FR15C0086I2 - Derives d'hydroxamate en tant qu'inhibiteurs de desacetylase - Google Patents

Derives d'hydroxamate en tant qu'inhibiteurs de desacetylase

Info

Publication number
FR15C0086I2
FR15C0086I2 FR15C0086C FR15C0086C FR15C0086I2 FR 15C0086 I2 FR15C0086 I2 FR 15C0086I2 FR 15C0086 C FR15C0086 C FR 15C0086C FR 15C0086 C FR15C0086 C FR 15C0086C FR 15C0086 I2 FR15C0086 I2 FR 15C0086I2
Authority
FR
France
Prior art keywords
desacetylase
inhibitors
hydroxamate derivatives
hydroxamate
derivatives
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.)
Active
Application number
FR15C0086C
Other languages
English (en)
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Novartis AG
Original Assignee
Novartis AG
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=26923760&utm_source=***_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=FR15C0086(I2) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Novartis AG filed Critical Novartis AG
Publication of FR15C0086I1 publication Critical patent/FR15C0086I1/fr
Application granted granted Critical
Publication of FR15C0086I2 publication Critical patent/FR15C0086I2/fr
Active legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04Indoles; Hydrogenated indoles
    • C07D209/10Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
    • C07D209/14Radicals substituted by nitrogen atoms, not forming part of a nitro radical
    • 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
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/622Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/626Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B
    • C04B35/63Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B using additives specially adapted for forming the products, e.g.. binder binders
    • C04B35/632Organic additives
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C259/00Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups
    • C07C259/04Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups without replacement of the other oxygen atom of the carboxyl group, e.g. hydroxamic acids
    • C07C259/06Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups without replacement of the other oxygen atom of the carboxyl group, e.g. hydroxamic acids having carbon atoms of hydroxamic groups bound to hydrogen atoms or to acyclic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04Indoles; Hydrogenated indoles
    • C07D209/10Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
    • C07D209/14Radicals substituted by nitrogen atoms, not forming part of a nitro radical
    • C07D209/16Tryptamines
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/64Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D295/00Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/04Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
    • C07D295/14Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D295/155Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals with the ring nitrogen atoms and the carbon atoms with three bonds to hetero atoms separated by carbocyclic rings or by carbon chains interrupted by carbocyclic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D307/00Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/77Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D307/78Benzo [b] furans; Hydrogenated benzo [b] furans
    • C07D307/79Benzo [b] furans; Hydrogenated benzo [b] furans with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the hetero ring
    • C07D307/81Radicals substituted by nitrogen atoms not forming part of a nitro radical
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/12Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Ceramic Engineering (AREA)
  • Manufacturing & Machinery (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Structural Engineering (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Medicinal Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Materials Engineering (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Indole Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Furan Compounds (AREA)
  • Heterocyclic Compounds That Contain Two Or More Ring Oxygen Atoms (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pyrane Compounds (AREA)
FR15C0086C 2000-09-01 2015-12-08 Derives d'hydroxamate en tant qu'inhibiteurs de desacetylase Active FR15C0086I2 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US22994300P 2000-09-01 2000-09-01
US29223201P 2001-05-18 2001-05-18
PCT/EP2001/010037 WO2002022577A2 (fr) 2000-09-01 2001-08-30 Inhibiteurs de desacetylase

Publications (2)

Publication Number Publication Date
FR15C0086I1 FR15C0086I1 (fr) 2016-01-15
FR15C0086I2 true FR15C0086I2 (fr) 2016-06-03

Family

ID=26923760

Family Applications (1)

Application Number Title Priority Date Filing Date
FR15C0086C Active FR15C0086I2 (fr) 2000-09-01 2015-12-08 Derives d'hydroxamate en tant qu'inhibiteurs de desacetylase

Country Status (36)

Country Link
US (5) US6552065B2 (fr)
EP (2) EP1318980B1 (fr)
JP (1) JP4012819B2 (fr)
KR (1) KR100585484B1 (fr)
CN (1) CN1300110C (fr)
AR (1) AR035057A1 (fr)
AT (1) ATE376999T1 (fr)
AU (2) AU8212901A (fr)
BE (1) BE2015C062I2 (fr)
BR (1) BRPI0113669B8 (fr)
CA (1) CA2420899C (fr)
CY (2) CY1107839T1 (fr)
CZ (1) CZ302707B6 (fr)
DE (1) DE60131179T2 (fr)
DK (1) DK1318980T3 (fr)
EC (1) ECSP034492A (fr)
ES (1) ES2292610T3 (fr)
FR (1) FR15C0086I2 (fr)
HK (1) HK1057746A1 (fr)
HU (2) HU229796B1 (fr)
IL (2) IL154574A0 (fr)
LU (1) LU92890I2 (fr)
MX (1) MXPA03001832A (fr)
MY (1) MY136892A (fr)
NL (1) NL300778I2 (fr)
NO (2) NO324942B1 (fr)
NZ (1) NZ524365A (fr)
PE (1) PE20020354A1 (fr)
PL (1) PL221738B1 (fr)
PT (1) PT1318980E (fr)
RU (1) RU2302408C3 (fr)
SI (1) SI1318980T1 (fr)
SK (1) SK287609B6 (fr)
TW (1) TWI286544B (fr)
WO (1) WO2002022577A2 (fr)
ZA (1) ZA200301423B (fr)

Families Citing this family (422)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6777217B1 (en) 1996-03-26 2004-08-17 President And Fellows Of Harvard College Histone deacetylases, and uses related thereto
US6822267B1 (en) * 1997-08-20 2004-11-23 Advantest Corporation Signal transmission circuit, CMOS semiconductor device, and circuit board
WO2001038322A1 (fr) 1999-11-23 2001-05-31 Methylgene, Inc. Inhibiteurs de l'histone deacetylase
US20030129724A1 (en) 2000-03-03 2003-07-10 Grozinger Christina M. Class II human histone deacetylases, and uses related thereto
PE20020354A1 (es) * 2000-09-01 2002-06-12 Novartis Ag Compuestos de hidroxamato como inhibidores de histona-desacetilasa (hda)
EP1598067B1 (fr) 2000-09-29 2009-05-06 TopoTarget UK Limited Derivées d'acide de carbamine contenant un group amide pour la traitement de malaria
US7312247B2 (en) * 2001-03-27 2007-12-25 Errant Gene Therapeutics, Llc Histone deacetylase inhibitors
US20040087657A1 (en) 2001-10-16 2004-05-06 Richon Victoria M. Treatment of neurodegenerative diseases and cancer of the brain using histone deacetylase inhibitors
CN100457183C (zh) * 2001-11-06 2009-02-04 诺瓦提斯公司 环氧酶-2抑制剂/组蛋白脱乙酰酶抑制剂的组合
EP1487426B1 (fr) 2002-03-04 2012-08-22 Sloan-kettering Institute For Cancer Research Procedes d'induction de differenciation terminale
US7148257B2 (en) 2002-03-04 2006-12-12 Merck Hdac Research, Llc Methods of treating mesothelioma with suberoylanilide hydroxamic acid
US7456219B2 (en) 2002-03-04 2008-11-25 Merck Hdac Research, Llc Polymorphs of suberoylanilide hydroxamic acid
NZ536116A (en) 2002-04-03 2007-01-26 Topotarget Uk Ltd Carbamic acid compounds comprising a piperazine linkage as HDAC inhibitors
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
CN100566711C (zh) * 2002-04-15 2009-12-09 斯隆-凯特林癌症研究院 治疗癌症的化合物及其用途
ATE476995T1 (de) * 2002-06-10 2010-08-15 Novartis Pharma Gmbh Epothilone enthaltende kombinationen und deren pharmazeutische verwendungen
CA2495354A1 (fr) * 2002-08-20 2004-03-04 Yamanouchi Pharmaceutical Co., Ltd. Agent inhibant la degradation de la matrice extracellulaire du cartilage articulaire
JP2006501267A (ja) * 2002-09-13 2006-01-12 バージニア コモンウェルス ユニバーシティー 白血病の処置のためのa)N−{5−[4−(4−メチル−ピペラジノ−メチル)−ベンゾイルアミド]−2−メチルフェニル}−4−(3−ピリジル)−2−ピリミジン−アミンおよびb)ヒストンデアセチラーゼインヒビターの組合せ剤
US7154002B1 (en) 2002-10-08 2006-12-26 Takeda San Diego, Inc. Histone deacetylase inhibitors
US7250514B1 (en) 2002-10-21 2007-07-31 Takeda San Diego, Inc. Histone deacetylase inhibitors
WO2004046107A1 (fr) * 2002-11-19 2004-06-03 Takeda Pharmaceutical Company Limited Derives d'indole servant d'antagoniste de somatostatine
AU2003296310A1 (en) 2002-12-06 2004-06-30 University Of South Florida Histone deacetylase inhibitor enhancement of trail-induced apoptosis
US7135493B2 (en) 2003-01-13 2006-11-14 Astellas Pharma Inc. HDAC inhibitor
WO2004065354A1 (fr) 2003-01-17 2004-08-05 Topotarget Uk Limited Composes d'acide carbamique comprenant une liaison ester ou cetone, utilises comme inhibiteurs de l'histone desacetylase
AU2003900608A0 (en) * 2003-02-11 2003-02-27 Fujisawa Pharmaceutical Co., Ltd. Hdac inhibitor
AU2003900587A0 (en) * 2003-02-11 2003-02-27 Fujisawa Pharmaceutical Co., Ltd. Hdac inhibitor
JP4790594B2 (ja) 2003-02-25 2011-10-12 トポターゲット ユーケー リミテッド Hdacインヒビターとしての、二環式ヘテロアリール基を含むヒドロキサム酸化合物
US7375228B2 (en) * 2003-03-17 2008-05-20 Takeda San Diego, Inc. Histone deacetylase inhibitors
US20070123580A1 (en) * 2003-05-21 2007-05-31 Atadja Peter W Combination of histone deacetylase inhibitors with chemotherapeutic agents
WO2005011598A2 (fr) 2003-07-31 2005-02-10 University Of South Florida Composition et methode de traitement de la leucemie
JP2007501775A (ja) * 2003-08-07 2007-02-01 ノバルティス アクチエンゲゼルシャフト 免疫抑制剤としてのヒストンデアセチラーゼ阻害剤
BRPI0413439A (pt) * 2003-08-08 2006-10-17 Novartis Ag combinações compreendendo estaurosporinas
DK1663194T3 (da) 2003-08-26 2010-07-19 Merck Hdac Res Llc Anvendelse af SAHA til behandling af mesotheliom
CN1964714B (zh) 2003-08-29 2011-09-28 Hdac默克研究有限责任公司 辛二酰苯胺异羟肟酸和吉西他滨在制备用于治疗癌症的药物中的用途
CN100455564C (zh) * 2003-09-12 2009-01-28 深圳微芯生物科技有限责任公司 组蛋白去乙酰化酶抑制剂及其药用制剂的制备和应用
CA2539000A1 (fr) * 2003-09-18 2005-03-24 Novartis Ag Combinaison d'un inhibiteur de l'histone desacetylase avec un ligand des recepteurs de mort
SI1673349T1 (sl) * 2003-09-22 2010-10-29 S Bio Pte Ltd Derivati benzimidazola: priprava in farmacevtske uporabe
US7781595B2 (en) 2003-09-22 2010-08-24 S*Bio Pte Ltd. Benzimidazole derivatives: preparation and pharmaceutical applications
AU2004273615B2 (en) * 2003-09-23 2009-01-15 Novartis Ag Combination of a VEGF receptor inhibitor with a chemotherapeutic agent
US20070167499A1 (en) * 2003-10-27 2007-07-19 A*Bio Pte Ltd. Biaryl linked hydroxamates: preparation and pharmaceutical applications
CA2552279C (fr) 2003-12-02 2014-07-15 The Ohio State University Research Foundation Acides gras a chaine courte lies a un motif de chelation zn<sp>2+</sp> utilises en tant que nouvelle classe d'inhibiteurs d'histone desacetylase
EP1541549A1 (fr) * 2003-12-12 2005-06-15 Exonhit Therapeutics S.A. Dérivés tricycliques d'hydroxamate et de benzamide, compositions et methodes
WO2005066151A2 (fr) * 2003-12-19 2005-07-21 Takeda San Diego, Inc. Inhibiteurs d'histone desacetylase
US20050159470A1 (en) * 2003-12-19 2005-07-21 Syrrx, Inc. Histone deacetylase inhibitors
US20050197336A1 (en) * 2004-03-08 2005-09-08 Miikana Therapeutics Corporation Inhibitors of histone deacetylase
US7345043B2 (en) * 2004-04-01 2008-03-18 Miikana Therapeutics Inhibitors of histone deacetylase
AR048927A1 (es) 2004-04-07 2006-06-14 Novartis Ag Compuestos heterociclicos como inhibidores de proteinas de apoptosis (iap); composiciones farmaceuticas que los contienen y su uso en el tratamiento de una enfermedad proliferativa
CA2574035A1 (fr) * 2004-07-19 2006-02-23 Sandro Belvedere Inhibiteurs de l'histone deacetylase
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
ITMI20041869A1 (it) 2004-10-01 2005-01-01 Dac Srl Nuovi inibitori delle istone deacetilasi
US8242175B2 (en) 2004-10-01 2012-08-14 Dac S.R.L. Class of histone deacetylase inhibitors
US20070021612A1 (en) * 2004-11-04 2007-01-25 University Of Notre Dame Du Lac Processes and compounds for preparing histone deacetylase inhibitors and intermediates thereof
US7235688B1 (en) 2004-11-04 2007-06-26 University Of Notre Dame Du Lac Process for preparing histone deacetylase inhibitors and intermediates thereof
JP2008524246A (ja) * 2004-12-16 2008-07-10 タケダ サン ディエゴ インコーポレイテッド ヒストンデアセチラーゼ阻害剤
US7772245B2 (en) 2005-02-14 2010-08-10 Miikana Therapeutics, Inc. Inhibitors of histone deacetylase
US7666880B2 (en) 2005-03-21 2010-02-23 S*Bio Pte Ltd. Imidazo[1,2-A]pyridine derivatives: preparation and pharmaceutical applications
CN101495116A (zh) 2005-03-22 2009-07-29 哈佛大学校长及研究员协会 蛋白降解病症的治疗
GB0509223D0 (en) * 2005-05-05 2005-06-15 Chroma Therapeutics Ltd Enzyme inhibitors
GB0509225D0 (en) 2005-05-05 2005-06-15 Chroma Therapeutics Ltd Inhibitors of enzymatic activity
JP2008540574A (ja) * 2005-05-11 2008-11-20 タケダ サン ディエゴ インコーポレイテッド ヒストンデアセチラーゼ阻害剤
TWI365068B (en) 2005-05-20 2012-06-01 Merck Sharp & Dohme Formulations of suberoylanilide hydroxamic acid and methods for producing same
GB0510390D0 (en) 2005-05-20 2005-06-29 Novartis Ag Organic compounds
CN101263121A (zh) * 2005-07-14 2008-09-10 塔克达圣地亚哥公司 组蛋白脱乙酰基酶抑制剂
WO2007016532A2 (fr) * 2005-08-02 2007-02-08 Novartis Ag Mutations et polymorphismes de hdac4
BRPI0614090A2 (pt) 2005-08-03 2011-03-09 Novartis Ag uso de inibidores da hdac para o tratamento do mieloma
CN101282718A (zh) * 2005-08-10 2008-10-08 诺瓦提斯公司 脱乙酰酶抑制剂的使用方法
CA2617979A1 (fr) * 2005-08-11 2007-02-22 Novartis Ag Combinaison de composes organiques
EP2258359A3 (fr) 2005-08-26 2011-04-06 Braincells, Inc. Neurogenèse par modulation des récepteurs muscariniques avec sabcomeline
US7678363B2 (en) 2005-08-26 2010-03-16 Braincells Inc Methods of treating psychiatric conditions comprising administration of muscarinic agents in combination with SSRIs
CA2620414A1 (fr) * 2005-08-26 2007-03-01 Methylgene Inc. Inhibiteurs d'analogues de benzodiazepine et de benzopiperazine de l'histone deacetylase
WO2007030455A2 (fr) * 2005-09-07 2007-03-15 Novartis Ag Mutations et polymorphismes de hdac10
WO2007030454A2 (fr) * 2005-09-07 2007-03-15 Novartis Ag Mutations et polymorphismes de hdac9
WO2007038073A2 (fr) * 2005-09-22 2007-04-05 Novartis Ag Mutations et polymorphismes de l’hdac11
WO2007038459A2 (fr) 2005-09-27 2007-04-05 Novartis Ag Composes de carboxyamine et leurs methodes d'utilisation
EP1940389A2 (fr) 2005-10-21 2008-07-09 Braincells, Inc. Modulation de la neurogenese par inhibition de la pde
WO2007047998A2 (fr) * 2005-10-21 2007-04-26 Novartis Ag Mutations et polymorphismes du gène de l'hdac2
RU2436572C2 (ru) 2005-10-24 2011-12-20 Новартис Аг Комбинация ингибиторов гистондеацетилазы и излучения
US20070112017A1 (en) 2005-10-31 2007-05-17 Braincells, Inc. Gaba receptor mediated modulation of neurogenesis
WO2007053502A2 (fr) * 2005-11-01 2007-05-10 Novartis Ag Mutations et polymorphismes de l'hdac5
WO2007058992A2 (fr) * 2005-11-14 2007-05-24 Novartis Ag Mutations et polymorphismes de hdac6
KR20080071600A (ko) 2005-11-21 2008-08-04 노파르티스 아게 Mtor 억제제를 사용하는 신경내분비 종양 치료법
US20070207950A1 (en) * 2005-12-21 2007-09-06 Duke University Methods and compositions for regulating HDAC6 activity
JP2009525955A (ja) * 2006-01-13 2009-07-16 タケダ サン ディエゴ インコーポレイテッド ヒストンデアセチラーゼ阻害剤
PL1981877T3 (pl) * 2006-02-07 2012-12-31 Astellas Pharma Inc Związki N-hydroksyakryloamidowe
WO2008091349A1 (fr) * 2006-02-14 2008-07-31 The President And Fellows Of Harvard College Inhibiteurs bifonctionnels d'histone déacétylase
US20100216734A1 (en) 2006-03-08 2010-08-26 Braincells, Inc. Modulation of neurogenesis by nootropic agents
GB0605120D0 (en) 2006-03-14 2006-04-26 Novartis Ag Organic Compounds
CN101415424B (zh) 2006-04-05 2012-12-05 诺瓦提斯公司 用于治疗癌症、包含bcr-abl/c-kit/pdgf-r tk抑制剂的组合
CA2645633A1 (fr) 2006-04-05 2007-11-01 Novartis Ag Combinaisons d'agents therapeutiques pour traiter un cancer
EP2450437B1 (fr) 2006-04-14 2017-05-17 Cell Signaling Technology, Inc. Défauts de gène et ALK kinase mutante dans des tumeurs solides humaines
US8168383B2 (en) 2006-04-14 2012-05-01 Cell Signaling Technology, Inc. Gene defects and mutant ALK kinase in human solid tumors
US20100137239A1 (en) 2006-04-24 2010-06-03 Gloucester Pharmaceuticals Gemcitabine combination therapy
US20090018142A9 (en) * 2006-05-02 2009-01-15 Zhengping Zhuang Use of phosphatases to treat tumors overexpressing N-CoR
BRPI0711385A2 (pt) 2006-05-09 2011-11-08 Novartis Ag combinação compreendendo um quelante de ferro e um agente anti-neoplástico e seu uso
EP2021000A2 (fr) 2006-05-09 2009-02-11 Braincells, Inc. Neurogenèse par modulation de l'angiotensine
MX2008014320A (es) 2006-05-09 2009-03-25 Braincells Inc Neurogenesis mediada por el receptor de 5-hidroxitriptamina.
WO2007146730A2 (fr) 2006-06-08 2007-12-21 Gloucester Pharmaceuticals Thérapie à base d'inhibiteurs de désacétylase (dac)
CN101466672B (zh) * 2006-06-12 2012-05-16 诺瓦提斯公司 N-羟基-3-[4-[[[2-(2-甲基-1h-吲哚-3-基)乙基]氨基]甲基]苯基]-2e-2-丙烯酰胺的盐
MX2008015901A (es) * 2006-06-12 2009-01-12 Novartis Ag Sales de n-hidroxi-3-[4-[[[2-(2-metil-1h-indol-3-il)etil]amino]met il]fenil]-2e-2-propenamida.
BRPI0712847A2 (pt) * 2006-06-12 2012-08-07 Novartis Ag processo para a produÇço de n-hidràxi-3-[4-[[2-(metil-1h-indol-3-il)e-til]amino]metil]f enil]-2e-2-propenamida e materiais de partida para este.
KR20140142335A (ko) * 2006-06-12 2014-12-11 노파르티스 아게 N-히드록시-3-〔4-〔〔〔2-(2-메틸-1h-인돌-3-일)에틸〕아미노〕메틸〕페닐〕-2e-2-프로펜아미드의 동질이상체
NZ572744A (en) * 2006-06-12 2011-05-27 Novartis Ag Process for making salts of n-hydroxy-3-[4-[[[2-(2-methyl-1h-indol-3-yl)ethyl]amino]methyl]phenyl]-2e-2-propenamide
US20100008923A1 (en) * 2006-06-26 2010-01-14 Novartis Ag Organic Compounds
EP2068872A1 (fr) 2006-09-08 2009-06-17 Braincells, Inc. Combinaisons contenant un dérivé de 4-acylaminopyridine
US20100184806A1 (en) 2006-09-19 2010-07-22 Braincells, Inc. Modulation of neurogenesis by ppar agents
ES2561835T3 (es) 2006-09-20 2016-03-01 Mei Pharma, Inc. Compuestos hidroxamato de imidazo[1,2-a]piridina que son inhibidores de la histona desacetilasa
JP2010504969A (ja) * 2006-09-28 2010-02-18 メルク エンド カムパニー インコーポレーテッド Sahaのアミン塩基塩及びその多形
BRPI0717564A2 (pt) 2006-09-29 2013-10-22 Novartis Ag Pirazolopirimidinas como inibidores de pi3k lipídeo cinase
GB0619753D0 (en) 2006-10-06 2006-11-15 Chroma Therapeutics Ltd Enzyme inhibitors
EA017198B1 (ru) 2006-10-30 2012-10-30 Хрома Терапьютикс Лтд. Гидроксаматы в качестве ингибиторов гистон-деацетилазы
EP2099443A4 (fr) * 2006-11-10 2010-05-05 Syndax Pharmaceuticals Inc Association de ligands de era+ et d'inhibiteurs de l'histone désacétylase dans le traitement du cancer
AU2007328281B2 (en) * 2006-12-04 2011-03-31 Novartis Ag Combination of an HDAC inhibitor and an antimetabolite
CA2671993A1 (fr) * 2006-12-15 2008-06-26 Astellas Pharma Inc. Composes de n-hydroxyacrylamide
WO2008086330A2 (fr) * 2007-01-10 2008-07-17 Novartis Ag Formulations d'inhibiteurs de la déacétylase
WO2008097561A1 (fr) 2007-02-06 2008-08-14 Lixte Biotechology Holdings, Inc. Oxabicycloheptanes et oxabicycloheptènes, leur préparation et leur utilisation
AU2008216327A1 (en) 2007-02-15 2008-08-21 Novartis Ag Combination of LBH589 with other therapeutic agents for treating cancer
US20100056522A1 (en) 2007-03-28 2010-03-04 Santen Pharmaceutical Co., Ltd. Intraocular pressure-lowering agent comprising compound having histone deacetylase inhibitor effect as active ingredient
CN101679220A (zh) * 2007-04-09 2010-03-24 梅特希尔基因公司 组蛋白脱乙酰酶抑制剂
BRPI0811112A2 (pt) * 2007-05-04 2014-12-23 Novartis Ag Uso de inibidores de hdac para o tratamento de cânceres gastrointestinais.
TW200911231A (en) * 2007-05-11 2009-03-16 Novartis Ag Use of HDAC inhibitors for the treatment of melanoma
AU2008260236A1 (en) * 2007-05-30 2008-12-11 Novartis Ag Use of HDAC inhibitors for the treatment of bone destruction
US7737175B2 (en) 2007-06-01 2010-06-15 Duke University Methods and compositions for regulating HDAC4 activity
AU2008284364A1 (en) * 2007-08-03 2009-02-12 Lixte Biotechnology, Inc. Use of phosphatases to treat neuroblastomas and medulloblastomas
CL2008002786A1 (es) * 2007-09-20 2009-05-15 Novartis Ag Torta farmceuticamente aceptable, formada por liofilizacion, que comprende: n-hidroxi-3-[4-[[[2-(2-metil-1h-indol-3-il]-etil]-amino]-metil]-fenil]-2e-2-propenamida o una sal, un regulador de ph seleciondo de lactato o acidop lactico, fodfato o acido fosforico o una combinacion y un agente de volumen; proceso de elaboracion.
CN101854804B (zh) 2007-10-01 2014-07-23 利克斯特生物技术公司 Hdac抑制剂
BRPI0817860A2 (pt) * 2007-10-22 2019-09-24 Orchid Res Laboratories Limited inibidores de histona deacetilase
CN101417967A (zh) * 2007-10-26 2009-04-29 浙江海正药业股份有限公司 组蛋白去乙酰酶抑制剂、其组合物及其应用
US20090131367A1 (en) * 2007-11-19 2009-05-21 The Regents Of The University Of Colorado Combinations of HDAC Inhibitors and Proteasome Inhibitors
US20110044952A1 (en) * 2007-11-27 2011-02-24 Ottawa Health Research Institute Amplification of cancer-specific oncolytic viral infection by histone deacetylase inhibitors
CA2708281A1 (fr) 2007-12-11 2009-08-27 Viamet Pharmaceuticals, Inc. Inhibiteurs de metalloenzymes utilisant des fractions de liaison a un metal en combinaison avec des fractions de ciblage
ITFI20070288A1 (it) 2007-12-21 2009-06-22 A I L Firenze Sezione Autonoma Inibitori delle deacetilasi istoniche
EP2100879A1 (fr) * 2008-03-13 2009-09-16 4Sc Ag Nouveaux composants d'acide hydroxamique tetrahydroisoquinoline/ isoindoline substitués N
ES2524259T3 (es) 2008-03-24 2014-12-04 Novartis Ag Inhibidores de metaloproteinasa de matriz a base de arilsulfonamida
MY150437A (en) * 2008-03-26 2014-01-30 Novartis Ag Hydroxamate-based inhibitors of deacetylases b
BRPI0915927A2 (pt) * 2008-07-18 2016-06-07 Novartis Ag uso de inibiodores de hdac para o tratamento da doença de hodgkin
RU2515611C2 (ru) 2008-07-23 2014-05-20 Президент Энд Феллоуз Оф Гарвард Колледж Ингибиторы деацетилазы и их применение
CA2730148C (fr) * 2008-08-01 2018-04-03 Lixte Biotechnology, Inc. Agents neuroprotecteurs pour la prevention et le traitement de maladies neurodegeneratives
CA2730428A1 (fr) * 2008-08-01 2010-02-04 Lixte Biotechnology, Inc. Procedes de regulation de la mitose cellulaire par inhibition de la phosphatase de serine/threonine
US8227473B2 (en) 2008-08-01 2012-07-24 Lixte Biotechnology, Inc. Oxabicycloheptanes and oxabicycloheptenes, their preparation and use
WO2010147612A1 (fr) 2009-06-18 2010-12-23 Lixte Biotechnology, Inc. Procédés de modulation de la régulation cellulaire par inhibition de p53
WO2010083617A1 (fr) 2009-01-21 2010-07-29 Oncalis Ag Pyrazolopyrimidines en tant qu'inhibiteurs de protéines kinases
ES2396023T3 (es) 2009-01-29 2013-02-18 Novartis Ag Bencimidazoles sustituidos para el tratamiento de astrocitomas
US20100216805A1 (en) 2009-02-25 2010-08-26 Braincells, Inc. Modulation of neurogenesis using d-cycloserine combinations
GB0903480D0 (en) * 2009-02-27 2009-04-08 Chroma Therapeutics Ltd Enzyme Inhibitors
KR101168801B1 (ko) 2009-03-27 2012-07-25 주식회사종근당 신규한 하이드록사메이트 유도체, 이의 제조방법, 및 이를 함유하는 약제학적 조성물
US7994357B2 (en) 2009-04-03 2011-08-09 Naturewise Biotech & Medicals Corporation Cinamic compounds and derivatives therefrom for the inhibition of histone deacetylase
EP2236503B1 (fr) 2009-04-03 2014-02-26 NatureWise Biotech & Medicals Corporation Composants cinnamiques et dérivés de celui-ci pour l'inhibition de l'histone désacétylase
EP2454267A2 (fr) 2009-07-16 2012-05-23 Royal College of Surgeons in Ireland Complexes métalliques ayant une double activité inhibitrice d'histone désacétylase et de liaison à l'adn
US8389526B2 (en) 2009-08-07 2013-03-05 Novartis Ag 3-heteroarylmethyl-imidazo[1,2-b]pyridazin-6-yl derivatives
WO2011019393A2 (fr) 2009-08-11 2011-02-17 President And Fellows Of Harvard College Inhibiteurs de hdac classe- et isoforme-spécifiques et utilisations de ceux-ci
JP5781510B2 (ja) 2009-08-12 2015-09-24 ノバルティス アーゲー ヘテロ環式ヒドラゾン化合物および癌および炎症の処置のためのそれらの使用
JP5819831B2 (ja) 2009-08-17 2015-11-24 インテリカイン, エルエルシー 複素環式化合物およびそれらの使用
WO2011020861A1 (fr) 2009-08-20 2011-02-24 Novartis Ag Composés d'oximes hétérocycliques
EP2470502A1 (fr) 2009-08-26 2012-07-04 Novartis AG Composés hétéroaryliques tétrasubstitués et leur utilisation comme modulateurs de mdm2 et/ou mdm4
US20110053925A1 (en) * 2009-08-28 2011-03-03 Novartis Ag Hydroxamate-Based Inhibitors of Deacetylases
AR077975A1 (es) 2009-08-28 2011-10-05 Irm Llc Derivados de pirazol pirimidina y composiciones como inhibidores de cinasa de proteina
PE20121471A1 (es) 2009-11-04 2012-11-01 Novartis Ag Derivados de sulfonamida heterociclicos utiles como inhibidores de mek
JP6220126B2 (ja) 2009-11-23 2017-10-25 セルリアン・ファーマ・インコーポレイテッド 治療的送達のためのシクロデキストリンに基づく重合体
EA201200823A1 (ru) 2009-12-08 2013-02-28 Новартис Аг Гетероциклические производные сульфонамидов
CU24130B1 (es) 2009-12-22 2015-09-29 Novartis Ag Isoquinolinonas y quinazolinonas sustituidas
US8440693B2 (en) 2009-12-22 2013-05-14 Novartis Ag Substituted isoquinolinones and quinazolinones
EP2638009A4 (fr) * 2010-01-08 2014-06-11 Harvard College Inhibiteurs fluorés de hdac et leurs utilisations
US8981084B2 (en) 2010-01-13 2015-03-17 Tempero Pharmaceuticals, Inc. Oxadiazole HDAC inhibitors
WO2011088181A1 (fr) 2010-01-13 2011-07-21 Tempero Pharmaceuticals, Inc. Composés et procédés
US20110178287A1 (en) 2010-01-19 2011-07-21 Cerulean Pharma Inc. Cyclodextrin-based polymers for therapeutic delivery
UY33236A (es) 2010-02-25 2011-09-30 Novartis Ag Inhibidores dimericos de las iap
US8217079B2 (en) 2010-03-26 2012-07-10 Italfarmaco Spa Method for treating Philadelphia-negative myeloproliferative syndromes
WO2011119995A2 (fr) 2010-03-26 2011-09-29 Cerulean Pharma Inc. Formulations et procédés d'utilisation
UA112517C2 (uk) 2010-07-06 2016-09-26 Новартіс Аг Тетрагідропіридопіримідинові похідні
EP2407164A1 (fr) 2010-07-14 2012-01-18 Dublin Institute of Technology Intellectual Property Ltd Complexes de cuivre II et de phenanthroline et leur utilisation dans le traitement du cancer
WO2012025701A1 (fr) * 2010-08-25 2012-03-01 Chroma Therapeutics Ltd. Dérivés d'ester de glycine alpha, alpha-disubstituée et leur utilisation comme inhibiteurs des hdac
WO2012025155A1 (fr) * 2010-08-26 2012-03-01 Novartis Ag Composés à base d'hydroxamate en tant qu'inhibiteurs des désacétylases
KR20140011301A (ko) * 2010-08-27 2014-01-28 노파르티스 아게 데아세틸라제의 히드록사메이트-기반 억제제
WO2012080260A1 (fr) 2010-12-13 2012-06-21 Novartis Ag Inhibiteurs iap dimériques
UY33794A (es) 2010-12-13 2012-07-31 Novartis Ag Inhibidores diméricos de las iap
WO2012097013A1 (fr) 2011-01-10 2012-07-19 Nimbus Iris, Inc. Inhibiteurs d'irak et leurs utilisation
TW201245115A (en) * 2011-01-24 2012-11-16 Chdi Foundation Inc Histone deacetylase inhibitors and compositions and methods of use thereof
JP2014505088A (ja) 2011-02-10 2014-02-27 ノバルティス アーゲー C−METチロシンキナーゼ阻害剤としての[1,2,4]トリアゾロ[4,3−b]ピリダジン化合物
WO2012116237A2 (fr) 2011-02-23 2012-08-30 Intellikine, Llc Composés hétérocycliques et leurs utilisations
AR085397A1 (es) 2011-02-23 2013-09-25 Intellikine Inc Combinacion de inhibidores de quinasa y sus usos
CN110063951A (zh) 2011-03-09 2019-07-30 赛伦诺科学有限公司 利用组蛋白脱乙酰酶抑制物改善受损的内源纤维蛋白溶解作用的化合物和方法
MX2013014398A (es) 2011-06-09 2014-03-21 Novartis Ag Derivados de sulfonamida heterociclicos.
PE20140604A1 (es) 2011-06-14 2014-05-13 Novartis Ag Combinacion de panobinostat y ruxolitinib en el tratamiento del cancer tal como una neoplasia mieloproliferativa
WO2012175520A1 (fr) 2011-06-20 2012-12-27 Novartis Ag Dérivés d'isoquinolinone substitués par un hydroxy
EP2721007B1 (fr) 2011-06-20 2015-04-29 Novartis AG Composés de cyclohexyl-isoquinolinone
CA2840315A1 (fr) 2011-06-27 2013-01-03 Novartis Ag Formes solides et sels de derives de tetrahydro-pyrido-pyrimidine
JP5957526B2 (ja) 2011-09-15 2016-07-27 ノバルティス アーゲー チロシンキナーゼとしての6−置換3−(キノリン−6−イルチオ)−[1,2,4]トリアゾロ[4,3−a]ピラジン
WO2013070996A1 (fr) 2011-11-11 2013-05-16 Novartis Ag Procédé de traitement d'une maladie proliférative
KR102091295B1 (ko) 2011-11-23 2020-03-19 어레이 바이오파마 인크. 제약 제제
CN103130673B (zh) * 2011-11-28 2017-05-03 重庆医药工业研究院有限责任公司 一种阿戈美拉晶型i的制备方法
US8969341B2 (en) 2011-11-29 2015-03-03 Novartis Ag Pyrazolopyrrolidine compounds
US9408885B2 (en) 2011-12-01 2016-08-09 Vib Vzw Combinations of therapeutic agents for treating melanoma
PL2794600T3 (pl) 2011-12-22 2018-06-29 Novartis Ag Pochodne 2,3-dihydro-benzo[1,4]oksazyny i powiązane związki jako inhibitory kinazy fosfoinozytydu-3 (PI3K) do leczenia np. reumatoidalnego zapalenia stawów
US20150148377A1 (en) 2011-12-22 2015-05-28 Novartis Ag Quinoline Derivatives
WO2013096060A1 (fr) 2011-12-23 2013-06-27 Novartis Ag Composés inhibiteurs de l'interaction entre bcl2 et des partenaires de liaison
US20130178520A1 (en) 2011-12-23 2013-07-11 Duke University Methods of treatment using arylcyclopropylamine compounds
KR20140107575A (ko) 2011-12-23 2014-09-04 노파르티스 아게 Bcl2와 결합 파트너의 상호작용을 억제하기 위한 화합물
CN104125954A (zh) 2011-12-23 2014-10-29 诺华股份有限公司 用于抑制bcl2与结合配偶体相互作用的化合物
JP2015503516A (ja) 2011-12-23 2015-02-02 ノバルティス アーゲー Bcl2と結合相手の相互作用を阻害するための化合物
US9126980B2 (en) 2011-12-23 2015-09-08 Novartis Ag Compounds for inhibiting the interaction of BCL2 with binding partners
JP2015504056A (ja) * 2011-12-29 2015-02-05 ファーマサイクリックス,インク. ヒストンデアセチラーゼ8の阻害剤としての珪皮酸ヒドロキシアミド
CA2861066C (fr) 2012-01-12 2024-01-02 Yale University Composes et procedes pour la degradation amelioree de proteines cibles et d'autres polypeptides par une e3 ubiquitine ligase
US8815926B2 (en) 2012-01-26 2014-08-26 Novartis Ag Substituted pyrrolo[3,4-D]imidazoles for the treatment of MDM2/4 mediated diseases
AR092790A1 (es) * 2012-02-01 2015-05-06 Euro Celtique Sa Derivados bencimidazolicos del acido hidroxamico
EP3964513A1 (fr) 2012-04-03 2022-03-09 Novartis AG Produits combinés comprenant des inhibiteurs de tyrosine kinase et leur utilisation
CN104302634B (zh) 2012-05-15 2017-02-08 诺华股份有限公司 用于抑制abl1、abl2和bcr‑abl1的活性的苯甲酰胺衍生物
SI2861579T1 (en) 2012-05-15 2018-05-31 Novartis Ag Benzamide derivatives for inhibiting the activity of ABL1, ABL2 and BCR-ABL1
EA201492005A1 (ru) 2012-05-15 2015-04-30 Новартис Аг Бензамидные производные для ингибирования активности abl1, abl2 и bcr-abl1
MX357305B (es) 2012-05-15 2018-07-04 Novartis Ag Compuestos y composiciones para inhibir la actividad de abl-1, abl-2, y bcr-abl1.
EP2855483B1 (fr) 2012-05-24 2017-10-25 Novartis AG Composés pyrrolopyrrolidinones
CN104582732A (zh) 2012-06-15 2015-04-29 布里格姆及妇女医院股份有限公司 治疗癌症的组合物及其制造方法
AR091773A1 (es) 2012-07-16 2015-02-25 Chdi Foundation Inc Inhibidores de la histona desacetilasa y composiciones y sus metodos de uso
EP2879675B1 (fr) 2012-08-06 2019-11-13 Duke University Composés et procédés pour le ciblage de hsp90
CA2885969C (fr) 2012-10-02 2021-04-06 Epitherapeutics Aps Derives de pyridine substitues et leurs compositions utiles comme inhibiteurs d'histone demethylases
EP3662911A1 (fr) 2012-10-30 2020-06-10 MEI Pharma, Inc. Combinaison d'azacitide et de pracinostat pour traiter le syndrome myélodysplasique (mds)
AU2013337247B2 (en) 2012-11-05 2018-08-09 Dana-Farber Cancer Institute, Inc. XBP1, CD138, and CS1 peptides, pharmaceutical compositions that include the peptides, and methods of using such peptides and compositions
US20150283136A1 (en) 2012-11-08 2015-10-08 Novartis Ag Pharmaceutical combination comprising a b-raf inhibitor and a histone deacetylase inhibitor and their use in the treatment of proliferative diseases
TW201422625A (zh) 2012-11-26 2014-06-16 Novartis Ag 二氫-吡啶并-□衍生物之固體形式
WO2014115077A1 (fr) 2013-01-22 2014-07-31 Novartis Ag Composés de purinone substitués
US9556180B2 (en) 2013-01-22 2017-01-31 Novartis Ag Pyrazolo[3,4-d]pyrimidinone compounds as inhibitors of the P53/MDM2 interaction
WO2014128612A1 (fr) 2013-02-20 2014-08-28 Novartis Ag Dérivés de quinazolin-4-one
US9650339B2 (en) 2013-02-27 2017-05-16 Gilead Sciences, Inc. Inhibitors of histone demethylases
CN105246482A (zh) 2013-03-15 2016-01-13 因特利凯有限责任公司 激酶抑制剂的组合及其用途
WO2014155268A2 (fr) 2013-03-25 2014-10-02 Novartis Ag Inhibiteurs de kinase tyrosine fgf-r et leur utilisation dans le traitement de maladies associées à un manque ou à une absence d'activité snf5
JP2016519684A (ja) 2013-04-08 2016-07-07 デニス エム ブラウン 準最適に投与された薬物療法の有効性を改善するための及び/又は副作用を低減するための方法および組成物
CA2909160C (fr) 2013-04-09 2021-05-25 Lixte Biotechnology, Inc. Formulations d'oxabicycloheptanes et d'oxabicycloheptenes
US9878986B2 (en) 2013-04-29 2018-01-30 Chong Kun Dang Pharmaceutical Corp. Compounds for selective histone deacetylase inhibitors, and pharmaceutical composition comprising the same
US20150018376A1 (en) 2013-05-17 2015-01-15 Novartis Ag Pyrimidin-4-yl)oxy)-1h-indole-1-carboxamide derivatives and use thereof
GB201311888D0 (en) 2013-07-03 2013-08-14 Glaxosmithkline Ip Dev Ltd Novel compounds
GB201311891D0 (en) 2013-07-03 2013-08-14 Glaxosmithkline Ip Dev Ltd Novel compound
UY35675A (es) 2013-07-24 2015-02-27 Novartis Ag Derivados sustituidos de quinazolin-4-ona
KR20160099081A (ko) 2013-07-26 2016-08-19 업데이트 파마 인코포레이트 비산트렌의 치료 효과 개선용 조합 방법
US9227969B2 (en) 2013-08-14 2016-01-05 Novartis Ag Compounds and compositions as inhibitors of MEK
WO2015022664A1 (fr) 2013-08-14 2015-02-19 Novartis Ag Composés et compositions utiles comme inhibiteurs de mek
WO2015022663A1 (fr) 2013-08-14 2015-02-19 Novartis Ag Composés et compositions utiles comme inhibiteurs de mek
KR20160060100A (ko) 2013-09-22 2016-05-27 칼리토르 사이언시즈, 엘엘씨 치환된 아미노피리미딘 화합물 및 이용 방법
WO2015048312A1 (fr) 2013-09-26 2015-04-02 Costim Pharmaceuticals Inc. Méthodes de traitement de cancers hématologiques
CN103467359B (zh) * 2013-09-27 2015-04-22 山东大学 一种含有吲哚的肉桂酰胺类组蛋白去乙酰化酶抑制剂及其制备方法和应用
TW201605450A (zh) 2013-12-03 2016-02-16 諾華公司 Mdm2抑制劑與BRAF抑制劑之組合及其用途
CN103664734B (zh) * 2013-12-10 2015-09-23 广州康缔安生物科技有限公司 杂环羟肟酸类化合物及其药用组合物和应用
TR201900057T4 (tr) 2013-12-12 2019-01-21 Chong Kun Dang Pharmaceutical Corp Selektif histon deasetilaz (HDAC) inhibitörleri olarak yeni azaindol deriveleri ve bunları içeren farmasötik bileşimler.
KR101685639B1 (ko) 2014-01-03 2016-12-12 주식회사 종근당 신규한 인돌 유도체 화합물 및 이를 포함하는 약제학적 조성물
JOP20200094A1 (ar) 2014-01-24 2017-06-16 Dana Farber Cancer Inst Inc جزيئات جسم مضاد لـ pd-1 واستخداماتها
JOP20200096A1 (ar) 2014-01-31 2017-06-16 Children’S Medical Center Corp جزيئات جسم مضاد لـ tim-3 واستخداماتها
ES2921874T3 (es) 2014-02-28 2022-09-01 Nimbus Lakshmi Inc Inhibidores de TYK2 y usos de los mismos
WO2015148714A1 (fr) 2014-03-25 2015-10-01 Duke University Ligands de récepteurs de la protéine de choc thermique 70 (hsp-70)
JP6517319B2 (ja) 2014-03-28 2019-05-22 キャリター・サイエンシーズ・リミテッド・ライアビリティ・カンパニーCalitor Sciences, Llc 置換されたヘテロアリール化合物および使用方法
EP3126345A1 (fr) 2014-03-31 2017-02-08 Gilead Sciences, Inc. Inhibiteurs d'histones déméthylases
AU2015241198A1 (en) 2014-04-03 2016-11-17 Invictus Oncology Pvt. Ltd. Supramolecular combinatorial therapeutics
JP6778114B2 (ja) 2014-04-14 2020-10-28 アルビナス・オペレーションズ・インコーポレイテッドArvinas Operations, Inc. イミド系タンパク質分解モジュレーター及び関連する使用方法
GB201409471D0 (en) 2014-05-28 2014-07-09 Euro Celtique Sa Pharmaceutical composition
GB201409488D0 (en) 2014-05-28 2014-07-09 Euro Celtique Sa Pharmaceutical composition
GB201409485D0 (en) 2014-05-28 2014-07-09 Euro Celtique Sa Pharmaceutical composition
WO2016011658A1 (fr) 2014-07-25 2016-01-28 Novartis Ag Polythérapie
US10195208B2 (en) 2014-07-31 2019-02-05 Novartis Ag Combination therapy
US10071164B2 (en) 2014-08-11 2018-09-11 Yale University Estrogen-related receptor alpha based protac compounds and associated methods of use
CN117088931A (zh) 2014-08-12 2023-11-21 莫纳什大学 定向淋巴的前药
EA201790154A1 (ru) 2014-08-27 2017-08-31 Джилид Сайэнс, Инк. Соединения и способы для ингибирования гистоновых деметилаз
EP2995630A1 (fr) 2014-09-09 2016-03-16 Dublin Institute of Technology Composés hybrides formés à partir de liquides ioniques et leurs utilisations dans des électrodes à sélectivité ionique
WO2016040892A1 (fr) 2014-09-13 2016-03-17 Novartis Ag Polythérapies
EP3200775B1 (fr) 2014-10-03 2019-11-20 Novartis AG Polythérapies
US20160251376A1 (en) 2015-02-27 2016-09-01 Nimbus Lakshmi, Inc. Tyk2 inhibitors and uses thereof
US10449211B2 (en) 2015-03-10 2019-10-22 Aduro Biotech, Inc. Compositions and methods for activating “stimulator of interferon gene”—dependent signalling
KR20170124602A (ko) 2015-03-13 2017-11-10 포르마 세라퓨틱스 인크. Hdac8 억제제로서의 알파-신나미드 화합물 및 조성물
PT3297992T (pt) 2015-05-22 2020-03-17 Chong Kun Dang Pharmaceutical Corp Compostos derivados de alquilo heterocíclicos como inibidores seletivos da histona desacetilase e composições farmacêuticas que compreendem os mesmos
WO2017004134A1 (fr) 2015-06-29 2017-01-05 Nimbus Iris, Inc. Inhibiteurs d'irak et leurs utilisations
WO2017004133A1 (fr) 2015-06-29 2017-01-05 Nimbus Iris, Inc. Inhibiteurs d'irak et utilisations de ceux-ci
CA2995036A1 (fr) 2015-08-06 2017-02-09 Dana-Farber Cancer Institute, Inc. Degradation modulable de proteine endogene
WO2017032281A1 (fr) * 2015-08-21 2017-03-02 苏州晶云药物科技有限公司 Nouvelles formes cristallines de lactate de panobinostat
WO2017040757A1 (fr) 2015-09-02 2017-03-09 Nimbus Lakshmi, Inc. Inhibiteurs de tyk2 et leurs utilisations
WO2017041139A1 (fr) 2015-09-08 2017-03-16 Monash University Promédicaments ciblant la lymphe
EP3347097B1 (fr) 2015-09-11 2021-02-24 Sunshine Lake Pharma Co., Ltd. Dérivés d' aminopyrimidine substitués en tant que modulateurs des kinases jak, flt3 et aurora
PT3364958T (pt) 2015-10-23 2023-04-10 Navitor Pharm Inc Moduladores de interação sestrina-gator2 e utilizações dos mesmos
CN108366992A (zh) 2015-11-02 2018-08-03 耶鲁大学 蛋白水解靶向嵌合体化合物及其制备和应用方法
ITUB20155193A1 (it) 2015-11-03 2017-05-03 Italfarmaco Spa Sospensioni orali di Givinostat fisicamente e chimicamente stabili
WO2017106332A1 (fr) 2015-12-14 2017-06-22 X4 Pharmaceuticals, Inc. Méthodes de traitement du cancer
CN109069426B (zh) 2015-12-14 2021-10-29 X4 制药有限公司 治疗癌症的方法
WO2017106352A1 (fr) 2015-12-14 2017-06-22 Raze Therapeutics, Inc. Inhibiteurs de caféine de mthfd2 et leurs utilisations
US10610527B2 (en) 2015-12-22 2020-04-07 X4 Pharmaceuticals, Inc. Methods for treating immunodeficiency disease
CN105732467A (zh) * 2016-01-13 2016-07-06 深圳市康立生生物科技有限公司 一种panobinostat(帕比司他)的制备方法
US10954220B2 (en) 2016-03-09 2021-03-23 Raze Therapeutics, Inc. 3-phosphoglycerate dehydrogenase inhibitors and uses thereof
PL3426244T3 (pl) 2016-03-09 2023-09-25 Raze Therapeutics, Inc. Inhibitory dehydrogenazy 3-fosfoglicerynianowej i ich zastosowania
SG10201913290QA (en) 2016-03-15 2020-03-30 Oryzon Genomics Sa Combinations of lsd1 inhibitors for the treatment of hematological malignancies
AU2017233898B2 (en) 2016-03-15 2022-12-15 Oryzon Genomics, S.A. Combinations of LSD1 inhibitors for use in the treatment of solid tumors
JP2019510785A (ja) 2016-04-08 2019-04-18 エックス4 ファーマシューティカルズ, インコーポレイテッド 癌を処置する方法
WO2017184956A1 (fr) 2016-04-22 2017-10-26 Duke University Composés et procédés de ciblage de hsp90
AR108257A1 (es) 2016-05-02 2018-08-01 Mei Pharma Inc Formas polimórficas de 3-[2-butil-1-(2-dietilamino-etil)-1h-bencimidazol-5-il]-n-hidroxi-acrilamida y usos de las mismas
WO2017197055A1 (fr) 2016-05-10 2017-11-16 C4 Therapeutics, Inc. Dégronimères hétérocycliques pour la dégradation de protéines cibles
CN109562113A (zh) 2016-05-10 2019-04-02 C4医药公司 用于靶蛋白降解的螺环降解决定子体
EP3455218A4 (fr) 2016-05-10 2019-12-18 C4 Therapeutics, Inc. Dégronimères de type glutarimide liés au carbone c3 pour la dégradation de protéines cibles
CA3027500A1 (fr) 2016-06-21 2017-12-28 X4 Pharmaceuticals, Inc. Inhibiteurs de cxcr4 et leurs utilisations
CA3027495A1 (fr) 2016-06-21 2017-12-28 X4 Pharmaceuticals, Inc. Inhibiteurs de cxcr4 et leurs utilisations
JP7054529B2 (ja) 2016-06-21 2022-04-14 エックス4 ファーマシューティカルズ, インコーポレイテッド Cxcr4阻害剤およびその使用
BR112018076812A2 (pt) * 2016-06-21 2021-09-28 The University Of Melbourne Ativadores da latência de hiv
WO2018015493A1 (fr) 2016-07-20 2018-01-25 Royal College Of Surgeons In Ireland Complexes métalliques ayant des applications thérapeutiques
CA3034666A1 (fr) 2016-08-23 2018-03-01 Oncopep, Inc. Vaccins peptidiques et durvalumab pour le traitement du cancer du sein
WO2018039203A1 (fr) 2016-08-23 2018-03-01 Oncopep, Inc. Vaccins peptidiques et durvalumab pour le traitement du myélome multiple
WO2018054960A1 (fr) 2016-09-21 2018-03-29 INSERM (Institut National de la Santé et de la Recherche Médicale) Procédés de prédiction et de traitement de la résistance à la chimiothérapie dans le lagc à npm-alk(+)
US10207998B2 (en) 2016-09-29 2019-02-19 Duke University Substituted benzimidazole and substituted benzothiazole inhibitors of transforming growth factor-β kinase and methods of use thereof
US10927083B2 (en) 2016-09-29 2021-02-23 Duke University Substituted benzimidazoles as inhibitors of transforming growth factor-β kinase
AU2016426574B2 (en) 2016-10-11 2023-07-13 Euro-Celtique S.A. Hodgkin lymphoma therapy
CA3039202A1 (fr) 2016-10-14 2018-04-19 Nimbus Lakshmi, Inc. Inhibiteurs de tyk2 et leurs utilisations
WO2018075937A1 (fr) 2016-10-21 2018-04-26 Nimbus Lakshmi, Inc. Inhibiteurs de tyk2 et leurs utilisations
US10414727B2 (en) 2016-11-08 2019-09-17 Navitor Pharmaceuticals, Inc. Phenyl amino piperidine mTORC inhibitors and uses thereof
JP2019535839A (ja) 2016-11-29 2019-12-12 ピュアテック ヘルス エルエルシー 治療剤の送達のためのエクソソーム
US11091451B2 (en) 2016-12-05 2021-08-17 Raze Therapeutics, Inc. SHMT inhibitors and uses thereof
CN110603261A (zh) 2016-12-23 2019-12-20 拜斯科阿迪有限公司 具有新型键结构的肽衍生物
US10624968B2 (en) 2017-01-06 2020-04-21 Bicyclerd Limited Compounds for treating cancer
CA3053006C (fr) 2017-02-08 2023-09-05 Dana-Farber Cancer Institute, Inc. Regulation de recepteurs d'antigenes chimeriques
AR111233A1 (es) 2017-03-08 2019-06-19 Nimbus Lakshmi Inc Inhibidores de tyk2, usos y métodos para la producción de los mismos
EP3375778A1 (fr) 2017-03-14 2018-09-19 Artax Biopharma Inc. Dérivés d'aryl-pipéridine
EP3375784A1 (fr) 2017-03-14 2018-09-19 Artax Biopharma Inc. Dérivés d'aza-dihydro-acridone
WO2018191146A1 (fr) 2017-04-10 2018-10-18 Navitor Pharmaceuticals, Inc. Inhibiteurs de rheb à base d'hétéroaryle et leurs utilisations
JOP20180036A1 (ar) 2017-04-18 2019-01-30 Vifor Int Ag أملاح لمثبطات فروبورتين جديدة
US10857196B2 (en) 2017-04-27 2020-12-08 Bicycletx Limited Bicyclic peptide ligands and uses thereof
UY37695A (es) 2017-04-28 2018-11-30 Novartis Ag Compuesto dinucleótido cíclico bis 2’-5’-rr-(3’f-a)(3’f-a) y usos del mismo
CN107141244B (zh) * 2017-05-08 2019-11-19 潍坊医学院 吲哚丁酸类组蛋白去乙酰酶抑制剂及其制备方法和应用
GB201709406D0 (en) 2017-06-13 2017-07-26 Euro-Cletique S A Compounds for treating TNBC
GB201709403D0 (en) 2017-06-13 2017-07-26 Euro Celtique Sa Compounds for treating sarcoma
GB201709405D0 (en) 2017-06-13 2017-07-26 Euro Celtique Sa Compounds for treating ovarian cancer
GB201709402D0 (en) 2017-06-13 2017-07-26 Euro Celtique Sa Compounds for treating t-pll
CN111032678A (zh) 2017-06-26 2020-04-17 拜西克尔德有限公司 具有可检测部分的双环肽配体和其用途
CN117946115A (zh) 2017-07-28 2024-04-30 武田药品工业株式会社 Tyk2抑制剂与其用途
KR101977970B1 (ko) 2017-08-04 2019-05-14 중원대학교 산학협력단 신규한 벤즈아미드계 유도체, 이의 제조방법 및 이를 유효성분으로 함유하는 암 예방 또는 치료용 약학 조성물
US20200291096A1 (en) 2017-08-14 2020-09-17 Bicyclerd Limited Bicyclic peptide ligand sting conjugates and uses thereof
EP3668550A1 (fr) 2017-08-14 2020-06-24 Bicyclerd Limited Conjugués peptide bicyclique-ligand ppr-a et leurs utilisations
US11883497B2 (en) 2017-08-29 2024-01-30 Puretech Lyt, Inc. Lymphatic system-directing lipid prodrugs
EP3684366A4 (fr) 2017-09-22 2021-09-08 Kymera Therapeutics, Inc. Ligands crbn et utilisations de ces derniers
AU2018338314A1 (en) 2017-09-22 2020-04-09 Kymera Therapeutics, Inc Protein degraders and uses thereof
EP3461480A1 (fr) 2017-09-27 2019-04-03 Onxeo Combinaison d'inhibiteurs de point de contrôle du cycle cellulaire de réponse à un dommage à l'adn et de belinostat pour traiter le cancer
EP3461488A1 (fr) 2017-09-27 2019-04-03 Onxeo Combinaison d'une molécule dbait et un inhibiteur de hdac pour le traitement du cancer
WO2019083960A1 (fr) 2017-10-24 2019-05-02 Oncopep, Inc. Vaccins peptidiques et inhibiteurs d'hdac pour le traitement du myélome multiple
EP3700901A1 (fr) 2017-10-24 2020-09-02 Genentech, Inc. Composés (4-hydroxypyrrolidin-2-yl)-hétérocycliques et leurs procédés d'utilisation
WO2019084030A1 (fr) 2017-10-24 2019-05-02 Genentech, Inc. Composés de (4-hydroxypyrrolidin-2-yl)-hydroxamate et leurs procédés d'utilisation
CA3079422A1 (fr) 2017-10-24 2019-05-02 Oncopep, Inc. Vaccins peptidiques et pembrolizumab pour le traitement du cancer du sein
US10683297B2 (en) 2017-11-19 2020-06-16 Calitor Sciences, Llc Substituted heteroaryl compounds and methods of use
US10537585B2 (en) 2017-12-18 2020-01-21 Dexcel Pharma Technologies Ltd. Compositions comprising dexamethasone
US11608345B1 (en) 2017-12-19 2023-03-21 Puretech Lyt, Inc. Lipid prodrugs of rapamycin and its analogs and uses thereof
US11304954B2 (en) 2017-12-19 2022-04-19 Puretech Lyt, Inc. Lipid prodrugs of mycophenolic acid and uses thereof
US11602534B2 (en) 2017-12-21 2023-03-14 Hefei Institutes Of Physical Science, Chinese Academy Of Sciences Pyrimidine derivative kinase inhibitors
JP2021508703A (ja) 2017-12-26 2021-03-11 カイメラ セラピューティクス, インコーポレイテッド Irak分解剤およびそれらの使用
EP3737666A4 (fr) 2018-01-12 2022-01-05 Kymera Therapeutics, Inc. Agents de dégradation de protéines et utilisations associées
EP3737675A4 (fr) 2018-01-12 2022-01-05 Kymera Therapeutics, Inc. Ligands crbn et leurs utilisations
AU2019209960B2 (en) 2018-01-20 2023-11-23 Sunshine Lake Pharma Co., Ltd. Substituted aminopyrimidine compounds and methods of use
CA3089769A1 (fr) 2018-01-29 2019-08-01 Merck Patent Gmbh Inhibiteurs de gcn2 et leurs utilisations
BR112020015328A2 (pt) 2018-01-29 2020-12-08 Merck Patent Gmbh Inibidores de gcn2 e usos dos mesmos
IL276608B2 (en) 2018-02-12 2024-04-01 Inimmune Corp TOLL-like receptor ligands
KR20200140262A (ko) 2018-02-27 2020-12-15 아텍스 바이오파마 인코포레이티드 Tcr-nck 상호 작용의 억제제로서의 크로멘 유도체
WO2019183523A1 (fr) 2018-03-23 2019-09-26 Genentech, Inc. Composés de dégradation hétéro-bifonctionnels et leur utilisation en tant que modulateurs de l'ubiquination ciblée (vhl)
CN112262134B (zh) 2018-04-13 2024-05-24 阿尔维纳斯运营股份有限公司 小脑蛋白配体和包括其的双官能化合物
IL278142B2 (en) 2018-04-24 2023-11-01 Merck Patent Gmbh Antiproliferative compounds and their uses
ES2969982T3 (es) 2018-04-24 2024-05-23 Vertex Pharma Compuestos de pteridinona y usos de los mismos
WO2019238886A1 (fr) 2018-06-13 2019-12-19 University Of Dundee Molécules bifonctionnelles pour le ciblage de l'usp14
US20210283139A1 (en) 2018-06-13 2021-09-16 Amphista Therapeutics Ltd Bifunctional molecules for targeting uchl5
CA3103185A1 (fr) 2018-06-13 2019-12-19 Amphista Therapeutics Ltd Molecules bifonctionnelles pour cibler rpn11
WO2019241789A1 (fr) 2018-06-15 2019-12-19 Navitor Pharmaceuticals, Inc. Analogues de la rapamycine et leurs utilisations
US11180531B2 (en) 2018-06-22 2021-11-23 Bicycletx Limited Bicyclic peptide ligands specific for Nectin-4
EP3817748A4 (fr) 2018-07-06 2022-08-24 Kymera Therapeutics, Inc. Ligands crbn tricycliques et leurs utilisations
CN108752255A (zh) * 2018-07-19 2018-11-06 重庆医科大学 一种帕比司他及其关键中间体的制备方法
EP3826988A4 (fr) 2018-07-24 2023-03-22 Hygia Pharmaceuticals, LLC Composés, dérivés et analogues contre le cancer
US10548889B1 (en) 2018-08-31 2020-02-04 X4 Pharmaceuticals, Inc. Compositions of CXCR4 inhibitors and methods of preparation and use
EP3846793B1 (fr) 2018-09-07 2024-01-24 PIC Therapeutics, Inc. Inhibiteurs d'eif4e et leurs utilisations
AU2019360941A1 (en) 2018-10-15 2021-04-29 Takeda Pharmaceutical Company Limited TYK2 inhibitors and uses thereof
WO2020084305A1 (fr) 2018-10-23 2020-04-30 Bicycletx Limited Ligands peptidiques bicycliques et leurs utilisations
CN109574936B (zh) * 2018-11-23 2022-02-22 沈阳药科大学 一种具有hdac6抑制活性的异羟肟酸类化合物及其应用
SG11202105424PA (en) 2018-11-30 2021-06-29 Kymera Therapeutics Inc Irak degraders and uses thereof
WO2020112937A1 (fr) 2018-11-30 2020-06-04 Nimbus Lakshmi, Inc. Inhibiteurs de tyk2 et leurs utilisations
CN113453679A (zh) 2018-12-20 2021-09-28 C4医药公司 靶向蛋白降解
EP3670659A1 (fr) 2018-12-20 2020-06-24 Abivax Biomarqueurs et leurs utilisations dans le traitement d'infections virales, d'inflammations ou du cancer
JP2022518505A (ja) 2019-01-23 2022-03-15 ニンバス ラクシュミ, インコーポレイテッド Tyk2阻害剤およびその使用
WO2020165600A1 (fr) 2019-02-14 2020-08-20 Bicycletx Limited Conjugués peptide-ligand bicyclique et leurs utilisations
WO2020201753A1 (fr) 2019-04-02 2020-10-08 Bicycletx Limited Conjugués de toxines bicycliques et leurs utilisations
SG11202110829YA (en) 2019-04-05 2021-10-28 Kymera Therapeutics Inc Stat degraders and uses thereof
MX2021014441A (es) 2019-05-31 2022-01-06 Ikena Oncology Inc Inhibidores del dominio asociado mejorador de la transcripcion (tead) y usos de los mismos.
GB201913121D0 (en) 2019-09-11 2019-10-23 Seald As Compositions and methods for treatment of cholangiocarcinoma
GB201913123D0 (en) 2019-09-11 2019-10-23 Seald As Compositions and methods for treatment of cholangiocarcinoma
EP4028385A4 (fr) 2019-09-11 2023-11-08 Vincere Biosciences, Inc. Inhibiteurs d'usp30 et utilisations de ceux-ci
GB201913122D0 (en) 2019-09-11 2019-10-23 Seald As Compositions and methods for treatment of cholangiocarcinoma
GB201913124D0 (en) 2019-09-11 2019-10-23 Seald As Compositions and methods for treatment of cholangiocarcinoma
CA3151988A1 (fr) 2019-09-25 2021-04-01 Wenxin Wang Compositions de nanoparticules pour la therapie genique
EP3798250A1 (fr) 2019-09-25 2021-03-31 University College Dublin Polymères cationiques hyperramifiés utiles en tant que vecteurs d'administration d'acide nucléique pour la transfection
AU2020380333A1 (en) * 2019-11-06 2022-04-07 Dana-Farber Cancer Institute, Inc. Selective histone deacetylase (HDAC) degraders and methods of use thereof
TW202134234A (zh) 2019-12-05 2021-09-16 美商奈維特製藥公司 雷帕黴素類似物及其用途
IL293917A (en) 2019-12-17 2022-08-01 Kymera Therapeutics Inc Iraq joints and their uses
EP4076524A4 (fr) 2019-12-17 2023-11-29 Kymera Therapeutics, Inc. Agents de dégradation d'irak et leurs utilisations
KR20220119094A (ko) 2019-12-19 2022-08-26 아비나스 오퍼레이션스, 인코포레이티드 안드로겐 수용체의 표적화된 분해를 위한 화합물 및 방법
WO2021133920A1 (fr) 2019-12-23 2021-07-01 Kymera Therapeutics, Inc. Agents de dégradation de smarca et leurs utilisations
WO2021148581A1 (fr) 2020-01-22 2021-07-29 Onxeo Nouvelle molécule dbait et son utilisation
CA3166908A1 (fr) 2020-02-05 2021-08-12 Daniel Kenneth BONNER Promedicaments lipidiques de neurosteroides
IT202000004075A1 (it) 2020-02-27 2021-08-27 Flamma Spa Processo per la preparazione di panobinostat
CA3170411A1 (fr) 2020-03-03 2021-09-10 Christopher L. Vandeusen Inhibiteurs d'eif4e et leurs utilisations
WO2021233534A1 (fr) 2020-05-20 2021-11-25 Pvac Medical Technologies Ltd Utilisation d'une substance et composition pharmaceutique associée, et traitements médicaux ou utilisations associées
WO2021185844A1 (fr) 2020-03-16 2021-09-23 Pvac Medical Technologies Ltd Utilisation d'une substance et composition pharmaceutique correspondante et traitements médicaux ou utilisations correspondants
CN115776887A (zh) 2020-03-19 2023-03-10 凯麦拉医疗公司 Mdm2降解剂和其用途
TW202210483A (zh) 2020-06-03 2022-03-16 美商凱麥拉醫療公司 Irak降解劑之結晶型
EP4192509A1 (fr) 2020-08-05 2023-06-14 Ellipses Pharma Ltd Traitement du cancer à l'aide d'un conjugué polymère contenant de la cyclodextrine-inhibiteur de la topoisomérase et d'un inhibiteur de parp
KR20230074721A (ko) 2020-08-17 2023-05-31 바이사이클티엑스 리미티드 Nectin-4에 특이적인 이환 콘쥬게이트 및 이의 용도
KR20230131189A (ko) 2020-12-02 2023-09-12 이케나 온콜로지, 인코포레이티드 Tead 억제제 및 이의 용도
WO2022120353A1 (fr) 2020-12-02 2022-06-09 Ikena Oncology, Inc. Inhibiteurs de tead et leurs utilisations
PE20240545A1 (es) 2020-12-18 2024-03-19 Amphista Therapeutics Ltd Moleculas bifuncionales novedosas para la degradacion de proteinas dirigidas
GB202020359D0 (en) 2020-12-22 2021-02-03 Midatech Pharma Wales Ltd Pharmaceutical compositions and use thereof in combination therapy for brain cancer
WO2022167445A1 (fr) 2021-02-02 2022-08-11 Liminal Biosciences Limited Antagonistes du gpr84 et leurs utilisations
JP2024505571A (ja) 2021-02-02 2024-02-06 リミナル・バイオサイエンシーズ・リミテッド Gpr84アンタゴニストおよびその使用
KR20230172548A (ko) 2021-04-16 2023-12-22 이케나 온콜로지, 인코포레이티드 Mek 억제제 및 이의 용도
AU2022334296A1 (en) 2021-08-25 2024-03-07 PIC Therapeutics, Inc. Eif4e inhibitors and uses thereof
US20230134932A1 (en) 2021-08-25 2023-05-04 PIC Therapeutics, Inc. Eif4e inhibitors and uses thereof
WO2023041805A1 (fr) 2021-09-20 2023-03-23 INSERM (Institut National de la Santé et de la Recherche Médicale) Procédés pour l'amélioration de l'efficacité d'une thérapie par inhibiteur de hdac et la prédiction de la réponse à un traitement comprenant un inhibiteur de hdac
GB2611043A (en) 2021-09-22 2023-03-29 Univ Dublin City A cis-platinum(II)-oligomer hybrid
WO2023089183A1 (fr) 2021-11-19 2023-05-25 Branca Bunus Limited Composition comprenant un agent thérapeutiquement actif enrobé dans un véhicule d'administration de médicament
WO2023114984A1 (fr) 2021-12-17 2023-06-22 Ikena Oncology, Inc. Inhibiteurs de tead et leurs utilisations
WO2023173053A1 (fr) 2022-03-10 2023-09-14 Ikena Oncology, Inc. Inhibiteurs de mek et leurs utilisations
WO2023173057A1 (fr) 2022-03-10 2023-09-14 Ikena Oncology, Inc. Inhibiteurs de mek et leurs utilisations
WO2023194441A1 (fr) 2022-04-05 2023-10-12 Istituto Nazionale Tumori Irccs - Fondazione G. Pascale Combinaison d'inhibiteurs de hdac et de statines pour une utilisation dans le traitement du cancer du pancréas
WO2023211889A1 (fr) 2022-04-25 2023-11-02 Ikena Oncology, Inc. Composés polymorphes et leurs utilisations
GB2617409A (en) 2022-04-27 2023-10-11 Cancertain Ltd Method for predicting responsiveness to therapy
TW202404581A (zh) 2022-05-25 2024-02-01 美商醫肯納腫瘤學公司 Mek抑制劑及其用途
WO2023242597A1 (fr) 2022-06-16 2023-12-21 Amphista Therapeutics Limited Molécules bifonctionnelles pour la dégradation ciblée de protéines
WO2024028365A1 (fr) 2022-08-02 2024-02-08 Liminal Biosciences Limited Antagonistes de gpr84 contenant de la pyridone substituée et leurs utilisations
WO2024030441A1 (fr) 2022-08-02 2024-02-08 National University Corporation Hokkaido University Procédés d'amélioration d'une thérapie cellulaire avec des complexes d'organites
WO2024028364A1 (fr) 2022-08-02 2024-02-08 Liminal Biosciences Limited Aryl-triazolyle et antagonistes de gpr84 apparentés et leurs utilisations
WO2024028363A1 (fr) 2022-08-02 2024-02-08 Liminal Biosciences Limited Hétéroaryl-carboxamide et antagonistes de gpr84 associés et leurs utilisations
WO2024041744A1 (fr) 2022-08-26 2024-02-29 Biodexa Ltd. Polythérapie pour le cancer du cerveau

Family Cites Families (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5700811A (en) * 1991-10-04 1997-12-23 Sloan-Kettering Institute For Cancer Research Potent inducers of terminal differentiation and method of use thereof
JP3342485B2 (ja) 1991-12-10 2002-11-11 塩野義製薬株式会社 芳香族スルホンアミド系ヒドロキサム酸誘導体
US5569668A (en) * 1995-03-29 1996-10-29 Webster; John M. Indole derivatives with antibacterial and antimycotic properties
US5722242A (en) * 1995-12-15 1998-03-03 Borealis Technical Limited Method and apparatus for improved vacuum diode heat pump
US6777217B1 (en) 1996-03-26 2004-08-17 President And Fellows Of Harvard College Histone deacetylases, and uses related thereto
JPH10182583A (ja) 1996-12-25 1998-07-07 Mitsui Chem Inc 新規ヒドロキサム酸誘導体
AUPO721997A0 (en) * 1997-06-06 1997-07-03 Queensland Institute Of Medical Research, The Anticancer compounds
US6127392A (en) * 1997-08-05 2000-10-03 American Home Products Corporation Anthranilic acid analogs
CA2297412A1 (fr) 1997-08-05 1999-02-18 John Anthony Butera Analogues d'acide anthranilique
DE69920247T2 (de) 1998-10-19 2005-09-29 Methylgene, Inc., Saint-Laurent Veränderung der dns methyltransferase durch kombinationstherapie
US6110922A (en) 1998-12-29 2000-08-29 Abbott Laboratories Cell adhesion-inhibiting antiinflammatory and immune-suppressive compounds
UA74781C2 (en) 1999-04-02 2006-02-15 Abbott Lab Antiinflammatory and immumosuppressive compounds inhibiting cell adhesion
EA007649B1 (ru) 1999-09-08 2006-12-29 Слоан-Кеттеринг Инститьют Фор Кэнсер Рисёч Ингибиторы гистондеацетилазы, вызывающие дифференцировку клеток, и их применение
GB9922173D0 (en) 1999-09-21 1999-11-17 Zeneca Ltd Chemical compounds
WO2001038322A1 (fr) * 1999-11-23 2001-05-31 Methylgene, Inc. Inhibiteurs de l'histone deacetylase
ES2260080T3 (es) 1999-12-08 2006-11-01 Axys Pharmaceuticals, Inc. Proteinas histono deacetilasa-8, acidos nucleicos y procedimiento de utilizacion.
TW427572U (en) * 1999-12-17 2001-03-21 Hon Hai Prec Ind Co Ltd Electrical connector
AU2001248701A1 (en) 2000-03-24 2001-10-03 Methylgene, Inc. Inhibitors of histone deacetylase
AU2001298014A1 (en) * 2000-03-24 2003-01-29 Methylgene, Inc. Inhibition of specific histone deacetylase isoforms
CA2423733A1 (fr) * 2000-08-31 2003-02-14 Terukage Hirata Nouveaux derives d'acide propenohydroxamique
PE20020354A1 (es) 2000-09-01 2002-06-12 Novartis Ag Compuestos de hidroxamato como inhibidores de histona-desacetilasa (hda)
US20040058903A1 (en) 2000-10-05 2004-03-25 Hisashi Takasugi Benzamide compounds as apo b secretion inhibitors
SE0101386D0 (sv) 2001-04-20 2001-04-20 Astrazeneca Ab New compounds
US6905669B2 (en) 2001-04-24 2005-06-14 Supergen, Inc. Compositions and methods for reestablishing gene transcription through inhibition of DNA methylation and histone deacetylase
EP1417169A2 (fr) 2001-08-11 2004-05-12 Bristol-Myers Squibb Pharma Company Modulateurs selectifs de recepteur d'oestrogene
US6706686B2 (en) * 2001-09-27 2004-03-16 The Regents Of The University Of Colorado Inhibition of histone deacetylase as a treatment for cardiac hypertrophy
DE10152764A1 (de) * 2001-10-29 2003-05-08 Linde Ag Ventil für kryogene Medien

Also Published As

Publication number Publication date
US6833384B2 (en) 2004-12-21
TWI286544B (en) 2007-09-11
IL154574A (en) 2010-02-17
JP4012819B2 (ja) 2007-11-21
CN1300110C (zh) 2007-02-14
NO20030867L (no) 2003-02-25
SK287609B6 (sk) 2011-04-05
SK2422003A3 (en) 2003-09-11
CZ302707B6 (cs) 2011-09-14
HU229796B1 (en) 2014-07-28
HUP0300880A2 (hu) 2003-08-28
US6552065B2 (en) 2003-04-22
CA2420899A1 (fr) 2002-03-21
US7067551B2 (en) 2006-06-27
AU2001282129B2 (en) 2005-08-25
AU8212901A (en) 2002-03-26
NO324942B1 (no) 2008-01-07
NL300778I2 (fr) 2016-06-30
MXPA03001832A (es) 2003-06-04
EP1870399A1 (fr) 2007-12-26
EP1318980A2 (fr) 2003-06-18
US20030018062A1 (en) 2003-01-23
CY2015053I2 (el) 2016-06-22
CZ2003573A3 (cs) 2003-06-18
AR035057A1 (es) 2004-04-14
IL154574A0 (en) 2003-09-17
KR100585484B1 (ko) 2006-06-07
PL221738B1 (pl) 2016-05-31
ES2292610T3 (es) 2008-03-16
BRPI0113669B1 (pt) 2017-06-06
CN1450991A (zh) 2003-10-22
MY136892A (en) 2008-11-28
BE2015C062I2 (fr) 2021-01-28
WO2002022577A3 (fr) 2002-09-06
SI1318980T1 (sl) 2008-08-31
KR20030031986A (ko) 2003-04-23
US20050085507A1 (en) 2005-04-21
FR15C0086I1 (fr) 2016-01-15
RU2302408C3 (ru) 2018-06-01
ECSP034492A (es) 2003-04-25
HUP0300880A3 (en) 2010-03-29
US20080176849A1 (en) 2008-07-24
PE20020354A1 (es) 2002-06-12
DK1318980T3 (da) 2008-02-11
LU92890I2 (fr) 2016-02-01
US20040024067A1 (en) 2004-02-05
PT1318980E (pt) 2008-01-17
DE60131179T2 (de) 2008-03-06
RU2302408C2 (ru) 2007-07-10
NZ524365A (en) 2004-11-26
DE60131179D1 (en) 2007-12-13
PL361408A1 (en) 2004-10-04
ZA200301423B (en) 2004-04-21
NO2015026I1 (no) 2015-12-10
HK1057746A1 (en) 2004-04-16
US20060189674A1 (en) 2006-08-24
ATE376999T1 (de) 2007-11-15
WO2002022577A2 (fr) 2002-03-21
BRPI0113669B8 (pt) 2021-05-25
CY2015053I1 (el) 2016-06-22
JP2004509105A (ja) 2004-03-25
NO20030867D0 (no) 2003-02-25
BR0113669A (pt) 2003-06-03
NO2015026I2 (no) 2015-12-28
HUS1500068I1 (hu) 2018-05-02
CA2420899C (fr) 2011-03-08
CY1107839T1 (el) 2013-06-19
EP1318980B1 (fr) 2007-10-31

Similar Documents

Publication Publication Date Title
FR15C0086I2 (fr) Derives d&#39;hydroxamate en tant qu&#39;inhibiteurs de desacetylase
FR20C1039I2 (fr) Derives de l&#39;uk-2a
AR028253A1 (es) Inhibidores de la glucogeno fosforilasa
AR028567A1 (es) Nuevos derivados de fenil-propargileter
DZ3439A1 (fr) Derives de 2-aminocarbonyl-9h-purine
NO20040198L (no) Dolastatin 10 derivater
MA26812A1 (fr) Pyrimidine-2,4,6-triones inhibitrices de metalloproteinases
MA26782A1 (fr) Pyrazolobenzodiazepines en tant qu&#39;inhibiteurs de cdk2.
MA27126A1 (fr) 3&#39;PROMEDICAMENTS DE 2&#39;-DESOXY- β-L-NUCLEOSIDES
MA26972A1 (fr) Derives du tetralone en tant qu&#39;agents anti-tumeur
AR028596A1 (es) Nuevos derivados de fenilglicina
PT1303521E (pt) Derivados de tetra-hidro-heterocicloazepinil-pirimidina
FR2813756B1 (fr) Dilueur pour la conservation de spermatozoides de porcins
FR2810318B1 (fr) Derives de diamano-phenothiazine
DE50114491D1 (de) Substituierte C-Cyclohexylmethylamin-Derivative
AR028602A1 (es) Derivados de pirrol
AR028282A1 (es) Derivados de aminofenil pirimidona
AR028607A1 (es) Derivados de 1,4-diazepan-2,5-diona
PT1322592E (pt) Derivados substituidos de 1-aminobutan-3-ol
ATE282021T1 (de) Substituierte aminomethyl-phenyl- cyclohexanderivate
MA27240A1 (fr) Derives d&#39;imidazoquinoleine
DE60031450D1 (de) Polymorph v von torasemid
PT1246791E (pt) Derivados de aminometilfenilciclo-hexanona
MA25653A1 (fr) Derives d&#39;amides heterocycliques.
AR028075A1 (es) Inhibidores de la peptido-desformilasa