JP2013544277A5 - - Google Patents

Download PDF

Info

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
MX2013005915A (es) 2010-12-01 2013-07-03 Pfizer Inhibidores de kat ii.
JP6440625B2 (ja) 2012-11-14 2018-12-19 ザ・ジョンズ・ホプキンス・ユニバーシティー 精神分裂病を処置するための方法および組成物
JP6442485B2 (ja) * 2014-04-23 2018-12-19 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
WO2016164754A1 (en) 2015-04-09 2016-10-13 Eisai R&D Management Co., Ltd. Fgfr4 inhibitors
WO2016164703A1 (en) 2015-04-09 2016-10-13 Eisai R & D Management Co., Ltd. Fgfr4 inhibitors
US10793582B2 (en) 2015-10-22 2020-10-06 Mitsubishi Tanabe Pharma Corporation Bicyclic heterocyclic compound
MX2021016133A (es) * 2019-06-20 2022-07-19 Univ Kentucky Res Found Moduladores de la neddilación de cullina mediada por dcn1/2 de tipo pirazolo piridona farmacéuticamente activos.
JP7717065B2 (ja) 2019-11-22 2025-08-01 インサイト コーポレーション Alk2阻害剤及びjak2阻害剤を含む併用療法
MX2022013657A (es) 2020-05-05 2023-02-01 Nuvalent Inc Quimioterápicos de éter macrocíclico heteroaromático.
EP4146205A4 (en) 2020-05-05 2024-05-29 Nuvalent, Inc. HETEROAROMATIC MACROCYCLIC ETHERS AS CHEMOTHERAPEUTIC AGENTS
WO2022165382A1 (en) * 2021-01-29 2022-08-04 Neurawell Therapeutics Phenylethylidenehydrazine combination therapies
CA3231813A1 (en) 2021-10-01 2023-04-06 Sibao CHEN Solid forms, pharmaceutical compositions and preparation of heteroaromatic macrocyclic ether compounds
WO2025096981A1 (en) * 2023-11-03 2025-05-08 Cellarity, Inc. Modulators of dcn-1 and methods of use thereof
WO2025096956A1 (en) 2023-11-03 2025-05-08 Cellarity, Inc. Dcn-1 modulating compounds 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
EP1644335A4 (en) * 2003-07-11 2008-06-04 Bristol Myers Squibb Co TETRAHYDROQUINOLINE DERIVATIVES COMPRISING MODULATORS OF CANNABINOID RECEPTORS
GT200500186A (es) 2004-07-07 2006-03-02 Regimenes anticonceptivos con antagonistas del receptor de progesterona y kits
JP2008517994A (ja) 2004-10-28 2008-05-29 ファルマシア・アンド・アップジョン・カンパニー・エルエルシー 新規医薬品
WO2007055941A2 (en) 2005-11-03 2007-05-18 Merck & Co., Inc. Histone deacetylase inhibitors with aryl-pyrazolyl motifs
CA2635209A1 (en) 2006-01-12 2007-08-02 Merck & Co., Inc. Fluorinated arylamide derivatives
WO2008012010A1 (en) 2006-07-27 2008-01-31 Ucb Pharma, S.A. Fused oxazoles & thiazoles as histamine h3- receptor ligands
EP2222662A4 (en) * 2007-11-15 2011-08-03 Univ Maryland INHIBITORS OF KYNURENINE AMINO TRANSFERASE
WO2009095752A1 (en) * 2008-01-29 2009-08-06 Glenmark Pharmaceuticals, S.A. Fused pyrazole derivatives as cannabinoid receptor modulators
US9293849B2 (en) 2008-07-30 2016-03-22 Bal Seal Engineering, Inc. Electrical connector using a canted coil multi-metallic wire
CA2763960C (en) * 2009-06-18 2014-07-08 Pfizer Inc. Bicyclic and tricyclic compounds as kat ii inhibitors

Similar Documents

Publication Publication Date Title
JP2013544277A5 (enExample)
JP2012530129A5 (enExample)
JP2009509920A5 (enExample)
HK1217486A1 (zh) 作爲β-分泌酶抑制剂的全氟化环丙基稠合的1,3-恶嗪-2-胺化合物以及其使用方法
GEP201706608B (en) 1 - arylcarbonyl - 4 - oxy – piperidine compounds useful for the treatment of neurodegenerative diseases
RU2015101532A (ru) Замещенные бициклические алкокси-пиразольные аналоги в качестве аллостерических модуляторов рецепторов mglur5
PH12019500004A1 (en) 5,7-dihydro-pyrrolo-pyridine derivatives for treating neurological and neurodegenerative diseases
JP2014051526A5 (enExample)
JP2014515008A5 (enExample)
TN2018000299A1 (en) Heterocyclic compound.
CA2834286A1 (en) Methods of treating alzheimer's disease, huntington's disease, autism, and other disorders
RU2015101512A (ru) Замещенные бициклические алкокси-пиразольные аналоги в качестве аллостерических модуляторов рецепторов mglur5
PH12013501556A1 (en) IMIDAZO[5,1-f][1,2,4]TRIAZINES FOR THE TREATMENT OF NEUROLOGICAL DISORDERS
JP2020502092A5 (enExample)
JP2015516429A5 (enExample)
CA2441565A1 (en) Bisarylamines as potassium channel openers
JP2013519728A5 (enExample)
SI2605652T1 (en) Diketones and hydroxyketones as catenin signaling pathways
RU2013142364A (ru) Замещенные производные 6,7-диалкокси-3-изохинолинола в качестве ингибиторов фосфодиэстеразы 10 (фдэ10а)
MX2016008842A (es) Derivados de n-fenil-lactama capaces de estimular la neurogenesis y su uso en el tratamiento de trastornos neurologicos.
JP2017522340A5 (enExample)
PH12018502211A1 (en) Prodrug of amino acid derivative
JP2015500842A5 (enExample)
ME02833B (me) Prekursor leka aminokiseline koja sadrži fluor
CN111511745A (zh) 吡唑并[1,5-a][1,3,5]三嗪-2-胺类衍生物、其制备方法及其在医药上的应用