|
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
|
|
US6541661B1
(en)
|
1999-11-23 |
2003-04-01 |
Methylgene, Inc. |
Inhibitors of 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)
|
|
JP2004509941A
(ja)
|
2000-09-29 |
2004-04-02 |
プロリフィクス リミテッド |
Hdacインヒビターとしてのアミド結合を含むカルバミン酸化合物
|
|
US7312247B2
(en)
*
|
2001-03-27 |
2007-12-25 |
Errant Gene Therapeutics, Llc |
Histone deacetylase inhibitors
|
|
EP1443928B1
(en)
|
2001-10-16 |
2011-07-27 |
Sloan-Kettering Institute For Cancer Research |
Treatment of neurodegenerative diseases and cancer of the brain
|
|
EP1443967B1
(en)
*
|
2001-11-06 |
2007-01-24 |
Novartis AG |
Cyclooxygenase-2 inhibitor/histone deacetylase inhibitor combination
|
|
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
|
|
MXPA04008577A
(es)
|
2002-03-04 |
2005-07-13 |
Aton Pharma Inc |
Metodos para inducir diferenciacion terminal.
|
|
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.
|
|
US7495022B2
(en)
|
2002-04-11 |
2009-02-24 |
Sk Chemicals Co., Ltd. |
α,β-unsaturated hydroxamic acid derivatives and their use as histone deacetylase inhibitors
|
|
US20040018968A1
(en)
*
|
2002-04-15 |
2004-01-29 |
George Sgouros |
Use of histone deacetylase inhibitors in combination with radiation for the treatment of cancer
|
|
PL372070A1
(en)
*
|
2002-06-10 |
2005-07-11 |
Novartis Ag |
Combinations comprising epothilones and pharmaceutical uses thereof
|
|
US20050272647A1
(en)
*
|
2002-08-20 |
2005-12-08 |
Noboru Yamaji |
Arthrodial cartilage extracellular matrix degradation inhibitor
|
|
BR0314112A
(pt)
*
|
2002-09-13 |
2005-07-12 |
Univ Virginia Commonwealth |
Combinação de a) n-{5-[4-(4-metil-piperazino-metil)-benzoilamido]-2-metil fenil}-4-(3-piridil)-2-pirimidina-amina e b) um inibidor de desacetilase de histona para o tratamento de leucemia
|
|
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
|
|
US20060223826A1
(en)
*
|
2002-11-19 |
2006-10-05 |
Takeda Pharmaceutical Company Limited Intellectual Property Department |
Indole derivatives as somatostatin agonists or antagonists
|
|
AU2003296310A1
(en)
|
2002-12-06 |
2004-06-30 |
University Of South Florida |
Histone deacetylase inhibitor enhancement of trail-induced apoptosis
|
|
TW200418806A
(en)
*
|
2003-01-13 |
2004-10-01 |
Fujisawa Pharmaceutical Co |
HDAC inhibitor
|
|
JP4612621B2
(ja)
|
2003-01-17 |
2011-01-12 |
トポターゲット ユーケー リミテッド |
Hdac阻害剤としてのエステル又はケトン結合を含むカルバミン酸化合物
|
|
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
|
|
CA2526908A1
(en)
*
|
2003-05-21 |
2004-12-02 |
Novartis Ag |
Combination of histone deacetylase inhibitors with chemotherapeutic agents
|
|
WO2005011598A2
(en)
*
|
2003-07-31 |
2005-02-10 |
University Of South Florida |
Leukemia treatment method and composition
|
|
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
|
|
WO2005014004A1
(en)
*
|
2003-08-08 |
2005-02-17 |
Novartis Ag |
Combinations comprising staurosporines
|
|
EP2201947A3
(en)
|
2003-08-26 |
2010-08-11 |
Merck HDAC Research, LLC |
Use of SAHA for treating mesothelioma
|
|
JP2007504131A
(ja)
|
2003-08-29 |
2007-03-01 |
エートン ファーマ インコーポレーティッド |
癌の組み合わせ処置法
|
|
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
|
|
PL1673349T3
(pl)
*
|
2003-09-22 |
2010-11-30 |
Mei Pharma Inc |
Pochodne benzimidazolu: wytwarzanie i zastosowania farmaceutyczne
|
|
TWI349664B
(en)
|
2003-09-22 |
2011-10-01 |
S Bio Pte Ltd |
Benzimidazole derivatives: preparation and pharmaceutical applications
|
|
MXPA06003163A
(es)
*
|
2003-09-23 |
2006-06-05 |
Novartis Ag |
Combinacion de un inhibidor de receptor de vegf con un agente quimioterapeutico.
|
|
US20070167499A1
(en)
*
|
2003-10-27 |
2007-07-19 |
A*Bio Pte Ltd. |
Biaryl linked hydroxamates: preparation and pharmaceutical applications
|
|
AU2004296764B2
(en)
*
|
2003-12-02 |
2011-04-28 |
The Ohio State University Research Foundation |
Zn2+ -chelating motif-tethered short -chain fatty acids as a novel class of histone deacetylase inhibitors
|
|
EP1541549A1
(en)
|
2003-12-12 |
2005-06-15 |
Exonhit Therapeutics S.A. |
Tricyclic hydroxamate and benzaminde derivatives, compositions and methods
|
|
WO2005065681A1
(en)
*
|
2003-12-19 |
2005-07-21 |
Takeda San Diego, Inc. |
N- hydroxy-3-(3-(1h-imidazol-2-yl)-phenyl)-acrylamide derivatives and related compounds as histone deacetylase (hdac) inhibitors for the treatment of cancer
|
|
WO2005066151A2
(en)
*
|
2003-12-19 |
2005-07-21 |
Takeda San Diego, 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
|
|
PL2253614T3
(pl)
|
2004-04-07 |
2013-03-29 |
Novartis Ag |
Inhibitory IAP
|
|
CA2574035A1
(en)
*
|
2004-07-19 |
2006-02-23 |
Sandro Belvedere |
Histone deacetylase inhibitors
|
|
MX2007001550A
(es)
*
|
2004-08-09 |
2007-04-10 |
Astellas Pharma Inc |
Compuestos de hidroxiamida que tienen actividad como inhibidores de histona desacetilasa (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
(en)
|
2004-12-16 |
2006-06-22 |
Takeda San Diego, Inc. |
Histone deacetylase inhibitors
|
|
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
|
|
EP3354265A1
(en)
|
2005-03-22 |
2018-08-01 |
President and Fellows of Harvard College |
Treatment of solid tumors
|
|
GB0509223D0
(en)
|
2005-05-05 |
2005-06-15 |
Chroma Therapeutics Ltd |
Enzyme inhibitors
|
|
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
|
|
GB0510390D0
(en)
|
2005-05-20 |
2005-06-29 |
Novartis Ag |
Organic compounds
|
|
TWI365068B
(en)
|
2005-05-20 |
2012-06-01 |
Merck Sharp & Dohme |
Formulations of suberoylanilide hydroxamic acid and methods for producing same
|
|
WO2007011626A2
(en)
|
2005-07-14 |
2007-01-25 |
Takeda San Diego, Inc. |
Histone deacetylase inhibitors
|
|
WO2007016532A2
(en)
*
|
2005-08-02 |
2007-02-08 |
Novartis Ag |
Mutations and polymorphisms of hdac4
|
|
JP5665271B2
(ja)
*
|
2005-08-03 |
2015-02-04 |
ノバルティス アーゲー |
骨髄腫の処置のためのhdac阻害剤の使用
|
|
US20090012066A1
(en)
*
|
2005-08-10 |
2009-01-08 |
Novartis Ag |
Method of Use of Deacetylase Inhibitors
|
|
US20080200489A1
(en)
*
|
2005-08-11 |
2008-08-21 |
Peter Wisdom Atadja |
Combination of Organic Compounds
|
|
WO2007025177A2
(en)
|
2005-08-26 |
2007-03-01 |
Braincells, Inc. |
Neurogenesis by muscarinic receptor modulation
|
|
EP2258359A3
(en)
|
2005-08-26 |
2011-04-06 |
Braincells, Inc. |
Neurogenesis by muscarinic receptor modulation with sabcomelin
|
|
US20070155730A1
(en)
*
|
2005-08-26 |
2007-07-05 |
Methylgene, Inc. |
Benzodiazepine And Benzopiperazine Analog Inhibitors Of Histone Deacetylase
|
|
WO2007030454A2
(en)
*
|
2005-09-07 |
2007-03-15 |
Novartis Ag |
Mutations and polymorphisms of hdac9
|
|
WO2007030455A2
(en)
*
|
2005-09-07 |
2007-03-15 |
Novartis Ag |
Mutations and polymorphisms of hdac10
|
|
WO2007038073A2
(en)
*
|
2005-09-22 |
2007-04-05 |
Novartis Ag |
Mutations and polymorphisms of hdac11
|
|
JP2009510073A
(ja)
|
2005-09-27 |
2009-03-12 |
ノバルティス アクチエンゲゼルシャフト |
カルボキシアミン化合物およびその使用方法
|
|
CA2625153A1
(en)
|
2005-10-21 |
2007-04-26 |
Braincells, Inc. |
Modulation of neurogenesis by pde inhibition
|
|
WO2007047998A2
(en)
*
|
2005-10-21 |
2007-04-26 |
Novartis Ag |
Mutations and polymorphisms of hdac2
|
|
AU2006306240A1
(en)
*
|
2005-10-24 |
2007-05-03 |
Novartis Ag |
Combination of histone deacetylase inhibitors and radiation
|
|
EP1942879A1
(en)
|
2005-10-31 |
2008-07-16 |
Braincells, Inc. |
Gaba receptor mediated modulation of neurogenesis
|
|
WO2007053502A2
(en)
*
|
2005-11-01 |
2007-05-10 |
Novartis Ag |
Mutations and polymorphisms of hdac5
|
|
WO2007058992A2
(en)
*
|
2005-11-14 |
2007-05-24 |
Novartis Ag |
Mutations and polymorphisms of hdac6
|
|
JP2009516671A
(ja)
|
2005-11-21 |
2009-04-23 |
ノバルティス アクチエンゲゼルシャフト |
mTOR阻害剤を使用する神経内分泌腫瘍処置
|
|
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
|
|
AU2007213018A1
(en)
|
2006-02-07 |
2007-08-16 |
Astellas Pharma Inc. |
N-hydroxyacrylamide compounds
|
|
CA2642273C
(en)
*
|
2006-02-14 |
2016-09-20 |
President And Fellows Of Harvard College |
Bifunctional histone deacetylase inhibitors
|
|
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
|
|
BRPI0709750A2
(pt)
|
2006-04-05 |
2011-07-26 |
Novartis Ag |
combinaÇÕes de agentes terapÊuticos para tratamento de cÂncer
|
|
CA2644143C
(en)
|
2006-04-05 |
2013-10-01 |
Novartis Ag |
Combinations comprising bcr-abl/c-kit/pdgf-r tk inhibitors for treating cancer
|
|
ES2637592T3
(es)
|
2006-04-14 |
2017-10-13 |
Cell Signaling Technology, Inc. |
Defectos de genes y quinasa ALK mutante en tumores sólidos humanos
|
|
US8168383B2
(en)
|
2006-04-14 |
2012-05-01 |
Cell Signaling Technology, Inc. |
Gene defects and mutant ALK kinase in human solid tumors
|
|
WO2007145704A2
(en)
|
2006-04-24 |
2007-12-21 |
Gloucester Pharmaceuticals |
Gemcitabine combination therapy
|
|
US20090018142A9
(en)
*
|
2006-05-02 |
2009-01-15 |
Zhengping Zhuang |
Use of phosphatases to treat tumors overexpressing N-CoR
|
|
EP2021000A2
(en)
|
2006-05-09 |
2009-02-11 |
Braincells, Inc. |
Neurogenesis by modulating angiotensin
|
|
AU2007247112B2
(en)
|
2006-05-09 |
2010-08-26 |
Novartis Ag |
Combination comprising an iron chelator and an anti-neoplastic agent and use thereof
|
|
US7678808B2
(en)
|
2006-05-09 |
2010-03-16 |
Braincells, Inc. |
5 HT receptor mediated neurogenesis
|
|
US8957027B2
(en)
|
2006-06-08 |
2015-02-17 |
Celgene Corporation |
Deacetylase inhibitor therapy
|
|
MX366213B
(es)
*
|
2006-06-12 |
2019-07-01 |
Novartis Ag Star |
Procesamiento para hacer n-hidroxi-3 [4-[[[2-(2-metil-1h-indol-3-i l)etil]amino]metil]fenil] -2e-2-propenamida y materiales de partida para la misma.
|
|
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
|
|
KR20090026282A
(ko)
|
2006-06-12 |
2009-03-12 |
노파르티스 아게 |
N-히드록시-3-[4-[[[2-(2-메틸-1h-인돌-3-일)에틸]아미노]메틸]페닐]-2e-2-프로펜아미드의 염을 제조하는 방법
|
|
SMP200900002B
(it)
*
|
2006-06-12 |
2010-01-19 |
Novartis Ag |
Sali di n-idrossi-3-[4-[[[2-(2-metil-1h-indol-3-il)etil]ammino]metil]fenil]-2e-2-propenammide
|
|
UA95289C2
(en)
*
|
2006-06-12 |
2011-07-25 |
Новартис Аг |
Salts of n-hydroxy-3-[4-[[[2-(2-methyl-1h-indol-3-yl)ethyl]amino]methyl]phenyl]-2e-2-propenamide
|
|
RU2009102275A
(ru)
*
|
2006-06-26 |
2010-08-10 |
Новартис АГ (CH) |
Органические соединения
|
|
CA2662491A1
(en)
|
2006-09-08 |
2008-03-13 |
Braincells, Inc. |
Combinations containing a 4-acylaminopyridine derivative
|
|
US20100184806A1
(en)
|
2006-09-19 |
2010-07-22 |
Braincells, Inc. |
Modulation of neurogenesis by ppar agents
|
|
WO2008036046A1
(en)
|
2006-09-20 |
2008-03-27 |
S*Bio Pte Ltd |
IMIDAZO[l,2-a]PYRIDINE HYDROXYMATE COMPOUNDS THAT ARE INHIBITORS OF HISTONE DEACETYLASE
|
|
EP2079304A4
(en)
*
|
2006-09-28 |
2010-01-06 |
Merck & Co Inc |
AMINBASE SALTS FROM SAHA AND POLYMORPHE DAVON
|
|
WO2008037477A1
(en)
|
2006-09-29 |
2008-04-03 |
Novartis Ag |
Pyrazolopyrimidines as p13k lipid kinase inhibitors
|
|
GB0619753D0
(en)
*
|
2006-10-06 |
2006-11-15 |
Chroma Therapeutics Ltd |
Enzyme inhibitors
|
|
EP2077999B1
(en)
|
2006-10-30 |
2014-07-30 |
Chroma Therapeutics Limited |
Hydroxamates as inhibitors of histone deacetylase
|
|
WO2008058287A1
(en)
*
|
2006-11-10 |
2008-05-15 |
Syndax Pharmaceuticals, Inc. |
COMBINATION OF ERα+ LIGANDS AND HISTONE DEACETYLASE INHIBITORS FOR THE TREATMENT OF CANCER
|
|
US8093220B2
(en)
*
|
2006-12-04 |
2012-01-10 |
Novartis Ag |
Combination of an HDAC inhibitor and an antimetabolite
|
|
WO2008075757A1
(en)
*
|
2006-12-15 |
2008-06-26 |
Astellas Pharma Inc. |
N-hydroxyacrylamide compounds
|
|
MX2009007343A
(es)
*
|
2007-01-10 |
2009-07-15 |
Novartis Ag |
Formulaciones de inhibidores de desacetilasa.
|
|
AU2008214299B2
(en)
|
2007-02-06 |
2014-01-09 |
Lixte Biotechnology, Inc. |
Oxabicycloheptanes and oxabicycloheptenes, their preparation and use
|
|
RU2009134223A
(ru)
|
2007-02-15 |
2011-03-20 |
Новартис АГ (CH) |
Комбинация lbh589 с другими терапевтическими средствами, предназначенная для лечения рака
|
|
CA2680838A1
(en)
|
2007-03-28 |
2008-10-16 |
Santen Pharmaceutical Co., Ltd. |
Intraocular pressure-lowering agent comprising compound having histone deacetylase inhibitory effect as active ingredient
|
|
EP2139850B1
(en)
*
|
2007-04-09 |
2018-09-12 |
MethylGene Inc. |
Inhibitors of histone deacetylase
|
|
MX2009011692A
(es)
*
|
2007-05-04 |
2009-11-10 |
Novartis Ag |
Uso de inhibidores de desacetilasa de histona (hdac) para el tratamiento de canceres gastrointestinales.
|
|
MX2009012179A
(es)
*
|
2007-05-11 |
2009-12-01 |
Novartis Ag |
Uso de inhibidores de desacetilasa de histona (hdac) para el tratamiento de melanoma.
|
|
CA2687274A1
(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
|
|
WO2009020565A1
(en)
*
|
2007-08-03 |
2009-02-12 |
Lixte Biotechnology, Inc. |
Use of phosphates to treat neuroblastomas and medullogastomas
|
|
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.
|
|
ES2628748T3
(es)
*
|
2007-10-01 |
2017-08-03 |
Lixte Biotechnology, Inc. |
Inhibidores de la HDAC
|
|
MX2010004402A
(es)
*
|
2007-10-22 |
2010-10-15 |
Orchid Res Lab Ltd |
Inhibidores de histona deacetilasa.
|
|
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
(en)
*
|
2007-11-19 |
2009-05-28 |
Syndax Pharmaceuticals, Inc. |
Combinations of hdac inhibitors and proteasome inhibitors
|
|
CA2706750A1
(en)
*
|
2007-11-27 |
2009-06-04 |
Ottawa Health Research Institute |
Amplification of cancer-specific oncolytic viral infection by histone deacetylase inhibitors
|
|
CA2708281A1
(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
(en)
*
|
2008-03-13 |
2009-09-16 |
4Sc Ag |
Novel N-substituted tetrahydroisoquinoline/isoindoline hydroxamic acid compounds
|
|
EA020114B1
(ru)
|
2008-03-24 |
2014-08-29 |
Новартис Аг |
Производные арилсульфонамида в качестве ингибиторов матриксной металлопротеазы
|
|
JP5330498B2
(ja)
*
|
2008-03-26 |
2013-10-30 |
ノバルティス アーゲー |
脱アセチル化酵素bのヒドロキサメートを基にした阻害剤
|
|
JP2011528662A
(ja)
*
|
2008-07-18 |
2011-11-24 |
ノバルティス アーゲー |
ホジキン病の治療のためのhdac阻害剤の使用
|
|
AU2009274549B2
(en)
|
2008-07-23 |
2014-05-01 |
Dana-Farber Cancer Institute, Inc. |
Deacetylase inhibitors and uses thereof
|
|
WO2010147612A1
(en)
|
2009-06-18 |
2010-12-23 |
Lixte Biotechnology, Inc. |
Methods of modulating cell regulation by inhibiting p53
|
|
US8227473B2
(en)
|
2008-08-01 |
2012-07-24 |
Lixte Biotechnology, Inc. |
Oxabicycloheptanes and oxabicycloheptenes, their preparation and use
|
|
AU2009277086B2
(en)
|
2008-08-01 |
2015-12-10 |
Lixte Biotechnology, Inc. |
Neuroprotective agents for the prevention and treatment of neurodegenerative diseases
|
|
WO2010014141A1
(en)
*
|
2008-08-01 |
2010-02-04 |
Lixte Biotechnology, Inc. |
Methods for regulating cell mitosis by inhibiting serine/threonine phosphatase
|
|
WO2010083617A1
(en)
|
2009-01-21 |
2010-07-29 |
Oncalis Ag |
Pyrazolopyrimidines as protein kinase inhibitors
|
|
HRP20121006T1
(hr)
|
2009-01-29 |
2013-01-31 |
Novartis Ag |
Supstituirani benzimidazoli za lijeäśenje astrocitoma
|
|
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
(en)
|
2009-04-03 |
2014-02-26 |
NatureWise Biotech & Medicals Corporation |
Cinamic compounds and derivatives therefrom for the inhibition of histone deacetylase
|
|
WO2011006908A2
(en)
|
2009-07-16 |
2011-01-20 |
Royal College Of Surgeons In Ireland |
Metal complexes having dual histone deacetylase inhibitory and dna-binding activity
|
|
US8389526B2
(en)
|
2009-08-07 |
2013-03-05 |
Novartis Ag |
3-heteroarylmethyl-imidazo[1,2-b]pyridazin-6-yl derivatives
|
|
WO2011019393A2
(en)
*
|
2009-08-11 |
2011-02-17 |
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
|
|
ES2709108T3
(es)
|
2009-08-17 |
2019-04-15 |
Intellikine Llc |
Compuestos heterocíclicos y usos de los mismos
|
|
EA201200318A1
(ru)
|
2009-08-20 |
2012-09-28 |
Новартис Аг |
Гетероциклические оксимы
|
|
US20120149661A1
(en)
|
2009-08-26 |
2012-06-14 |
Novartis Ag |
Tetra-substituted heteroaryl compounds and their use as mdm2 and/or mdm4 modulators
|
|
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
|
|
EA201200651A1
(ru)
|
2009-11-04 |
2012-12-28 |
Новартис Аг |
Гетероциклические сульфонамидные производные, применимые в качестве ингибиторов мек
|
|
AU2010321533A1
(en)
|
2009-11-23 |
2012-05-31 |
Cerulean Pharma Inc. |
Cyclodextrin-based polymers for therapeutic delivery
|
|
AU2012265844A1
(en)
|
2009-12-08 |
2013-05-02 |
Novartis Ag |
Heterocyclic sulfonamide derivatives
|
|
PE20121384A1
(es)
|
2009-12-08 |
2012-10-13 |
Novartis Ag |
Derivados de sulfonamida heterociclicos
|
|
US8440693B2
(en)
|
2009-12-22 |
2013-05-14 |
Novartis Ag |
Substituted isoquinolinones and quinazolinones
|
|
CU24130B1
(es)
|
2009-12-22 |
2015-09-29 |
Novartis Ag |
Isoquinolinonas y quinazolinonas sustituidas
|
|
EP2638009A4
(en)
*
|
2010-01-08 |
2014-06-11 |
Harvard College |
FLUORINATED HDAC HEMMER AND USES THEREOF
|
|
EP2523664A4
(en)
|
2010-01-13 |
2013-06-26 |
Tempero Pharmaceuticals Inc |
COMPOUNDS AND METHODS
|
|
ES2560627T3
(es)
|
2010-01-13 |
2016-02-22 |
Tempero Pharmaceuticals, Inc. |
Compuestos y procedimientos para la inhibición de HDAC
|
|
WO2011090940A1
(en)
|
2010-01-19 |
2011-07-28 |
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
|
|
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
(en)
|
2010-07-14 |
2012-01-18 |
Dublin Institute of Technology Intellectual Property Ltd |
Copper II complexes of phenanthroline and their use in cancer treatment
|
|
WO2012025701A1
(en)
*
|
2010-08-25 |
2012-03-01 |
Chroma Therapeutics Ltd. |
Alpha, alpha - di substituted glycine ester derivatives and their use as hdac inhibitors
|
|
WO2012025155A1
(en)
*
|
2010-08-26 |
2012-03-01 |
Novartis Ag |
Hydroxamate-based inhibitors of deacetylases
|
|
WO2012025164A1
(en)
*
|
2010-08-27 |
2012-03-01 |
Novartis Ag |
Hydroxamate-based inhibitors of deacetylases
|
|
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
(en)
|
2011-01-10 |
2017-10-11 |
Nimbus Iris, Inc. |
Irak inhibitors and uses thereof
|
|
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
|
|
CA2828483A1
(en)
|
2011-02-23 |
2012-11-01 |
Intellikine, Llc |
Combination of kinase inhibitors and uses thereof
|
|
EP2678016B1
(en)
|
2011-02-23 |
2016-08-10 |
Intellikine, LLC |
Heterocyclic compounds and uses thereof
|
|
US20140051716A1
(en)
|
2011-03-09 |
2014-02-20 |
Cereno Scientific Ab |
Compounds and methods for improving impaired endogenous fibrinolysis using histone deacetylase inhibitors
|
|
CA2844407A1
(en)
|
2011-06-14 |
2012-12-20 |
Novartis Ag |
Combination of panobinostat and ruxolitinib in the treatment of cancer such as a myeloproliferative neoplasm
|
|
US8859586B2
(en)
|
2011-06-20 |
2014-10-14 |
Novartis Ag |
Cyclohexyl isoquinolinone compounds
|
|
EP2721008B1
(en)
|
2011-06-20 |
2015-04-29 |
Novartis AG |
Hydroxy substituted isoquinolinone derivatives as p53 (mdm2 or mdm4) inhibitors
|
|
EA201490164A1
(ru)
|
2011-06-27 |
2014-04-30 |
Новартис Аг |
Твердые формы и соли производных тетрагидропиридопиримидина
|
|
EP3795145A3
(en)
|
2011-08-17 |
2021-06-09 |
Dennis M. Brown |
Compositions and methods to improve the therapeutic benefit of suboptimally administered chemical compounds including substituted hexitols such as dibromodulcitol
|
|
WO2013038362A1
(en)
|
2011-09-15 |
2013-03-21 |
Novartis Ag |
6 - substituted 3 - (quinolin- 6 - ylthio) - [1,2,4] triazolo [4, 3 -a] pyradines as tyrosine kinase
|
|
RU2622015C2
(ru)
|
2011-11-11 |
2017-06-08 |
Новартис Аг |
Способ лечения пролиферативного заболевания
|
|
JP6216325B2
(ja)
|
2011-11-23 |
2017-10-18 |
ノバルティス アーゲー |
医薬製剤
|
|
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
|
|
SG11201402237WA
(en)
|
2011-12-22 |
2014-09-26 |
Novartis Ag |
Dihydro-benzo-oxazine and dihydro-pyrido-oxazine derivatives
|
|
US20150148377A1
(en)
|
2011-12-22 |
2015-05-28 |
Novartis Ag |
Quinoline Derivatives
|
|
EP2794590A1
(en)
|
2011-12-23 |
2014-10-29 |
Novartis AG |
Compounds for inhibiting the interaction of bcl2 with binding partners
|
|
AU2012355624A1
(en)
|
2011-12-23 |
2014-07-17 |
Novartis Ag |
Compounds for inhibiting the interaction of BCL2 with binding partners
|
|
CA2859862A1
(en)
|
2011-12-23 |
2013-06-27 |
Novartis Ag |
Compounds for inhibiting the interaction of bcl2 with binding partners
|
|
US20130178520A1
(en)
|
2011-12-23 |
2013-07-11 |
Duke University |
Methods of treatment using arylcyclopropylamine compounds
|
|
KR20140107578A
(ko)
|
2011-12-23 |
2014-09-04 |
노파르티스 아게 |
Bcl2와 결합 파트너의 상호작용을 억제하기 위한 화합물
|
|
KR20140104047A
(ko)
|
2011-12-23 |
2014-08-27 |
노파르티스 아게 |
Bcl2와 결합 파트너의 상호작용을 억제하기 위한 화합물
|
|
EP2797875A4
(en)
*
|
2011-12-29 |
2015-09-02 |
Pharmacyclics Inc |
CINNAMIC ACID HYDROXYAMIDES AS HISTONE DEACETYLASE INHIBITORS 8
|
|
KR102438072B1
(ko)
|
2012-01-12 |
2022-08-31 |
예일 유니버시티 |
E3 유비퀴틴 리가아제에 의한 표적 단백질 및 다른 폴리펩티드의 증진된 분해를 위한 화합물 및 방법
|
|
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
|
|
MX371119B
(es)
|
2012-04-03 |
2020-01-17 |
Novartis Ag |
Productos de combinacion con los inhibidores de cinasa de tirosina y su uso.
|
|
AP3613A
(en)
|
2012-05-15 |
2016-02-29 |
Novartis Ag |
Benzamide derivatives for inhibiting the activity of abl1, abl2 and bcr-abl1 abl1abl2 bcr-abl1
|
|
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
|
|
US9278981B2
(en)
|
2012-05-15 |
2016-03-08 |
Novartis Ag |
Compounds and compositions for inhibiting the activity of ABL1, ABL2 and BCR-ABL1
|
|
PT2900637T
(pt)
|
2012-05-15 |
2017-11-15 |
Novartis Ag |
Derivados de amida de pirimidina, piridina e pirazina substituídos com tiazole ou imidazole e compostos relacionados como inibidores de abl1, abl2 e bcr-abl1 para tratamento do cancro, infecções virais específicas e disturbios do snc específicos
|
|
CN104321325B
(zh)
|
2012-05-24 |
2016-11-16 |
诺华股份有限公司 |
吡咯并吡咯烷酮化合物
|
|
AU2013274101B2
(en)
|
2012-06-15 |
2017-09-07 |
The Brigham And Women's Hospital, Inc. |
Compositions for treating cancer and methods for making the same
|
|
AR091773A1
(es)
|
2012-07-16 |
2015-02-25 |
Chdi Foundation Inc |
Inhibidores de la histona desacetilasa y composiciones y sus metodos de uso
|
|
US9738643B2
(en)
|
2012-08-06 |
2017-08-22 |
Duke University |
Substituted indazoles for targeting Hsp90
|
|
HUE033380T2
(en)
|
2012-10-02 |
2017-11-28 |
Gilead Sciences Inc |
Inhibitors of histone demethylases
|
|
WO2014070948A1
(en)
|
2012-10-30 |
2014-05-08 |
Mei Pharma, Inc. |
Combination therapies
|
|
JP6374392B2
(ja)
|
2012-11-05 |
2018-08-15 |
デイナ ファーバー キャンサー インスティチュート,インコーポレイテッド |
Xbp1、cd138およびcs1ペプチド、該ペプチドを含有する薬学的組成物、ならびにかかるペプチドおよび組成物を使用する方法
|
|
RU2015121367A
(ru)
|
2012-11-08 |
2017-01-10 |
Новартис Аг |
Фармацевтическая комбинация, содержащая ингибитор b-raf и ингибитор деацетилазы гистонов, и ее применение при лечении пролиферативных заболеваний
|
|
TW201422625A
(zh)
|
2012-11-26 |
2014-06-16 |
Novartis Ag |
二氫-吡啶并-□衍生物之固體形式
|
|
WO2014115080A1
(en)
|
2013-01-22 |
2014-07-31 |
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
(en)
|
2013-02-20 |
2014-08-28 |
Novartis Ag |
Quinazolin-4-one derivatives
|
|
MX2015011097A
(es)
|
2013-02-27 |
2016-03-09 |
Epitherapeutics Aps |
Inhibidores de histona desmetilasas.
|
|
WO2014151147A1
(en)
|
2013-03-15 |
2014-09-25 |
Intellikine, Llc |
Combination of kinase inhibitors and uses thereof
|
|
WO2014155268A2
(en)
|
2013-03-25 |
2014-10-02 |
Novartis Ag |
Fgf-r tyrosine kinase activity inhibitors - use in diseases associated with lack of or reduced snf5 activity
|
|
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
|
|
EA201591931A1
(ru)
|
2013-04-09 |
2016-05-31 |
Ликсте Байотекнолоджи, Инк. |
Композиции оксабициклогептанов и оксабициклогептенов
|
|
PT2991982T
(pt)
*
|
2013-04-29 |
2018-11-28 |
Chong Kun Dang Pharmaceutical Corp |
Novos compostos para inibidores seletivos de histonadesacetilase e composição farmacêutica que os compreende
|
|
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
|
|
CN105764501A
(zh)
|
2013-07-26 |
2016-07-13 |
现代化制药公司 |
改善比生群治疗效益的组合物
|
|
WO2015022664A1
(en)
|
2013-08-14 |
2015-02-19 |
Novartis Ag |
Compounds and compositions as inhibitors of mek
|
|
WO2015022663A1
(en)
|
2013-08-14 |
2015-02-19 |
Novartis Ag |
Compounds and compositions as inhibitors of mek
|
|
US9227969B2
(en)
|
2013-08-14 |
2016-01-05 |
Novartis Ag |
Compounds and compositions as inhibitors of MEK
|
|
CA2918938C
(en)
|
2013-09-22 |
2021-05-18 |
Calitor Sciences, Llc |
Substituted aminopyrimidine compounds and methods of use
|
|
WO2015048312A1
(en)
|
2013-09-26 |
2015-04-02 |
Costim Pharmaceuticals Inc. |
Methods for treating hematologic cancers
|
|
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
|
|
HRP20181965T1
(hr)
|
2013-12-12 |
2019-02-08 |
Chong Kun Dang Pharmaceutical Corp. |
Novi derivati azaindola kao selektivni inhibitori histonske deacetilaze (hdac) i farmaceutski pripravci koji ih sadrže
|
|
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
|
|
EP4019518A1
(en)
|
2014-02-28 |
2022-06-29 |
Nimbus Lakshmi, Inc. |
Tyk2 inhibitors and uses thereof
|
|
EP3116909B1
(en)
|
2014-03-14 |
2019-11-13 |
Novartis Ag |
Antibody molecules to lag-3 and uses thereof
|
|
WO2015148714A1
(en)
|
2014-03-25 |
2015-10-01 |
Duke University |
Heat shock protein 70 (hsp-70) receptor ligands
|
|
AU2015235880B2
(en)
|
2014-03-28 |
2018-11-01 |
Sunshine Lake Pharma Co., Ltd. |
Substituted heteroaryl compounds and methods of use
|
|
CA2943824A1
(en)
|
2014-03-31 |
2015-10-08 |
Gilead Sciences, Inc. |
Inhibitors of histone demethylases
|
|
KR20160132496A
(ko)
|
2014-04-03 |
2016-11-18 |
인빅터스 온콜로지 피비티. 엘티디. |
초분자 조합 치료제
|
|
US20180228907A1
(en)
|
2014-04-14 |
2018-08-16 |
Arvinas, Inc. |
Cereblon ligands and bifunctional compounds comprising the same
|
|
EP3131588B1
(en)
|
2014-04-14 |
2025-11-05 |
Arvinas Operations, Inc. |
Imide-based modulators of proteolysis and associated methods of use
|
|
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
|
|
GB201409471D0
(en)
|
2014-05-28 |
2014-07-09 |
Euro Celtique Sa |
Pharmaceutical composition
|
|
WO2016011658A1
(en)
|
2014-07-25 |
2016-01-28 |
Novartis Ag |
Combination therapy
|
|
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
|
|
CN112430250A
(zh)
|
2014-08-12 |
2021-03-02 |
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
(en)
|
2014-09-09 |
2016-03-16 |
Dublin Institute of Technology |
Hybrid compounds formed from ionic liquids and uses thereof in ion selective electrodes
|
|
AU2015314756A1
(en)
|
2014-09-13 |
2017-03-16 |
Novartis Ag |
Combination therapies of alk inhibitors
|
|
EP3662903A3
(en)
|
2014-10-03 |
2020-10-14 |
Novartis AG |
Combination therapies
|
|
WO2016067035A1
(en)
|
2014-10-29 |
2016-05-06 |
Bicycle Therapeutics Limited |
Bicyclic peptide ligands specific for mt1-mmp
|
|
EP3262049B1
(en)
|
2015-02-27 |
2022-07-20 |
Nimbus Lakshmi, Inc. |
Tyk2 inhibitors and uses thereof
|
|
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
|
|
MX2017011778A
(es)
|
2015-03-13 |
2017-12-04 |
Forma Therapeutics Inc |
Compuestos y composiciones de alfa-cinamida como inhibidores de histona desacetilasa 8 (hdac8).
|
|
KR20230175343A
(ko)
|
2015-03-18 |
2023-12-29 |
아비나스 오퍼레이션스, 인코포레이티드 |
타겟화된 단백질들의 향상된 분해를 위한 화합물들 및 방법들
|
|
WO2016190630A1
(en)
|
2015-05-22 |
2016-12-01 |
Chong Kun Dang Pharmaceutical Corp. |
Heterocyclicalkyl derivative compounds as selective histone deacetylase inhibitors and pharmaceutical compositions comprising the same
|
|
WO2017004134A1
(en)
|
2015-06-29 |
2017-01-05 |
Nimbus Iris, Inc. |
Irak inhibitors and uses thereof
|
|
WO2017004133A1
(en)
|
2015-06-29 |
2017-01-05 |
Nimbus Iris, Inc. |
Irak inhibitors and uses thereof
|
|
AU2016301196B2
(en)
|
2015-08-06 |
2022-09-08 |
Dana-Farber Cancer Institute, Inc. |
Tunable endogenous protein degradation
|
|
WO2017032281A1
(zh)
*
|
2015-08-21 |
2017-03-02 |
苏州晶云药物科技有限公司 |
帕比司他乳酸盐的新晶型
|
|
TWI707852B
(zh)
|
2015-09-02 |
2020-10-21 |
美商林伯士拉克許米公司 |
Tyk2 抑制劑及其用途
|
|
WO2017041139A1
(en)
|
2015-09-08 |
2017-03-16 |
Monash University |
Lymph directing prodrugs
|
|
WO2017044434A1
(en)
|
2015-09-11 |
2017-03-16 |
Sunshine Lake Pharma Co., Ltd. |
Substituted heteroaryl compounds and methods of use
|
|
HRP20230331T1
(hr)
|
2015-10-23 |
2023-07-07 |
Navitor Pharmaceuticals, Inc. |
Modulatori interakcije sestrin-gator2 i njihova uporaba
|
|
KR20180097530A
(ko)
|
2015-11-02 |
2018-08-31 |
예일 유니버시티 |
단백질분해 표적화 키메라 화합물(Proteolysis Targeting Chimera compound) 및 그의 제조 및 사용 방법
|
|
ITUB20155193A1
(it)
|
2015-11-03 |
2017-05-03 |
Italfarmaco Spa |
Sospensioni orali di Givinostat fisicamente e chimicamente stabili
|
|
JP6864296B2
(ja)
|
2015-12-14 |
2021-04-28 |
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
|
|
WO2017106332A1
(en)
|
2015-12-14 |
2017-06-22 |
X4 Pharmaceuticals, Inc. |
Methods for treating cancer
|
|
WO2017106352A1
(en)
|
2015-12-14 |
2017-06-22 |
Raze Therapeutics, Inc. |
Caffeine inhibitors of mthfd2 and uses thereof
|
|
SI3393468T1
(sl)
|
2015-12-22 |
2023-01-31 |
X4 Pharmaceuticals, Inc. |
Postopki za zdravljenje bolezni imunske pomanjkljivosti
|
|
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
|
|
US11014882B2
(en)
*
|
2016-03-09 |
2021-05-25 |
Raze Therapeutics, Inc. |
3-phosphoglycerate dehydrogenase inhibitors and uses thereof
|
|
LT3426243T
(lt)
|
2016-03-09 |
2021-08-10 |
Raze Therapeutics, Inc. |
3-fosfogliceratdehidrogenazės inhibitoriai ir jų panaudojimas
|
|
WO2017157825A1
(en)
|
2016-03-15 |
2017-09-21 |
F. Hoffmann-La Roche Ag |
Combinations of lsd1 inhibitors for use in the treatment of solid tumors
|
|
WO2017157813A1
(en)
|
2016-03-15 |
2017-09-21 |
F. Hoffmann-La Roche Ag |
Combinations of lsd1 inhibitors for the treatment of hematological malignancies
|
|
CA3019394A1
(en)
|
2016-04-08 |
2017-10-12 |
X4 Pharmaceuticals, Inc. |
Methods for treating cancer
|
|
WO2017184956A1
(en)
|
2016-04-22 |
2017-10-26 |
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
|
|
EP4491236A3
(en)
|
2016-05-10 |
2025-04-02 |
C4 Therapeutics, Inc. |
Heterocyclic degronimers for target protein degradation
|
|
WO2017197046A1
(en)
|
2016-05-10 |
2017-11-16 |
C4 Therapeutics, Inc. |
C3-carbon linked glutarimide degronimers for target protein degradation
|
|
EP3454862B1
(en)
|
2016-05-10 |
2024-09-11 |
C4 Therapeutics, Inc. |
Spirocyclic degronimers for target protein degradation
|
|
WO2017197051A1
(en)
|
2016-05-10 |
2017-11-16 |
C4 Therapeutics, Inc. |
Amine-linked c3-glutarimide degronimers for target protein degradation
|
|
EP3484858A4
(en)
*
|
2016-06-21 |
2020-02-26 |
The University of Melbourne |
HIV LATENCY ACTIVATORS
|
|
WO2017223229A1
(en)
|
2016-06-21 |
2017-12-28 |
X4 Pharmaceuticals, Inc. |
Cxcr4 inhibitors and uses thereof
|
|
EP3808748A1
(en)
|
2016-06-21 |
2021-04-21 |
X4 Pharmaceuticals, Inc. |
Substituted piperidines as cxcr4-inhibitors
|
|
JP6994767B2
(ja)
|
2016-06-21 |
2022-01-14 |
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
|
|
WO2018015493A1
(en)
|
2016-07-20 |
2018-01-25 |
Royal College Of Surgeons In Ireland |
Metal complexes having therapeutic applications
|
|
WO2018039203A1
(en)
|
2016-08-23 |
2018-03-01 |
Oncopep, Inc. |
Peptide vaccines and durvalumab for treating multiple myeloma
|
|
WO2018039205A1
(en)
|
2016-08-23 |
2018-03-01 |
Oncopep, Inc. |
Peptide vaccines and durvalumab for treating breast cancer
|
|
WO2018054960A1
(en)
|
2016-09-21 |
2018-03-29 |
INSERM (Institut National de la Santé et de la Recherche Médicale) |
Methods for predicting and treating resistance to chemotherapy in npm-alk(+) alcl
|
|
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
|
|
WO2018068832A1
(en)
|
2016-10-11 |
2018-04-19 |
Euro-Celtique S.A. |
Hodgkin lymphoma therapy
|
|
JP7082130B2
(ja)
|
2016-10-14 |
2022-06-07 |
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
|
|
AU2017345736B2
(en)
|
2016-10-21 |
2022-04-07 |
Takeda Pharmaceutical Company Limited |
TYK2 inhibitors and uses thereof
|
|
WO2018089499A1
(en)
|
2016-11-08 |
2018-05-17 |
Navitor Pharmaceuticals, Inc. |
PHENYL AMINO PIPERIDINE mTORC INHIBITORS AND USES THEREOF
|
|
CA3043768A1
(en)
|
2016-11-29 |
2018-06-07 |
PureTech Health LLC |
Exosomes for delivery of therapeutic agents
|
|
WO2018106636A1
(en)
|
2016-12-05 |
2018-06-14 |
Raze Therapeutics, Inc. |
Shmt inhibitors and uses thereof
|
|
JP7246309B2
(ja)
|
2016-12-08 |
2023-03-27 |
リクスト・バイオテクノロジー,インコーポレイテッド |
免疫応答を調節するためのオキサビシクロヘプタン
|
|
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
|
|
ES2985986T3
(es)
|
2017-01-06 |
2024-11-08 |
Bicyclerd Ltd |
Conjugado biciclo para tratar el cáncer
|
|
AU2018215212B2
(en)
|
2017-01-31 |
2022-06-02 |
Arvinas Operations, Inc. |
Cereblon ligands and bifunctional compounds comprising the same
|
|
JP7227912B2
(ja)
|
2017-02-08 |
2023-02-24 |
ダナ-ファーバー キャンサー インスティテュート,インコーポレイテッド |
キメラ抗原受容体の調節
|
|
EP4338802A3
(en)
|
2017-03-08 |
2024-09-04 |
Takeda Pharmaceutical Company Limited |
Tyk2 inhibitors, uses, and methods for production thereof
|
|
EP3375778A1
(en)
|
2017-03-14 |
2018-09-19 |
Artax Biopharma Inc. |
Aryl-piperidine derivatives
|
|
EP3375784A1
(en)
|
2017-03-14 |
2018-09-19 |
Artax Biopharma Inc. |
Aza-dihydro-acridone derivatives
|
|
WO2018191146A1
(en)
|
2017-04-10 |
2018-10-18 |
Navitor Pharmaceuticals, Inc. |
Heteroaryl rheb inhibitors and uses thereof
|
|
JOP20180036A1
(ar)
|
2017-04-18 |
2019-01-30 |
Vifor Int Ag |
أملاح لمثبطات فروبورتين جديدة
|
|
EP3615550A1
(en)
|
2017-04-27 |
2020-03-04 |
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
|
|
GB201709402D0
(en)
|
2017-06-13 |
2017-07-26 |
Euro Celtique Sa |
Compounds for treating t-pll
|
|
GB201709405D0
(en)
|
2017-06-13 |
2017-07-26 |
Euro Celtique Sa |
Compounds for treating ovarian cancer
|
|
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
|
|
EP3645549A1
(en)
|
2017-06-26 |
2020-05-06 |
BicycleRD Limited |
Bicyclic peptide ligands with detectable moieties and uses thereof
|
|
CN111194317A
(zh)
|
2017-07-28 |
2020-05-22 |
林伯士拉克许米公司 |
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
|
|
CN111183147B
(zh)
|
2017-08-04 |
2024-07-05 |
拜斯科技术开发有限公司 |
Cd137特异性的双环肽配体
|
|
EP3668550A1
(en)
|
2017-08-14 |
2020-06-24 |
Bicyclerd Limited |
Bicyclic peptide ligand prr-a conjugates and uses thereof
|
|
US20200291096A1
(en)
|
2017-08-14 |
2020-09-17 |
Bicyclerd Limited |
Bicyclic peptide ligand sting conjugates and uses thereof
|
|
WO2019046491A1
(en)
|
2017-08-29 |
2019-03-07 |
Ariya Therapeutics, Inc. |
LIPIDIC PRODRUGS DIRECTING TO THE LYMPHATIC SYSTEM
|
|
US11883497B2
(en)
|
2017-08-29 |
2024-01-30 |
Puretech Lyt, Inc. |
Lymphatic system-directing lipid prodrugs
|
|
EP4624467A2
(en)
|
2017-09-22 |
2025-10-01 |
Kymera Therapeutics, Inc. |
Protein degraders and uses thereof
|
|
US11358948B2
(en)
|
2017-09-22 |
2022-06-14 |
Kymera Therapeutics, Inc. |
CRBN ligands and uses thereof
|
|
EP3461480A1
(en)
|
2017-09-27 |
2019-04-03 |
Onxeo |
Combination of a dna damage response cell cycle checkpoint inhibitors and belinostat for treating cancer
|
|
EP3461488A1
(en)
|
2017-09-27 |
2019-04-03 |
Onxeo |
Combination of a dbait molecule and a hdac inhibitor for treating cancer
|
|
WO2019084030A1
(en)
|
2017-10-24 |
2019-05-02 |
Genentech, Inc. |
(4-HYDROXYPYRROLIDIN-2-YL) -HYDROXAMATE COMPOUNDS AND METHODS OF USE
|
|
WO2019084026A1
(en)
|
2017-10-24 |
2019-05-02 |
Genentech, Inc. |
(4-HYDROXYPYRROLIDIN-2-YL) -HETEROCYCLIC COMPOUNDS AND METHODS OF USE
|
|
WO2019083960A1
(en)
|
2017-10-24 |
2019-05-02 |
Oncopep, Inc. |
PEPTIDE VACCINES AND HDAC INHIBITORS FOR THE TREATMENT OF MULTIPLE MYELOMA
|
|
WO2019083962A1
(en)
|
2017-10-24 |
2019-05-02 |
Oncopep, Inc. |
PEPTIDE AND PEMBROLIZUMAB VACCINES FOR THE TREATMENT OF BREAST CANCER
|
|
JP7254076B2
(ja)
|
2017-11-19 |
2023-04-07 |
サンシャイン・レイク・ファーマ・カンパニー・リミテッド |
置換ヘテロアリール化合物及び使用方法
|
|
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
|
|
US11602534B2
(en)
|
2017-12-21 |
2023-03-14 |
Hefei Institutes Of Physical Science, Chinese Academy Of Sciences |
Pyrimidine derivative kinase inhibitors
|
|
IL315310A
(en)
|
2017-12-26 |
2024-10-01 |
Kymera Therapeutics Inc |
Irak degraders and uses thereof
|
|
EP3737675A4
(en)
|
2018-01-12 |
2022-01-05 |
Kymera Therapeutics, Inc. |
Crbn ligands and uses thereof
|
|
WO2019140380A1
(en)
|
2018-01-12 |
2019-07-18 |
Kymera Therapeutics, Inc. |
Protein degraders and uses thereof
|
|
US10751339B2
(en)
|
2018-01-20 |
2020-08-25 |
Sunshine Lake Pharma Co., Ltd. |
Substituted aminopyrimidine compounds and methods of use
|
|
TWI816742B
(zh)
|
2018-01-29 |
2023-10-01 |
美商維泰克斯製藥公司 |
Gcn2抑制劑及其用途
|
|
MX2020007797A
(es)
|
2018-01-29 |
2020-09-18 |
Merck Patent Gmbh |
Inhibidores de la cinasa 2 de control general no desrepresible (gcn2) y usos de los mismos.
|
|
KR102895036B1
(ko)
|
2018-02-12 |
2025-12-03 |
이니뮨 코퍼레이션 |
톨-유사 수용체 리간드
|
|
EP3755725A1
(en)
|
2018-02-23 |
2020-12-30 |
BicycleTX Limited |
Multimeric bicyclic peptide ligands
|
|
CN112189009B
(zh)
|
2018-02-27 |
2023-09-29 |
阿塔克斯生物制药有限公司 |
作为tcr-nck相互作用的抑制剂的色烯衍生物
|
|
WO2019183523A1
(en)
|
2018-03-23 |
2019-09-26 |
Genentech, Inc. |
Hetero-bifunctional degrader compounds and their use as modulators of targeted ubiquination (vhl)
|
|
WO2019199816A1
(en)
|
2018-04-13 |
2019-10-17 |
Arvinas Operations, Inc. |
Cereblon ligands and bifunctional compounds comprising the same
|
|
IL301501B2
(en)
|
2018-04-24 |
2024-10-01 |
Vertex Pharma |
Antiproliferation compounds and uses thereof
|
|
TWI884914B
(zh)
|
2018-04-24 |
2025-06-01 |
美商維泰克斯製藥公司 |
喋啶酮化合物及其用途
|
|
WO2019238886A1
(en)
|
2018-06-13 |
2019-12-19 |
University Of Dundee |
Bifunctional molecules for targeting usp14
|
|
EP3807272A1
(en)
|
2018-06-13 |
2021-04-21 |
Amphista Therapeutics Ltd |
Bifunctional molecules for targeting rpn11
|
|
EP3807263A1
(en)
|
2018-06-13 |
2021-04-21 |
Amphista Therapeutics Ltd |
Bifunctional molecules for targeting uchl5
|
|
CN117843659A
(zh)
|
2018-06-15 |
2024-04-09 |
詹森药业有限公司 |
雷帕霉素类似物和其用途
|
|
IL279489B2
(en)
|
2018-06-22 |
2025-10-01 |
Bicycletx Ltd |
Bicyclic peptide ligands specific for nectin-4, a drug conjugate containing the peptide ligands and a pharmaceutical composition containing the drug conjugate
|
|
US12454520B2
(en)
|
2018-07-06 |
2025-10-28 |
Kymera Therapeutics, Inc. |
Protein degraders and uses thereof
|
|
WO2020010177A1
(en)
|
2018-07-06 |
2020-01-09 |
Kymera Therapeutics, Inc. |
Tricyclic crbn ligands and uses thereof
|
|
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
|
|
US12220423B2
(en)
|
2018-07-24 |
2025-02-11 |
Hygia Pharmaceuticals, Llc |
Compounds, derivatives, and analogs for cancer
|
|
US10548889B1
(en)
|
2018-08-31 |
2020-02-04 |
X4 Pharmaceuticals, Inc. |
Compositions of CXCR4 inhibitors and methods of preparation and use
|
|
EP3846793B1
(en)
|
2018-09-07 |
2024-01-24 |
PIC Therapeutics, Inc. |
Eif4e inhibitors and uses thereof
|
|
CN113271940A
(zh)
|
2018-10-15 |
2021-08-17 |
林伯士拉克许米公司 |
Tyk2抑制剂和其用途
|
|
JP2022512779A
(ja)
|
2018-10-23 |
2022-02-07 |
バイスクルテクス・リミテッド |
二環式ペプチドリガンドおよびその使用
|
|
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
|
|
KR102891608B1
(ko)
|
2018-11-30 |
2025-11-28 |
카이메라 쎄라퓨틱스 인코포레이티드 |
Irak 분해제 및 이의 용도
|
|
WO2020112937A1
(en)
|
2018-11-30 |
2020-06-04 |
Nimbus Lakshmi, Inc. |
Tyk2 inhibitors and uses thereof
|
|
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
|
|
GB201820325D0
(en)
|
2018-12-13 |
2019-01-30 |
Bicyclerd Ltd |
Bicyclic peptide ligands specific for psma
|
|
WO2020128912A1
(en)
|
2018-12-18 |
2020-06-25 |
Mundipharma International Corporation Limited |
Compounds for treating lymphoma or a t-cell malignant disease
|
|
EP3670659A1
(en)
|
2018-12-20 |
2020-06-24 |
Abivax |
Biomarkers, and uses in treatment of viral infections, inflammations, or cancer
|
|
CN120698983A
(zh)
|
2018-12-20 |
2025-09-26 |
C4医药公司 |
靶向蛋白降解
|
|
EP3897849A1
(en)
|
2018-12-21 |
2021-10-27 |
BicycleTx Limited |
Bicyclic peptide ligands specific for pd-l1
|
|
WO2020154474A1
(en)
|
2019-01-23 |
2020-07-30 |
Nimbus Lakshmi, Inc. |
Tyk2 inhibitors and uses thereof
|
|
WO2020165600A1
(en)
|
2019-02-14 |
2020-08-20 |
Bicycletx Limited |
Bicyclic peptide ligand sting conjugates and uses thereof
|
|
EP3946462A1
(en)
|
2019-04-02 |
2022-02-09 |
BicycleTX Limited |
Bicycle toxin conjugates and uses thereof
|
|
KR20220006139A
(ko)
|
2019-04-05 |
2022-01-14 |
카이메라 쎄라퓨틱스 인코포레이티드 |
Stat 분해제 및 이의 용도
|
|
CA3141826A1
(en)
|
2019-05-31 |
2020-12-03 |
Ikena Oncology, Inc. |
Tead inhibitors and uses thereof
|
|
GB201913121D0
(en)
|
2019-09-11 |
2019-10-23 |
Seald As |
Compositions and methods for treatment of cholangiocarcinoma
|
|
CA3150492A1
(en)
|
2019-09-11 |
2021-03-18 |
Donna L. Romero |
USP30 INHIBITORS AND USES THEREOF
|
|
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
|
|
GB201913122D0
(en)
|
2019-09-11 |
2019-10-23 |
Seald As |
Compositions and methods for treatment of cholangiocarcinoma
|
|
MX2022002877A
(es)
|
2019-09-13 |
2022-08-08 |
Nimbus Saturn Inc |
Antagonistas de cinasa progenitora hematopoyetica 1 (hpk1) y sus usos.
|
|
BR112022005412A2
(pt)
|
2019-09-25 |
2022-06-21 |
Univ Dublin |
Composições nanoparticuladas para terapia gênica
|
|
EP3798250A1
(en)
|
2019-09-25 |
2021-03-31 |
University College Dublin |
Hyperbranched cationic polymers useful as nucleic acid delivery vectors for transfecting
|
|
US20220401564A1
(en)
*
|
2019-11-06 |
2022-12-22 |
Dana-Farber Cancer Institute, Inc. |
Selective histone deacetylase (hdac) degraders and methods of use thereof
|
|
KR20220128345A
(ko)
|
2019-12-05 |
2022-09-20 |
아나쿠리아 테라퓨틱스, 인코포레이티드 |
라파마이신 유사체 및 이의 용도
|
|
EP4076520A4
(en)
|
2019-12-17 |
2024-03-27 |
Kymera Therapeutics, Inc. |
Irak degraders and uses thereof
|
|
WO2021127283A2
(en)
|
2019-12-17 |
2021-06-24 |
Kymera Therapeutics, Inc. |
Irak degraders and uses thereof
|
|
CN118059104A
(zh)
|
2019-12-19 |
2024-05-24 |
阿尔维纳斯运营股份有限公司 |
用于雄激素受体的靶向降解的化合物和方法
|
|
WO2021133920A1
(en)
|
2019-12-23 |
2021-07-01 |
Kymera Therapeutics, Inc. |
Smarca degraders and uses thereof
|
|
WO2021148581A1
(en)
|
2020-01-22 |
2021-07-29 |
Onxeo |
Novel dbait molecule and its use
|
|
AU2021217172A1
(en)
|
2020-02-05 |
2022-09-22 |
Monash University |
Lipid prodrugs of neurosteroids
|
|
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
|
|
CN115515585A
(zh)
|
2020-03-10 |
2022-12-23 |
X4 制药有限公司 |
用于治疗中性粒细胞减少症的方法
|
|
WO2021233534A1
(en)
|
2020-05-20 |
2021-11-25 |
Pvac Medical Technologies Ltd |
Use of substance and pharmaceutical composition thereof, and medical treatments or uses thereof
|
|
WO2021185844A1
(en)
|
2020-03-16 |
2021-09-23 |
Pvac Medical Technologies Ltd |
Use of substance and pharmaceutical composition thereof, and medical treatments or uses thereof
|
|
IL296451A
(en)
|
2020-03-19 |
2022-11-01 |
Kymera Therapeutics Inc |
Mdm2 degraders and uses thereof
|
|
WO2021211776A1
(en)
|
2020-04-15 |
2021-10-21 |
California Institute Of Technology |
Thermal control of t-cell immunotherapy through molecular and physical actuation
|
|
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
|
|
EP4161521A4
(en)
|
2020-06-03 |
2024-07-10 |
Kymera Therapeutics, Inc. |
DEUTERED IRAQ DEGRADERS AND USES THEREOF
|
|
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
|
|
IL300450A
(en)
|
2020-08-17 |
2023-04-01 |
Bicycletx Ltd |
Bicyclic conjugates specific to nectin-4 and uses thereof
|
|
US11999964B2
(en)
|
2020-08-28 |
2024-06-04 |
California Institute Of Technology |
Synthetic mammalian signaling circuits for robust cell population control
|
|
JP2023546996A
(ja)
|
2020-10-23 |
2023-11-08 |
ニンバス クロソー, インコーポレイテッド |
Ctps1阻害剤およびその使用
|
|
WO2022120353A1
(en)
|
2020-12-02 |
2022-06-09 |
Ikena Oncology, Inc. |
Tead inhibitors and uses thereof
|
|
KR20230131189A
(ko)
|
2020-12-02 |
2023-09-12 |
이케나 온콜로지, 인코포레이티드 |
Tead 억제제 및 이의 용도
|
|
KR20230137889A
(ko)
|
2020-12-18 |
2023-10-05 |
암피스타 테라퓨틱스 엘티디 |
표적화된 단백질 분해를 위한 신규의 2기능성 분자
|
|
GB202020359D0
(en)
|
2020-12-22 |
2021-02-03 |
Midatech Pharma Wales Ltd |
Pharmaceutical compositions and use thereof in combination therapy for brain cancer
|
|
CN116867758A
(zh)
|
2020-12-30 |
2023-10-10 |
凯麦拉医疗公司 |
Irak降解剂和其用途
|
|
CA3206501A1
(en)
|
2021-02-02 |
2022-08-11 |
Shaun Abbott |
Gpr84 antagonists and uses thereof
|
|
EP4288430A1
(en)
|
2021-02-02 |
2023-12-13 |
Liminal Biosciences Limited |
Gpr84 antagonists and uses thereof
|
|
MX2023009527A
(es)
|
2021-02-15 |
2023-08-24 |
Kymera Therapeutics Inc |
Degradadores de la cinasa 4 asociada al receptor de interleucina 1 (irak4) y usos de los mismos.
|
|
WO2022217276A1
(en)
|
2021-04-09 |
2022-10-13 |
Nimbus Clio, Inc. |
Cbl-b modulators and uses thereof
|
|
KR20230172548A
(ko)
|
2021-04-16 |
2023-12-22 |
이케나 온콜로지, 인코포레이티드 |
Mek 억제제 및 이의 용도
|
|
AU2022271290A1
(en)
|
2021-05-07 |
2023-11-23 |
Kymera Therapeutics, Inc. |
Cdk2 degraders and uses thereof
|
|
WO2023028238A1
(en)
|
2021-08-25 |
2023-03-02 |
PIC Therapeutics, Inc. |
Eif4e inhibitors and uses thereof
|
|
IL310924A
(en)
|
2021-08-25 |
2024-04-01 |
Pic Therapeutics Inc |
Eif4e inhibitors and uses thereof
|
|
EP4405680A1
(en)
|
2021-09-20 |
2024-07-31 |
Institut National de la Santé et de la Recherche Médicale (INSERM) |
Methods for improving the efficacy of hdac inhibitor therapy and predicting the response to treatment with hdac inhibitor
|
|
GB2611043A
(en)
|
2021-09-22 |
2023-03-29 |
Univ Dublin City |
A cis-platinum(II)-oligomer hybrid
|
|
IL312397A
(en)
|
2021-10-29 |
2024-06-01 |
Kymera Therapeutics Inc |
IRAK4 subunits and their synthesis
|
|
EP4433031A1
(en)
|
2021-11-19 |
2024-09-25 |
Branca Bunus Limited |
A composition comprising a therapeutically active agent packaged within a drug delivery vehicle
|
|
WO2023114984A1
(en)
|
2021-12-17 |
2023-06-22 |
Ikena Oncology, Inc. |
Tead inhibitors and uses thereof
|
|
US12091411B2
(en)
|
2022-01-31 |
2024-09-17 |
Kymera Therapeutics, Inc. |
IRAK degraders and uses thereof
|
|
WO2023173057A1
(en)
|
2022-03-10 |
2023-09-14 |
Ikena Oncology, Inc. |
Mek inhibitors and uses thereof
|
|
WO2023173053A1
(en)
|
2022-03-10 |
2023-09-14 |
Ikena Oncology, Inc. |
Mek inhibitors and uses thereof
|
|
EP4504165A1
(en)
|
2022-04-05 |
2025-02-12 |
Istituto Nazionale Tumori IRCCS - Fondazione G. Pascale |
Combination of hdac inhibitors and statins for use in the treatment of pancreatic cancer
|
|
GB2617409B
(en)
|
2022-04-27 |
2024-06-26 |
Cancertain Ltd |
Method for predicting responsiveness to therapy
|
|
WO2023211889A1
(en)
|
2022-04-25 |
2023-11-02 |
Ikena Oncology, Inc. |
Polymorphic compounds and uses thereof
|
|
CA3252253A1
(en)
|
2022-05-25 |
2023-11-30 |
Ikena Oncology, Inc. |
Mek inhibitors and uses thereof
|
|
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
|
|
IL318576A
(en)
|
2022-08-02 |
2025-03-01 |
Liminal Biosciences Ltd |
Pyridoxine-substituted GPR84 antagonists and their uses
|
|
EP4565684A1
(en)
|
2022-08-02 |
2025-06-11 |
National University Corporation Hokkaido University |
Methods of improving cellular therapy with organelle complexes
|
|
AU2023317740A1
(en)
|
2022-08-02 |
2025-03-13 |
Liminal Biosciences Limited |
Heteroaryl carboxamide and related gpr84 antagonists and uses thereof
|
|
KR20250057801A
(ko)
|
2022-08-02 |
2025-04-29 |
리미널 바이오사이언시스 리미티드 |
아릴-트라이아졸릴 및 관련 gpr84 길항제 및 이의 용도
|
|
WO2024041744A1
(en)
|
2022-08-26 |
2024-02-29 |
Biodexa Ltd. |
Combination therapy for brain cancer
|
|
WO2024112894A1
(en)
|
2022-11-22 |
2024-05-30 |
PIC Therapeutics, Inc. |
Eif4e inhibitors and uses thereof
|
|
EP4676454A1
(en)
|
2023-03-03 |
2026-01-14 |
iOnctura SA |
Combination of roginolisib and hdac inhibitor in the treatment of haematological malignancy
|
|
AU2024312190A1
(en)
|
2023-06-23 |
2025-07-03 |
Kymera Therapeutics, Inc. |
Irak degraders and uses thereof
|
|
WO2025026925A1
(en)
|
2023-07-28 |
2025-02-06 |
Ospedale San Raffaele S.R.L. |
Gtf2i inhibitors and uses thereof
|
|
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
(en)
|
2023-09-21 |
2025-03-27 |
Takeda Pharmaceutical Company Limited |
Tyk2 inhibitors for use in the treatment of inflammatory bowel disease
|
|
WO2025078542A1
(en)
|
2023-10-11 |
2025-04-17 |
Technological University Dublin |
Coumarin-metal complexes and uses thereof
|
|
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
|