1 (https=)
RU (1) RU2693404C2 (https=)
SG (1) SG11201600004SA (https=)
SI (1) SI3027602T1 (https=)
TW (1) TW201504224A (https=)
UA (1) UA117020C2 (https=)
UY (1) UY35653A (https=)
WO (1) WO2015011396A1 (https=)
ZA (1) ZA201600415B (https=)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105237509A (zh) * 2015-11-20 2016-01-13 江苏瑞邦农药厂有限公司 一种2,2-二氟-1,3-苯并二恶茂的合成方法
EP3454856B1 (en) 2016-05-10 2024-09-11 C4 Therapeutics, Inc. Heterocyclic degronimers for target protein degradation
CN109641874A (zh) 2016-05-10 2019-04-16 C4医药公司 用于靶蛋白降解的c3-碳连接的戊二酰亚胺降解决定子体
CN109790143A (zh) 2016-05-10 2019-05-21 C4医药公司 用于靶蛋白降解的胺连接的c3-戊二酰亚胺降解决定子体
ES2990061T3 (es) 2016-05-10 2024-11-28 C4 Therapeutics Inc Degronímeros espirocíclicos para la degradación de proteínas diana
AU2018208458B2 (en) * 2017-01-10 2020-07-16 ETH Zürich Cell-protective compounds and their use
TWI743346B (zh) 2017-03-31 2021-10-21 國立大學法人東京大學 諾羅病毒抗體
CN110769822A (zh) 2017-06-20 2020-02-07 C4医药公司 用于蛋白降解的n/o-连接的降解决定子和降解决定子体
CN108409580A (zh) * 2018-02-01 2018-08-17 浙江工业大学 一种苄胺类化合物的合成方法
CN120698983A (zh) 2018-12-20 2025-09-26 C4医药公司 靶向蛋白降解
CN116997544A (zh) * 2021-03-24 2023-11-03 法国施维雅药厂 用于合成5-{5-氯-2-[(3s)-3-[(吗啉-4-基)甲基]-3,4-二氢异喹啉-2(1h)-羰基]苯基}-1,2-二甲基-1h-吡咯-3-甲酸衍生物的新方法及其在生产药物化合物中的应用
US20250387504A1 (en) 2022-05-20 2025-12-25 Novartis Ag Antibody-drug conjugates of antineoplastic compounds and methods of use thereof
PY24103486A (es) 2023-11-22 2025-06-06 Servier Lab Conjugados de anticuerpo anti-cd74-fármaco y métodos de uso de los mismos
AR134424A1 (es) 2023-11-22 2026-01-14 Novartis Ag Conjugados de anticuerpo anti-cd7-fármaco y métodos de uso de los mismos

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2298832T3 (es) 2003-10-24 2008-05-16 Glaxo Group Limited Compuestos heterociclicos.
TW200533398A (en) * 2004-03-29 2005-10-16 Bristol Myers Squibb Co Novel therapeutic agents for the treatment of migraine
AU2005277223C1 (en) * 2004-08-20 2009-05-21 The Regents Of The University Of Michigan Small molecule inhibitors of anti-apoptotic Bcl-2 family members and the uses thereof
GB0522908D0 (en) 2005-11-10 2005-12-21 Merck Sharp & Dohme Therapeutic agents
JP2014521595A (ja) * 2011-05-25 2014-08-28 ブリストル−マイヤーズ スクイブ カンパニー 抗アポトーシスBcl阻害剤として有用な置換スルホンアミド
US9126980B2 (en) * 2011-12-23 2015-09-08 Novartis Ag Compounds for inhibiting the interaction of BCL2 with binding partners
EP2794592A1 (en) * 2011-12-23 2014-10-29 Novartis AG Compounds for inhibiting the interaction of bcl2 with binding partners
BR112014015308A8 (pt) * 2011-12-23 2017-06-13 Novartis Ag compostos para inibição da interação de bcl2 com contrapartes de ligação
WO2013096051A1 (en) * 2011-12-23 2013-06-27 Novartis Ag Compounds for inhibiting the interaction of bcl2 with binding partners
EP2794591A1 (en) * 2011-12-23 2014-10-29 Novartis AG Compounds for inhibiting the interaction of bcl2 with binding partners
FR2986002B1 (fr) 2012-01-24 2014-02-21 Servier Lab Nouveaux derives d'indolizine, leur procede de preparation et les compositions pharmaceutiques qui les contiennent

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