JP2021502400A - 置換ピロロピリミジンjak阻害剤ならびにこれを作製および使用する方法 - Google Patents

置換ピロロピリミジンjak阻害剤ならびにこれを作製および使用する方法 Download PDF

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JP2021502400A
JP2021502400A JP2020526289A JP2020526289A JP2021502400A JP 2021502400 A JP2021502400 A JP 2021502400A JP 2020526289 A JP2020526289 A JP 2020526289A JP 2020526289 A JP2020526289 A JP 2020526289A JP 2021502400 A JP2021502400 A JP 2021502400A
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disease
alkyl
syndrome
autoimmune
fibrosis
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デイヴィッド ランドルフ アンダーソン
デイヴィッド ランドルフ アンダーソン
スーザン ランディス ホッカーマン
スーザン ランディス ホッカーマン
ジェイムズ ロバート ブリン
ジェイムズ ロバート ブリン
エリック ジョン ジェイコブセン
エリック ジョン ジェイコブセン
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アクラリス セラピューティクス,インコーポレイテッド
アクラリス セラピューティクス,インコーポレイテッド
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Publication of JP2021502400A publication Critical patent/JP2021502400A/ja
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    • C07ORGANIC CHEMISTRY
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    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
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    • A61K31/437Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
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JP2020526289A 2017-11-03 2018-11-02 置換ピロロピリミジンjak阻害剤ならびにこれを作製および使用する方法 Pending JP2021502400A (ja)

Priority Applications (1)

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JP2023198813A JP7607732B2 (ja) 2017-11-03 2023-11-24 置換ピロロピリミジンjak阻害剤ならびにこれを作製および使用する方法

Applications Claiming Priority (5)

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US201762581428P 2017-11-03 2017-11-03
US62/581,428 2017-11-03
US201862670448P 2018-05-11 2018-05-11
US62/670,448 2018-05-11
PCT/US2018/059071 WO2019090158A1 (en) 2017-11-03 2018-11-02 Substituted pyrrolopyrimidine jak inhibitors and methods of making and using the same

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JP2021502400A true JP2021502400A (ja) 2021-01-28
JP2021502400A5 JP2021502400A5 (https=) 2021-11-25

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JP2023198813A Active JP7607732B2 (ja) 2017-11-03 2023-11-24 置換ピロロピリミジンjak阻害剤ならびにこれを作製および使用する方法

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US (4) US10981906B2 (https=)
EP (1) EP3710431A4 (https=)
JP (2) JP2021502400A (https=)
KR (1) KR102821964B1 (https=)
CN (2) CN119119039A (https=)
AU (2) AU2018360059B2 (https=)
BR (1) BR112020008850A2 (https=)
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Cited By (1)

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JP2024509383A (ja) * 2021-02-18 2024-03-01 アクラリス セラピューティクス,インコーポレイテッド アトピー性皮膚炎及びその他の皮膚状態の治療のためのjak1/3阻害剤の局所製剤及びその使用方法

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MY200629A (en) 2017-08-01 2024-01-06 Theravance Biopharma R&D Ip Llc Pyrazolo and triazolo bicyclic compounds as jak kinase inhibitors
EP3710431A4 (en) 2017-11-03 2021-07-07 Aclaris Therapeutics, Inc. SUBSTITUTED PYRROLOPYRIMIDINE-BASED JAK INHIBITORS AND THEIR MANUFACTURING AND USE PROCEDURES
MD3773593T2 (ro) 2018-03-30 2024-10-31 Incyte Corp Tratament hidradenitei supurative utilizând inhibitori ai JAK
WO2020033955A1 (en) 2018-08-10 2020-02-13 Aclaris Therapeutics, Inc. Pyrrolopyrimidine itk inhibitors
CA3125039A1 (en) 2019-01-23 2020-07-30 Theravance Biopharma R&D Ip, Llc Imidazo[1,5-a]pyridine, 1,2,4-triazolo[4,3-a]pyridine and imidazo[1,5-a]pyrazine as jak inhibitors
WO2020223728A1 (en) 2019-05-02 2020-11-05 Aclaris Therapeutics, Inc. Substituted pyrrolopyridines as jak inhibitors
CN114787363A (zh) 2019-10-01 2022-07-22 恩派瑞安神经科学公司 对真菌进行遗传工程化以调节色胺表达
AU2021350089A1 (en) * 2020-09-25 2023-04-13 Aclaris Therapeutics, Inc. Crystalline polymorph form a of a jak inhibitor and methods for its preparation
CN117279915A (zh) * 2021-02-18 2023-12-22 阿克拉瑞斯治疗股份有限公司 Jak1/3抑制剂的局部制剂及其用于特异性皮炎和其他皮肤病况的治疗的方法
WO2022199599A1 (zh) * 2021-03-23 2022-09-29 凯复(苏州)生物医药有限公司 丙烯酰基取代的化合物、包含其的药物组合物及其用途
EP4457336A4 (en) 2021-12-31 2026-01-14 Empyrean Neuroscience Inc ORGANISMS GENETICALLY MODIFIED TO PRODUCE PSYCHOTROPIC ALKALOIDS
WO2023151069A1 (zh) * 2022-02-14 2023-08-17 湖南南新制药股份有限公司 吡咯并[2,3-d]六元杂芳环衍生物、其制备方法和药物用途
WO2023165562A1 (zh) * 2022-03-02 2023-09-07 南京明德新药研发有限公司 含氮杂环类化合物及其应用
US12564326B2 (en) 2022-10-25 2026-03-03 GE Precision Healthcare LLC Non-invasive bilirubin detection using induced photoreaction
WO2025038910A1 (en) * 2023-08-16 2025-02-20 Aclaris Therapeutics, Inc. Crystalline polymorph form a of a jak inhibitor and methods for its preparation

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