CN115335039A - 胱天蛋白酶6抑制剂和其用途 - Google Patents

胱天蛋白酶6抑制剂和其用途 Download PDF

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CN115335039A
CN115335039A CN202080092870.XA CN202080092870A CN115335039A CN 115335039 A CN115335039 A CN 115335039A CN 202080092870 A CN202080092870 A CN 202080092870A CN 115335039 A CN115335039 A CN 115335039A
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A·R·伦斯洛
M·R·阿尔金
R·J·奈茨
R·吴
P·李
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Shanghua Innovation Co ltd
University of California San Diego UCSD
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University of California San Diego UCSD
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    • C07C311/01Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms
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    • C07C311/08Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton having the nitrogen atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
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    • C07D211/36Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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    • A61K31/41641,3-Diazoles
    • A61K31/41881,3-Diazoles condensed with other heterocyclic ring systems, e.g. biotin, sorbinil
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    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445Non condensed piperidines, e.g. piperocaine
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    • A61K31/454Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
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    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/47Quinolines; Isoquinolines
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    • C07D215/16Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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    • C07D215/16Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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CN202080092870.XA 2019-11-22 2020-11-20 胱天蛋白酶6抑制剂和其用途 Pending CN115335039A (zh)

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US201962939263P 2019-11-22 2019-11-22
US62/939,263 2019-11-22
PCT/US2020/061659 WO2021102361A1 (en) 2019-11-22 2020-11-20 Caspase 6 inhibitors and uses thereof

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US (1) US20250263366A2 (https=)
EP (1) EP4061341A4 (https=)
JP (2) JP7734663B2 (https=)
KR (1) KR20220159346A (https=)
CN (1) CN115335039A (https=)
AU (1) AU2020386639A1 (https=)
BR (1) BR112022009881A2 (https=)
CA (1) CA3162470A1 (https=)
IL (1) IL293222A (https=)
MX (1) MX2022006052A (https=)
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AU2022328634A1 (en) 2021-08-18 2024-02-22 Chemocentryx, Inc. Aryl sulfonyl compounds as ccr6 inhibitors
WO2023023532A2 (en) 2021-08-18 2023-02-23 Chemocentryx, Inc. Aryl sulfonyl (hydroxy) piperidines as ccr6 inhibitors
KR20250030560A (ko) * 2023-08-25 2025-03-05 재단법인 아산사회복지재단 Htra 활성제를 유효성분으로 포함하는 퇴행성 질환의 예방 또는 치료용 약학적 조성물 및 htra 활성 조절제의 스크리닝 방법

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CN105189456A (zh) * 2013-03-15 2015-12-23 亚瑞克西斯制药公司 Kras g12c的共价抑制剂
WO2016020732A1 (en) * 2014-08-05 2016-02-11 The University Of British Columbia Modulators of caspase-6

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PT2322525E (pt) 2006-04-21 2013-12-26 Novartis Ag Derivados de purina para utilização como agonistas do recetor de adenosina a2a
WO2009089011A2 (en) * 2008-01-08 2009-07-16 Sirtris Pharmaceuticals, Inc. Resveratrol formulations
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PE20190710A1 (es) 2014-10-24 2019-05-17 Bristol Myers Squibb Co Compuestos de indol carboxamida utiles como inhibidores de cinasas
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CN104860891A (zh) * 2014-02-25 2015-08-26 上海海雁医药科技有限公司 芳氨基嘧啶类化合物及其应用以及由其制备的药物组合物和药用组合物
WO2016020732A1 (en) * 2014-08-05 2016-02-11 The University Of British Columbia Modulators of caspase-6

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US20250263366A2 (en) 2025-08-21
US20230202974A1 (en) 2023-06-29
KR20220159346A (ko) 2022-12-02
JP2023502268A (ja) 2023-01-23
EP4061341A1 (en) 2022-09-28
WO2021102361A1 (en) 2021-05-27
AU2020386639A1 (en) 2022-06-02
CA3162470A1 (en) 2021-05-27
JP2025183238A (ja) 2025-12-16
JP7734663B2 (ja) 2025-09-05
IL293222A (en) 2022-07-01
MX2022006052A (es) 2022-08-15
BR112022009881A2 (pt) 2022-10-11

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