JP2013544277A5 - - Google Patents

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Publication number
JP2013544277A5
JP2013544277A5 JP2013541446A JP2013541446A JP2013544277A5 JP 2013544277 A5 JP2013544277 A5 JP 2013544277A5 JP 2013541446 A JP2013541446 A JP 2013541446A JP 2013541446 A JP2013541446 A JP 2013541446A JP 2013544277 A5 JP2013544277 A5 JP 2013544277A5
Authority
JP
Japan
Prior art keywords
alkyl
aryl
cycloalkyl
pharmaceutically acceptable
heteroaryl
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
JP2013541446A
Other languages
English (en)
Japanese (ja)
Other versions
JP2013544277A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/IB2011/055158 external-priority patent/WO2012073143A1/en
Publication of JP2013544277A publication Critical patent/JP2013544277A/ja
Publication of JP2013544277A5 publication Critical patent/JP2013544277A5/ja
Ceased legal-status Critical Current

Links

JP2013541446A 2010-12-01 2011-11-17 Katii阻害剤 Ceased JP2013544277A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US41880210P 2010-12-01 2010-12-01
US61/418,802 2010-12-01
PCT/IB2011/055158 WO2012073143A1 (en) 2010-12-01 2011-11-17 Kat ii inhibitors

Publications (2)

Publication Number Publication Date
JP2013544277A JP2013544277A (ja) 2013-12-12
JP2013544277A5 true JP2013544277A5 (enExample) 2014-09-25

Family

ID=45444662

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2013541446A Ceased JP2013544277A (ja) 2010-12-01 2011-11-17 Katii阻害剤

Country Status (13)

Country Link
US (2) US8598200B2 (enExample)
EP (1) EP2646443B1 (enExample)
JP (1) JP2013544277A (enExample)
KR (1) KR101544290B1 (enExample)
CN (1) CN103228660A (enExample)
AU (1) AU2011336214B2 (enExample)
CA (1) CA2819102A1 (enExample)
DK (1) DK2646443T3 (enExample)
ES (1) ES2524423T3 (enExample)
MX (1) MX2013005773A (enExample)
SG (1) SG190207A1 (enExample)
WO (1) WO2012073143A1 (enExample)
ZA (1) ZA201303360B (enExample)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101522803B1 (ko) 2010-12-01 2015-05-26 화이자 인코포레이티드 Kat ii 억제제
WO2014078568A1 (en) 2012-11-14 2014-05-22 The Johns Hopkins University Methods and compositions for treating schizophrenia
WO2015163339A1 (ja) * 2014-04-23 2015-10-29 田辺三菱製薬株式会社 新規二環性または三環性複素環化合物
WO2016164703A1 (en) 2015-04-09 2016-10-13 Eisai R & D Management Co., Ltd. Fgfr4 inhibitors
WO2016164754A1 (en) 2015-04-09 2016-10-13 Eisai R&D Management Co., Ltd. Fgfr4 inhibitors
EP3372601B1 (en) * 2015-10-22 2022-09-21 Mitsubishi Tanabe Pharma Corporation Novel bicyclic heterocyclic compound
CN114599650A (zh) * 2019-06-20 2022-06-07 肯塔基大学研究基金会 DCN1/2介导的cullin类泛素化修饰的药学活性吡唑并-吡啶酮调节剂
CR20220280A (es) 2019-11-22 2022-09-02 Incyte Corp Terapia de combinación que comprende un inhibidor de alk2 y un inhibidor de jak2
CN115916754A (zh) 2020-05-05 2023-04-04 纽威伦特公司 杂芳族大环醚化学治疗剂
BR112022022530A2 (pt) 2020-05-05 2023-02-23 Nuvalent Inc Composto, composição farmacêutica, método de tratamento de câncer, método de inibição seletiva, método de redução de um nível de ros1 ou alk
WO2022165382A1 (en) * 2021-01-29 2022-08-04 Neurawell Therapeutics Phenylethylidenehydrazine combination therapies
MX2024003738A (es) 2021-10-01 2024-06-19 Nuvalent Inc Formas solidas, composiciones farmaceuticas y preparacion de compuestos de eter macrociclico heteroaromatico.
WO2025096956A1 (en) 2023-11-03 2025-05-08 Cellarity, Inc. Dcn-1 modulating compounds and methods of use thereof
US12435087B2 (en) 2023-11-03 2025-10-07 Cellarity, Inc. Modulators of DCN-1 and methods of use thereof

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4282361A (en) 1978-03-16 1981-08-04 Massachusetts Institute Of Technology Synthesis for 7-alkylamino-3-methylpyrazolo [4,3-d]pyrimidines
US5519055A (en) * 1993-08-06 1996-05-21 University Of Maryland At Baltimore Substituted kynurenines and process for their preparation
US7276608B2 (en) * 2003-07-11 2007-10-02 Bristol-Myers Squibb Company Tetrahydroquinoline derivatives as cannabinoid receptor modulators
GT200500186A (es) 2004-07-07 2006-03-02 Regimenes anticonceptivos con antagonistas del receptor de progesterona y kits
WO2006046135A2 (en) 2004-10-28 2006-05-04 Pharmacia & Upjohn Company Llc Pyrazolo[4,3-d] pyrimidine derivatives useful as pde-5 inhibitors
CA2626897A1 (en) 2005-11-03 2007-05-18 Joshua Close Histone deacetylase inhibitors with aryl-pyrazolyl motifs
US20090012075A1 (en) 2006-01-12 2009-01-08 Miller Thomas A Fluorinated Arylamide Derivatives
EP2049548A1 (en) 2006-07-27 2009-04-22 UCB Pharma, S.A. Fused oxazoles & thiazoles as histamine h3- receptor ligands
WO2009064836A2 (en) * 2007-11-15 2009-05-22 University Of Maryland, Baltimore Kynurenine-aminotransferase inhibitors
WO2009095752A1 (en) * 2008-01-29 2009-08-06 Glenmark Pharmaceuticals, S.A. Fused pyrazole derivatives as cannabinoid receptor modulators
WO2010014688A2 (en) 2008-07-30 2010-02-04 Bal Seal Engineering Canted coil multi-metallic wire
DK2443092T3 (en) * 2009-06-18 2015-04-27 Pfizer Bicyclic and tricyclic compounds as CAT-II inhibitors

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