JP2004518651A5 - - Google Patents

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Publication number
JP2004518651A5
JP2004518651A5 JP2002549678A JP2002549678A JP2004518651A5 JP 2004518651 A5 JP2004518651 A5 JP 2004518651A5 JP 2002549678 A JP2002549678 A JP 2002549678A JP 2002549678 A JP2002549678 A JP 2002549678A JP 2004518651 A5 JP2004518651 A5 JP 2004518651A5
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JP
Japan
Prior art keywords
cycloalkyl
het
group
pyrazolo
pyrimidinyl
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
JP2002549678A
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English (en)
Japanese (ja)
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JP2004518651A (ja
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Publication date
Application filed filed Critical
Priority claimed from PCT/US2001/044210 external-priority patent/WO2002048147A2/en
Publication of JP2004518651A publication Critical patent/JP2004518651A/ja
Publication of JP2004518651A5 publication Critical patent/JP2004518651A5/ja
Ceased legal-status Critical Current

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JP2002549678A 2000-12-15 2001-11-26 治療用化合物 Ceased JP2004518651A (ja)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US25576300P 2000-12-15 2000-12-15
US27428401P 2001-03-08 2001-03-08
US31508901P 2001-08-27 2001-08-27
PCT/US2001/044210 WO2002048147A2 (en) 2000-12-15 2001-11-26 Pyrazolopyridines

Publications (2)

Publication Number Publication Date
JP2004518651A JP2004518651A (ja) 2004-06-24
JP2004518651A5 true JP2004518651A5 (enExample) 2005-12-22

Family

ID=27400896

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2002549678A Ceased JP2004518651A (ja) 2000-12-15 2001-11-26 治療用化合物

Country Status (8)

Country Link
US (3) US6919352B2 (enExample)
EP (1) EP1341788B1 (enExample)
JP (1) JP2004518651A (enExample)
AT (1) ATE301653T1 (enExample)
AU (1) AU2002239344A1 (enExample)
DE (1) DE60112609T2 (enExample)
ES (1) ES2245380T3 (enExample)
WO (1) WO2002048147A2 (enExample)

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CN103649079B (zh) 2010-12-22 2016-11-16 Abbvie公司 丙型肝炎抑制剂及其用途
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AU2016358100B2 (en) 2015-11-19 2021-05-27 Incyte Corporation Heterocyclic compounds as immunomodulators
TW201726623A (zh) 2015-12-17 2017-08-01 英塞特公司 作為免疫調節劑之雜環化合物
TWI850624B (zh) 2015-12-22 2024-08-01 美商英塞特公司 作為免疫調節劑之雜環化合物
TW201808950A (zh) 2016-05-06 2018-03-16 英塞特公司 作為免疫調節劑之雜環化合物
US20170342060A1 (en) 2016-05-26 2017-11-30 Incyte Corporation Heterocyclic compounds as immunomodulators
DK3472167T3 (da) 2016-06-20 2022-09-05 Incyte Corp Heterocykliske forbindelser som immunomodulatorer
EP3484866B1 (en) 2016-07-14 2022-09-07 Incyte Corporation Heterocyclic compounds as immunomodulators
EP3504198B1 (en) 2016-08-29 2023-01-25 Incyte Corporation Heterocyclic compounds as immunomodulators
EP3558973B1 (en) 2016-12-22 2021-09-15 Incyte Corporation Pyridine derivatives as immunomodulators
ES2929193T3 (es) 2016-12-22 2022-11-25 Incyte Corp Derivados de tetrahidro imidazo[4,5-c]piridina como inductores de la internalización de PD-L1
EP3558963B1 (en) 2016-12-22 2022-03-23 Incyte Corporation Bicyclic heteroaromatic compounds as immunomodulators
ES2874756T3 (es) 2016-12-22 2021-11-05 Incyte Corp Derivados de triazolo[1,5-A]piridina como inmunomoduladores
IL295660A (en) 2016-12-22 2022-10-01 Incyte Corp Benzooxazole derivatives as immunomodulators
RS64055B1 (sr) 2018-03-30 2023-04-28 Incyte Corp Heterociklična jedinjenja kao imunomodulatori
EP4219492B1 (en) 2018-05-11 2024-11-27 Incyte Corporation Heterocyclic compounds as immunomodulators
JP7665593B2 (ja) 2019-08-09 2025-04-21 インサイト・コーポレイション Pd-1/pd-l1阻害剤の塩
EP4037773A1 (en) 2019-09-30 2022-08-10 Incyte Corporation Pyrido[3,2-d]pyrimidine compounds as immunomodulators
BR112022009031A2 (pt) 2019-11-11 2022-10-11 Incyte Corp Sais e formas cristalinas de um inibidor de pd-1/pd-l1
DE102020125641A1 (de) * 2020-09-25 2022-03-31 Creative Therapeutics Gmbh Wirkstoffe und Arzneimittel für die Therapie von Viruserkrankungen, insbesondere Corona-Infektionen, insbesondere COVID-19
WO2022099018A1 (en) 2020-11-06 2022-05-12 Incyte Corporation Process of preparing a pd-1/pd-l1 inhibitor
EP4240739A1 (en) 2020-11-06 2023-09-13 Incyte Corporation Process for making a pd-1/pd-l1 inhibitor and salts and crystalline forms thereof
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