JP2017522352A5 - - Google Patents

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Publication number
JP2017522352A5
JP2017522352A5 JP2017505440A JP2017505440A JP2017522352A5 JP 2017522352 A5 JP2017522352 A5 JP 2017522352A5 JP 2017505440 A JP2017505440 A JP 2017505440A JP 2017505440 A JP2017505440 A JP 2017505440A JP 2017522352 A5 JP2017522352 A5 JP 2017522352A5
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JP
Japan
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formula
compound
group
salt
independently represent
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JP2017505440A
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English (en)
Japanese (ja)
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JP2017522352A (ja
JP6529575B2 (ja
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Priority claimed from PCT/EP2015/067271 external-priority patent/WO2016016242A1/en
Publication of JP2017522352A publication Critical patent/JP2017522352A/ja
Publication of JP2017522352A5 publication Critical patent/JP2017522352A5/ja
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JP2017505440A 2014-08-01 2015-07-28 置換オキセタンおよびそれらのカテプシンcの阻害薬としての使用 Active JP6529575B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP14179458 2014-08-01
EP14179458.6 2014-08-01
PCT/EP2015/067271 WO2016016242A1 (en) 2014-08-01 2015-07-28 Substituted oxetanes and their use as inhibitors of cathepsin c

Publications (3)

Publication Number Publication Date
JP2017522352A JP2017522352A (ja) 2017-08-10
JP2017522352A5 true JP2017522352A5 (en:Method) 2018-09-06
JP6529575B2 JP6529575B2 (ja) 2019-06-12

Family

ID=51266130

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2017505440A Active JP6529575B2 (ja) 2014-08-01 2015-07-28 置換オキセタンおよびそれらのカテプシンcの阻害薬としての使用

Country Status (4)

Country Link
US (1) US9440960B2 (en:Method)
EP (1) EP3174879B1 (en:Method)
JP (1) JP6529575B2 (en:Method)
WO (1) WO2016016242A1 (en:Method)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NO2699580T3 (en:Method) 2014-01-24 2018-02-24
KR20200118103A (ko) * 2018-02-07 2020-10-14 인스메드 인코포레이티드 Anca 관련 혈관염을 치료하기 위한 특정 (2s)-n-[(1s)-1-시아노-2-페닐에틸]-1,4-옥사제판-2-카복스아미드
FI3758708T3 (fi) 2018-03-01 2025-02-18 Astrazeneca Ab (2s)-{(1s)-1-syano-2-[4-(3-metyyli-2-okso-2,3-dihydro-1,3-bentsoksatsol-5-yyli)fenyyli]etyyli}-1,4-oksatsepaani-2-karboksamidia käsittäviä farmaseuttisia koostumuksia
KR20210032431A (ko) 2018-07-17 2021-03-24 인스메드 인코포레이티드 루푸스 신염을 치료하기 위한 특정 (2s)-n-[(1s)-1-시아노-2-페닐에틸]-1,4-옥사제판-2-카복스아미드
WO2022020245A1 (en) 2020-07-20 2022-01-27 Insmed, Inc. Methods for extracting neutrophil serine proteases and treating dipeptidyl peptidase 1-mediated conditions
LT4129989T (lt) 2020-08-26 2024-12-27 Haisco Pharmaceuticals Pte. Ltd. Nitrilo darinys, kuris veikia kaip dipeptidilpeptidazės 1 inhibitorius ir jo panaudojimas
KR20230093251A (ko) 2020-09-10 2023-06-27 프리시릭스 엔.브이. Fap에 대한 항체 단편
AU2022218443B2 (en) * 2021-02-05 2025-03-13 Shanghai Fosun Pharmaceutical Industrial Development Co., Ltd. Fused ring derivatives containing 1,4-oxazepane
WO2023203135A1 (en) 2022-04-22 2023-10-26 Precirix N.V. Improved radiolabelled antibody
JP2025517625A (ja) 2022-05-02 2025-06-10 プレシリックス・ナームローゼ・ベンノートシヤープ プレターゲティング
JP2026503035A (ja) 2023-01-06 2026-01-27 インスメッド インコーポレイテッド 新規な可逆性dpp1阻害剤及びその用途
WO2024193695A1 (zh) 2023-03-23 2024-09-26 西藏海思科制药有限公司 一种二肽基肽酶小分子抑制剂的药物组合物
WO2025002093A1 (zh) 2023-06-27 2025-01-02 西藏海思科制药有限公司 一种dpp1抑制剂中间体及其制备方法及在医药中的用途

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US4125727A (en) 1976-10-18 1978-11-14 American Cyanamid Company Method of preparing imidazoisoindolediones
US6960597B2 (en) 2000-06-30 2005-11-01 Orth-Mcneil Pharmaceutical, Inc. Aza-bridged-bicyclic amino acid derivatives as α4 integrin antagonists
ATE409482T1 (de) 2001-03-02 2008-10-15 Merck Frosst Canada Ltd Cathepsincystein-proteasehemmer
US20070099958A1 (en) * 2003-06-18 2007-05-03 Prozymex A/S Protease inhibitors
TW200528440A (en) 2003-10-31 2005-09-01 Fujisawa Pharmaceutical Co 2-cyanopyrrolidinecarboxamide compound
US20060223846A1 (en) 2005-03-08 2006-10-05 Dyatkin Alexey B Aza-bridged-bicyclic amino acid derivatives as alpha4 integrin antagonists
WO2006102535A2 (en) * 2005-03-22 2006-09-28 Celera Genomics Sulfonyl containing compounds as cysteine protease inhibitors
WO2009047829A1 (ja) 2007-10-12 2009-04-16 Fujitsu Limited Ip電話自動試験システム及び方法
MX2010006110A (es) 2007-12-12 2010-06-25 Astrazeneca Ab Peptidil-nitrilos y usos de los mismos como inhibidores de la dipeptidil-peptidasa i.
KR20120034639A (ko) 2009-05-07 2012-04-12 아스트라제네카 아베 치환된 1-시아노에틸헤테로시클릴카르복스아미드 화합물 750
WO2010142985A1 (en) * 2009-06-10 2010-12-16 Astrazeneca Ab Substituted n-[1-cyano-2-(phenyl)ethyl]piperidin-2-ylcarboxmide compounds 761
US8524710B2 (en) * 2010-11-05 2013-09-03 Hoffmann-La Roche Inc. Pyrrolidine derivatives
WO2012119941A1 (en) 2011-03-04 2012-09-13 Prozymex A/S Peptidyl nitrilcompounds as peptidase inhibitors
US8999975B2 (en) 2011-09-19 2015-04-07 Boehringer Ingelheim International Gmbh Substituted N- [1-cyano-2- (phenyl) ethyl] -2-azabicyclo [2.2.1] heptane-3-carboxamide inhibitors of cathepsin C
PL2970283T3 (pl) * 2013-03-14 2021-05-31 Boehringer Ingelheim International Gmbh Podstawione (benzylocyjanometylo)amidy kwasu 2-aza-bicyklo[2.2.1]heptano-3-karboksylowego będące inhibitorami katepsyny c
JP2017526716A (ja) * 2014-09-12 2017-09-14 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 カテプシンcのスピロ環状阻害剤

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