HK1145831A1 - Methods of synthesis of certain n-hydroxy-3-(3-phenylsulfamoyl-phenyl)- acrylamide compounds n--3-(3--)- - Google Patents

Methods of synthesis of certain n-hydroxy-3-(3-phenylsulfamoyl-phenyl)- acrylamide compounds n--3-(3--)-

Info

Publication number
HK1145831A1
HK1145831A1 HK11100011.2A HK11100011A HK1145831A1 HK 1145831 A1 HK1145831 A1 HK 1145831A1 HK 11100011 A HK11100011 A HK 11100011A HK 1145831 A1 HK1145831 A1 HK 1145831A1
Authority
HK
Hong Kong
Prior art keywords
phenylsulfamoyl
hydroxy
phenyl
synthesis
methods
Prior art date
Application number
HK11100011.2A
Other languages
English (en)
Chinese (zh)
Inventor
Helge A Reisch
Peter Leeming
Prasad S Raje
Original Assignee
Topotarget Uk Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Topotarget Uk Ltd filed Critical Topotarget Uk Ltd
Publication of HK1145831A1 publication Critical patent/HK1145831A1/xx

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C303/00Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides
    • C07C303/36Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of amides of sulfonic acids
    • C07C303/40Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of amides of sulfonic acids by reactions not involving the formation of sulfonamide groups
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/06Antipsoriatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P33/00Antiparasitic agents
    • A61P33/02Antiprotozoals, e.g. for leishmaniasis, trichomoniasis, toxoplasmosis
    • A61P33/06Antimalarials
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Veterinary Medicine (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Dermatology (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
HK11100011.2A 2007-09-25 2011-01-03 Methods of synthesis of certain n-hydroxy-3-(3-phenylsulfamoyl-phenyl)- acrylamide compounds n--3-(3--)- HK1145831A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US97488007P 2007-09-25 2007-09-25
PCT/GB2008/003226 WO2009040517A2 (fr) 2007-09-25 2008-09-23 Procédés de synthèse de certains composés d'acide hydroxamique

Publications (1)

Publication Number Publication Date
HK1145831A1 true HK1145831A1 (en) 2011-05-06

Family

ID=40293778

Family Applications (1)

Application Number Title Priority Date Filing Date
HK11100011.2A HK1145831A1 (en) 2007-09-25 2011-01-03 Methods of synthesis of certain n-hydroxy-3-(3-phenylsulfamoyl-phenyl)- acrylamide compounds n--3-(3--)-

Country Status (8)

Country Link
US (1) US8642809B2 (fr)
EP (1) EP2203421B1 (fr)
JP (1) JP2010540426A (fr)
CN (1) CN101868446A (fr)
CA (1) CA2700173C (fr)
HK (1) HK1145831A1 (fr)
MX (1) MX2010003230A (fr)
WO (1) WO2009040517A2 (fr)

Families Citing this family (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2385829B1 (fr) 2009-01-09 2018-08-01 Board of Regents of the University of Texas System Composés pro-neurogéniques
US8362277B2 (en) 2009-01-09 2013-01-29 Board Of Regents Of The University Of Texas System Pro-neurogenic compounds
US9962368B2 (en) 2009-01-09 2018-05-08 Board Of Regents Of The University Of Texas System Pro-neurogenic compounds
US9162980B2 (en) 2009-01-09 2015-10-20 Board Of Regents Of The University Of Texas System Anti-depression compounds
EP2451790A4 (fr) * 2009-07-07 2012-12-26 Anthem Biosciences Private Ltd Inhibiteurs de l histone désacétylase
BR112013000414A2 (pt) 2010-07-07 2016-05-17 Univ Texas compostos proneurogênicos
CN102531972A (zh) * 2010-12-31 2012-07-04 北京万全阳光医药科技有限公司 抗肿瘤药物Belinostat的中间体的制备方法
CN102786448B (zh) * 2012-08-09 2014-03-12 深圳万乐药业有限公司 一种合成belinostat的方法
US9701676B2 (en) 2012-08-24 2017-07-11 Board Of Regents Of The University Of Texas System Pro-neurogenic compounds
WO2015070237A1 (fr) 2013-11-11 2015-05-14 Board Of Regents Of The University Of Texas System Produits chimiques neuroprotecteurs et leurs procédés d'identification et d'utilisation
WO2015070234A2 (fr) 2013-11-11 2015-05-14 Board Of Regents Of The University Of Texas System Composés neuroprotecteurs et leur utilisation
CN103724239A (zh) * 2013-12-31 2014-04-16 无锡万全医药技术有限公司 一种3-(3-苯基氨磺酰基-苯基)-丙烯酸酯的制备方法
CN103787924A (zh) * 2014-01-14 2014-05-14 北京万全德众医药生物技术有限公司 抗肿瘤药物Belinostat的一种新纯化方法
CN104478769B (zh) * 2014-12-22 2016-01-06 深圳万乐药业有限公司 一种适合工业化生产的贝利司他合成方法
CN105367455B (zh) * 2015-12-18 2017-10-24 深圳万乐药业有限公司 一种贝利司他异构体的制备方法
AU2017233898B2 (en) 2016-03-15 2022-12-15 Oryzon Genomics, S.A. Combinations of LSD1 inhibitors for use in the treatment of solid tumors
WO2017157813A1 (fr) 2016-03-15 2017-09-21 F. Hoffmann-La Roche Ag Combinaisons d'inhibiteurs de lsd1 pour le traitement des malignités hématologiques
WO2017199264A1 (fr) * 2016-05-17 2017-11-23 Biophore India Pharmaceuticals Pvt. Ltd. Nouveau procédé de préparation du belinostat
JP2019523273A (ja) * 2016-07-26 2019-08-22 フレゼニウス・カビ・オンコロジー・リミテッド ベリノスタットの多形形態、およびその調製のためのプロセス
WO2018029699A1 (fr) * 2016-08-11 2018-02-15 Msn Research & Development Center Formes à l'état solide de (2e)-n-hydroxy-3-[3- (phénylsulfamoyl) phényl] prop-2-énamide et leur procédé de préparation
CN106565552A (zh) * 2016-10-31 2017-04-19 瑞阳制药有限公司 贝利司他结晶体及其制备方法
RU2748835C1 (ru) 2017-11-27 2021-05-31 Совет Научных И Прикладных Исследований Индол(сульфонил)-n-гидроксибензамидные производные в качестве селективных ингибиторов hdac
CN108033902B (zh) * 2017-12-26 2020-07-07 深圳万乐药业有限公司 一种高纯度贝利司他顺式异构体的制备方法
CN109265377B (zh) * 2018-10-25 2021-01-22 瑞阳制药股份有限公司 贝利司他的绿色合成方法
CN109336788A (zh) * 2018-10-31 2019-02-15 安徽省庆云医药股份有限公司 一种贝利司他的制备方法
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
CN115636774B (zh) * 2022-12-01 2023-12-22 南开大学 一种贝利司他的合成方法

Family Cites Families (92)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4642316A (en) * 1985-05-20 1987-02-10 Warner-Lambert Company Parenteral phenytoin preparations
US6071923A (en) * 1994-09-16 2000-06-06 Bar-Ilan University Retinoyloxy aryl-substituted alkylene butyrates useful for the treatment of cancer and other proliferative diseases
US5730977A (en) 1995-08-21 1998-03-24 Mitsui Toatsu Chemicals, Inc. Anti-VEGF human monoclonal antibody
EP0827742A1 (fr) 1996-09-04 1998-03-11 Vrije Universiteit Brussel Utilisation des inhibiteurs de l'histone déacétylase pour le traitement de la fibrose ou de la cirrhose
HUP0103985A2 (hu) * 1998-10-13 2002-02-28 Fujisawa Pharmaceutical Co., Ltd. Ciklikus tetrapeptid, és annak felhasználása
US20070148228A1 (en) * 1999-02-22 2007-06-28 Merrion Research I Limited Solid oral dosage form containing an enhancer
MXPA01010891A (es) * 1999-04-28 2002-11-07 Univ Texas Composiciones y metodos para el tratamiento contra el cancer mediante la inhibicion selectiva del factor de crecimiento endotelial vascular (vegf).
DK1233958T3 (da) * 1999-11-23 2011-10-17 Methylgene Inc Hæmmere af histondeacetylase
GB0023983D0 (en) * 2000-09-29 2000-11-15 Prolifix Ltd Therapeutic compounds
ATE430567T1 (de) 2000-09-29 2009-05-15 Topotarget Uk Ltd Carbaminsäurederivate enthaltend eine amidgruppe zur behandlung von malaria
WO2002030879A2 (fr) * 2000-09-29 2002-04-18 Prolifix Limited Composes d'acide carbamique comprenant une liaison sulfonamide en tant qu'inhibiteurs de hdac
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
DE60227658D1 (de) 2001-05-02 2008-08-28 Univ California Verfahren zur behandlung neurodegenerativer, psychiatrischer und anderer störungen mit deacetylaseinhibitoren
WO2003016254A1 (fr) * 2001-08-09 2003-02-27 Ono Pharmaceutical Co., Ltd. Composes derives d'acide carboxylique et medicaments comprenant ces composes comme principe actif
RU2298414C2 (ru) 2001-08-21 2007-05-10 Астеллас Фарма Инк. Медицинское применение ингибитора гистоновой дезацетилазы и способ оценки его противоопухолевого действия
US6897220B2 (en) * 2001-09-14 2005-05-24 Methylgene, Inc. Inhibitors of histone deacetylase
EP1293205A1 (fr) 2001-09-18 2003-03-19 G2M Cancer Drugs AG Acide valproique et ses dérivés pour la polythérapie du cancer humain et pour le traitement de la métastase de tumeurs et de la maladie residuelle imperceptible
ATE382343T1 (de) * 2002-01-11 2008-01-15 Matthias Rath Polyphenole enthaltende pharmazeutische nahrungsmittelergänzungsformel und ihre anwendung in der krebsbehandlung
AU2003215112A1 (en) 2002-02-07 2003-09-02 Axys Pharmaceuticals Novel bicyclic hydroxamates as inhibitors of histone deacetylase
CA2476434A1 (fr) * 2002-02-15 2003-08-28 Sloan-Kettering Institute For Cancer Research Methode de traitement des maladies mediees par la thioredoxine (trx)
US20050288227A1 (en) * 2002-02-15 2005-12-29 Marks Paul A Use of thioredoxin measurements for diagnostics and treatments
US20070060614A1 (en) * 2002-03-04 2007-03-15 Bacopoulos Nicholas G Methods of treating cancer with hdac inhibitors
US7148257B2 (en) * 2002-03-04 2006-12-12 Merck Hdac Research, Llc Methods of treating mesothelioma with suberoylanilide hydroxamic acid
PL372239A1 (en) * 2002-03-04 2005-07-11 Aton Pharma, Inc. Methods of inducing terminal differentiation
US20040132825A1 (en) * 2002-03-04 2004-07-08 Bacopoulos Nicholas G. Methods of treating cancer with HDAC inhibitors
EP1485353B1 (fr) 2002-03-13 2011-08-24 Janssen Pharmaceutica NV Nouveaux inhibiteurs de l'histone deacetylase
US7629343B2 (en) 2002-04-03 2009-12-08 Topotarget Uk Limited Carbamic acid compounds comprising a piperazine linkage as HDAC inhibitors
TWI319387B (en) 2002-04-05 2010-01-11 Astrazeneca Ab Benzamide derivatives
WO2003087066A1 (fr) * 2002-04-11 2003-10-23 Sk Chemicals, Co., Ltd. Derives d'acide hydroxamique $g(a),$g(b)-insatures et leur utilisation comme inhibiteurs de l'histone desacetylase
WO2003088954A1 (fr) * 2002-04-15 2003-10-30 Sloan-Kettering Institute For Cancer Research Polytherapie pour le traitement de cancer
US8883148B2 (en) * 2002-04-26 2014-11-11 Asan Laboratories Company (Cayman), Limited Prevention of joint destruction
GB0209715D0 (en) 2002-04-27 2002-06-05 Astrazeneca Ab Chemical compounds
DE10233412A1 (de) 2002-07-23 2004-02-12 4Sc Ag Neue Verbindungen als Histondeacetylase-Inhibitoren
WO2004013130A1 (fr) 2002-08-02 2004-02-12 Argenta Discovery Limited Acides substitues thienylhydroxamiques utilises en tant qu'inhibiteurs d'histone desacetylase
GB0226370D0 (en) 2002-11-12 2002-12-18 Novartis Ag Organic compounds
US20080004311A1 (en) * 2002-11-12 2008-01-03 Alcon, Inc. Histone deacetylase inhibitors for treating degenerative diseases of the eye
ITMI20030025A1 (it) 2003-01-10 2004-07-11 Italfarmaco Spa Derivati dell'acido idrossammico ad attivita' antinfiammatoria.
US7135493B2 (en) 2003-01-13 2006-11-14 Astellas Pharma Inc. HDAC inhibitor
US20050222013A1 (en) * 2003-01-16 2005-10-06 Georgetown University Methods for the use of inhibitors of histone deacetylase as synergistic agents in cancer therapy
TW200424174A (en) 2003-02-06 2004-11-16 Hoffmann La Roche New TP diamide
AU2003900608A0 (en) 2003-02-11 2003-02-27 Fujisawa Pharmaceutical Co., Ltd. Hdac inhibitor
US7244751B2 (en) 2003-02-14 2007-07-17 Shenzhen Chipscreen Biosciences Ltd. Histone deacetylase inhibitors of novel benzamide derivatives with potent differentiation and anti-proliferation activity
EP1597390A4 (fr) 2003-02-18 2006-12-27 Maxcyte Inc Introduction d'antigenes dans des cellules par electroporation
CA2518318A1 (fr) 2003-03-17 2004-09-30 Takeda San Diego, Inc. Inhibiteurs d'histone deacetylase
TW200424187A (en) 2003-04-04 2004-11-16 Hoffmann La Roche New oxime derivatives and their use as pharmaceutically active agents
AU2004230889B2 (en) 2003-04-07 2008-03-13 Pharmacyclics Llc Hydroxamates as therapeutic agents
US20040220242A1 (en) * 2003-05-02 2004-11-04 Leland Shapiro Inhibitors of serine protease activity, methods and compositions for treatment of nitric oxide induced clinical conditions
JP5416338B2 (ja) 2003-05-09 2014-02-12 デューク ユニバーシティ Cd20特異的抗体およびその使用方法
CN1791396A (zh) 2003-05-21 2006-06-21 诺瓦提斯公司 组蛋白脱乙酰基酶抑制剂与化疗剂的组合
EP1491188A1 (fr) * 2003-06-25 2004-12-29 G2M Cancer Drugs AG Utilisation topique de l'acide valproique pour traiter des maladies de la peau
ATE462426T1 (de) * 2003-08-26 2010-04-15 Merck Hdac Res Llc Verwendung von saha zur behandlung von mesotheliom
CA2535889A1 (fr) 2003-08-29 2005-03-17 Aton Pharma, Inc. Methodes combinees de traitement du cancer
JP2007511212A (ja) * 2003-11-14 2007-05-10 ホルム,ペル・ゾンネ 新規アデノウイルス、それをコードする核酸及びその使用
WO2005051430A1 (fr) * 2003-11-14 2005-06-09 Per Sonne Holm Nouvelle utilisation d'adenovirus et d'acides nucleiques les codant
AU2003290412A1 (en) 2003-12-30 2005-07-21 Council Of Scientific And Industrial Research Arginine hydrochloride enhances chaperone-like activity of alpha crystallin
GB0401876D0 (en) * 2004-01-28 2004-03-03 Vereniging Het Nl Kanker I New use for cancer antigen
WO2005085864A1 (fr) * 2004-02-27 2005-09-15 The Government Of The United States Of America, Asrepresented By The Secretary Of The Department Of Health And Human Services Essais pharmacodynamiques à cytométrie de flux
PT1591109E (pt) * 2004-04-30 2008-09-05 Desitin Arzneimittel Gmbh Formulação exibindo libertação bifásica compreendendo um inibidor da desacetilase de histona
PL1781321T3 (pl) 2004-08-02 2014-07-31 Zenyth Operations Pty Ltd Sposób leczenia raka zawierający antagonistę VEGF-B
JPWO2006014024A1 (ja) * 2004-08-06 2008-05-01 小野薬品工業株式会社 精神神経系疾患治療剤
CN101001851B (zh) * 2004-08-09 2011-04-20 安斯泰来制药有限公司 具有作为组蛋白脱乙酰酶(hdac)抑制剂的活性的羟基酰胺化合物
WO2006060382A2 (fr) * 2004-11-30 2006-06-08 Trustees Of The University Of Pennsylvania Utilisation d'inhibiteurs de hdac et/ou dnmt dans le traitement d'une lesion ischemique
FR2879204B1 (fr) 2004-12-15 2007-02-16 Lab Francais Du Fractionnement Anticorps cytotoxique dirige contre les proliferations hematopoietiques lymphoides de type b.
EP1830864A2 (fr) * 2004-12-31 2007-09-12 Per Sonne Holm Adenovirus a region e1 absente et leur utilisation
MX2007008781A (es) * 2005-01-21 2007-09-11 Astex Therapeutics Ltd Compuestos farmaceuticos.
NZ599464A (en) * 2005-02-03 2014-03-28 Topotarget Uk Ltd Combination therapies using hdac inhibitors
US20060229237A1 (en) * 2005-04-07 2006-10-12 Yih-Lin Chung Treatment of gastrointestinal distress
GB0509225D0 (en) * 2005-05-05 2005-06-15 Chroma Therapeutics Ltd Inhibitors of enzymatic activity
CN102579417B (zh) 2005-05-13 2014-11-26 托波塔吉特英国有限公司 Hdac抑制剂的药物制剂
EP1743654A1 (fr) * 2005-07-15 2007-01-17 TopoTarget Germany AG Utilisation d'inhibiteurs d'histone déacetylase avec des composés AINS pour traiter le cancer et/ou les maladies inflammatoires
CA2619568A1 (fr) * 2005-08-19 2007-03-01 Government Of The United States Of America, Represented By The Secretary , Department Of Health And Human Services Formulations topiques d'inhibiteurs d'histone desacetylase et procedes d'utilisation de celles-ci
RU2008108221A (ru) * 2005-09-07 2009-10-20 Плекссикон, Инк. (Us) Соединения, активные в отношении ppar (рецепторов активаторов пролиферации пероксисом)
WO2007049262A1 (fr) 2005-10-27 2007-05-03 Berand Limited Procedes et compositions pour favoriser la croissance neuronale et le traitement de l'asociabilite et des troubles affectifs
AU2006313517B2 (en) * 2005-11-10 2013-06-27 Topotarget Uk Limited Histone deacetylase (HDAC) inhibitors (PXD101) for the treatment of cancer alone or in combination with chemotherapeutic agent
US8445198B2 (en) * 2005-12-01 2013-05-21 Medical Prognosis Institute Methods, kits and devices for identifying biomarkers of treatment response and use thereof to predict treatment efficacy
KR101415354B1 (ko) * 2006-02-22 2014-07-04 4에스체 악티엔게젤샤프트 Eg5 키네신 조절제로서의 인돌로피리딘
MX2008010799A (es) * 2006-02-22 2008-11-06 4Sc Ag Indolopiridinas como moduladores de quinesina eg5.
GB0606096D0 (en) 2006-03-27 2006-05-03 Cbmm Sa Screening method
EP1839656A1 (fr) * 2006-03-31 2007-10-03 TopoTarget Germany AG Utilisation d'acide valproic pour le traitement topique de doux de modérer vulgaris d'acné
EP2026805A1 (fr) * 2006-05-08 2009-02-25 Astex Therapeutics Limited Combinaisons pharmaceutiques de dérivés de diazole pour le traitement du cancer
JP2009539862A (ja) * 2006-06-09 2009-11-19 メリオン リサーチ Iii リミテッド 強化剤を含む固体経口投与剤形
WO2008011603A2 (fr) * 2006-07-20 2008-01-24 Wisconsin Alumni Research Foundation Modulation de la voie du signal notch1 pour le traitement de tumeurs neuroendocrines
JP2010509370A (ja) * 2006-11-10 2010-03-25 シンダックス ファーマシューティカルズ,インク. 癌の治療用のERα+リガンドとヒストンデアセチラーゼ阻害剤との組み合わせ
US8796330B2 (en) * 2006-12-19 2014-08-05 Methylgene Inc. Inhibitors of histone deacetylase and prodrugs thereof
WO2008090534A1 (fr) 2007-01-26 2008-07-31 Berand Limited Procédés et compositions destinés à l'inhibition d'un gain de poids excessif, la réduction de comportements alimentaires inappropriés et l'inhibition de l'hyperphagie pour le traitement de l'obésité
US7915245B2 (en) * 2007-02-01 2011-03-29 The Board Of Regents Of The University Of Texas System Methods and compositions of trail-death receptor agonists/activators
WO2008101121A2 (fr) * 2007-02-14 2008-08-21 Dana-Farber Cancer Institute, Inc. Procédés et compositions concernant la régulation de promoteurs par les protéines muc1 et klf
WO2008136838A1 (fr) * 2007-05-04 2008-11-13 Trustees Of Dartmouth College Nouveaux dérivés d'amide de cddo et leurs procédés d'utilisation
WO2008154402A2 (fr) * 2007-06-06 2008-12-18 University Of Maryland, Baltimore Inhibiteurs de hdac et médicaments ciblant une hormone pour le traitement du cancer
US20090246198A1 (en) * 2008-03-31 2009-10-01 Takeda Pharmaceutical Company Limited Mapk/erk kinase inhibitors and methods of use thereof
US20090270497A1 (en) * 2008-04-24 2009-10-29 Pharmacyclics, Inc. Treatment of Non-Localized Inflammation with pan-HDAC Inhibitors
WO2009137649A2 (fr) * 2008-05-07 2009-11-12 The Trustees Of The University Of Pennsylvania Procédés de traitement du cancer de la thyroïde

Also Published As

Publication number Publication date
US8642809B2 (en) 2014-02-04
JP2010540426A (ja) 2010-12-24
CA2700173A1 (fr) 2009-04-02
US20100286279A1 (en) 2010-11-11
EP2203421A2 (fr) 2010-07-07
WO2009040517A3 (fr) 2009-06-25
CN101868446A (zh) 2010-10-20
WO2009040517A2 (fr) 2009-04-02
CA2700173C (fr) 2016-10-11
MX2010003230A (es) 2010-04-07
EP2203421B1 (fr) 2014-05-07

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