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LU92890I2 - Panobinstat ou un sel pharmaceutiquement acceptable, ou un dérivé de celui-ci (farydak) - Google Patents

Panobinstat ou un sel pharmaceutiquement acceptable, ou un dérivé de celui-ci (farydak) Download PDF

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Publication number
LU92890I2
LU92890I2 LU92890C LU92890C LU92890I2 LU 92890 I2 LU92890 I2 LU 92890I2 LU 92890 C LU92890 C LU 92890C LU 92890 C LU92890 C LU 92890C LU 92890 I2 LU92890 I2 LU 92890I2
Authority
LU
Luxembourg
Prior art keywords
panobinstat
farydak
derivative
pharmaceutically acceptable
acceptable salt
Prior art date
Application number
LU92890C
Other languages
English (en)
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=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=LU92890(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 LU92890I2 publication Critical patent/LU92890I2/fr

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    • 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)
  • Health & Medical Sciences (AREA)
  • Manufacturing & Machinery (AREA)
  • Veterinary Medicine (AREA)
  • Structural Engineering (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • General Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (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)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Furan Compounds (AREA)
  • Pyrane Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Heterocyclic Compounds That Contain Two Or More Ring Oxygen Atoms (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
LU92890C 2000-09-01 2015-12-01 Panobinstat ou un sel pharmaceutiquement acceptable, ou un dérivé de celui-ci (farydak) LU92890I2 (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 (1)

Publication Number Publication Date
LU92890I2 true LU92890I2 (fr) 2016-02-01

Family

ID=26923760

Family Applications (1)

Application Number Title Priority Date Filing Date
LU92890C LU92890I2 (fr) 2000-09-01 2015-12-01 Panobinstat ou un sel pharmaceutiquement acceptable, ou un dérivé de celui-ci (farydak)

Country Status (35)

Country Link
US (5) US6552065B2 (fr)
EP (2) EP1870399A1 (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)
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 (462)

* 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
EP1233958B1 (fr) 1999-11-23 2011-06-29 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
EP1443928B1 (fr) 2001-10-16 2011-07-27 Sloan-Kettering Institute For Cancer Research Traitement des maladies neurodegeneratives et du cancer du cerveau
DE60217895T2 (de) * 2001-11-06 2007-07-05 Novartis Ag Kombination cyclooxygenase-2 inhibitor/ histone deacetylase inhibitor
BR0308250A (pt) 2002-03-04 2005-01-11 Aton Pharma Inc Métodos de indução de diferenciação terminal
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
MXPA04009490A (es) 2002-04-03 2005-06-08 Topo Target Uk Ltd Compuesto de acido carbamico que comprenden un enlace de piperazina como inhibidores de histona desacetilasa.
AU2003219595A1 (en) 2002-04-11 2003-10-27 In2Gen Co., Ltd. Alpha,Beta-UNSATURATED HYDROXAMIC ACID DERIVATIVES AND THEIR USE AS HISTONE DEACETYLASE INHIBITORS
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
BR0311714A (pt) * 2002-06-10 2005-03-01 Novartis Ag Combinações que compreendem epotilonas e seus usos farmacêuticos
JP4804004B2 (ja) * 2002-08-20 2011-10-26 アステラス製薬株式会社 関節軟骨細胞外マトリクス分解阻害剤
US20060100140A1 (en) * 2002-09-13 2006-05-11 Paul Dent Combination of a) n-{5-[4-(4-methyl-piperazino-methyl)-benzoylamido]2-methylphenyl}-4- (3-pyridyl)-2-pyrimidine-amine and b) a histone deacetylase inhibitor for the treatment of leukemia
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
AR042064A1 (es) * 2002-11-19 2005-06-08 Takeda Pharmaceutical Compuestos de amina con actividad inhibidora de la union al receptor de somastotina
WO2004052292A2 (fr) 2002-12-06 2004-06-24 University Of South Florida Amelioration de l'apoptose induite par trail au moyen d'un inhibiteur de l'histone deacetylase
TW200418806A (en) * 2003-01-13 2004-10-01 Fujisawa Pharmaceutical Co HDAC inhibitor
AU2004205372B2 (en) 2003-01-17 2011-02-24 Topotarget Uk Limited Hydroxamic acid compounds comprising an ester or ketone linkage as HDAC inhibitors
AU2003900587A0 (en) * 2003-02-11 2003-02-27 Fujisawa Pharmaceutical Co., Ltd. Hdac inhibitor
AU2003900608A0 (en) * 2003-02-11 2003-02-27 Fujisawa Pharmaceutical Co., Ltd. Hdac inhibitor
AU2004215624B2 (en) 2003-02-25 2011-06-02 Topotarget Uk Limited Hydroxamic acid compounds comprising a bicyclic heteroaryl group as HDAC inhibitors
US7169801B2 (en) 2003-03-17 2007-01-30 Takeda San Diego, Inc. Histone deacetylase inhibitors
MXPA05012464A (es) * 2003-05-21 2006-01-30 Novartis Ag Combinacion de inhibidores de deacetilasa de histona con agentes quimioterapeuticos.
WO2005011598A2 (fr) 2003-07-31 2005-02-10 University Of South Florida Composition et methode de traitement de la leucemie
WO2005013958A1 (fr) * 2003-08-07 2005-02-17 Novartis Ag Inhibiteurs d'histone deacetylase utilises comme immunosuppresseurs
EP1653973A1 (fr) * 2003-08-08 2006-05-10 Novartis AG Combinaisons contenant des staurosporines
CA2535806C (fr) 2003-08-26 2009-02-17 Aton Pharma, Inc. Procede pour traiter le cancer au moyen d'inhibiteurs d'hdac
CN101856348A (zh) 2003-08-29 2010-10-13 斯隆-凯特林癌症研究所 联合治疗癌症的方法
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
BRPI0414506A (pt) * 2003-09-18 2006-11-07 Novartis Ag combinação de um inibidor de histona desacetilase com um ligante de receptor de morte
SI1673349T1 (sl) * 2003-09-22 2010-10-29 S Bio Pte Ltd Derivati benzimidazola: priprava in farmacevtske uporabe
DE602004027932D1 (de) 2003-09-22 2010-08-12 S Bio Pte Ltd Benzimidazolderivate: herstellung und pharmazeutische anwendungen
KR20060097000A (ko) * 2003-09-23 2006-09-13 노파르티스 아게 화학요법제와 vegf 수용체 저해제의 배합물
US20070167499A1 (en) * 2003-10-27 2007-07-19 A*Bio Pte Ltd. Biaryl linked hydroxamates: preparation and pharmaceutical applications
EP1696898B1 (fr) * 2003-12-02 2015-11-18 The Ohio State University Research Foundation Acides gras a chaine courte lies a un motif de chelation zn 2+ 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
US20050159470A1 (en) * 2003-12-19 2005-07-21 Syrrx, Inc. Histone deacetylase inhibitors
WO2005066151A2 (fr) * 2003-12-19 2005-07-21 Takeda San Diego, Inc. Inhibiteurs d'histone desacetylase
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
PL2253614T3 (pl) 2004-04-07 2013-03-29 Novartis Ag Inhibitory IAP
CA2574035A1 (fr) * 2004-07-19 2006-02-23 Sandro Belvedere Inhibiteurs de l'histone deacetylase
EP1776357A1 (fr) * 2004-08-09 2007-04-25 Astellas Pharma Inc. Composés d'hydroxyamide présentant une activité en tant qu'inhibiteurs d'histone désacétylase (hdac)
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
WO2006066133A2 (fr) 2004-12-16 2006-06-22 Takeda San Diego, Inc. Inhibiteurs d'histone desacetylase
CA2596015A1 (fr) 2005-02-14 2006-08-24 Sampath K. Anandan Composes heterocycliques fusionnes utiles comme inhibiteurs de l'histone deacetylase
US7666880B2 (en) * 2005-03-21 2010-02-23 S*Bio Pte Ltd. Imidazo[1,2-A]pyridine derivatives: preparation and pharmaceutical applications
AU2006226861B2 (en) 2005-03-22 2012-08-16 Dana-Farber Cancer Institute, Inc. Treatment of protein degradation disorders
GB0509225D0 (en) 2005-05-05 2005-06-15 Chroma Therapeutics Ltd Inhibitors of enzymatic activity
GB0509223D0 (en) * 2005-05-05 2005-06-15 Chroma Therapeutics Ltd Enzyme inhibitors
US7642253B2 (en) 2005-05-11 2010-01-05 Takeda San Diego, Inc. Histone deacetylase inhibitors
GB0510390D0 (en) 2005-05-20 2005-06-29 Novartis Ag Organic compounds
TWI415603B (zh) 2005-05-20 2013-11-21 Merck Sharp & Dohme 1,8-辛二醯基苯胺羥胺酸(suberoylanilide hydroxamic acid)之調配物及其製配方法
WO2007011626A2 (fr) * 2005-07-14 2007-01-25 Takeda San Diego, Inc. Inhibiteurs de l'histone deacetylase
WO2007016532A2 (fr) * 2005-08-02 2007-02-08 Novartis Ag Mutations et polymorphismes de hdac4
ES2545076T3 (es) 2005-08-03 2015-09-08 Novartis Ag Uso del inhibidor de HDAC panobinostat para el tratamiento de mieloma
EP1915141A1 (fr) * 2005-08-10 2008-04-30 Novartis AG Procede d'utilisation d'inhibiteurs de la desacetylase
US20080200489A1 (en) * 2005-08-11 2008-08-21 Peter Wisdom Atadja Combination of Organic Compounds
EP1928437A2 (fr) 2005-08-26 2008-06-11 Braincells, Inc. Neurogenese par modulation du recepteur muscarinique
WO2007022638A1 (fr) * 2005-08-26 2007-03-01 Methylgene Inc. Inhibiteurs d'analogues de benzodiazepine et de benzopiperazine de l'histone deacetylase
EP2258359A3 (fr) 2005-08-26 2011-04-06 Braincells, Inc. Neurogenèse par modulation des récepteurs muscariniques avec sabcomeline
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
EP1996550A2 (fr) 2005-09-27 2008-12-03 Novartis AG Composes carboxamines et leur utilisation pour le traitement de maladies liees a la hdac
WO2007047998A2 (fr) * 2005-10-21 2007-04-26 Novartis Ag Mutations et polymorphismes du gène de l'hdac2
JP2009512711A (ja) 2005-10-21 2009-03-26 ブレインセルス,インコーポレイティド Pde阻害による神経新生の調節
JP2009512732A (ja) 2005-10-24 2009-03-26 ノバルティス アクチエンゲゼルシャフト ヒストンデアセチラーゼ阻害剤および照射の組合せ
WO2007053596A1 (fr) 2005-10-31 2007-05-10 Braincells, Inc. Modulation de la neurogenese dont la mediation est assuree par recepteur gaba
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
NO346575B1 (no) 2005-11-21 2022-10-17 Novartis Ag Anvendelse av 40-O-(2-hydroksyetyl)-rapamycin i behandling av carcinoid eller småøyet celle cancer
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
JP5218057B2 (ja) * 2006-02-07 2013-06-26 アステラス製薬株式会社 N−ヒドロキシアクリルアミド化合物
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
RU2447891C2 (ru) 2006-04-05 2012-04-20 Новартис Аг Комбинации терапевтических средств, предназначенные для лечения рака
CA2644143C (fr) 2006-04-05 2013-10-01 Novartis Ag Combinaisosns comprenant des inhibiteurs de bcr-abl/c-kit/pdgf-r tk pour le traitement du cancer
US8168383B2 (en) 2006-04-14 2012-05-01 Cell Signaling Technology, Inc. Gene defects and mutant ALK kinase in human solid tumors
EP2447359B1 (fr) 2006-04-14 2015-11-04 Cell Signaling Technology, Inc. Défauts de gène et ALK kinase mutante dans des tumeurs solides humaines
EP2012801A4 (fr) 2006-04-24 2009-08-05 Gloucester Pharmaceuticals Inc Thérapie de combinaison de gemcitabine
US20090018142A9 (en) * 2006-05-02 2009-01-15 Zhengping Zhuang Use of phosphatases to treat tumors overexpressing N-CoR
EP2026813A2 (fr) 2006-05-09 2009-02-25 Braincells, Inc. Neurogenèse induite par le récepteur 5ht
WO2007134136A2 (fr) 2006-05-09 2007-11-22 Braincells, Inc. Neurogenèse par modulation de l'angiotensine
EP2026800A1 (fr) 2006-05-09 2009-02-25 Novartis AG Combinaison comprenant un chélatant du fer et un agent antinéoplasique et ses applications
US8957027B2 (en) 2006-06-08 2015-02-17 Celgene Corporation Deacetylase inhibitor therapy
EA017984B1 (ru) * 2006-06-12 2013-04-30 Новартис Аг Кристаллические безводные формы лактата n-гидрокси-3-[4-[[[2-(2-метил-1h-индол-3-ил)этил]амино]метил]фенил]-2e-2-акриламида
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.
JP2009540005A (ja) * 2006-06-12 2009-11-19 ノバルティス アクチエンゲゼルシャフト N−ヒドロキシ−3−[4−[[[2−(2−メチル−1h−インドール−3−イル)エチル]アミノ]メチル]フェニル]−2e−2−プロペンアミドの塩
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
EP2032532B8 (fr) * 2006-06-12 2015-07-01 Novartis AG Procédé de fabrication des sels de N-hydroxy-3-[4-[[[2-(2-méthyl-1H-indol-3-yl)éthyl]amino]méthyl]phényl]-2E-2-propénamide
EP2034978A1 (fr) * 2006-06-26 2009-03-18 Novartis AG Composés organiques
WO2008030651A1 (fr) 2006-09-08 2008-03-13 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
WO2008036046A1 (fr) 2006-09-20 2008-03-27 S*Bio Pte Ltd COMPOSÉS D'HYDROXYMATE D'IMIDAZO[l,2-a]PYRIDINE QUI SONT DES INHIBITEURS D'HISTONE DÉSACÉTYLASE
US20100035991A1 (en) * 2006-09-28 2010-02-11 Mckeown Arlene Amide base salts of saha and polymorphis thereof
MX2009003185A (es) 2006-09-29 2009-04-03 Novartis Ag Pirazolopirimidinas como inhibidores de lipido cinasa pi3k.
GB0619753D0 (en) 2006-10-06 2006-11-15 Chroma Therapeutics Ltd Enzyme inhibitors
CN101553475B (zh) 2006-10-30 2013-04-24 色品疗法有限公司 作为组蛋白脱乙酰基酶抑制剂的异羟肟酸
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
MY148893A (en) 2006-12-04 2013-06-14 Novartis Ag Combination of an hdac inhibitor and an antimetabolite
KR20090099561A (ko) * 2006-12-15 2009-09-22 아스텔라스세이야쿠 가부시키가이샤 N-히드록시아크릴아미드 화합물
KR20090098920A (ko) * 2007-01-10 2009-09-17 노파르티스 아게 데아세틸라제 억제제의 제제
EA023804B1 (ru) 2007-02-06 2016-07-29 Ликсте Байотекнолоджи, Инк. Оксабициклогептаны, их получение и применение
CN101626758A (zh) 2007-02-15 2010-01-13 诺瓦提斯公司 用于治疗癌症的lbh589和其他治疗剂的组合
EP2135620A4 (fr) 2007-03-28 2010-12-29 Santen Pharmaceutical Co Ltd Agent hypotenseur oculaire comprenant un composé capable d'inhiber une histone désacétylase comme principe actif
EP2139850B1 (fr) 2007-04-09 2018-09-12 MethylGene Inc. Inhibiteurs d'histone déacétylase
CA2683554A1 (fr) * 2007-05-04 2008-11-13 Novartis Ag Utilisation d'inhibiteurs de la hdac pour le traitement des cancers gastro-intestinaux
KR20100016376A (ko) * 2007-05-11 2010-02-12 노파르티스 아게 흑색종의 치료를 위한 hdac 억제제의 용도
JP2010529028A (ja) * 2007-05-30 2010-08-26 ノバルティス アーゲー 骨破壊の処置のためのhdac阻害剤の使用
US7737175B2 (en) 2007-06-01 2010-06-15 Duke University Methods and compositions for regulating HDAC4 activity
CA2718472A1 (fr) * 2007-08-03 2009-02-12 Lixte Biotechnology, Inc. Utilisation de phosphates pour traiter des neuroblastomes et des medulloblastomes
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.
WO2009045440A1 (fr) 2007-10-01 2009-04-09 Lixte Biotechnology Holdings, Inc. Inhibiteurs de hdac
RU2453536C2 (ru) * 2007-10-22 2012-06-20 Оркид Рисерч Лабораториз Лимитед Ингибиторы гистондезацетилазы
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
WO2009067453A1 (fr) * 2007-11-19 2009-05-28 Syndax Pharmaceuticals, Inc. Combinaisons d'inhibiteurs de la hdac et d'inhibiteurs de protéasomes
WO2009067808A1 (fr) * 2007-11-27 2009-06-04 Ottawa Health Research Institute Amplification d'une infection par un virus oncolytique spécifique au cancer par des inhibiteurs d'histone désacétylase
AU2008350907A1 (en) 2007-12-11 2009-08-27 Viamet Pharmaceuticals, Inc. Metalloenzyme inhibitors using metal binding moieties in combination with targeting moieties
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
WO2009118292A1 (fr) 2008-03-24 2009-10-01 Novartis Ag Inhibiteurs de métalloprotéases matricielles à base d'arylsulfonamides
EP2628726A1 (fr) 2008-03-26 2013-08-21 Novartis AG Inhibiteurs à hydroxamate de désacétylases B
US20110118309A1 (en) * 2008-07-18 2011-05-19 Peter Wisdom Atadja Use of hdac inhibitors for the treatment of hodgkin's disease
WO2010011296A2 (fr) 2008-07-23 2010-01-28 President And Fellows Of Harvard College Inhibiteurs de désacétylase et leurs utilisations
WO2010014141A1 (fr) * 2008-08-01 2010-02-04 Lixte Biotechnology, Inc. Procédés de régulation de la mitose cellulaire par inhibition de la phosphatase de sérine/thréonine
WO2010014220A1 (fr) 2008-08-01 2010-02-04 Lixte Biotechnology, Inc. Agents neuroprotecteurs pour la prévention et le traitement de maladies neurodégénératives
WO2010147612A1 (fr) 2009-06-18 2010-12-23 Lixte Biotechnology, Inc. Procédés de modulation de la régulation cellulaire par inhibition de p53
US8227473B2 (en) * 2008-08-01 2012-07-24 Lixte Biotechnology, Inc. Oxabicycloheptanes and oxabicycloheptenes, their preparation and use
WO2010083617A1 (fr) 2009-01-21 2010-07-29 Oncalis Ag Pyrazolopyrimidines en tant qu'inhibiteurs de protéines kinases
PT2391366E (pt) 2009-01-29 2013-02-05 Novartis Ag Benzimidazoles substituídos para o tratamento de astrocitomas
WO2010099217A1 (fr) 2009-02-25 2010-09-02 Braincells, Inc. Modulation de neurogenèse à l'aide de combinaisons de d-cyclosérine
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
ES2473792T3 (es) 2009-04-03 2014-07-07 Naturewise Biotech & Medicals Corporation Compuestos cin�micos y derivados de los mismos para la inhibición de la histona desacetilasa
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
US8716344B2 (en) 2009-08-11 2014-05-06 President And Fellows Of Harvard College Class- and isoform-specific HDAC inhibitors and uses thereof
BR112012003262A8 (pt) 2009-08-12 2016-05-17 Novartis Ag compostos de hidrazona heterocíclica e seus usos para tratar câncer e inflamação
PE20121148A1 (es) 2009-08-17 2012-09-07 Intellikine Llc Compuestos heterociclicos y usos de los mismos
BR112012008061A2 (pt) 2009-08-20 2016-03-01 Novartis Ag compostos de oxima heterocíclica
IN2012DN01693A (fr) 2009-08-26 2015-06-05 Novartis Ag
AR077975A1 (es) 2009-08-28 2011-10-05 Irm Llc Derivados de pirazol pirimidina y composiciones como inhibidores de cinasa de proteina
US20110053925A1 (en) * 2009-08-28 2011-03-03 Novartis Ag Hydroxamate-Based Inhibitors of Deacetylases
BR112012010519A2 (pt) 2009-11-04 2017-12-05 Novartis Ag derivados de sulfonamida heterocíclicos
MX2012005987A (es) 2009-11-23 2012-06-25 Cerulean Pharma Inc Polimeros a base de ciclodextrina para administracion terapeutica.
ES2484171T3 (es) 2009-12-08 2014-08-11 Novartis Ag Derivados de sulfonamidas heterocíclicas
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
US20130040998A1 (en) * 2010-01-08 2013-02-14 Dana-Farber Cancer Institute, Inc. Fluorinated hdac inhibitors and uses thereof
EP2533783B8 (fr) 2010-01-13 2015-12-16 Tempero Pharmaceuticals, Inc. COMPOSÉS ET PROCÉDÉS pour l' inhibition d' HDAC
JP2013517281A (ja) 2010-01-13 2013-05-16 テンペロ、ファーマシューティカルズ、インコーポレイテッド 化合物及び方法
WO2011090940A1 (fr) 2010-01-19 2011-07-28 Cerulean Pharma Inc. Polymères à base de cyclodextrine pour administration thérapeutique
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
US20110237686A1 (en) 2010-03-26 2011-09-29 Cerulean Pharma Inc Formulations and methods of use
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
EA201390292A1 (ru) * 2010-08-27 2013-08-30 Новартис Аг Ингибиторы деацетилазы на основе гидроксамата
UY33794A (es) 2010-12-13 2012-07-31 Novartis Ag Inhibidores diméricos de las iap
US20130266590A1 (en) 2010-12-13 2013-10-10 Novartis Ag Dimeric iap inhibitors
EP2663312B1 (fr) 2011-01-10 2017-10-11 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
EP2673277A1 (fr) 2011-02-10 2013-12-18 Novartis AG Composés de [1, 2, 4]triazolo [4, 3 -b]pyridazine en tant qu'inhibiteurs de la tyrosine kinase c-met
TWI592411B (zh) 2011-02-23 2017-07-21 英特爾立秦有限責任公司 激酶抑制劑之組合及其用途
JP5808826B2 (ja) 2011-02-23 2015-11-10 インテリカイン, エルエルシー 複素環化合物およびその使用
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
IN2014DN00123A (fr) 2011-06-09 2015-05-22 Novartis Ag
MX344580B (es) 2011-06-14 2016-12-20 Novartis Ag Combinacion de panobinostat y ruxolitinib en el tratamiento del cancer tal como una neoplasia mieloproliferativa.
US8859535B2 (en) 2011-06-20 2014-10-14 Novartis Ag Hydroxy substituted isoquinolinone derivatives
EP2721007B1 (fr) 2011-06-20 2015-04-29 Novartis AG Composés de cyclohexyl-isoquinolinone
KR20140025530A (ko) 2011-06-27 2014-03-04 노파르티스 아게 테트라히드로-피리도-피리미딘 유도체의 고체 형태 및 염
US12194002B2 (en) 2011-08-17 2025-01-14 Dennis Brown Compositions and methods to improve the therapeutic benefit of suboptimally administered chemical compounds including substituted hexitols such as dibromodulcitol
EP2755976B1 (fr) 2011-09-15 2018-07-18 Novartis AG 3-(quinolin-6-ylthio)-[1,2,4]triazolo[4,3-a]pyradines substituées en position 6 à activité tyrosine kinase
AU2012335663B2 (en) 2011-11-11 2015-12-24 Array Biopharma Inc. Method of treating a proliferative disease
AR088936A1 (es) 2011-11-23 2014-07-16 Novartis Ag Formulaciones farmaceuticas
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
US20150148377A1 (en) 2011-12-22 2015-05-28 Novartis Ag Quinoline Derivatives
PT2794600T (pt) 2011-12-22 2018-03-13 Novartis Ag Derivados de 2,3-di-hidro-benzo[1,4]oxazina e compostos relacionados como inibidores de fosfoinositídeo-3-cinase (pi3k) para o tratamento de, por exemplo, artrite reumatoide
EA201491268A1 (ru) 2011-12-23 2014-11-28 Новартис Аг Соединения и композиции для ингибирования взаимодействия bcl2 с партнерами по связыванию
US20130178520A1 (en) 2011-12-23 2013-07-11 Duke University Methods of treatment using arylcyclopropylamine compounds
CN104136428A (zh) 2011-12-23 2014-11-05 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
CA2859867A1 (fr) 2011-12-23 2013-06-27 Novartis Ag Composes pour inhiber l'interaction de bcl-2 avec des partenaires de liaison
JP2015503518A (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
JP2015503519A (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
CA2862259A1 (fr) * 2011-12-29 2013-07-04 Pharmacyclics, Inc. Hydroxyamides d'acide cinnamique en tant qu'inhibiteurs d'histone desacetylase 8
EP3608317A1 (fr) 2012-01-12 2020-02-12 Yale University Composés et procédés pour la dégradation améliorée de protéines cibles et d'autres polypeptides par une e3 ubiquitine ligase
UY34591A (es) 2012-01-26 2013-09-02 Novartis Ag Compuestos de imidazopirrolidinona
TWI573792B (zh) 2012-02-01 2017-03-11 歐陸斯迪公司 新穎治療劑
JP2015512425A (ja) 2012-04-03 2015-04-27 ノバルティス アーゲー チロシンキナーゼ阻害剤との組合せ製品及びそれらの使用
CN104379574B (zh) 2012-05-15 2017-03-01 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
BR112014027584B1 (pt) 2012-05-15 2023-01-24 Novartis Ag Uso de inibidores da atividade de abl1, abl2 e bcr-abl1, e composição farmacêutica
SG11201407152XA (en) 2012-05-15 2014-11-27 Novartis Ag Benzamide derivatives for inhibiting the activity of abl1, abl2 and bcr-abl1
EA201492007A1 (ru) 2012-05-15 2015-03-31 Новартис Аг Производные бензамида для ингибирования активности abl1, abl2 и bcr-abl1
US9365576B2 (en) 2012-05-24 2016-06-14 Novartis Ag Pyrrolopyrrolidinone compounds
JP6427097B2 (ja) 2012-06-15 2018-11-21 ザ ブリガム アンド ウィメンズ ホスピタル インコーポレイテッドThe Brigham and Women’s Hospital, Inc. 癌を処置するための組成物および該組成物を製造するための方法
AR091773A1 (es) 2012-07-16 2015-02-25 Chdi Foundation Inc Inhibidores de la histona desacetilasa y composiciones y sus metodos de uso
WO2014025395A1 (fr) 2012-08-06 2014-02-13 Duke University Composés et procédés pour le ciblage de hsp90
PT2903968T (pt) 2012-10-02 2017-03-13 Gilead Sciences Inc Inibidores de desmetilases de histonas
PL2914254T3 (pl) 2012-10-30 2020-09-07 Mei Pharma, Inc. Terapie skojarzone w leczeniu nowotworów chemoodpornych
US9950047B2 (en) 2012-11-05 2018-04-24 Dana-Farber Cancer Institute, Inc. XBP1, CD138, and CS1 peptides, pharmaceutical compositions that include the peptides, and methods of using such peptides and compositions
CN104994850A (zh) 2012-11-08 2015-10-21 诺华股份有限公司 包含b-raf抑制剂和组蛋白脱乙酰基酶抑制剂的药物组合以及其在治疗增生性疾病中的用途
TW201422625A (zh) 2012-11-26 2014-06-16 Novartis Ag 二氫-吡啶并-□衍生物之固體形式
US9556180B2 (en) 2013-01-22 2017-01-31 Novartis Ag Pyrazolo[3,4-d]pyrimidinone compounds as inhibitors of the P53/MDM2 interaction
US9403827B2 (en) 2013-01-22 2016-08-02 Novartis Ag Substituted purinone compounds
WO2014128612A1 (fr) 2013-02-20 2014-08-28 Novartis Ag Dérivés de quinazolin-4-one
EP2961736B1 (fr) 2013-02-27 2018-04-11 Gilead Sciences, Inc. Inhibiteurs d'histone déméthylases
WO2014151147A1 (fr) 2013-03-15 2014-09-25 Intellikine, Llc Combinaison d'inhibiteurs de kinase et ses utilisations
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
EP2983674A4 (fr) 2013-04-08 2017-05-10 Dennis M. Brown Bénéfice thérapeutique de composés chimiques administrés de façon sous-optimale
WO2014168941A1 (fr) 2013-04-09 2014-10-16 Lixte Biotechnology, Inc. Formulations d'oxabicycloheptanes et d'oxabicycloheptènes
NZ712696A (en) 2013-04-29 2016-07-29 Chong Kun Dang Pharm Corp Novel 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
AU2014293011A1 (en) 2013-07-26 2016-03-17 Race Oncology Ltd. Compositions to improve the therapeutic benefit of bisantrene
WO2015022663A1 (fr) 2013-08-14 2015-02-19 Novartis Ag Composés et compositions utiles comme inhibiteurs de mek
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
JP6494634B2 (ja) 2013-09-22 2019-04-03 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 置換されているアミノピリミジン化合物および使用方法
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
WO2015084804A1 (fr) 2013-12-03 2015-06-11 Novartis Ag Combinaison d'un inhibiteur de mdm2 et d'un inhibiteur de braf, et leur utilisation
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
US9650379B2 (en) 2013-12-12 2017-05-16 Chong Kun Dang Pharmaceutical Corp. Azaindole derivatives as selective histone deacetylase (HDAC) inhibitors and pharmaceutical compositions comprising the same
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
EP3110820B1 (fr) 2014-02-28 2022-04-06 Nimbus Lakshmi, Inc. Inhibiteurs de tyk2 et leurs utilisations
LT3116909T (lt) 2014-03-14 2020-02-10 Novartis Ag Antikūno molekulės prieš lag-3 ir jų panaudojimas
WO2015148714A1 (fr) 2014-03-25 2015-10-01 Duke University Ligands de récepteurs de la protéine de choc thermique 70 (hsp-70)
EP3312164B1 (fr) 2014-03-28 2020-12-09 Calitor Sciences, LLC Composés d'hétéroaryle substitués et procédés d'utilisation
EP3126345A1 (fr) 2014-03-31 2017-02-08 Gilead Sciences, Inc. Inhibiteurs d'histones déméthylases
US10426753B2 (en) 2014-04-03 2019-10-01 Invictus Oncology Pvt. Ltd. Supramolecular combinatorial therapeutics
WO2015160845A2 (fr) 2014-04-14 2015-10-22 Arvinas, Inc. Modulateurs de la protéolyse, à base d'imide, et procédés d'utilisation associés
US20180228907A1 (en) 2014-04-14 2018-08-16 Arvinas, Inc. Cereblon ligands and bifunctional compounds comprising the same
GB201409485D0 (en) 2014-05-28 2014-07-09 Euro Celtique Sa Pharmaceutical composition
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
WO2016011658A1 (fr) 2014-07-25 2016-01-28 Novartis Ag Polythérapie
AU2015294889B2 (en) 2014-07-31 2018-03-15 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
WO2016023082A1 (fr) 2014-08-12 2016-02-18 Monash University Promédicaments de transport vers le système lymphatique
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
CA2960824A1 (fr) 2014-09-13 2016-03-17 Novartis Ag Therapies combinees d'inhibiteurs d'alk
ES2774448T3 (es) 2014-10-03 2020-07-21 Novartis Ag Terapias de combinación
HRP20210809T8 (hr) 2014-10-29 2021-09-17 Bicyclerd Limited Biciklični peptidni ligandi specifični za mt1-mmp
TWI744225B (zh) 2015-02-27 2021-11-01 美商林伯士拉克許米公司 酪胺酸蛋白質激酶2(tyk2)抑制劑及其用途
JP6692826B2 (ja) 2015-03-10 2020-05-13 アドゥロ バイオテック,インク. 「インターフェロン遺伝子刺激因子」依存性シグナル伝達の活性化のための組成物及び方法
BR112017019453A2 (pt) 2015-03-13 2018-05-15 Forma Therapeutics Inc compostos e composições de alfa-cinamida como inibidores de hdac8
HK1249058A1 (zh) 2015-03-18 2018-10-26 Arvinas, Inc. 用於增强靶向蛋白质降解的化合物和方法
WO2016190630A1 (fr) 2015-05-22 2016-12-01 Chong Kun Dang Pharmaceutical Corp. Composés dérivés d'alkyle hétérocycliques à utiliser en tant qu'inhibiteurs de l'histone désacétylase et compositions pharmaceutiques les comprenant
WO2017004133A1 (fr) 2015-06-29 2017-01-05 Nimbus Iris, Inc. Inhibiteurs d'irak et utilisations de ceux-ci
WO2017004134A1 (fr) 2015-06-29 2017-01-05 Nimbus Iris, Inc. Inhibiteurs d'irak et leurs utilisations
EP3331905B1 (fr) 2015-08-06 2022-10-05 Dana-Farber Cancer Institute, Inc. Dégradation de protéines ciblées destinée à atténuer une thérapie par transfert adoptif de cellules t associée des réponses inflammatoires indésirables
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
JP7118888B2 (ja) 2015-09-08 2022-08-16 モナッシュ ユニバーシティ リンパ指向性プロドラッグ
JP2018527362A (ja) 2015-09-11 2018-09-20 サンシャイン・レイク・ファーマ・カンパニー・リミテッドSunshine Lake Pharma Co.,Ltd. 置換されたヘテロアリール化合物および使用方法
CN121102186A (zh) 2015-10-23 2025-12-12 纳维托制药有限公司 Sestrin-gator2相互作用的调节剂和其用途
EP3370715A4 (fr) 2015-11-02 2019-05-15 Yale University Composés chimères de ciblage de protéolyse et procédés de préparation et d'utilisation de ceux-ci
ITUB20155193A1 (it) 2015-11-03 2017-05-03 Italfarmaco Spa Sospensioni orali di Givinostat fisicamente e chimicamente stabili
CA3008272A1 (fr) 2015-12-14 2017-06-22 X4 Pharmaceuticals, Inc. Methodes de traitement du cancer
JP6958820B2 (ja) 2015-12-14 2021-11-02 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 がんを処置する方法
EP3389664A4 (fr) 2015-12-14 2020-01-08 Raze Therapeutics Inc. Inhibiteurs de caféine de mthfd2 et leurs utilisations
JP7055380B2 (ja) 2015-12-22 2022-04-18 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 免疫不全疾患を処置するための方法
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
SI3426243T1 (sl) 2016-03-09 2021-11-30 Raze Therapeutics, Inc. Zaviralci 3-fosfoglicerat dehidrogenaze in uporabe le-teh
EP4234552A3 (fr) 2016-03-09 2023-10-18 Raze Therapeutics, Inc. Inhibiteurs de la 3-phosphoglycérate déshydrogénase et leurs utilisations
SG10201913290QA (en) 2016-03-15 2020-03-30 Oryzon Genomics Sa Combinations of lsd1 inhibitors for the treatment of hematological malignancies
CN109195593A (zh) 2016-03-15 2019-01-11 奥莱松基因组股份有限公司 用于治疗实体瘤的lsd1抑制剂的组合
US11337969B2 (en) 2016-04-08 2022-05-24 X4 Pharmaceuticals, Inc. Methods for treating cancer
US11261187B2 (en) 2016-04-22 2022-03-01 Duke University Compounds and methods for targeting 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
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
EP4483875A3 (fr) 2016-05-10 2025-04-02 C4 Therapeutics, Inc. Dégronimères spirocycliques pour la dégradation de protéines cibles
CN109790143A (zh) 2016-05-10 2019-05-21 C4医药公司 用于靶蛋白降解的胺连接的c3-戊二酰亚胺降解决定子体
CN109562107A (zh) 2016-05-10 2019-04-02 C4医药公司 用于靶蛋白降解的杂环降解决定子体
WO2017223229A1 (fr) 2016-06-21 2017-12-28 X4 Pharmaceuticals, Inc. Inhibiteurs de cxcr4 et leurs utilisations
CN109641859A (zh) * 2016-06-21 2019-04-16 墨尔本大学 Hiv潜伏的激活剂
CN116554168B (zh) 2016-06-21 2025-09-23 X4制药有限公司 Cxcr4抑制剂及其用途
CN109641838A (zh) 2016-06-21 2019-04-16 X4 制药有限公司 Cxcr4抑制剂及其用途
WO2018015493A1 (fr) 2016-07-20 2018-01-25 Royal College Of Surgeons In Ireland Complexes métalliques ayant des applications thérapeutiques
WO2018039205A1 (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(+)
US10927083B2 (en) 2016-09-29 2021-02-23 Duke University Substituted benzimidazoles as inhibitors of transforming growth factor-β kinase
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
CA3040155C (fr) 2016-10-11 2024-01-16 Euro-Celtique S.A. Compose d'utilisation dans le traitement du lymphome de hodgkin
EP3848370B1 (fr) 2016-10-14 2025-05-07 Takeda Pharmaceutical Company Limited Inhibiteurs de tyk2 et leurs utilisations
EP3528816A4 (fr) 2016-10-21 2020-04-08 Nimbus Lakshmi, Inc. Inhibiteurs de tyk2 et leurs utilisations
WO2018089499A1 (fr) 2016-11-08 2018-05-17 Navitor Pharmaceuticals, Inc. Inhibiteurs de la phényl amino pipéridine mtorc et leurs utilisations
US20180193270A1 (en) 2016-11-29 2018-07-12 PureTech Health LLC Exosomes for delivery of therapeutic agents
US11091451B2 (en) 2016-12-05 2021-08-17 Raze Therapeutics, Inc. SHMT inhibitors and uses thereof
MX2019006694A (es) 2016-12-08 2019-08-21 Lixte Biotechnology Inc Oxabicicloheptanos para la modulacion de la respuesta inmunitaria.
EP3559018A1 (fr) 2016-12-23 2019-10-30 Bicyclerd Limited Dérivés peptidiques ayant de nouvelles structures de liaison
US10624968B2 (en) 2017-01-06 2020-04-21 Bicyclerd Limited Compounds for treating cancer
CA3050309A1 (fr) 2017-01-31 2018-08-09 Arvinas Operations, Inc. Ligands de cereblon et composes bifonctionnels les contenant
WO2018148440A1 (fr) 2017-02-08 2018-08-16 Dana-Farber Cancer Institute, Inc. Régulation de récepteurs d'antigènes chimériques
TW202515876A (zh) 2017-03-08 2025-04-16 日商武田藥品工業股份有限公司 Tyk2抑制劑及其用途
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
WO2018197893A1 (fr) 2017-04-27 2018-11-01 Bicycletx Limited Ligands peptidiques bicycliques et leurs utilisations
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
GB201709405D0 (en) 2017-06-13 2017-07-26 Euro Celtique Sa Compounds for treating ovarian cancer
GB201709403D0 (en) 2017-06-13 2017-07-26 Euro Celtique Sa Compounds for treating sarcoma
GB201709402D0 (en) 2017-06-13 2017-07-26 Euro Celtique Sa Compounds for treating t-pll
GB201709406D0 (en) 2017-06-13 2017-07-26 Euro-Cletique S A Compounds for treating TNBC
CN118440096A (zh) 2017-06-20 2024-08-06 C4医药公司 用于蛋白降解的n/o-连接的降解决定子和降解决定子体
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
CN117946114A (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
WO2019025811A1 (fr) 2017-08-04 2019-02-07 Bicycletx Limited Ligands peptidiques bicycliques spécifiques de cd137
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
US20200283482A1 (en) 2017-08-14 2020-09-10 Bicyclerd Limited Bicyclic peptide ligand prr-a conjugates and uses thereof
EP4306524A3 (fr) 2017-08-29 2024-09-11 PureTech LYT, Inc. Promédicaments lipidiques dirigeant le système lymphatique
US11883497B2 (en) 2017-08-29 2024-01-30 Puretech Lyt, Inc. Lymphatic system-directing lipid prodrugs
US11358948B2 (en) 2017-09-22 2022-06-14 Kymera Therapeutics, Inc. CRBN ligands and uses thereof
IL273432B (en) 2017-09-22 2022-09-01 Kymera Therapeutics Inc Protein compounds and their uses
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
WO2019084026A1 (fr) 2017-10-24 2019-05-02 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
WO2019083962A1 (fr) 2017-10-24 2019-05-02 Oncopep, Inc. Vaccins peptidiques et pembrolizumab pour le traitement du cancer du sein
WO2019083960A1 (fr) 2017-10-24 2019-05-02 Oncopep, Inc. Vaccins peptidiques et inhibiteurs d'hdac pour le traitement du myélome multiple
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
US11304954B2 (en) 2017-12-19 2022-04-19 Puretech Lyt, Inc. Lipid prodrugs of mycophenolic acid and uses thereof
US11608345B1 (en) 2017-12-19 2023-03-21 Puretech Lyt, Inc. Lipid prodrugs of rapamycin and its analogs and uses thereof
EP3730483B1 (fr) 2017-12-21 2023-08-30 Hefei Institutes of Physical Science, Chinese Academy of Sciences Classe d'inhibiteurs de kinase dérivés de pyrimidine
IL315310A (en) 2017-12-26 2024-10-01 Kymera Therapeutics Inc Irak degraders and uses thereof
EP3737675A4 (fr) 2018-01-12 2022-01-05 Kymera Therapeutics, Inc. Ligands crbn et leurs utilisations
WO2019140380A1 (fr) 2018-01-12 2019-07-18 Kymera Therapeutics, Inc. Agents de dégradation de protéines et utilisations associées
US10751339B2 (en) 2018-01-20 2020-08-25 Sunshine Lake Pharma Co., Ltd. Substituted aminopyrimidine compounds and methods of use
SG11202006701TA (en) 2018-01-29 2020-08-28 Merck Patent Gmbh Gcn2 inhibitors and uses thereof
CN111867581B (zh) 2018-01-29 2023-12-26 默克专利股份有限公司 Gcn2抑制剂及其用途
EA202091931A1 (ru) 2018-02-12 2020-11-05 Иниммьюн Корпорейшн ЛИГАНДЫ Toll-ПОДОБНЫХ РЕЦЕПТОРОВ
MX2020008791A (es) 2018-02-23 2021-01-08 Bicycletx Ltd Ligandos de peptidos biciclicos multimericos.
EP3759086A1 (fr) 2018-02-27 2021-01-06 Artax Biopharma Inc. Dérivés de chromène en tant qu'inhibiteurs de l'interaction tcr-nck
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)
KR20210003804A (ko) 2018-04-13 2021-01-12 아비나스 오퍼레이션스, 인코포레이티드 세레브론 리간드 및 이를 포함하는 2작용성 화합물
JP7479293B2 (ja) 2018-04-24 2024-05-08 バーテックス ファーマシューティカルズ インコーポレイテッド プテリジノン化合物およびその使用
EP3784666B1 (fr) 2018-04-24 2022-03-16 Merck Patent GmbH Composés antiprolifératifs et leurs utilisations
JP2021533181A (ja) 2018-06-13 2021-12-02 アンフィスタ セラピューティクス リミテッド UchL5を標的化するための二機能性分子
JP2021527137A (ja) 2018-06-13 2021-10-11 アンフィスタ セラピューティクス リミテッド Rpn11を標的化するための二機能性分子
WO2019238886A1 (fr) 2018-06-13 2019-12-19 University Of Dundee Molécules bifonctionnelles pour le ciblage de l'usp14
HUE067446T2 (hu) 2018-06-15 2024-10-28 Janssen Pharmaceutica Nv Rapamicin analógok és alkalmazásaik
US11180531B2 (en) 2018-06-22 2021-11-23 Bicycletx Limited Bicyclic peptide ligands specific for Nectin-4
WO2020010177A1 (fr) 2018-07-06 2020-01-09 Kymera Therapeutics, Inc. Ligands crbn tricycliques et leurs utilisations
EP3817822A4 (fr) 2018-07-06 2022-07-27 Kymera Therapeutics, Inc. Agents de dégradation de protéines 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
US11414431B2 (en) 2018-10-15 2022-08-16 Nimbus Lakshmi, Inc. Substituted pyrazolo[1,5-a]pyrimidines as TYK2 inhibitors
EP3870597A1 (fr) 2018-10-23 2021-09-01 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
JP7530360B2 (ja) 2018-11-30 2024-08-07 武田薬品工業株式会社 Tyk2阻害剤およびその使用
CA3119773A1 (fr) 2018-11-30 2020-06-04 Kymera Therapeutics, Inc. Agents de degradation de kinases de type irak et leurs utilisations
GB201820325D0 (en) 2018-12-13 2019-01-30 Bicyclerd Ltd Bicyclic peptide ligands specific for psma
GB201820295D0 (en) 2018-12-13 2019-01-30 Bicyclerd Ltd Bicyclic peptide ligands specific for MT1-MMP
GB201820288D0 (en) 2018-12-13 2019-01-30 Bicycle Tx Ltd Bicycle peptide ligaands specific for MT1-MMP
JP2022522928A (ja) 2018-12-18 2022-04-21 ムンディファーマ・インターナショナル・コーポレーション・リミテッド 多発性骨髄腫を治療するための化合物
EP3670659A1 (fr) 2018-12-20 2020-06-24 Abivax Biomarqueurs et leurs utilisations dans le traitement d'infections virales, d'inflammations ou du cancer
CN113453679B (zh) 2018-12-20 2025-07-08 C4医药公司 靶向蛋白降解
EP3897849A1 (fr) 2018-12-21 2021-10-27 BicycleTx Limited Ligands peptidiques bicycliques spécifiques pour pd-l1
CA3126034A1 (fr) 2019-01-23 2020-07-30 Nimbus Lakshmi, Inc. Inhibiteurs de tyk2 et leurs utilisations
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
CN120574283A (zh) 2019-04-05 2025-09-02 凯麦拉医疗公司 Stat降解剂和其用途
TW202108559A (zh) 2019-05-31 2021-03-01 美商醫肯納腫瘤學公司 Tead抑制劑及其用途
WO2020251972A1 (fr) 2019-06-10 2020-12-17 Kymera Therapeutics, Inc. Agents de dégradation de smarca et leurs utilisations
GB201913124D0 (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
GB201913121D0 (en) 2019-09-11 2019-10-23 Seald As Compositions and methods for treatment of cholangiocarcinoma
US11845724B2 (en) 2019-09-11 2023-12-19 Vincere Biosciences, Inc. USP30 inhibitors and uses thereof
GB201913122D0 (en) 2019-09-11 2019-10-23 Seald As Compositions and methods for treatment of cholangiocarcinoma
WO2021050964A1 (fr) 2019-09-13 2021-03-18 Nimbus Saturn, Inc. Antagonistes de hpk1 et leurs utilisations
EP4034152A1 (fr) 2019-09-25 2022-08-03 University College Dublin Compositions de nanoparticules pour la thérapie génique
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
CA3152582A1 (fr) * 2019-11-06 2021-05-14 Dana-Farber Cancer Institute, Inc. Agents de degradation selectif de l'histone deacetylase (hdac) et leurs procedes d'utilisation
CA3163680A1 (fr) 2019-12-05 2021-06-10 David John O'neill Analogues de la rapamycine et leurs utilisations
EP4076524A4 (fr) 2019-12-17 2023-11-29 Kymera Therapeutics, Inc. Agents de dégradation d'irak et leurs utilisations
JP2023509366A (ja) 2019-12-17 2023-03-08 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
PE20221582A1 (es) 2019-12-19 2022-10-06 Arvinas Operations Inc Compuestos y metodos para la degradacion dirigida de receptor de androgenos
CN115297931A (zh) 2019-12-23 2022-11-04 凯麦拉医疗公司 Smarca降解剂和其用途
WO2021148581A1 (fr) 2020-01-22 2021-07-29 Onxeo Nouvelle molécule dbait et son utilisation
WO2021159021A1 (fr) 2020-02-05 2021-08-12 Puretech Lyt, Inc. Promédicaments lipidiques de neurostéroïdes
IT202000004075A1 (it) * 2020-02-27 2021-08-27 Flamma Spa Processo per la preparazione di panobinostat
TW202146393A (zh) 2020-03-03 2021-12-16 美商皮克醫療公司 Eif4e抑制劑及其用途
EP4117662A4 (fr) 2020-03-10 2024-04-03 X4 Pharmaceuticals, Inc. Méthodes de traitement de la neutropénie
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
US12528785B2 (en) 2020-03-19 2026-01-20 Kymera Therapeutics, Inc. MDM2 degraders and uses thereof
CN115768890A (zh) 2020-04-15 2023-03-07 加州理工学院 通过分子和物理启动对t细胞免疫疗法的热控制
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
US20230250110A1 (en) 2020-06-03 2023-08-10 Kymera Therapeutics, Inc. Deuterated irak degraders and uses thereof
CA3189761A1 (fr) 2020-08-03 2022-02-10 Gemma Mudd Lieurs a base de peptides
JP2023536346A (ja) 2020-08-05 2023-08-24 エリプシーズ ファーマ リミテッド シクロデキストリン含有ポリマートポイソメラーゼ阻害剤コンジュゲートおよびparp阻害剤を用いた癌の処置
MX2023001588A (es) 2020-08-17 2023-05-03 Bicycletx Ltd Conjugados biciclo específicos para nectina-4 y usos de estos.
US11999964B2 (en) 2020-08-28 2024-06-04 California Institute Of Technology Synthetic mammalian signaling circuits for robust cell population control
US12331046B2 (en) 2020-10-23 2025-06-17 Nimbus Clotho, Inc. CTPS1 inhibitors and uses thereof
WO2022120353A1 (fr) 2020-12-02 2022-06-09 Ikena Oncology, Inc. Inhibiteurs de tead et leurs utilisations
CN117015531A (zh) 2020-12-02 2023-11-07 医肯纳肿瘤学公司 Tead抑制剂及其用途
WO2022129925A1 (fr) 2020-12-18 2022-06-23 Amphista Therapeutics Limited Nouvelles molécules bifonctionnelles pour la dégradation ciblée de protéines
GB202020359D0 (en) 2020-12-22 2021-02-03 Midatech Pharma Wales Ltd Pharmaceutical compositions and use thereof in combination therapy for brain cancer
TW202241891A (zh) 2020-12-30 2022-11-01 美商凱麥拉醫療公司 Irak降解劑及其用途
BR112023015584A2 (pt) 2021-02-02 2023-10-24 Liminal Biosciences Ltd Antagonistas de gpr84 e usos dos mesmos
EP4288427A1 (fr) 2021-02-02 2023-12-13 Liminal Biosciences Limited Antagonistes de gpr84 et leurs utilisations
US12171768B2 (en) 2021-02-15 2024-12-24 Kymera Therapeutics, Inc. IRAK4 degraders and uses thereof
KR20240007155A (ko) 2021-04-09 2024-01-16 님버스 클리오, 인코포레이티드 Cbl-b 조절제 및 이의 용도
WO2022221866A1 (fr) 2021-04-16 2022-10-20 Ikena Oncology, Inc. Inhibiteurs de mek et leurs utilisations
IL308314A (en) 2021-05-07 2024-01-01 Kymera Therapeutics Inc CDK2 compounds and their uses
JP2024532276A (ja) 2021-08-25 2024-09-05 ピク セラピューティクス, インコーポレイテッド eIF4E阻害剤及びその使用
US12234231B2 (en) 2021-08-25 2025-02-25 PIC Therapeutics, Inc. EIF4E inhibitors and uses thereof
EP4405680A1 (fr) 2021-09-20 2024-07-31 Institut National de la Santé et de la Recherche Médicale (INSERM) 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
AR127505A1 (es) 2021-10-29 2024-01-31 Kymera Therapeutics Inc Degradadores irak-4 y síntesis de los mismos
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
WO2023147594A2 (fr) 2022-01-31 2023-08-03 Kymera Therapeutics, Inc. Agents de dégradation d'irak 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
GB2617409B (en) 2022-04-27 2024-06-26 Cancertain Ltd Method for predicting responsiveness to therapy
WO2023211889A1 (fr) 2022-04-25 2023-11-02 Ikena Oncology, Inc. Composés polymorphes et leurs utilisations
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
CN119384408A (zh) 2022-06-16 2025-01-28 安菲斯塔治疗有限责任公司 用于靶向蛋白降解的双功能分子
KR20250057801A (ko) 2022-08-02 2025-04-29 리미널 바이오사이언시스 리미티드 아릴-트라이아졸릴 및 관련 gpr84 길항제 및 이의 용도
IL318710A (en) 2022-08-02 2025-03-01 Univ Hokkaido Nat Univ Corp Methods for improving cellular therapy with organelle complexes
KR20250056924A (ko) 2022-08-02 2025-04-28 리미널 바이오사이언시스 리미티드 치환된 피리돈 gpr84 길항제 및 이의 용도
CN120019047A (zh) 2022-08-02 2025-05-16 里米诺生物科学有限公司 杂芳基甲酰胺和相关gpr84拮抗剂及其用途
WO2024041744A1 (fr) 2022-08-26 2024-02-29 Biodexa Ltd. Polythérapie pour le cancer du cerveau
WO2024112894A1 (fr) 2022-11-22 2024-05-30 PIC Therapeutics, Inc. Inhibiteurs d'eif4e et leurs utilisations
EP4676454A1 (fr) 2023-03-03 2026-01-14 iOnctura SA Combinaison de roginolisib et d'un inhibiteur de hdac dans le traitement d'une malignité hématologique
CN120865251A (zh) 2023-06-23 2025-10-31 凯麦拉医疗公司 Irak降解剂及其用途
WO2025026925A1 (fr) 2023-07-28 2025-02-06 Ospedale San Raffaele S.R.L. Inhibiteurs de gtf2i et leurs utilisations
CN119490449B (zh) * 2023-08-16 2025-11-21 沈阳药科大学 含n-苄基-2-(5-苯基吡啶-2-基)乙酰胺的异羟肟酸类化合物及制备方法和应用
WO2025062372A1 (fr) 2023-09-21 2025-03-27 Takeda Pharmaceutical Company Limited Inhibiteurs de tyk2 destinés à être utilisés dans le traitement d'une maladie inflammatoire de l'intestin
WO2025078542A1 (fr) 2023-10-11 2025-04-17 Technological University Dublin Complexes coumarine-métal et leurs utilisations
CN118027033A (zh) * 2024-01-26 2024-05-14 四川大学 一种hdac6抑制剂及其制备方法和在抗炎和溃疡性结肠炎中的用途

Family Cites Families (28)

* 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
EP0570594B1 (fr) 1991-12-10 1997-07-30 Shionogi & Co., Ltd. Derive d'acide hydroxamique a base de sulfonamide aromatique
GB9215665D0 (en) * 1992-07-23 1992-09-09 British Bio Technology Compounds
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
CN1273579A (zh) 1997-08-05 2000-11-15 美国家用产品公司 氨茴酸类似物
EP1123111B1 (fr) 1998-10-19 2004-09-15 Methylgene, Inc. Modulation de l'expression de l'adn methyltransferase par therapie combinee
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
CN1378450A (zh) 1999-09-08 2002-11-06 斯隆-凯特林癌症研究院 新型细胞分化剂和组蛋白脱乙酰基酶抑制剂及其使用方法
GB9922173D0 (en) 1999-09-21 1999-11-17 Zeneca Ltd Chemical compounds
EP1233958B1 (fr) 1999-11-23 2011-06-29 MethylGene Inc. Inhibiteurs de l'histone deacetylase
AU1959001A (en) 1999-12-08 2001-06-18 Axys Pharmaceuticals, Inc. Histone deacetylase-8 proteins, nucleic acids, and methods of use
TW427572U (en) * 1999-12-17 2001-03-21 Hon Hai Prec Ind Co Ltd Electrical connector
US7288567B2 (en) 2000-03-24 2007-10-30 Methylgene Inc. Inhibitors of histone deacetylase
CA2408385A1 (fr) 2000-03-24 2001-09-24 Methylgene, Inc. Inhibition d'isoformes de deacetylase d'histones specifiques
AU2001280167A1 (en) 2000-08-31 2002-03-13 Wakunaga Pharmaceutical Co.,Ltd Novel propenohydroxamic acid derivatives
PE20020354A1 (es) * 2000-09-01 2002-06-12 Novartis Ag Compuestos de hidroxamato como inhibidores de histona-desacetilasa (hda)
CA2425097A1 (fr) 2000-10-05 2002-04-11 Fujisawa Pharmaceutical Co., Ltd. Composes a base de benzamide, inhibiteurs des secretions d'apolipoproteine b
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
AU2002323098A1 (en) 2001-08-11 2003-03-03 Bristol-Myers Squibb Pharma Company Selective estrogen receptor modulators
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

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