JP2017527532A5 - - Google Patents

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JP2017527532A5
JP2017527532A5 JP2016575738A JP2016575738A JP2017527532A5 JP 2017527532 A5 JP2017527532 A5 JP 2017527532A5 JP 2016575738 A JP2016575738 A JP 2016575738A JP 2016575738 A JP2016575738 A JP 2016575738A JP 2017527532 A5 JP2017527532 A5 JP 2017527532A5
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alkyl
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aryl
haloalkyl
salt
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JP2016575738A
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JP6503386B2 (ja
JP2017527532A (ja
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Priority claimed from PCT/EP2015/065134 external-priority patent/WO2016001376A1/en
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JP2016575738A 2014-07-03 2015-07-02 MDM2−p53阻害剤としての新しいスピロ[3H−インドール−3,2’−ピロリジン]−2(1H)−オン化合物および誘導体 Active JP6503386B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP14175620 2014-07-03
EP14175620.5 2014-07-03
PCT/EP2015/065134 WO2016001376A1 (en) 2014-07-03 2015-07-02 New spiro[3h-indole-3,2´-pyrrolidin]-2(1h)-one compounds and derivatives as mdm2-p53 inhibitors

Publications (3)

Publication Number Publication Date
JP2017527532A JP2017527532A (ja) 2017-09-21
JP2017527532A5 true JP2017527532A5 (enExample) 2018-08-16
JP6503386B2 JP6503386B2 (ja) 2019-04-17

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JP2016575738A Active JP6503386B2 (ja) 2014-07-03 2015-07-02 MDM2−p53阻害剤としての新しいスピロ[3H−インドール−3,2’−ピロリジン]−2(1H)−オン化合物および誘導体

Country Status (4)

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US (1) US10576064B2 (enExample)
EP (1) EP3164401B1 (enExample)
JP (1) JP6503386B2 (enExample)
WO (1) WO2016001376A1 (enExample)

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JP6503386B2 (ja) 2014-07-03 2019-04-17 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング MDM2−p53阻害剤としての新しいスピロ[3H−インドール−3,2’−ピロリジン]−2(1H)−オン化合物および誘導体
EA038071B1 (ru) 2014-08-21 2021-07-01 Бёрингер Ингельхайм Интернациональ Гмбх СОЕДИНЕНИЕ СПИРО[3H-ИНДОЛ-3,2'-ПИРРОЛИДИН]-2(1H)-ОНА И ЕГО ПРОИЗВОДНЫЕ В КАЧЕСТВЕ ИНГИБИТОРОВ MDM2-p53
PT3359542T (pt) 2015-10-09 2021-05-25 Boehringer Ingelheim Int Compostos de espiro[3h-indole-3,2¿-pirrolidin]-2(1h)-ona e derivados como inibidores de mdm2-p53
CN113788818A (zh) 2016-04-06 2021-12-14 密执安大学评议会 Mdm2蛋白质降解剂
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IL298633A (en) 2020-06-02 2023-01-01 Boehringer Ingelheim Int Cyclic 2-amino-3-cyanothiophenes and their implications for cancer therapy
WO2023056069A1 (en) 2021-09-30 2023-04-06 Angiex, Inc. Degrader-antibody conjugates and methods of using same
EP4441056A1 (en) 2021-12-01 2024-10-09 Boehringer Ingelheim International GmbH Annulated 2-amino-3-cyano thiophenes and derivatives for the treatment of cancer
US20250129096A1 (en) 2021-12-01 2025-04-24 Boehringer Ingelheim Int'l GmbH Corp. Annulated 2-amino-3-cyano thiophenes and derivatives for the treatment of cancer
WO2023099620A1 (en) 2021-12-01 2023-06-08 Boehringer Ingelheim International Gmbh Kras degrading compounds comprising annulated 2-amino-3-cyano thiophenes
US20250313553A1 (en) 2021-12-01 2025-10-09 Boehringer Ingelheim Int'l GmbH Corp. Annulated 2-amino-3-cyano thiophenes and derivatives for the treatment of cancer
KR20240128852A (ko) 2021-12-01 2024-08-27 베링거 인겔하임 인터내셔날 게엠베하 암 치료를 위한 고리형 2-아미노-3-시아노 티오펜 및 유도체
US20250352535A1 (en) * 2022-06-06 2025-11-20 Kymera Therapeutics, Inc. Mdm2 degraders and uses thereof
US11944604B1 (en) 2023-03-10 2024-04-02 King Saud University Nanoformulation of spriooxindole and methods for treating hepatocellular carcinoma
WO2024240858A1 (en) 2023-05-23 2024-11-28 Valerio Therapeutics Protac molecules directed against dna damage repair system and uses thereof
TW202511268A (zh) 2023-05-30 2025-03-16 德商百靈佳殷格翰國際股份有限公司 用於治療癌症之螺環狀2-胺基-3-氰基噻吩及衍生物

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CN103910746B (zh) 2014-02-28 2016-08-03 中山大学 一类海洋真菌来源的Berkeleyones化合物及其制备方法和应用
WO2015155332A1 (en) 2014-04-11 2015-10-15 Boehringer Ingelheim International Gmbh Spiro[3h-indole-3,2'-pyrrolidin]-2(1h)-one derivatives and their use as mdm2-p53 inhibitors
JP6503386B2 (ja) 2014-07-03 2019-04-17 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング MDM2−p53阻害剤としての新しいスピロ[3H−インドール−3,2’−ピロリジン]−2(1H)−オン化合物および誘導体
EA038071B1 (ru) 2014-08-21 2021-07-01 Бёрингер Ингельхайм Интернациональ Гмбх СОЕДИНЕНИЕ СПИРО[3H-ИНДОЛ-3,2'-ПИРРОЛИДИН]-2(1H)-ОНА И ЕГО ПРОИЗВОДНЫЕ В КАЧЕСТВЕ ИНГИБИТОРОВ MDM2-p53
NO2721710T3 (enExample) 2014-08-21 2018-03-31
PT3359542T (pt) 2015-10-09 2021-05-25 Boehringer Ingelheim Int Compostos de espiro[3h-indole-3,2¿-pirrolidin]-2(1h)-ona e derivados como inibidores de mdm2-p53

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