SG11201706146UA - 3-alkyl-4-amido-bicyclic [4,5,0] hydroxamic acids as hdac inhibitors - Google Patents
3-alkyl-4-amido-bicyclic [4,5,0] hydroxamic acids as hdac inhibitorsInfo
- Publication number
- SG11201706146UA SG11201706146UA SG11201706146UA SG11201706146UA SG11201706146UA SG 11201706146U A SG11201706146U A SG 11201706146UA SG 11201706146U A SG11201706146U A SG 11201706146UA SG 11201706146U A SG11201706146U A SG 11201706146UA SG 11201706146U A SG11201706146U A SG 11201706146UA
- Authority
- SG
- Singapore
- Prior art keywords
- amido
- bicyclic
- alkyl
- hdac inhibitors
- hydroxamic acids
- Prior art date
Links
Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/553—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having at least one nitrogen and one oxygen as ring hetero atoms, e.g. loxapine, staurosporine
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- C07D243/14—1,4-Benzodiazepines; Hydrogenated 1,4-benzodiazepines
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- C07D267/12—Seven-membered rings having the hetero atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems
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- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
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Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
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US201562110716P | 2015-02-02 | 2015-02-02 | |
US201562205438P | 2015-08-14 | 2015-08-14 | |
PCT/US2016/016201 WO2016126725A1 (en) | 2015-02-02 | 2016-02-02 | 3-alkyl-4-amido-bicyclic [4,5,0] hydroxamic acids as hdac inhibitors |
Publications (1)
Publication Number | Publication Date |
---|---|
SG11201706146UA true SG11201706146UA (en) | 2017-08-30 |
Family
ID=55353351
Family Applications (4)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SG11201706146UA SG11201706146UA (en) | 2015-02-02 | 2016-02-02 | 3-alkyl-4-amido-bicyclic [4,5,0] hydroxamic acids as hdac inhibitors |
SG10202100915RA SG10202100915RA (en) | 2015-02-02 | 2016-02-02 | 3-alkyl-4-amido-bicyclic [4,5,0] hydroxamic acids as hdac inhibitors |
SG10202100916PA SG10202100916PA (en) | 2015-02-02 | 2016-02-02 | 3-aryl-4-amido-bicyclic [4,5,0] hydroxamic acids as hdac inhibitors |
SG11201708622UA SG11201708622UA (en) | 2015-02-02 | 2016-02-02 | 3-aryl-4-amido-bicyclic [4,5,0] hydroxamic acids as hdac inhibitors |
Family Applications After (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SG10202100915RA SG10202100915RA (en) | 2015-02-02 | 2016-02-02 | 3-alkyl-4-amido-bicyclic [4,5,0] hydroxamic acids as hdac inhibitors |
SG10202100916PA SG10202100916PA (en) | 2015-02-02 | 2016-02-02 | 3-aryl-4-amido-bicyclic [4,5,0] hydroxamic acids as hdac inhibitors |
SG11201708622UA SG11201708622UA (en) | 2015-02-02 | 2016-02-02 | 3-aryl-4-amido-bicyclic [4,5,0] hydroxamic acids as hdac inhibitors |
Country Status (27)
Country | Link |
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US (32) | US10112915B2 (zh) |
EP (3) | EP3292116B8 (zh) |
JP (1) | JP6668362B2 (zh) |
KR (1) | KR102633628B1 (zh) |
CN (3) | CN107873023B (zh) |
AU (4) | AU2016215431B2 (zh) |
BR (1) | BR112017016493B1 (zh) |
CA (2) | CA2990165C (zh) |
CL (1) | CL2017001968A1 (zh) |
CO (1) | CO2017007863A2 (zh) |
DK (1) | DK3292116T3 (zh) |
EA (2) | EA201792673A1 (zh) |
EC (1) | ECSP17055491A (zh) |
ES (2) | ES2770123T3 (zh) |
HK (2) | HK1251550A1 (zh) |
HU (1) | HUE057623T2 (zh) |
IL (4) | IL280856B (zh) |
MA (1) | MA42032A (zh) |
MX (2) | MX373137B (zh) |
MY (1) | MY191591A (zh) |
PH (1) | PH12017501383B1 (zh) |
PL (1) | PL3292116T3 (zh) |
PT (1) | PT3292116T (zh) |
SA (1) | SA517382027B1 (zh) |
SG (4) | SG11201706146UA (zh) |
TW (6) | TW201629026A (zh) |
WO (4) | WO2016126724A1 (zh) |
Families Citing this family (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
IL280856B (en) | 2015-02-02 | 2022-09-01 | Forma Therapeutics Inc | 3-alkyl-4-amido-bicyclic [4,5,0] hydroxamic acids as hdac inhibitors |
TW201636329A (zh) | 2015-02-02 | 2016-10-16 | 佛瑪治療公司 | 作為hdac抑制劑之雙環[4,6,0]異羥肟酸 |
TW201639811A (zh) | 2015-03-13 | 2016-11-16 | 佛瑪治療公司 | 作為HDAC8抑制劑之α-桂皮醯胺化合物與組成物 |
US10029995B2 (en) | 2015-09-03 | 2018-07-24 | Forma Therapeutics, Inc. | [6,6] fused bicyclic HDAC8 inhibitors |
EP3472131B1 (en) | 2016-06-17 | 2020-02-19 | Forma Therapeutics, Inc. | 2-spiro-5- and 6-hydroxamic acid indanes as hdac inhibitors |
US10357493B2 (en) | 2017-03-10 | 2019-07-23 | Selenity Therapeutics (Bermuda), Ltd. | Metalloenzyme inhibitor compounds |
TWI794232B (zh) * | 2017-05-17 | 2023-03-01 | 美商戴納立製藥公司 | 激酶抑制劑及其用途 |
US11161825B2 (en) * | 2017-08-15 | 2021-11-02 | Bayer Aktiengesellschaft | 4-oxo-2,3,4,5-tetrahydro-1H-1,5-benzodiazepine-7-carboxamides |
WO2020096916A2 (en) | 2018-11-08 | 2020-05-14 | Merck Sharp & Dohme Corp. | Inhibitors of histone deacetylase useful for the treatment or prevention of hiv infection |
CN111848591B (zh) * | 2019-04-25 | 2022-03-18 | 成都先导药物开发股份有限公司 | Hdac抑制剂及其制备方法和用途 |
US11453661B2 (en) * | 2019-09-27 | 2022-09-27 | Takeda Pharmaceutical Company Limited | Heterocyclic compound |
CN113527206B (zh) * | 2020-04-17 | 2022-12-30 | 上海中泽医药科技有限公司 | 一种苯并氮杂环类化合物、其制备方法及用途 |
UY39484A (es) | 2020-11-02 | 2022-06-30 | Novartis Ag | Inhibidores de interleucina-17 |
CN112691706A (zh) * | 2020-12-23 | 2021-04-23 | 中触媒新材料股份有限公司 | 一种乙醇制乙腈催化剂的再生方法 |
IL307883A (en) | 2021-04-23 | 2023-12-01 | Tenaya Therapeutics Inc | HDAC6 inhibitors for use in the treatment of dilated myocardial disease |
IL308152A (en) | 2021-05-04 | 2024-01-01 | Tenaya Therapeutics Inc | 2-fluoroalkyl-4,3,1-oxadiazol-5-yl-thiazole, HDAC6 inhibitors for use in the treatment of metabolic disease and HFPEF |
TWI829329B (zh) * | 2021-09-06 | 2024-01-11 | 臺北醫學大學 | 組蛋白去乙醯化酶6和熱休克蛋白90之雙重抑制劑 |
WO2023081328A1 (en) * | 2021-11-04 | 2023-05-11 | Valo Health, Inc. | Histone deacetylase 6 inhibitor compounds and uses thereof |
WO2024104823A1 (en) | 2022-11-16 | 2024-05-23 | Basf Se | New substituted tetrahydrobenzoxazepine |
WO2024104822A1 (en) | 2022-11-16 | 2024-05-23 | Basf Se | Substituted tetrahydrobenzodiazepine as fungicides |
WO2024229406A1 (en) | 2023-05-04 | 2024-11-07 | Revolution Medicines, Inc. | Combination therapy for a ras related disease or disorder |
US20250049810A1 (en) | 2023-08-07 | 2025-02-13 | Revolution Medicines, Inc. | Methods of treating a ras protein-related disease or disorder |
Family Cites Families (212)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2557425C2 (de) | 1975-12-19 | 1987-03-19 | C.H. Boehringer Sohn, 6507 Ingelheim | 11-Oxo-11-H-pyrido[2,1-b]-chinazolin-2-carbonsäure und ihre Salze, Verfahren zu ihrer Herstellung und Arzneimittel |
DE3704203A1 (de) | 1987-02-11 | 1988-08-25 | Boehringer Ingelheim Kg | Verwendung von oxochinazolinderivaten bei der behandlung der hyperurikaemie |
US5244911A (en) | 1991-03-28 | 1993-09-14 | Eli Lilly And Company | 6-heterocyclic-4-amino-1,2,2a,3,4,5-hexahydrobenz(cd)indoles and pharmaceutical use thereof |
US5153185A (en) | 1991-04-16 | 1992-10-06 | Merck & Co., Inc. | 2-phenanthridonyl carbapenems |
US5294610A (en) | 1992-10-15 | 1994-03-15 | Merck & Co. Inc. | 2-(aza-9-fluorenonyl)carbapenem antibacterial agents |
US5262564A (en) | 1992-10-30 | 1993-11-16 | Octamer, Inc. | Sulfinic acid adducts of organo nitroso compounds useful as retroviral inactivating agents anti-retroviral agents and anti-tumor agents |
EP0638071B1 (en) | 1992-12-28 | 1997-04-09 | Eisai Co., Ltd. | Heterocyclic carbonic acid derivatives which bind to retinoid receptors (rar) |
EP0695184B1 (en) | 1993-01-15 | 1999-04-21 | Agouron Pharmaceuticals, Inc. | Hiv protease inhibitors |
US5384317A (en) | 1993-08-02 | 1995-01-24 | Merck & Co., Inc. | Bridged biphenyl carbapenem compounds, compositions containing such compounds and methods of use |
US6872542B1 (en) | 1993-11-18 | 2005-03-29 | Siga Pharmaceuticals, Inc. | Treatment or prophylaxis of diseases caused by pilus-forming bacteria |
US6420127B1 (en) | 1994-11-18 | 2002-07-16 | Washington University | Compounds and pharmaceutical compositions for the treatment and prophylaxis of bacterial infections |
JPH09505309A (ja) | 1993-11-18 | 1997-05-27 | ワシントン・ユニバーシティ | 細菌感染の治療および予防のための化合物および医薬組成物 |
US6110913A (en) | 1994-01-04 | 2000-08-29 | Novo Nordisk A/S | N-substituted azaheterocyclic carboxylic acids and esters thereof |
US5532261A (en) | 1994-12-12 | 1996-07-02 | Merck & Co., Inc. | Carbapenem antibiotics, compositions containing such compounds and methods of use |
US5719144A (en) | 1995-02-22 | 1998-02-17 | Merck & Co., Inc. | Fibrinogen receptor antagonists |
CA2201477C (en) | 1995-08-02 | 2005-05-03 | Javier Bartroli | New pyrimidone derivatives with antifungal activity |
US5728844A (en) | 1995-08-29 | 1998-03-17 | Celgene Corporation | Immunotherapeutic agents |
WO1997048786A1 (de) | 1996-06-19 | 1997-12-24 | Call Hans Peter | Mehrkomponentensystem zur verwendung mit waschaktiven substanzen |
US6566384B1 (en) | 1996-08-07 | 2003-05-20 | Darwin Discovery Ltd. | Hydroxamic and carboxylic acid derivatives having MMP and TNF inhibitory activity |
DE19726241A1 (de) | 1997-06-20 | 1998-12-24 | Call Krimhild | Erweitertes enzymatisches Multikomponentensystem zur Behandlung von Abwässern, zur Herstellung von Holzverbundstoffen, zum Deinken von Altpapier, Colour stripping von Altpapier, zum Einsatz als Oxidationssystem bei der organischen Synthese und zum Einsatz bei der Kohleverflüssigung |
IL121748A0 (en) | 1997-09-11 | 1998-02-22 | Yeda Res & Dev | Vanadium complexes of hydroxamates and pharmaceutical compositions comprising them |
US6403632B1 (en) | 2000-03-01 | 2002-06-11 | Bristol Myers Squibb Pharma Co | Lactam metalloprotease inhibitors |
US6180640B1 (en) | 1998-06-25 | 2001-01-30 | Sepracor, Inc. | Di- and tetra-hydroquinoline-indole antimicrobial agents, uses and compositions related thereto |
JP2000044562A (ja) | 1998-07-31 | 2000-02-15 | Kyowa Hakko Kogyo Co Ltd | ピロロフタルイミド誘導体 |
US6288099B1 (en) | 1998-12-04 | 2001-09-11 | American Home Products Corporation | Substituted benzofuranoindoles and indenoindoles as novel potassium channel openers |
EP1135393A2 (en) | 1998-12-04 | 2001-09-26 | American Home Products Corporation | Substituted benzofuranoindoles and indenoindoles as novel potassium channel openers |
US6946473B2 (en) | 1999-01-27 | 2005-09-20 | Wyeth Holdings Corporation | Preparation and use of acetylenic ortho-sulfonamido and phosphinic acid amido bicyclic heteroaryl hydroxamic acids as TACE inhibitors |
JP2000357809A (ja) | 1999-06-15 | 2000-12-26 | Fuji Photo Film Co Ltd | 光電変換材料、光電変換素子及びポリメチン色素 |
JP4162106B2 (ja) | 1999-06-17 | 2008-10-08 | 富士フイルム株式会社 | 光電変換素子および光電気化学電池ならびに金属錯体色素 |
AU6525300A (en) | 1999-08-13 | 2001-03-13 | Sepracor, Inc. | Spirocyclic ligands for sigma receptors, and libraries and methods of use thereof |
JP2001226269A (ja) | 2000-02-18 | 2001-08-21 | Takeda Chem Ind Ltd | メラニン凝集ホルモン拮抗剤 |
FR2809391B1 (fr) | 2000-05-29 | 2003-05-09 | Rhodia Chimie Sa | Nouveau mortier phosphomagnesien, procede d'obtention de ce mortier |
ES2572332T3 (es) | 2000-10-31 | 2016-05-31 | Rensselaer Polytech Inst | 2,6-metano-3-benzazocinas sustituidas en posición 8 y morfinanos sustituidos en posición 3 como ligandos de receptores opioides |
AU2002214222A1 (en) | 2000-11-01 | 2002-05-15 | Yeda Research And Development Co..Ltd. | Pharmaceutical compositions comprising organic vanadium complexes for treatment of ischemia |
JP2004514669A (ja) | 2000-11-07 | 2004-05-20 | ブリストル−マイヤーズ スクイブ カンパニー | セリンプロテアーゼ阻害剤として有用な酸誘導体 |
US7214690B2 (en) | 2001-02-23 | 2007-05-08 | Ligand Pharmaceuticals Incorporated | Tricyclic quinolinone and tricyclic quinoline androgen receptor modulator compounds and methods |
IN192526B (zh) | 2001-09-25 | 2004-04-24 | Ranbaxy Lab | |
FR2832711B1 (fr) | 2001-11-26 | 2004-01-30 | Warner Lambert Co | Derives de triazolo [4,3-a] pyrido [2,3-d] pyrimidin-5-ones, compositions les contenant, procede de preparation et utilisation |
TW200301698A (en) | 2001-12-21 | 2003-07-16 | Bristol Myers Squibb Co | Acridone inhibitors of IMPDH enzyme |
DE60320957D1 (en) | 2002-03-13 | 2008-06-26 | Janssen Pharmaceutica Nv | Sulfonylderivate als histone-deacetylase-inhibitoren |
WO2003087059A2 (en) | 2002-04-08 | 2003-10-23 | Sun Pharmaceutical Industries Limited | (e)-oxime ether derivative of 5,6-dihydro-benzo[5,6]cyclohepta[1,2-b]pyridin-11-one |
TW200404796A (en) | 2002-08-19 | 2004-04-01 | Ono Pharmaceutical Co | Nitrogen-containing compound |
AU2003255845A1 (en) | 2002-08-22 | 2004-03-11 | Piramed Limited | Phosphadidylinositol 3,5-biphosphate inhibitors as anti-viral agents |
EP1556053A4 (en) | 2002-10-31 | 2006-04-19 | Amgen Inc | ANTI-INFLAMMATORY AGENTS |
BR0317528A (pt) | 2002-12-20 | 2005-11-22 | Basf Ag | Uso dos compostos, métodos para o controle de insetos, aracnìdeos ou nematodos, e para a proteção de plantas em crescimento contra o ataque ou a infestação por insetos, aracnìdeos ou nematodos, compostos, e, composições |
JP2004210716A (ja) | 2002-12-27 | 2004-07-29 | Dai Ichi Seiyaku Co Ltd | ジアミド誘導体 |
WO2004063156A1 (en) | 2003-01-08 | 2004-07-29 | Biovitrum Ab | Novel indole derivates as fabp-4 inhibitors |
US7704756B2 (en) | 2003-01-21 | 2010-04-27 | Novartis Vaccines And Diagnostics, Inc. | Fluorogenic dyes |
US7241775B2 (en) | 2003-03-24 | 2007-07-10 | Sanofi-Aventis Deutschland Gmbh | Composition, process of making, and medical use of substituted 4-phenyltetrahydroisoquinolines |
WO2004096139A2 (en) | 2003-04-24 | 2004-11-11 | Incyte Corporation | Aza spiro alkane derivatives as inhibitors of metalloproteases |
GB0313766D0 (en) | 2003-06-13 | 2003-07-23 | Xenova Ltd | Pharmaceutical compounds |
ATE433974T1 (de) | 2003-09-19 | 2009-07-15 | Gilead Sciences Inc | Azachinolinolphosphonatverbindungen als integraseinhibitoren |
US8227636B2 (en) * | 2004-04-05 | 2012-07-24 | Merck Hdac Research, Llc | Histone deacetylase inhibitor prodrugs |
US7705017B2 (en) | 2004-05-03 | 2010-04-27 | En Vivo Pharmaceuticals, Inc. | Compounds for treatment of neurodegenerative diseases |
CN1953982B (zh) | 2004-05-17 | 2011-07-06 | 泰博特克药品有限公司 | 4-取代-1,5-二氢-吡啶并[3,2-b]吲哚-2-酮 |
WO2005121139A1 (en) | 2004-06-09 | 2005-12-22 | Altana Pharma Ag | Substituted tricyclic benzimidazoles |
WO2005123089A2 (en) | 2004-06-10 | 2005-12-29 | Kalypsys, Inc. | Multicyclic sulfonamide compounds as inhibitors of histone deacetylase for the treatment of disease |
AR051041A1 (es) | 2004-10-04 | 2006-12-13 | Altana Pharma Ag | Bencimidazoles triciclicos condensados |
UY29198A1 (es) | 2004-11-09 | 2006-05-31 | Cancer Rec Tech Ltd | Derivados sustituidos de quinazolinona y derivados sustituidos de quinazolina-2, 4-diona, composiciones conteniéndolos, procedimientos de preparación y aplicaciones |
WO2006065842A2 (en) | 2004-12-13 | 2006-06-22 | Synta Pharmaceuticals Corp. | 5,6,7,8-tetrahydroquinolines and related compounds and uses thereof |
CA2596355C (en) | 2005-01-31 | 2015-01-06 | Ception Therapeutics, Inc. | Tumor necrosis factor inhibitors |
EP3354265A1 (en) | 2005-03-22 | 2018-08-01 | President and Fellows of Harvard College | Treatment of solid tumors |
GB0509223D0 (en) | 2005-05-05 | 2005-06-15 | Chroma Therapeutics Ltd | Enzyme inhibitors |
AR057061A1 (es) | 2005-06-16 | 2007-11-14 | Altana Pharma Ag | Espiro-bencimidazoles farmaceuticamente activos y su uso en la fabricacion de medicamentos |
JP2008543867A (ja) | 2005-06-17 | 2008-12-04 | ワイス | セロトニン阻害剤ならびに5−ht1aアゴニストおよびアンタゴニストとして有用な三環系化合物 |
EP1904454A2 (en) | 2005-06-22 | 2008-04-02 | Nycomed GmbH | Process for the production of intermadiates for the preparation of tricyclic benzimidazoles |
US7456195B2 (en) | 2005-06-24 | 2008-11-25 | Bristol-Myers Squibb Company | Phenylglycinamide and pyridylglycinamide derivatives useful as anticoagulants |
CA2619518A1 (en) | 2005-08-22 | 2007-03-01 | Nycomed Gmbh | Isotopically substituted benzimidazole derivatives |
EP1940805A4 (en) | 2005-08-26 | 2009-11-11 | Methylgene Inc | BENZODIAZEPIN AND BENZOPIPERAZINANALOGA AS INHIBITORS OF HISTONDEACETYLASE |
GB0518237D0 (en) | 2005-09-07 | 2005-10-19 | Angeletti P Ist Richerche Bio | Therapeutic compounds |
US8119655B2 (en) | 2005-10-07 | 2012-02-21 | Takeda Pharmaceutical Company Limited | Kinase inhibitors |
GB0522881D0 (en) | 2005-11-10 | 2005-12-21 | Angeletti P Ist Richerche Bio | Therapeutic compounds |
US8518964B2 (en) | 2005-11-22 | 2013-08-27 | Merck Sharp & Dohme Corp. | Tricyclic compounds useful as inhibitors of kinases |
AR057579A1 (es) | 2005-11-23 | 2007-12-05 | Merck & Co Inc | Compuestos espirociclicos como inhibidores de histona de acetilasa (hdac) |
CA2632444A1 (en) | 2005-12-19 | 2007-06-28 | Boehringer Ingelheim International Gmbh | Use of aminoalcohol derivatives for the treatment of overactive bladder |
DE102005061655A1 (de) | 2005-12-22 | 2007-06-28 | Merck Patent Gmbh | Diazepinone |
AR059036A1 (es) | 2006-01-17 | 2008-03-12 | Schering Corp | Compuestos para el tratamiento de trastornos inflamatorios |
EP1991247B1 (en) | 2006-02-14 | 2015-10-14 | President and Fellows of Harvard College | Bifunctional histone deacetylase inhibitors |
WO2007100536A1 (en) | 2006-02-24 | 2007-09-07 | Wyeth | DIHYDROSPIRO[DIBENZO[A,D][7]ANNULENE-5,4'-IMIDAZOL] COMPOUNDS FOR THE INHIBITION OF β-SECRETASE |
US8338416B2 (en) | 2006-03-16 | 2012-12-25 | Pharmacylics, Inc. | Indole derivatives as inhibitors of histone deacetylase |
WO2007115409A1 (en) | 2006-04-10 | 2007-10-18 | Painceptor Pharma Corporation | Compositions and methods for modulating gated ion channels |
EP2035042A2 (en) | 2006-06-12 | 2009-03-18 | Viamet Pharmaceuticals, Inc. | Metallo-hydrolase inhibitors using metal binding moieties in combination with targeting moieties |
US20070293530A1 (en) | 2006-06-14 | 2007-12-20 | Methylgene Inc. | Sulfamide and sulfamate derivatives as histone deacetylase inhibitors |
CN101108859A (zh) | 2006-07-17 | 2008-01-23 | 上海恒瑞医药有限公司 | 长春碱类化合物、其制备方法及其在医药上的用途 |
CN101495186A (zh) | 2006-07-26 | 2009-07-29 | 诺瓦提斯公司 | 十一异戊二烯基焦磷酸酯合酶的抑制剂 |
US20100173332A1 (en) | 2006-09-07 | 2010-07-08 | Auckland Uniservices Limited | Method for the Fluorescent Detection of Nitroreductase Activity Using Nitro-Substituted Aromatic Compounds |
WO2008048648A2 (en) | 2006-10-17 | 2008-04-24 | Acadia Pharmaceuticals Inc. | Cb1-modulating compounds and their use |
WO2008046155A1 (en) | 2006-10-20 | 2008-04-24 | Dia-B Tech Limited | Methods for regulating glucose homeostasis and agents therefor |
CN105481788A (zh) | 2006-10-28 | 2016-04-13 | 梅特希尔基因公司 | 组蛋白脱乙酰酶抑制剂 |
WO2008053131A1 (en) | 2006-10-30 | 2008-05-08 | Chroma Therapeutics Ltd. | Hydroxamates as inhibitors of histone deacetylase |
WO2008061160A1 (en) | 2006-11-14 | 2008-05-22 | Pharmacyclics, Inc. | Uses of selective inhibitors of hdac8 for treatment of inflammatory conditions |
US7820711B2 (en) | 2006-11-14 | 2010-10-26 | Pharmacyclics Inc. | Uses of selective inhibitors of HDAC8 for treatment of T-cell proliferative disorders |
US7951795B2 (en) | 2006-12-08 | 2011-05-31 | Merck Sharp & Dohme Corp. | Constrained spirocyclic compounds as CGRP receptor antagonists |
WO2008071765A1 (en) | 2006-12-14 | 2008-06-19 | Nycomed Gmbh | Pharmaceutically active spiro-substituted benzimidazole derivatives |
WO2008074858A1 (en) | 2006-12-21 | 2008-06-26 | Nycomed Gmbh | Intermediates and process for the production of 5-substituted tricyclic benzimidazoles |
BRPI0806447A2 (pt) | 2007-02-09 | 2011-09-06 | Forest Laboratoires Holdings Ltd | formulação de compostos heterocìclicos, método para tratar condição inflamatória ou alérgica e forma amorfa sustancialmente pura de um composto |
WO2008101186A1 (en) | 2007-02-15 | 2008-08-21 | The J. David Gladstone Institutes | Inhibitors for hdac8 |
DE102007013854A1 (de) | 2007-03-20 | 2008-09-25 | Merck Patent Gmbh | Tetrahydrochinoline |
DE102007013856A1 (de) | 2007-03-20 | 2008-09-25 | Merck Patent Gmbh | Substituierte Tetrahydropyrrolochinoline |
DE102007013855A1 (de) | 2007-03-20 | 2008-09-25 | Merck Patent Gmbh | Substituierte Tetrahydrochinoline |
US20090105283A1 (en) | 2007-04-11 | 2009-04-23 | Dmitry Koltun | 3-HYDROQUINAZOLIN-4-ONE DERIVATIVES FOR USE AS STEAROYL CoA DESATURASE INHIBITORS |
US20080255161A1 (en) | 2007-04-11 | 2008-10-16 | Dmitry Koltun | 3-HYDROQUINAZOLIN-4-ONE DERIVATIVES FOR USE AS STEAROYL CoA DESATURASE INHIBITORS |
MX2009012847A (es) | 2007-06-13 | 2009-12-08 | Bristol Myers Squibb Co | Analogos dipeptidicos como inhibidores de factores de coagulacion. |
WO2009015208A1 (en) | 2007-07-23 | 2009-01-29 | Replidyne, Inc. | Antibacterial amide and sulfonamide substituted heterocyclic urea compounds |
ES2403284T3 (es) | 2008-01-09 | 2013-05-17 | Array Biopharma, Inc. | Pirimidil ciclopentanos como inhibidores de la proteína quinasa AKT |
US8987468B2 (en) | 2008-02-04 | 2015-03-24 | The Translational Genomics Research Institute | Compounds, pharmaceutical compositions and methods of use of hydroxamic acid derivatives |
EP2244709A4 (en) | 2008-02-07 | 2012-02-29 | Synta Pharmaceuticals Corp | TOPICAL FORMULATIONS FOR THE TREATMENT OF PSORIASIS |
JP2009191041A (ja) | 2008-02-18 | 2009-08-27 | Univ Of Tokyo | ヒドロキシメチルケトン誘導体 |
EP2100879A1 (en) | 2008-03-13 | 2009-09-16 | 4Sc Ag | Novel N-substituted tetrahydroisoquinoline/isoindoline hydroxamic acid compounds |
US8436005B2 (en) | 2008-04-03 | 2013-05-07 | Abbott Laboratories | Macrocyclic pyrimidine derivatives |
US8980877B2 (en) | 2008-04-15 | 2015-03-17 | Dac S.R.L. | Spirocyclic derivatives as histone deacetylase inhibitors |
EP2110377A1 (en) | 2008-04-15 | 2009-10-21 | DAC S.r.l. | Spirocyclic derivatives as histone deacetylase inhibitors |
EP2311840A1 (en) | 2009-10-13 | 2011-04-20 | DAC S.r.l. | Spirocyclic derivatives as histone deacetylase inhibitors |
WO2009137503A1 (en) | 2008-05-05 | 2009-11-12 | Envivo Pharmaceuticals, Inc. | Hdac inhibitors and uses thereof |
WO2009137492A1 (en) | 2008-05-05 | 2009-11-12 | Abbott Laboratories | Heteroaryl-fused macrocyclic pyrimidine derivatives |
US8058427B2 (en) | 2008-06-12 | 2011-11-15 | National Health Research Institutes | Coumarin compounds and their use for treating cancer |
EP2303888B1 (en) | 2008-06-12 | 2015-05-06 | President and Fellows of Harvard College | Compounds for antimicrobial intervention |
US9265734B2 (en) | 2008-09-03 | 2016-02-23 | Biomarin Pharmaceutical Inc. | Compositions including 6-aminohexanoic acid derivatives as HDAC inhibitors |
AU2009291602B2 (en) | 2008-09-11 | 2013-02-14 | Amgen Inc. | Spiro-tetracyclic ring compounds as betasecretase modulators and methods of use |
AR073630A1 (es) | 2008-10-07 | 2010-11-17 | Schering Corp | Analogos de espiroaminooxazolina como moduladores de los receptores adrenergicos alfa2c |
US9040528B2 (en) | 2008-10-14 | 2015-05-26 | Astrazeneca Ab | Chemical compounds 542 |
ES2565611T3 (es) | 2008-10-14 | 2016-04-05 | Entasis Therapeutics Limited | Compuestos heteroaromáticos espirocíclicos y condensados para el tratamiento de infecciones bacterianas |
CA2740389A1 (en) | 2008-10-15 | 2010-05-20 | Gilead Sciences, Inc. | 3-hydroquinazolin-4-one derivatives for use as stearoyl coa desaturase inhibitors |
GB2465405A (en) | 2008-11-10 | 2010-05-19 | Univ Basel | Triazine, pyrimidine and pyridine analogues and their use in therapy |
EP2355825A2 (en) | 2008-11-10 | 2011-08-17 | Schering Corporation | Compounds for the treatment of inflammatory disorders |
RU2470934C1 (ru) | 2008-11-11 | 2012-12-27 | Дзе Ил Фармасьютикал Ко., Лтд. | Новое трициклическое производное или его фармацевтически приемлемые соли, способ их получения и содержащая их фармацевтическая композиция |
US20110319416A1 (en) | 2009-01-28 | 2011-12-29 | Emory University | Subunit Selective NMDA Receptor Antagonists For The Treatment Of Neurological Conditions |
TW201038569A (en) | 2009-02-16 | 2010-11-01 | Abbott Gmbh & Co Kg | Heterocyclic compounds, pharmaceutical compositions containing them, and their use in therapy |
CN109651342A (zh) | 2009-03-27 | 2019-04-19 | 默沙东公司 | 丙型肝炎病毒复制的抑制剂 |
CA2758149A1 (en) | 2009-04-09 | 2010-10-14 | Boehringer Ingelheim International Gmbh | Inhibitors of hiv replication |
WO2010125469A1 (en) | 2009-04-29 | 2010-11-04 | Glenmark Pharmaceuticals, S.A. | Pyrimidinedione-fused heterocyclic compounds as trpa1 modulators |
WO2010151317A1 (en) | 2009-06-22 | 2010-12-29 | Millennium Pharmaceuticals, Inc. | Substituted hydroxamic acids and uses thereof |
JP5798115B2 (ja) * | 2009-06-22 | 2015-10-21 | ミレニアム ファーマシューティカルズ, インコーポレイテッドMillennium Pharmaceuticals, Inc. | 置換ヒドロキサム酸およびその使用 |
AU2010263113B2 (en) | 2009-06-23 | 2015-11-26 | Translational Drug Development, Llc | Benzamide derivatives |
EP2266985A1 (en) | 2009-06-26 | 2010-12-29 | Deutsches Krebsforschungszentrum Stiftung des öffentlichen Rechts | Tricyclic Pyrimidine Derivatives as Wnt antagonists |
WO2011002520A2 (en) | 2009-07-02 | 2011-01-06 | Angion Biomedica Corp. | Small molecule inhibitors of parp activity |
ES2736200T3 (es) | 2009-07-22 | 2019-12-26 | Univ Illinois | Inhibidores de HDAC y métodos terapéuticos que utilizan los mismos |
IN2012DN03217A (zh) | 2009-09-16 | 2015-10-23 | Cylene Pharmaceuticals Inc | |
MY184074A (en) | 2009-09-28 | 2021-03-17 | Hoffmann La Roche | Benzoxazepin p13k inhibitors compounds and methods of use |
KR20140034948A (ko) | 2009-09-28 | 2014-03-20 | 에프. 호프만-라 로슈 아게 | 벤즈옥세핀 pi3k 억제제 화합물 및 사용 방법 |
EP2305643A1 (en) | 2009-10-02 | 2011-04-06 | Ikerchem, S.L. | New histone deacetylase inhibitors based simultaneously on trisubstituted 1h-pyrroles and aromatic and heteroaromatic spacers |
US9221773B2 (en) | 2009-12-22 | 2015-12-29 | The Translational Genomics Research Institute | Benzamide derivatives |
US8198290B2 (en) | 2009-12-23 | 2012-06-12 | Berry And Associates, Inc. | Methoxatin derivatives |
WO2011084991A2 (en) | 2010-01-08 | 2011-07-14 | President And Fellows Of Harvard College | Fluorinated hdac inhibitors and uses thereof |
KR101781663B1 (ko) | 2010-01-13 | 2017-09-25 | 템페로 파마슈티칼즈, 인크. | 히스톤 데아세틸라제 효소를 억제하기 위한 화합물 및 이를 제조하는 방법 |
JP2011148714A (ja) | 2010-01-19 | 2011-08-04 | Nippon Soda Co Ltd | 病害防除方法 |
EA026514B1 (ru) | 2010-01-22 | 2017-04-28 | Эситайлон Фармасьютикалз Инк. | Соединения обратного амида в качестве ингибиторов протеиндеацетилазы и способы их применения |
US8519122B2 (en) | 2010-02-12 | 2013-08-27 | The Regents Of The University Of California | Compositions and methods for modification of biomolecules |
WO2011106632A1 (en) | 2010-02-26 | 2011-09-01 | Millennium Pharmaceuticals, Inc. | Substituted hydroxamic acids and uses thereof |
US8546588B2 (en) | 2010-02-26 | 2013-10-01 | Millennium Pharmaceuticals, Inc. | Substituted hydroxamic acids and uses thereof |
US8946223B2 (en) | 2010-04-12 | 2015-02-03 | Millennium Pharmaceuticals, Inc. | Substituted hydroxamic acids and uses thereof |
JO3131B1 (ar) | 2010-04-27 | 2017-09-20 | Glaxosmithkline Llc | مركبات كيميائية |
WO2011146591A1 (en) | 2010-05-19 | 2011-11-24 | Millennium Pharmaceuticals, Inc. | Substituted hydroxamic acids and uses thereof |
US8685969B2 (en) | 2010-06-16 | 2014-04-01 | Bristol-Myers Squibb Company | Carboline carboxamide compounds useful as kinase inhibitors |
WO2012012322A1 (en) | 2010-07-19 | 2012-01-26 | Millennium Pharmaceuticals, Inc. | Substituted hydroxamic acids and uses thereof |
US20120015942A1 (en) | 2010-07-19 | 2012-01-19 | Millennium Pharmaceuticals, Inc. | Substituted hydroxamic acids and uses thereof |
US20130210899A1 (en) | 2010-07-30 | 2013-08-15 | The Regents Of The University Of California | Method and Therapeutic for the Treatment and Regulation of Memory Formation |
WO2012027564A1 (en) | 2010-08-26 | 2012-03-01 | Millennium Pharmaceuticals, Inc. | Substituted hydroxamic acids and uses thereof |
WO2012031993A1 (en) | 2010-09-09 | 2012-03-15 | F. Hoffmann-La Roche Ag | Novel n-hydroxy-benzamides for the treatment of cancer |
AU2011311531B2 (en) | 2010-10-08 | 2014-11-20 | Life Sciences Research Partners Vzw | HDAC inhibitors to treat Charcot-Marie-Tooth disease |
WO2012045194A1 (en) | 2010-10-09 | 2012-04-12 | Abbott Laboratories | Benzodiazepinones as fak inhibitors for treatment of cancer |
US8765773B2 (en) | 2010-10-18 | 2014-07-01 | Millennium Pharmaceuticals, Inc. | Substituted hydroxamic acids and uses thereof |
AU2011319685B2 (en) | 2010-10-22 | 2016-02-04 | Le Centre National De La Recherche Scientifique | Pochoxime conjugates useful for the treatment of HSP90 related pathologies |
JP6041808B2 (ja) | 2010-11-16 | 2016-12-14 | アセチロン ファーマシューティカルズ インコーポレイテッドAcetylon Pharmaceuticals,Inc. | 蛋白質脱アセチル化酵素抑制剤としてのピリミジン水酸基アミド化合物およびその利用方法 |
CN102558200A (zh) | 2010-12-21 | 2012-07-11 | 复旦大学 | 长春碱类衍生物、其制备方法及其在医药上的用途 |
WO2012088015A2 (en) | 2010-12-22 | 2012-06-28 | Millennium Pharmaceuticals, Inc. | Substituted hydroxamic acids and uses thereof |
WO2012085003A1 (en) | 2010-12-22 | 2012-06-28 | Katholieke Universiteit Leuven, K.U. Leuven R&D | 2-hydroxyisoquinoline-1,3(2h,4h)-diones and related compounds useful as hiv replication inhibitors |
US8980909B2 (en) | 2011-01-12 | 2015-03-17 | Crystal Biopharmaceutical Llc | HDAC inhibiting derivatives of camptothecin |
US9029391B2 (en) | 2011-01-24 | 2015-05-12 | Viiv Healthcare Uk Limited | Isoquinoline compounds and methods for treating HIV |
WO2012106343A2 (en) | 2011-02-01 | 2012-08-09 | The Board Of Trustees Of The University Of Illinois | Hdac inhibitors and therapeutic methods using the same |
EP2670750B1 (en) | 2011-02-02 | 2016-09-14 | Fibrogen, Inc. | Naphthyridine derivatives as inhibitors of hypoxia inducible factor |
WO2012109165A1 (en) | 2011-02-07 | 2012-08-16 | Amgen Inc. | 5-amino-oxazepine and 5-amino-thiazepane compounds as beta-secretase antagonists and methods of use |
WO2012112525A1 (en) | 2011-02-14 | 2012-08-23 | Alkermes, Inc. | PERIPHERIALLY ACTING μ OPIOID ANTAGONISTS |
US8962859B2 (en) | 2011-02-15 | 2015-02-24 | Amgen Inc. | Spiro-amino-imidazo-fused heterocyclic compounds as beta-secretase modulators and methods of use |
WO2012110860A1 (en) | 2011-02-17 | 2012-08-23 | Glenmark Pharmaceuticals S.A. | TRICYCLIC COMPOUNDS AS mPGES-1 INHIBITORS |
WO2012117421A1 (en) | 2011-03-02 | 2012-09-07 | Orchid Research Laboratories Ltd | Histone deacetylase inhibitors |
WO2012126901A1 (en) | 2011-03-21 | 2012-09-27 | F. Hoffmann-La Roche Ag | Benzoxazepin compounds selective for pi3k p110 delta and methods of use |
CN102838625B (zh) | 2011-06-22 | 2015-04-15 | 中国科学院上海药物研究所 | 四氢吡啶并噻唑类化合物、其制备方法、包含该化合物的药物组合物及其用途 |
EP2723338A2 (en) | 2011-06-24 | 2014-04-30 | The Trustees of Stevens Institute of Technology | Selective inhibitors of histone deacetylase isoform 6 and methods thereof |
WO2013006408A1 (en) | 2011-07-01 | 2013-01-10 | Tempero Pharmaceuticals, Inc. | Compounds and methods |
JP6047563B2 (ja) | 2011-07-08 | 2016-12-21 | ノバルティス アーゲー | 新規トリフルオロメチル−オキサジアゾール誘導体および疾患の治療におけるその使用 |
WO2013009827A1 (en) | 2011-07-13 | 2013-01-17 | Tempero Pharmaceuticals, Inc. | Methods of treatment |
US9512083B2 (en) | 2011-07-20 | 2016-12-06 | The General Hospital Corporation | Histone deacetylase 6 selective inhibitors for the treatment of bone disease |
SG2014012926A (en) | 2011-08-30 | 2014-06-27 | Chdi Foundation Inc | Kynurenine-3-monooxygenase inhibitors, pharmaceutical compositions, and methods of use thereof |
WO2013044092A1 (en) | 2011-09-21 | 2013-03-28 | Amgen Inc. | Amino-oxazines and amino-dihydrothiazine compounds as beta-secretase modulators and methods of use |
US20140241990A1 (en) | 2011-09-30 | 2014-08-28 | Tufts University | Methods of using adenosine a1 receptor activation for treating depression |
EP2763531A4 (en) | 2011-10-03 | 2015-11-18 | Univ Columbia | NEW MOLECULES FOR THE SELECTIVE INHIBITION OF HISTONDEACETYLASE 6 IN RELATION TO HISTONDEACETYLASE 1 |
JP6224600B2 (ja) | 2011-10-18 | 2017-11-01 | エコール ポリテクニーク フェデラル ドゥ ローザンヌ(エーペーエフエル) | 電気化学および/または光電子デバイス用化合物 |
WO2013059582A2 (en) | 2011-10-20 | 2013-04-25 | Nupotential, Inc. | Small molecule inhibitors of histone deacteylases |
ES2671387T3 (es) | 2011-12-11 | 2018-06-06 | Viamet Pharmaceuticals (NC), Inc. | Compuestos inhibidores de metaloenzimas |
EA030609B8 (ru) | 2011-12-15 | 2018-10-31 | Алкермес Фарма Айэленд Лимитед | Композиции бупренорфина и антагонистов мю-опиоидных рецепторов |
WO2013134467A1 (en) | 2012-03-07 | 2013-09-12 | H. Lee Moffitt Cancer Center And Research Institute, Inc. | Selective histone deactylase 6 inhibitors |
GB2503789A (en) | 2012-05-15 | 2014-01-08 | Syngenta Participations Ag | Quinazoline derivatives as antifungal agents |
EP2872474B1 (en) | 2012-07-10 | 2022-01-19 | Georgia State University Research Foundation, Inc. | Anthraquinone analogs and methods of making and using thereof |
WO2014011902A1 (en) | 2012-07-11 | 2014-01-16 | Nimbus Iris, Inc. | Irak inhibitors and uses thereof |
US20140018361A1 (en) | 2012-07-11 | 2014-01-16 | Nimbus Iris, Inc. | Irak inhibitors and uses thereof |
WO2014018919A1 (en) | 2012-07-27 | 2014-01-30 | The Regents Of The University Of California | Seriniquinones, melanoma-specific anticancer agents |
BR112015004648A2 (pt) | 2012-09-05 | 2017-07-04 | Bayer Cropscience Ag | amidas de ácidos bicicloaril carboxílicos com atividade herbicida |
ES2625959T3 (es) | 2012-09-28 | 2017-07-21 | Bayer Pharma Aktiengesellschaft | 5-Aril-triazolo-azepinas inhibidoras de la proteína BET |
US9403850B2 (en) | 2013-01-10 | 2016-08-02 | VenatoRx Pharmaceuticals, Inc. | Beta-lactamase inhibitors |
JP6321685B2 (ja) | 2013-02-25 | 2018-05-09 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツングMerck Patent Gesellschaft mit beschraenkter Haftung | 2−アミノ−3,4−ジヒドロ−キナゾリン誘導体、およびそのカテプシンd阻害剤としての使用 |
WO2014134127A1 (en) | 2013-02-26 | 2014-09-04 | Northeastern University | Cannabinergic nitrate esters and related analogs |
MY184756A (en) | 2013-04-29 | 2021-04-20 | Chong Kun Dang Pharmaceutical Corp | Novel compounds for selective histone deacetylase inhibitors, and pharmaceutical composition comprising the same |
JP6353032B2 (ja) | 2013-04-30 | 2018-07-04 | 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 | ジアミノピラジン化合物、前記化合物を含有する医薬、その使用、およびその調製方法 |
US9278963B2 (en) | 2013-10-10 | 2016-03-08 | Acetylon Pharmaceuticals, Inc. | Pyrimidine hydroxy amide compounds as histone deacetylase inhibitors |
RU2660897C2 (ru) | 2014-03-12 | 2018-07-11 | Чонг Кун Данг Фармасьютикал Корп. | Новые соединения в качестве ингибиторов гистондеацетилазы 6 и содержащие их фармацевтические композиции |
TW201636329A (zh) | 2015-02-02 | 2016-10-16 | 佛瑪治療公司 | 作為hdac抑制劑之雙環[4,6,0]異羥肟酸 |
IL280856B (en) | 2015-02-02 | 2022-09-01 | Forma Therapeutics Inc | 3-alkyl-4-amido-bicyclic [4,5,0] hydroxamic acids as hdac inhibitors |
GB201505133D0 (en) * | 2015-03-26 | 2015-05-06 | Egerton Charles E And Scott Harden Simon | Self-propelled water board apparatus |
WO2016168660A1 (en) | 2015-04-17 | 2016-10-20 | Forma Therapeutics, Inc. | 3-spiro-7-hydroxamic acid tetralins as hdac inhibitors |
FI3362445T3 (fi) | 2015-10-12 | 2023-03-21 | Chong Kun Dang Pharmaceutical Corp | Oksadiatsoliamiinijohdannaisyhdisteitä histonideasetylaasi 6:n inhibiittoreina ja niitä käsittävä farmaseuttinen koostumus |
EP3472131B1 (en) | 2016-06-17 | 2020-02-19 | Forma Therapeutics, Inc. | 2-spiro-5- and 6-hydroxamic acid indanes as hdac inhibitors |
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