US6117641A
(en)
|
1996-04-11 |
2000-09-12 |
Mitotix, Inc. |
Assays and reagents for identifying anti-fungal agents and uses related thereto
|
US6727082B1
(en)
|
1996-04-11 |
2004-04-27 |
Gpc Biotech Inc. |
Assays and reagents for identifying anti-fungal agents, and uses related thereto
|
ATE220110T1
(de)
|
1996-04-11 |
2002-07-15 |
Mitotix Inc |
Assays und reaganzien zur identifizierung von fungiziden wirkstoffen und ihre verwendungen
|
CA2260216A1
(en)
|
1996-07-15 |
1998-01-22 |
Bristol-Myers Squibb Company |
Thiadioxobenzodiazepine inhibitors of farnesyl protein transferase
|
EP1019529A4
(en)
*
|
1997-08-27 |
2002-09-11 |
Merck & Co Inc |
METHOD FOR TREATING CANCER
|
AU735366B2
(en)
*
|
1997-09-29 |
2001-07-05 |
Bristol-Myers Squibb Company |
Inhibitors of farnesyl protein transferase
|
US6458783B1
(en)
*
|
1997-09-29 |
2002-10-01 |
Bristol-Myers Squibb Company |
Non-imidazole benzodiazepine inhibitors of farnesyl protein transferase
|
DE69829412T2
(de)
*
|
1997-12-22 |
2005-07-28 |
Bayer Pharmaceuticals Corp., West Haven |
Hemmung der raf-kinase unter verwendung von symmetrisch und unsymmetrisch substituierten harnstoffen
|
US6071903A
(en)
*
|
1998-01-27 |
2000-06-06 |
American Cyanamid Company |
2,3,4,5-tetrahydro-1H-[1,4]-benzodiazepine-3-hydroxyamic acids
|
US6423519B1
(en)
|
1998-07-15 |
2002-07-23 |
Gpc Biotech Inc. |
Compositions and methods for inhibiting fungal growth
|
US6316436B1
(en)
|
1998-12-08 |
2001-11-13 |
Merck & Co., Inc. |
Inhibitors of prenyl-protein transferase
|
WO2000034437A2
(en)
|
1998-12-08 |
2000-06-15 |
Merck & Co., Inc. |
Inhibitors of prenyl-protein transferase
|
US8124630B2
(en)
|
1999-01-13 |
2012-02-28 |
Bayer Healthcare Llc |
ω-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors
|
IL144144A0
(en)
|
1999-01-13 |
2002-05-23 |
Bayer Ag |
Omega-carboxy aryl substituted diphenyl ureas as p38 kinase inhibitors
|
JP2002535253A
(ja)
*
|
1999-01-21 |
2002-10-22 |
ブリストル−マイヤーズ スクイブ カンパニー |
rasファルネシルトランスフェラーゼインヒビターおよびスルホブチルエーテル−7−β−シクロデキストリンまたは2−ヒドロキシプロピル−β−シクロデキストリンの複合体、ならびにその製造方法
|
JP2003524618A
(ja)
*
|
1999-03-03 |
2003-08-19 |
メルク エンド カムパニー インコーポレーテッド |
プレニル蛋白トランスフェラーゼ阻害剤
|
CN101481359A
(zh)
|
1999-04-15 |
2009-07-15 |
布里斯托尔-迈尔斯斯奎布公司 |
环状蛋白酪氨酸激酶抑制剂
|
US7125875B2
(en)
|
1999-04-15 |
2006-10-24 |
Bristol-Myers Squibb Company |
Cyclic protein tyrosine kinase inhibitors
|
US20060025388A1
(en)
|
1999-04-30 |
2006-02-02 |
Glick Gary D |
Compositions and methods relating to novel compounds and targets thereof
|
EP1187605A4
(en)
*
|
1999-06-18 |
2004-05-26 |
Thyreos Corp |
TREATMENT OF NON-MALIGNANT CONDITIONS WITH RAS ANTAGONISTS
|
US20020115696A1
(en)
|
1999-06-18 |
2002-08-22 |
Yoel Kloog |
Treatment of post-angioplasty restenosis and atherosclerosis with ras antagonists
|
EP1194400A1
(en)
|
1999-06-30 |
2002-04-10 |
Prescient Neuropharma Inc. |
2-aminoindane analogs
|
FR2796943A1
(fr)
*
|
1999-07-30 |
2001-02-02 |
Aventis Pharma Sa |
Derives de benzoxazinnes, leur procede de preparation et leur utilisation en therapeutique
|
EP1088821A1
(en)
*
|
1999-09-28 |
2001-04-04 |
Applied Research Systems ARS Holding N.V. |
Pharmaceutically active sulfonamide derivatives
|
US6100395A
(en)
*
|
2000-01-10 |
2000-08-08 |
Bristol-Myers Squibb Company |
Reductive alkylation of secondary amines with hydrosilane
|
JP2003523381A
(ja)
|
2000-02-24 |
2003-08-05 |
ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ |
投与レジメン
|
TWI310684B
(en)
*
|
2000-03-27 |
2009-06-11 |
Bristol Myers Squibb Co |
Synergistic pharmaceutical kits for treating cancer
|
EP1283055A4
(en)
*
|
2000-04-07 |
2003-05-07 |
Takeda Chemical Industries Ltd |
SOLUBLE PROMOTORS OF THE SECRETION OF BETA AMYLOID PROTEIN PRECURSORS
|
US7153958B2
(en)
*
|
2000-11-21 |
2006-12-26 |
Janssen Pharmaceutica N.V. |
Farnesyl transferase inhibiting benzoheterocyclic derivatives
|
AU2002218311A1
(en)
*
|
2000-11-28 |
2002-06-11 |
Janssen Pharmaceutica N.V. |
Farnesyl protein transferase inhibitors for the treatment of inflammatory bowel disease
|
WO2002051834A1
(en)
*
|
2000-12-27 |
2002-07-04 |
Janssen Pharmaceutica N.V. |
Farnesyl transferase inhibiting 4-heterocyclyl-quinoline and quinazoline derivatives
|
ATE319704T1
(de)
*
|
2000-12-27 |
2006-03-15 |
Janssen Pharmaceutica Nv |
Farnesyltransferase hemmende, in der 4-stellung substituierte chinolin- und chinazolinderivate
|
AU2002236813A1
(en)
*
|
2001-01-22 |
2002-07-30 |
Schering Corporation |
Treatment of malaria with farnesyl protein transferase inhibitors
|
PT1353668E
(pt)
|
2001-01-25 |
2008-06-30 |
Bristol Myers Squibb Co |
Processos de preparação de substâncias farmacêutica contendo substâncias análogas à epotilona para o tratamento de cancro
|
US7759323B2
(en)
|
2001-05-22 |
2010-07-20 |
Eisai R & D Management Co., Ltd. |
Highly purified antiendotoxin compound
|
EP1288713A1
(en)
*
|
2001-08-29 |
2003-03-05 |
Chugai Photo Chemical Co. Ltd. |
Processing agent for silver halide color photosensitive material and processing method thereof
|
US20030134846A1
(en)
*
|
2001-10-09 |
2003-07-17 |
Schering Corporation |
Treatment of trypanosoma brucei with farnesyl protein transferase inhibitors
|
US7074921B2
(en)
*
|
2001-11-13 |
2006-07-11 |
Bristol Myers Squibb Company |
Process for the preparation of 3,7-disubstituted-2,3,4,5-tetrahydro-1H-1,4-benzodiazepine compounds
|
AU2003209116A1
(en)
|
2002-02-11 |
2003-09-04 |
Bayer Pharmaceuticals Corporation |
Aryl ureas with angiogenesis inhibiting activity
|
EP1580188B9
(en)
|
2002-02-11 |
2012-05-23 |
Bayer HealthCare, LLC |
Aryl ureas as kinase inhibitors
|
AU2003214110A1
(en)
*
|
2002-03-15 |
2003-09-29 |
Ciba Specialty Chemicals Holding Inc. |
4-aminopyrimidines and their use for the antimicrobial treatment of surfaces
|
US7405234B2
(en)
*
|
2002-05-17 |
2008-07-29 |
Bristol-Myers Squibb Company |
Bicyclic modulators of androgen receptor function
|
CA2487866A1
(en)
*
|
2002-06-07 |
2003-12-18 |
Cortical Pty Ltd |
Napththalene derivatives which inhibit the cytokine or biological activity of macrophage migration inhibitory factor (mif)
|
WO2003106628A2
(en)
*
|
2002-06-17 |
2003-12-24 |
Bristol-Myers Squibb Company |
Benzodiazepine inhibitors of mitochondial f1f0 atp hydrolase and methods of inhibiting f1f0 atp hydrolase
|
US20040142888A1
(en)
*
|
2002-08-07 |
2004-07-22 |
Veeraswamy Manne |
Modulators of RabGGT and methods of use thereof
|
US7632858B2
(en)
*
|
2002-11-15 |
2009-12-15 |
Bristol-Myers Squibb Company |
Open chain prolyl urea-related modulators of androgen receptor function
|
JP2004346059A
(ja)
*
|
2003-01-28 |
2004-12-09 |
Takeda Chem Ind Ltd |
受容体作動薬
|
CA2514547A1
(en)
*
|
2003-01-28 |
2004-08-12 |
Takeda Pharmaceutical Company Limited |
Receptor agonists
|
US7157446B2
(en)
*
|
2003-05-02 |
2007-01-02 |
Bristol Myers Squibb Company |
Complex of ras-farnesyltransferase inhibitor, a cyclodextrin, and ethanol
|
PL1626714T3
(pl)
|
2003-05-20 |
2007-12-31 |
Bayer Healthcare Llc |
Diarylowe pochodne mocznika do schorzeń, w których pośredniczy PDGFR
|
ME00294B
(me)
|
2003-07-23 |
2011-05-10 |
Bayer Pharmaceuticals Corp |
Fluoro supstituisana omega-karaboksiaril difenil urea za liječenje i prevenciju bolesti i stanja bolesti
|
US7417026B2
(en)
|
2003-08-13 |
2008-08-26 |
Children's Hospital Medical Center |
Mobilization of hematopoietic cells
|
US20050069553A1
(en)
|
2003-08-13 |
2005-03-31 |
Yi Zheng |
Chimeric peptides for the regulation of GTPases
|
US7256208B2
(en)
*
|
2003-11-13 |
2007-08-14 |
Bristol-Myers Squibb Company |
Monocyclic N-Aryl hydantoin modulators of androgen receptor function
|
JP4691041B2
(ja)
|
2003-11-20 |
2011-06-01 |
チルドレンズ ホスピタル メディカル センター |
Gtpアーゼ阻害剤および使用方法
|
US7820702B2
(en)
*
|
2004-02-04 |
2010-10-26 |
Bristol-Myers Squibb Company |
Sulfonylpyrrolidine modulators of androgen receptor function and method
|
US20050182105A1
(en)
*
|
2004-02-04 |
2005-08-18 |
Nirschl Alexandra A. |
Method of using 3-cyano-4-arylpyridine derivatives as modulators of androgen receptor function
|
US7378426B2
(en)
|
2004-03-01 |
2008-05-27 |
Bristol-Myers Squibb Company |
Fused heterotricyclic compounds as inhibitors of 17β-hydroxysteroid dehydrogenase 3
|
US7625923B2
(en)
|
2004-03-04 |
2009-12-01 |
Bristol-Myers Squibb Company |
Bicyclic modulators of androgen receptor function
|
US7388027B2
(en)
*
|
2004-03-04 |
2008-06-17 |
Bristol-Myers Squibb Company |
Bicyclic compounds as modulators of androgen receptor function and method
|
US7696241B2
(en)
*
|
2004-03-04 |
2010-04-13 |
Bristol-Myers Squibb Company |
Bicyclic compounds as modulators of androgen receptor function and method
|
US20060106060A1
(en)
*
|
2004-03-18 |
2006-05-18 |
The Brigham And Women's Hospital, Inc. |
Methods for the treatment of synucleinopathies (Lansbury)
|
US20050272722A1
(en)
*
|
2004-03-18 |
2005-12-08 |
The Brigham And Women's Hospital, Inc. |
Methods for the treatment of synucleinopathies
|
CA2559285A1
(en)
*
|
2004-03-18 |
2005-09-29 |
Brigham And Women's Hospital, Inc. |
Methods for the treatment of synucleinopathies
|
US20070293539A1
(en)
*
|
2004-03-18 |
2007-12-20 |
Lansbury Peter T |
Methods for the treatment of synucleinopathies
|
WO2005089496A2
(en)
*
|
2004-03-18 |
2005-09-29 |
The Brigham And Women's Hospital, Inc. |
Methods for the treatment of synucleinopathies
|
US20050272068A1
(en)
*
|
2004-03-18 |
2005-12-08 |
The Brigham And Women's Hospital, Inc. |
UCH-L1 expression and cancer therapy
|
US7323455B2
(en)
*
|
2004-03-24 |
2008-01-29 |
Wyeth |
7-aryl 1,5-dihydro-4,1-benzoxazepin-2(3H)-one derivatives and their use as progesterone receptor modulators
|
US20050272723A1
(en)
*
|
2004-04-27 |
2005-12-08 |
The Regents Of The University Of Michigan |
Methods and compositions for treating diseases and conditions associated with mitochondrial function
|
US10675326B2
(en)
|
2004-10-07 |
2020-06-09 |
The Board Of Trustees Of The University Of Illinois |
Compositions comprising cupredoxins for treating cancer
|
DK1815247T3
(da)
|
2004-11-05 |
2013-03-11 |
Janssen Pharmaceutica Nv |
Terapeutisk anvendelse af farnesyltransferaseinhibitorer og fremgangsmåder til overvågning af deres effektivitet
|
TW200631609A
(en)
|
2004-11-18 |
2006-09-16 |
Bristol Myers Squibb Co |
Enteric coated bead comprising ixabepilone, and preparation and administration thereof
|
US20060194821A1
(en)
*
|
2005-02-18 |
2006-08-31 |
The Brigham And Women's Hospital, Inc. |
Compounds inhibiting the aggregation of superoxide dismutase-1
|
EP1867639A1
(en)
*
|
2005-03-25 |
2007-12-19 |
Kissei Pharmaceutical Co., Ltd. |
Urea derivative, medicinal composition containing the same, and medicinal use of these
|
US20060235006A1
(en)
*
|
2005-04-13 |
2006-10-19 |
Lee Francis Y |
Combinations, methods and compositions for treating cancer
|
US20060235028A1
(en)
*
|
2005-04-14 |
2006-10-19 |
Li James J |
Inhibitors of 11-beta hydroxysteroid dehydrogenase type I
|
EP1909795B1
(en)
*
|
2005-06-09 |
2011-04-13 |
Bristol-Myers Squibb Company |
Pharmaceutical composition for use in treating individuals exhibiting mutant kit protein
|
US20060281788A1
(en)
|
2005-06-10 |
2006-12-14 |
Baumann Christian A |
Synergistic modulation of flt3 kinase using a flt3 inhibitor and a farnesyl transferase inhibitor
|
JP2009508809A
(ja)
|
2005-07-29 |
2009-03-05 |
チルドレンズ ホスピタル メディカル センター |
RAC−1GTPaseのGTPase阻害因子とその使用方法およびその結晶構造
|
EP1934203B1
(en)
*
|
2005-08-25 |
2010-08-18 |
Schering Corporation |
3,4-dihydro-2H-benzo[1,4]oxazine and 3,4-dihydro-2H-benzo[1,4]thiazine COMPOUNDS AS ALPHA2C ADRENORECEPTOR AGONISTS
|
US7700592B2
(en)
|
2005-08-25 |
2010-04-20 |
Schering Corporation |
α2C adrenoreceptor agonists
|
PL1948607T3
(pl)
|
2005-09-16 |
2010-09-30 |
Janssen Pharmaceutica Nv |
Cyklopropyloaminy jako modulatory receptora histaminowego H3
|
EP1955073A2
(en)
*
|
2005-11-15 |
2008-08-13 |
Brystol-Myers Squibb Company |
Methods of identifying and treating individuals exhibiting mdr-1 overexpression with protein tyrosine kinase inhibitors and combinations thereof
|
NZ570530A
(en)
*
|
2006-02-14 |
2011-09-30 |
Vertex Pharma |
Pharmaceutical compositions comprising 6-oxo-6,7,8,9-tetrahydro-5H-pyrimido[4,5-b][1,4)diazepine derivatives
|
MX2008013533A
(es)
|
2006-04-20 |
2009-01-15 |
Janssen Pharmaceutica Nv |
Compuestos heterociclicos como inhibidores de c-fms cinasa.
|
US8697716B2
(en)
|
2006-04-20 |
2014-04-15 |
Janssen Pharmaceutica Nv |
Method of inhibiting C-KIT kinase
|
JP5331679B2
(ja)
|
2006-04-20 |
2013-10-30 |
ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ |
c−fmsキナーゼの阻害剤
|
AU2007329375A1
(en)
|
2006-12-04 |
2008-06-12 |
The Board Of Trustees Of The University Of Illinois |
Compositions and methods to treat cancer with cupredoxins and CpG rich DNA
|
ES2620818T3
(es)
|
2006-12-14 |
2017-06-29 |
Janssen Pharmaceutica N.V. |
Procedimiento para la preparación de derivados de piperazinil y diazepanil benzamida
|
WO2008089135A2
(en)
*
|
2007-01-12 |
2008-07-24 |
University Of South Florida |
Identification of biomarkers predictive of dasatinib effects in cancer cells
|
KR20090114414A
(ko)
|
2007-02-08 |
2009-11-03 |
더 보드 오브 트러스티즈 오브 더 유니버시티 오브 일리노이 |
쿠프레독신으로 암을 예방하는 조성물과 방법
|
KR20100017766A
(ko)
*
|
2007-05-10 |
2010-02-16 |
에이엠알 테크놀로지, 인크. |
아릴- 및 헤테로아릴-치환된 테트라히드로벤조-1,4-디아제핀 및 노르에피네프린, 도파민 및 세로토닌의 재흡수를 차단하기 위한 이의 용도
|
WO2008144981A1
(fr)
*
|
2007-05-25 |
2008-12-04 |
Topharman Shanghai Co., Ltd. |
Procédés et intermédiaires pour préparer une 4-acétyl-2,3,4,5-tétrahydro-1h-1,4-benzodiazépine
|
MY148609A
(en)
|
2007-06-05 |
2013-05-15 |
Merck Sharp & Dohme |
Polycyclic indazole derivatives and their use as erk inhibitors for the treatment of cancer
|
JO3240B1
(ar)
|
2007-10-17 |
2018-03-08 |
Janssen Pharmaceutica Nv |
c-fms مثبطات كيناز
|
EP2234608A2
(en)
|
2007-12-11 |
2010-10-06 |
Viamet Pharmaceuticals, Inc. |
Metalloenzyme inhibitors using metal binding moieties in combination with targeting moieties
|
US8232402B2
(en)
*
|
2008-03-12 |
2012-07-31 |
Link Medicine Corporation |
Quinolinone farnesyl transferase inhibitors for the treatment of synucleinopathies and other indications
|
AU2009243756B2
(en)
*
|
2008-05-05 |
2013-06-27 |
Sanofi-Aventis |
Acylamino-substituted fused cyclopentanecarboxylic acid derivatives and their use as pharmaceuticals
|
US8119129B2
(en)
*
|
2008-08-01 |
2012-02-21 |
Bristol-Myers Squibb Company |
Combination of anti-CTLA4 antibody with dasatinib for the treatment of proliferative diseases
|
US20110060005A1
(en)
*
|
2008-11-13 |
2011-03-10 |
Link Medicine Corporation |
Treatment of mitochondrial disorders using a farnesyl transferase inhibitor
|
US20100331363A1
(en)
*
|
2008-11-13 |
2010-12-30 |
Link Medicine Corporation |
Treatment of mitochondrial disorders using a farnesyl transferase inhibitor
|
BRPI0920927A2
(pt)
*
|
2008-11-13 |
2019-09-24 |
Link Medicine Corp |
derivados de azaquinolinona e usos dos mesmos
|
CN102459248A
(zh)
*
|
2009-05-26 |
2012-05-16 |
埃克塞里艾克西斯公司 |
作为PI3K/mTOR抑制剂的苯并氧杂环庚三烯以及它们使用与制造方法
|
MX2011013016A
(es)
|
2009-06-05 |
2012-04-20 |
Link Medicine Corp |
Derivados de aminopirrolidinona y usos de los mismos.
|
ES2768990T3
(es)
|
2009-07-20 |
2020-06-24 |
Bristol Myers Squibb Co |
Combinación de anticuerpos anti-CTLA4 con gemcitabina para el tratamiento sinérgico de enfermedades proliferativas
|
WO2011041152A1
(en)
|
2009-09-30 |
2011-04-07 |
Schering Corporation |
Novel compounds that are erk inhibitors
|
AU2010322286B2
(en)
|
2009-11-17 |
2014-06-05 |
The Regents Of The University Of Michigan |
1,4-benzodiazepine-2,5-diones and related compounds with therapeutic properties
|
EP2730561B1
(en)
|
2010-04-06 |
2015-10-14 |
Nippon Soda Co., Ltd. |
Methods to prepare haloalkyl nitrogen-containing heterocyclic compounds
|
AU2014201037B9
(en)
*
|
2010-04-06 |
2015-11-19 |
Nippon Soda Co., Ltd. |
Nitrogen-containing heterocyclic compound and method for producing same
|
US8999957B2
(en)
|
2010-06-24 |
2015-04-07 |
Merck Sharp & Dohme Corp. |
Heterocyclic compounds as ERK inhibitors
|
WO2012030685A2
(en)
|
2010-09-01 |
2012-03-08 |
Schering Corporation |
Indazole derivatives useful as erk inhibitors
|
WO2012087772A1
(en)
|
2010-12-21 |
2012-06-28 |
Schering Corporation |
Indazole derivatives useful as erk inhibitors
|
US8846006B2
(en)
|
2011-01-20 |
2014-09-30 |
Board Of Regents, The University Of Texas System |
MRI markers, delivery and extraction systems, and methods of manufacture and use thereof
|
CN102863474A
(zh)
|
2011-07-09 |
2013-01-09 |
陈小平 |
一类治疗细胞增殖性疾病的铂化合物、其制备方法和应用
|
CN102993239A
(zh)
|
2011-09-19 |
2013-03-27 |
陈小平 |
离去基团含氨基或烷胺基的丁二酸衍生物的铂类化合物
|
WO2013064231A1
(en)
|
2011-10-31 |
2013-05-10 |
Phenex Pharmaceuticals Ag |
SEVEN-MEMBERED SULFONAMIDES AS MODULATORS OF RAR-RELATED ORPHAN RECEPTOR-GAMMA (RORγ, NR1F3)
|
US9980942B2
(en)
|
2012-05-02 |
2018-05-29 |
Children's Hospital Medical Center |
Rejuvenation of precursor cells
|
EP2880039B1
(en)
|
2012-07-31 |
2017-01-04 |
Dow Global Technologies LLC |
Method of making an olefin polymerization catalyst activator
|
JP6359537B2
(ja)
|
2012-08-07 |
2018-07-18 |
ヤンセン ファーマシューティカ エヌ.ベー. |
複素環エステル誘導体の調製プロセス
|
JOP20180012A1
(ar)
|
2012-08-07 |
2019-01-30 |
Janssen Pharmaceutica Nv |
عملية السلفنة باستخدام نونافلوروبوتانيسولفونيل فلوريد
|
WO2014075391A1
(zh)
|
2012-11-17 |
2014-05-22 |
北京市丰硕维康技术开发有限责任公司 |
离去基团是含氨基或烷氨基的丙二酸衍生物的铂类化合物
|
UY35464A
(es)
|
2013-03-15 |
2014-10-31 |
Araxes Pharma Llc |
Inhibidores covalentes de kras g12c.
|
EP2970121B1
(en)
*
|
2013-03-15 |
2017-12-13 |
Araxes Pharma LLC |
Covalent inhibitors of kras g12c
|
TWI659021B
(zh)
|
2013-10-10 |
2019-05-11 |
亞瑞克西斯製藥公司 |
Kras g12c之抑制劑
|
US10028503B2
(en)
|
2014-06-18 |
2018-07-24 |
Children's Hospital Medical Center |
Platelet storage methods and compositions for same
|
EP3161127A4
(en)
|
2014-06-27 |
2018-06-06 |
The Regents of the University of California |
Cultured mammalian limbal stem cells, methods for generating the same, and uses thereof
|
ES2898765T3
(es)
|
2015-04-10 |
2022-03-08 |
Araxes Pharma Llc |
Compuestos de quinazolina sustituidos y métodos de uso de los mismos
|
MX2017013275A
(es)
|
2015-04-15 |
2018-01-26 |
Araxes Pharma Llc |
Inhibidores triciclicos fusionados de kras y metodos de uso de los mismos.
|
US10144724B2
(en)
|
2015-07-22 |
2018-12-04 |
Araxes Pharma Llc |
Substituted quinazoline compounds and methods of use thereof
|
DK3277842T5
(da)
|
2015-08-17 |
2020-08-31 |
Kura Oncology Inc |
Fremgangsmåder til at behandle kræftpatienter med farnesyl-transferase-inhibitorer
|
EP3356347A1
(en)
|
2015-09-28 |
2018-08-08 |
Araxes Pharma LLC |
Inhibitors of kras g12c mutant proteins
|
US10730867B2
(en)
|
2015-09-28 |
2020-08-04 |
Araxes Pharma Llc |
Inhibitors of KRAS G12C mutant proteins
|
WO2017058792A1
(en)
|
2015-09-28 |
2017-04-06 |
Araxes Pharma Llc |
Inhibitors of kras g12c mutant proteins
|
EP3356351A1
(en)
|
2015-09-28 |
2018-08-08 |
Araxes Pharma LLC |
Inhibitors of kras g12c mutant proteins
|
WO2017058728A1
(en)
|
2015-09-28 |
2017-04-06 |
Araxes Pharma Llc |
Inhibitors of kras g12c mutant proteins
|
EP3356339A1
(en)
|
2015-09-28 |
2018-08-08 |
Araxes Pharma LLC |
Inhibitors of kras g12c mutant proteins
|
WO2017058915A1
(en)
|
2015-09-28 |
2017-04-06 |
Araxes Pharma Llc |
Inhibitors of kras g12c mutant proteins
|
AU2016355433C1
(en)
|
2015-11-16 |
2021-12-16 |
Araxes Pharma Llc |
2-substituted quinazoline compounds comprising a substituted heterocyclic group and methods of use thereof
|
US20190119758A1
(en)
|
2016-04-22 |
2019-04-25 |
Kura Oncology, Inc. |
Methods of selecting cancer patients for treatment with farnesyltransferase inhibitors
|
EP4067347B1
(en)
*
|
2016-05-24 |
2024-06-19 |
Genentech, Inc. |
Heterocyclic inhibitors of cbp/ep300 for the treatment of cancer
|
US10646488B2
(en)
|
2016-07-13 |
2020-05-12 |
Araxes Pharma Llc |
Conjugates of cereblon binding compounds and G12C mutant KRAS, HRAS or NRAS protein modulating compounds and methods of use thereof
|
EP3519402A1
(en)
|
2016-09-29 |
2019-08-07 |
Araxes Pharma LLC |
Inhibitors of kras g12c mutant proteins
|
WO2018068017A1
(en)
|
2016-10-07 |
2018-04-12 |
Araxes Pharma Llc |
Heterocyclic compounds as inhibitors of ras and methods of use thereof
|
MY190861A
(en)
|
2016-11-03 |
2022-05-12 |
Kura Oncology Inc |
Farnesyltransferase inhibitors for use in methods of treating cancer
|
WO2018140512A1
(en)
|
2017-01-26 |
2018-08-02 |
Araxes Pharma Llc |
Fused bicyclic benzoheteroaromatic compounds and methods of use thereof
|
US11358959B2
(en)
|
2017-01-26 |
2022-06-14 |
Araxes Pharma Llc |
Benzothiophene and benzothiazole compounds and methods of use thereof
|
EP3573971A1
(en)
|
2017-01-26 |
2019-12-04 |
Araxes Pharma LLC |
1-(3-(6-(3-hydroxynaphthalen-1-yl)benzofuran-2-yl)azetidin-1yl)prop-2-en-1-one derivatives and similar compounds as kras g12c modulators for treating cancer
|
EP3573970A1
(en)
|
2017-01-26 |
2019-12-04 |
Araxes Pharma LLC |
1-(6-(3-hydroxynaphthalen-1-yl)quinazolin-2-yl)azetidin-1-yl)prop-2-en-1-one derivatives and similar compounds as kras g12c inhibitors for the treatment of cancer
|
JP7327802B2
(ja)
|
2017-01-26 |
2023-08-16 |
アラクセス ファーマ エルエルシー |
縮合ヘテロ-ヘテロ二環式化合物およびその使用方法
|
US9956215B1
(en)
|
2017-02-21 |
2018-05-01 |
Kura Oncology, Inc. |
Methods of treating cancer with farnesyltransferase inhibitors
|
TWI693074B
(zh)
|
2017-02-21 |
2020-05-11 |
美商庫拉腫瘤技術股份有限公司 |
以法呢基轉移酶(farnesyltransferase)抑制劑治療癌症之方法
|
MX2019013954A
(es)
|
2017-05-25 |
2020-08-31 |
Araxes Pharma Llc |
Inhibidores covalentes de kras.
|
CN110869357A
(zh)
|
2017-05-25 |
2020-03-06 |
亚瑞克西斯制药公司 |
化合物及其用于治疗癌症的使用方法
|
WO2018218069A1
(en)
|
2017-05-25 |
2018-11-29 |
Araxes Pharma Llc |
Quinazoline derivatives as modulators of mutant kras, hras or nras
|
US10806730B2
(en)
|
2017-08-07 |
2020-10-20 |
Kura Oncology, Inc. |
Methods of treating cancer with farnesyltransferase inhibitors
|
WO2019032489A1
(en)
|
2017-08-07 |
2019-02-14 |
Kura Oncology, Inc. |
METHODS OF TREATING CANCER WITH FARNESYLTRANSFERASE INHIBITORS
|
TWI795440B
(zh)
|
2017-09-15 |
2023-03-11 |
美商佛瑪治療公司 |
作為CBP/p300抑制劑之四氫─咪唑並喹啉化合物
|
WO2019113269A1
(en)
|
2017-12-08 |
2019-06-13 |
Kura Oncology, Inc. |
Methods of treating cancer patients with farnesyltransferase inhibitors
|
MX2020014303A
(es)
|
2018-06-29 |
2021-03-25 |
Forma Therapeutics Inc |
Inhibición de la proteína de union a creb (cbp).
|
AU2019312670B2
(en)
|
2018-08-01 |
2025-01-02 |
Araxes Pharma Llc |
Heterocyclic spiro compounds and methods of use thereof for the treatment of cancer
|
UY38427A
(es)
|
2018-10-26 |
2020-05-29 |
Novartis Ag |
Métodos y composiciones para terapia con células oculares
|
CN113286591A
(zh)
|
2018-11-01 |
2021-08-20 |
库拉肿瘤学公司 |
用法尼基转移酶抑制剂治疗癌症的方法
|
SG11202106599WA
(en)
|
2018-12-21 |
2021-07-29 |
Kura Oncology Inc |
Therapies for squamous cell carcinomas
|
US20220142983A1
(en)
|
2019-03-01 |
2022-05-12 |
Kura Oncology, Inc. |
Methods of treating cancer with farnesyltransferase inhibitors
|
WO2020190604A1
(en)
|
2019-03-15 |
2020-09-24 |
Kura Oncology, Inc. |
Methods of treating cancer patients with farnesyltransferase inhibitors
|
SG11202110472WA
(en)
|
2019-03-29 |
2021-10-28 |
Kura Oncology Inc |
Methods of treating squamous cell carcinomas with farnesyltransferase inhibitors
|
TW202102218A
(zh)
|
2019-04-01 |
2021-01-16 |
美商庫拉腫瘤技術股份有限公司 |
以法呢基(farnesyl)轉移酶抑制劑治療癌症的方法
|
US20220305001A1
(en)
|
2019-05-02 |
2022-09-29 |
Kura Oncology, Inc. |
Methods of treating acute myeloid leukemia with farnesyltransferase inhibitors
|
CA3141604A1
(en)
*
|
2019-05-20 |
2020-11-26 |
1200 Pharma Llc |
Kras g12c inhibitors and uses thereof
|
EP4013402B1
(en)
|
2019-08-16 |
2024-11-06 |
Children's Hospital Medical Center |
Cdc-42 inhibitors for use in the treatment of age-related depression, sarcopenia or frailty
|
EP4142879A1
(en)
|
2020-04-27 |
2023-03-08 |
Novartis AG |
Methods and compositions for ocular cell therapy
|
US11801243B2
(en)
|
2020-09-23 |
2023-10-31 |
Forma Therapeutics, Inc. |
Bromodomain inhibitors for androgen receptor-driven cancers
|
US11795168B2
(en)
|
2020-09-23 |
2023-10-24 |
Forma Therapeutics, Inc. |
Inhibiting cyclic amp-responsive element-binding protein (CREB) binding protein (CBP)
|
CN115745960B
(zh)
*
|
2021-09-02 |
2024-08-30 |
中国科学院上海药物研究所 |
一类含喹啉酮酰胺的化合物及其制备方法、药物组合物和用途
|
CN114230529A
(zh)
*
|
2021-11-03 |
2022-03-25 |
河南大学 |
四氢喹喔啉磺酰胺衍生物及其制备方法与用途
|
CN118556044A
(zh)
*
|
2022-01-29 |
2024-08-27 |
江苏恒瑞医药股份有限公司 |
稠杂环类化合物、其制备方法及其在医药上的应用
|
WO2024097606A1
(en)
*
|
2022-10-31 |
2024-05-10 |
Eli Lilly And Company |
Ahr agonists
|