JP2018509380A5 - - Google Patents

Download PDF

Info

Publication number
JP2018509380A5
JP2018509380A5 JP2017532715A JP2017532715A JP2018509380A5 JP 2018509380 A5 JP2018509380 A5 JP 2018509380A5 JP 2017532715 A JP2017532715 A JP 2017532715A JP 2017532715 A JP2017532715 A JP 2017532715A JP 2018509380 A5 JP2018509380 A5 JP 2018509380A5
Authority
JP
Japan
Prior art keywords
cancer
pharmaceutically acceptable
solvate
hydrate
following formula
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.)
Granted
Application number
JP2017532715A
Other languages
English (en)
Japanese (ja)
Other versions
JP2018509380A (ja
JP6650942B2 (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/EP2015/080022 external-priority patent/WO2016097001A1/en
Publication of JP2018509380A publication Critical patent/JP2018509380A/ja
Publication of JP2018509380A5 publication Critical patent/JP2018509380A5/ja
Application granted granted Critical
Publication of JP6650942B2 publication Critical patent/JP6650942B2/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2017532715A 2014-12-17 2015-12-16 N−(4−ヒドロキシ−4−メチル−シクロへキシル)−4−フェニル−ベンゼンスルホンアミド化合物、及びn−(4−ヒドロキシ−4−メチル−シクロへキシル)−4−(2−ピリジル)−ベンゼンスルホンアミド化合物、ならびにこれらの治療上の使用 Active JP6650942B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GB201422469 2014-12-17
GB1422469.5 2014-12-17
PCT/EP2015/080022 WO2016097001A1 (en) 2014-12-17 2015-12-16 N-(4-hydroxy-4-methyl-cyclohexyl)-4-phenyl-benzenesulfonamide and n-(4-hydroxy-4-methyl-cyclohexyl)-4-(2-pyridyl)-benzenesulfonamide compounds and their therapeutic use

Publications (3)

Publication Number Publication Date
JP2018509380A JP2018509380A (ja) 2018-04-05
JP2018509380A5 true JP2018509380A5 (cg-RX-API-DMAC7.html) 2019-01-24
JP6650942B2 JP6650942B2 (ja) 2020-02-19

Family

ID=54850187

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2017532715A Active JP6650942B2 (ja) 2014-12-17 2015-12-16 N−(4−ヒドロキシ−4−メチル−シクロへキシル)−4−フェニル−ベンゼンスルホンアミド化合物、及びn−(4−ヒドロキシ−4−メチル−シクロへキシル)−4−(2−ピリジル)−ベンゼンスルホンアミド化合物、ならびにこれらの治療上の使用

Country Status (13)

Country Link
US (2) US10005733B2 (cg-RX-API-DMAC7.html)
EP (1) EP3262028B1 (cg-RX-API-DMAC7.html)
JP (1) JP6650942B2 (cg-RX-API-DMAC7.html)
CN (1) CN107108508B (cg-RX-API-DMAC7.html)
AU (1) AU2015367528B2 (cg-RX-API-DMAC7.html)
CA (1) CA2970578C (cg-RX-API-DMAC7.html)
ES (1) ES2899852T3 (cg-RX-API-DMAC7.html)
HR (1) HRP20211877T1 (cg-RX-API-DMAC7.html)
HU (1) HUE057569T2 (cg-RX-API-DMAC7.html)
LT (1) LT3262028T (cg-RX-API-DMAC7.html)
MA (1) MA41587A (cg-RX-API-DMAC7.html)
SI (1) SI3262028T1 (cg-RX-API-DMAC7.html)
WO (1) WO2016097001A1 (cg-RX-API-DMAC7.html)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB201311361D0 (en) 2013-06-26 2013-08-14 Pimco 2664 Ltd Compounds and their therapeutic use
EP3262028B1 (en) 2014-12-17 2021-10-27 Pimco 2664 Limited N-(4-hydroxy-4-methyl-cyclohexyl)-4-phenyl-benzenesulfonamide and n-(-4hydroxy-4-methyl-cyclohexyl)-4-(2-pyridyl)-benzenesulfonamide compounds and their therapeutic use
GB201813312D0 (en) 2018-08-15 2018-09-26 Modern Biosciences Ltd Compounds and their therapeutic use
GB201905520D0 (en) 2019-04-18 2019-06-05 Modern Biosciences Ltd Compounds and their therapeutic use
EP4431090A1 (en) 2023-03-15 2024-09-18 Istesso 1 Limited Solfonamides acting as mitochondrial complex i modulator compounds
GB202308547D0 (en) 2023-06-08 2023-07-26 Istesso 2 Ltd Tnf inhibitor combination therapies
GB202309515D0 (en) 2023-06-23 2023-08-09 Istesso 2 Ltd JAK inhibitor and IL-6 inhibitor combination therapies
GB202315822D0 (en) 2023-10-16 2023-11-29 Istesso 3 Ltd Anti-fibrotic combination therapeutics
GB202317050D0 (en) 2023-11-07 2023-12-20 Istesso 2 Ltd Disease modifying anti-rheumatic drug combination therapies
EP4647071A1 (en) * 2024-05-10 2025-11-12 Istesso Therapeutics Limited Mitochondrial complex i modulator for use in the treatment of arthritis

Family Cites Families (58)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB597810A (en) 1943-04-12 1948-02-04 Gen Printing Ink Corp Improvements in or relating to derivatives of diphenyl
DE1046220B (de) 1956-04-21 1958-12-11 Bayer Ag Verfahren zur Herstellung von Monoazofarbstoffen und deren Metallkomplexverbindungen
US4119784A (en) 1977-07-01 1978-10-10 American Cyanamid Company Anionic substituted sulfonamido biphenyls
DE3000519A1 (de) 1979-02-01 1980-08-14 Byk Gulden Lomberg Chem Fab Sulfonamido-alkansaeuren, ihre verwendung und herstellung sowie sie enthaltende arzneimittel
DE3535167A1 (de) 1985-10-02 1987-04-09 Boehringer Mannheim Gmbh Neue sulfonyl-phenyl(alkyl)amine, verfahren zu ihrer herstellung sowie arzneimittel
IL118325A0 (en) 1995-05-25 1996-10-31 Pont Merck And Pharmaceutical Integrin receptor antagonists and pharmaceutical compositions containing them
AU1118097A (en) 1995-10-30 1997-05-22 Smithkline Beecham Corporation Protease inhibitors
US5760028A (en) 1995-12-22 1998-06-02 The Dupont Merck Pharmaceutical Company Integrin receptor antagonists
AU2421797A (en) 1996-03-15 1997-10-01 Du Pont Pharmaceuticals Company Spirocycle integrin inhibitors
PL331338A1 (en) 1996-07-22 1999-07-05 Monsanto Co Thiosulphonamidic metaloprotease inhibitors
AU731737B2 (en) 1996-10-16 2001-04-05 Wyeth Holdings Corporation The preparation and use of ortho-sulfonamido aryl hydroxamic acids as matrix metalloproteinase and tace inhibitors
AU5362998A (en) 1996-11-27 1998-06-22 Du Pont Pharmaceuticals Company Novel integrin receptor antagonists
AU6780398A (en) 1997-03-28 1998-10-22 Du Pont Merck Pharmaceutical Company, The Heterocyclic integrin inhibitor prodrugs
HUP0002951A3 (en) 1997-05-08 2002-10-28 Smithkline Beecham Corp Bis-aminomethylcarbonyl compounds as protease inhibitors and pharmaceutical compositions containing them
DE19719621A1 (de) 1997-05-09 1998-11-12 Hoechst Ag Sulfonylaminocarbonsäuren
DE59802394D1 (de) 1997-05-09 2002-01-24 Hoechst Ag Substituierte Diaminocarbonsäuren
US6291425B1 (en) 1999-09-01 2001-09-18 Guilford Pharmaceuticals Inc. Compounds, methods and pharmaceutical compositions for treating cellular damage, such as neural or cardiovascular tissue damage
AP1269A (en) 1998-01-23 2004-04-03 Aventis Pharma Deutschland Gmbh Novel salfonamide derivatives as inhibitors of bone resorption and as inhibitors of cell adhesion.
EP1053226A1 (en) 1998-02-04 2000-11-22 Novartis AG Sulfonylamino derivatives which inhibit matrix-degrading metalloproteinases
JPH11246527A (ja) 1998-03-02 1999-09-14 Shionogi & Co Ltd Mmp−8阻害剤
DE19815547C1 (de) 1998-04-07 1999-12-02 Joachim Schmidt Haftmittel für Zahnprothesen
EP0960882A1 (en) 1998-05-19 1999-12-01 Hoechst Marion Roussel Deutschland GmbH Thienyl substituted acylguanidines as inhibitors of bone resorption and vitronectin receptor antagonists
WO2001070720A2 (en) 2000-03-21 2001-09-27 The Procter & Gamble Company Carbocyclic side chain containing, n-substituted metalloprotease inhibitors
WO2001090077A1 (en) 2000-05-19 2001-11-29 Guilford Pharmaceuticals, Inc. Sulfonamide and carbamide derivatives of 6(5h)phenanthridinones and their uses
AU2002228316A1 (en) 2001-01-29 2002-08-12 Insight Strategy And Marketing Ltd Carbazole derivatives and their uses as heparanase inhibitors
JPWO2002074298A1 (ja) 2001-03-21 2004-07-08 小野薬品工業株式会社 Il−6産生阻害剤
JP2004535390A (ja) 2001-05-07 2004-11-25 スミスクライン・ビーチャム・コーポレイション スルホンアミド
NZ541950A (en) 2001-08-09 2007-02-23 Ono Pharmaceutical Co Carboxylic acid derivative compounds and drugs comprising these compounds as the active ingredient
GB0126157D0 (en) 2001-10-31 2002-01-02 Univ Aberdeen Therapeutic compounds
AU2003221160A1 (en) 2002-03-27 2003-10-08 Shionogi And Co., Ltd. Decomposition inhibitor for extracellular matrix of cartilage
ATE469903T1 (de) 2002-09-04 2010-06-15 Schering Corp Zur behandlung von krebserkrankungen geeignete pyrazolopyrimidine
DE10251170A1 (de) 2002-10-31 2004-05-13 Boehringer Ingelheim Pharma Gmbh & Co. Kg Neue Beta-Agonisten, Verfahren zu deren Herstellung und deren Verwendung als Arzneimittel
WO2004073619A2 (en) 2003-02-14 2004-09-02 Smithkline Beecham Corporation Ccr8 antagonists
DK1638544T3 (da) 2003-05-07 2008-03-31 Univ Aberdeen Ketoner og reducerede ketoner som terapeutiske midler til behandling af knogletilstande
JPWO2004106290A1 (ja) 2003-05-14 2006-07-20 キッセイ薬品工業株式会社 アミノアルコール誘導体、それを含有する医薬組成物およびそれらの用途
PE20050948A1 (es) 2003-09-09 2005-12-16 Japan Tobacco Inc Compuestos de carbamoil-amina como inhibidores de la dipeptidil peptidasa iv
GB0324792D0 (en) 2003-10-23 2003-11-26 Sterix Ltd Compound
EP1696915A1 (en) 2003-12-19 2006-09-06 Pfizer, Inc. Benzenesulfonylamino-pyridin-2-yl derivatives and related compounds as inhibitors of 11-beta-hydroxysteroid dehydrogenase type 1 (11-beta-hsd-1) for the treatment of diabetes and obesity
WO2005080367A1 (en) 2004-02-12 2005-09-01 Pharmagene Laboratories Limited Ep2 receptor agonists
GB0405193D0 (en) 2004-03-08 2004-04-21 Medical Res Council Compounds
EP1756025A1 (en) 2004-05-05 2007-02-28 Novo Nordisk A/S Sulfonamide derivatives
GB0412553D0 (en) 2004-06-04 2004-07-07 Univ Aberdeen Therapeutic agents for the treatment of bone conditions
WO2005123089A2 (en) 2004-06-10 2005-12-29 Kalypsys, Inc. Multicyclic sulfonamide compounds as inhibitors of histone deacetylase for the treatment of disease
RS20070076A (sr) 2004-10-29 2008-09-29 Astrazeneca Ab., Novi derivati sulfonamida kao modulatori glukokortikoidnog receptora za lečenje zapaljenskih bolesti
EP1659113A1 (en) 2004-11-08 2006-05-24 Evotec AG Inhibitors of 11beta-hydroxy steroid dehydrogenase type 1 (11beta-HSD1)
KR20080016649A (ko) 2005-06-16 2008-02-21 화이자 인코포레이티드 N-(피리딘-2-일)-술폰아미드 유도체
WO2007008541A2 (en) 2005-07-08 2007-01-18 Kalypsys, Inc. Cellular cholesterol absorption modifiers
TW200720261A (en) 2005-08-31 2007-06-01 Sankyo Co Phenylene derivatives
SI1945632T1 (sl) 2005-11-08 2014-03-31 Vertex Pharmaceuticals Incorporated Heterocikliäśni modulatorji za prenaĺ alce z atp-vezavno kaseto
EP1984344B1 (en) 2005-12-29 2012-09-26 Lexicon Pharmaceuticals, Inc. Multicyclic amino acid derivatives and methods of their use
US7560597B2 (en) 2007-03-08 2009-07-14 The University Court Of The University Of Aberdeen 2′,4′-dichloro-biphenyl-4-yl-hydroxy-ketones and related compounds and their use as therapeutic agents
GB0705400D0 (en) 2007-03-21 2007-05-02 Univ Aberdeen Therapeutic compounds andm their use
WO2010025235A1 (en) 2008-08-29 2010-03-04 Regents Of The University Of Michigan Selective ligands for the dopamine 3 (d3) receptor and methods of using the same
TWI453207B (zh) 2008-09-08 2014-09-21 Signal Pharm Llc 胺基三唑并吡啶,其組合物及使用其之治療方法
GB0817207D0 (en) 2008-09-19 2008-10-29 Pimco 2664 Ltd therapeutic apsac compounds and their use
GB0817208D0 (en) 2008-09-19 2008-10-29 Pimco 2664 Ltd Therapeutic apsap compounds and their use
GB201311361D0 (en) 2013-06-26 2013-08-14 Pimco 2664 Ltd Compounds and their therapeutic use
EP3262028B1 (en) 2014-12-17 2021-10-27 Pimco 2664 Limited N-(4-hydroxy-4-methyl-cyclohexyl)-4-phenyl-benzenesulfonamide and n-(-4hydroxy-4-methyl-cyclohexyl)-4-(2-pyridyl)-benzenesulfonamide compounds and their therapeutic use

Similar Documents

Publication Publication Date Title
JP2018509380A5 (cg-RX-API-DMAC7.html)
JP2016529218A5 (cg-RX-API-DMAC7.html)
HRP20211877T1 (hr) Spojevi n-(4-hidroksi-4-metil-cikloheksil)-4-fenil-benzensulfonamida i n-(4-hidroksi-4-metil-cikloheksil)-4- (2-piridil)-benzensulfonamida i njihova terapijska uporaba
HRP20171611T1 (hr) N-(4-hidroksi-4-metil-cikloheksil)-4-fenil-benzensulfonamidi i n-(4-hidroksi-4-metil-cikloheksil)-4-(2-piridil)-benzensulfonamidi i njihova terapeutska primjena
Rothenberg et al. Redifferentiation of iodine-refractory BRAF V600E-mutant metastatic papillary thyroid cancer with dabrafenib—response
MX384828B (es) Formas solidas cristalinas de n-{4-[(6,7-dimetoxiquinolin-4-il)oxi]fenil}-n'-(4-fluorofenil)ciclopropan-1,1-dicarboxamida, procesos para elaboracion y metodos de uso.
JP2017538677A5 (cg-RX-API-DMAC7.html)
JP2019532084A5 (cg-RX-API-DMAC7.html)
JP2016508505A5 (cg-RX-API-DMAC7.html)
JP2014508752A5 (cg-RX-API-DMAC7.html)
MX393599B (es) Rad1901 para usarse en el tratamiento de cancer en sujetos con cancer positivo a receptor de estrogeno alfa resistente a farmaco
JP2017511311A5 (cg-RX-API-DMAC7.html)
JP2017537080A5 (cg-RX-API-DMAC7.html)
JP2015508103A5 (cg-RX-API-DMAC7.html)
JP2019529518A5 (cg-RX-API-DMAC7.html)
JP2017520613A5 (cg-RX-API-DMAC7.html)
JP2015512943A5 (cg-RX-API-DMAC7.html)
MY189345A (en) Heteroaryl derivative or pharmaceutically acceptable salt thereof, preparation method therefor, and pharmaceutical composition for preventing or treating diseases associated with pi3 kinases, containing same as active ingredient
JP2017530171A5 (cg-RX-API-DMAC7.html)
JP2017517520A5 (cg-RX-API-DMAC7.html)
JP2015502926A5 (cg-RX-API-DMAC7.html)
JP2020502268A5 (cg-RX-API-DMAC7.html)
JP2016504325A5 (cg-RX-API-DMAC7.html)
JP2020515582A5 (cg-RX-API-DMAC7.html)
JP2016534048A5 (cg-RX-API-DMAC7.html)