ATE272633T1
(de)
*
|
1998-12-23 |
2004-08-15 |
Lilly Co Eli |
Aromatische amiden
|
DE10023485A1
(de)
*
|
2000-05-09 |
2001-11-22 |
Schering Ag |
Anthranylalkyl- und -cycloalkylamide und deren Verwendung als Arzneimittel
|
DE10023486C1
(de)
|
2000-05-09 |
2002-03-14 |
Schering Ag |
Ortho substituierte Anthranilsäureamide und deren Verwendung als Arzneimittel
|
DE10023484A1
(de)
*
|
2000-05-09 |
2001-11-22 |
Schering Ag |
Anthranylamide und deren Verwendung als Arzneimittel
|
JP3886897B2
(ja)
|
2000-06-21 |
2007-02-28 |
エフ.ホフマン−ラ ロシュ アーゲー |
ベンゾチアゾール誘導体
|
WO2002046172A2
(en)
*
|
2000-12-07 |
2002-06-13 |
Cv Therapeutics, Inc. |
Substituted 1, 3, 5-triazines and pyrimidines as abca-1 elevating compounds against coronary artery disease or atherosclerosis
|
US20030134836A1
(en)
|
2001-01-12 |
2003-07-17 |
Amgen Inc. |
Substituted arylamine derivatives and methods of use
|
US6995162B2
(en)
*
|
2001-01-12 |
2006-02-07 |
Amgen Inc. |
Substituted alkylamine derivatives and methods of use
|
US7105682B2
(en)
|
2001-01-12 |
2006-09-12 |
Amgen Inc. |
Substituted amine derivatives and methods of use
|
US20020147198A1
(en)
*
|
2001-01-12 |
2002-10-10 |
Guoqing Chen |
Substituted arylamine derivatives and methods of use
|
US7102009B2
(en)
*
|
2001-01-12 |
2006-09-05 |
Amgen Inc. |
Substituted amine derivatives and methods of use
|
US6878714B2
(en)
|
2001-01-12 |
2005-04-12 |
Amgen Inc. |
Substituted alkylamine derivatives and methods of use
|
CA2994779C
(en)
|
2001-02-19 |
2020-08-25 |
Novartis Ag |
Use of 40-o-(2-hydroxyethyl)-rapamycin for inhibiting growth of a solid tumour of the brain other than lymphatic cancer
|
US6864255B2
(en)
|
2001-04-11 |
2005-03-08 |
Amgen Inc. |
Substituted triazinyl amide derivatives and methods of use
|
US7459470B2
(en)
|
2001-05-08 |
2008-12-02 |
Schering Ag |
N-oxide anthranylamide derivatives and their use as medicaments
|
DE10123587B4
(de)
*
|
2001-05-08 |
2005-04-07 |
Schering Ag |
Cyanoanthranylamid-Derivate und deren Verwendung als Arzneimittel
|
EP1387838B1
(de)
|
2001-05-08 |
2006-04-19 |
Schering Aktiengesellschaft |
Cyanoanthranylamid-derivate und deren verwendung als arzneimittel
|
IL158783A0
(en)
*
|
2001-05-08 |
2004-05-12 |
Schering Ag |
Selective anthranilamide pyridine amides as inhibitors of vegfr-2 and vegfr-3
|
DE10123573B4
(de)
*
|
2001-05-08 |
2005-06-02 |
Schering Ag |
N-Oxidanthranylamid-Derivate und deren Verwendung als Arzneimittel
|
BR0209647A
(pt)
|
2001-05-16 |
2004-07-27 |
Novartis Ag |
Combinação que compreende n-{5-[4-(4-metil-piperazino-metil)-benzoilamido]-2-metil fenil}-4-(3-piridil)-2-pirimidina-amina e um agente quimioterapêutico
|
WO2002100833A1
(fr)
*
|
2001-06-12 |
2002-12-19 |
Sumitomo Pharmaceuticals Company, Limited |
Inhibiteurs de rho kinase
|
TWI315982B
(en)
|
2001-07-19 |
2009-10-21 |
Novartis Ag |
Combinations comprising epothilones and pharmaceutical uses thereof
|
US7132438B2
(en)
|
2001-10-09 |
2006-11-07 |
Amgen Inc. |
Benzimidazole derivatives
|
GB0126902D0
(en)
*
|
2001-11-08 |
2002-01-02 |
Novartis Ag |
Organic compounds
|
GB0206215D0
(en)
|
2002-03-15 |
2002-05-01 |
Novartis Ag |
Organic compounds
|
PL372103A1
(en)
|
2002-05-16 |
2005-07-11 |
Novartis Ag |
Use of edg receptor binding agents in cancer
|
US7307088B2
(en)
|
2002-07-09 |
2007-12-11 |
Amgen Inc. |
Substituted anthranilic amide derivatives and methods of use
|
US7094789B2
(en)
|
2002-07-22 |
2006-08-22 |
Asahi Kasei Pharma Corporation |
5-substituted isoquinoline derivatives
|
DE10235690A1
(de)
*
|
2002-07-31 |
2004-02-19 |
Schering Ag |
VEGFR-2 und VEGFR-3 inhibitorische Anthranylamidpyridinamide
|
US7615565B2
(en)
|
2002-07-31 |
2009-11-10 |
Bayer Schering Pharma Aktiengesellschaft |
VEGFR-2 and VEGFR-3 inhibitory anthranilamide pyridines
|
US7338956B2
(en)
|
2002-08-07 |
2008-03-04 |
Sanofi-Aventis Deutschland Gmbh |
Acylamino-substituted heteroaromatic compounds and their use as pharmaceuticals
|
EP1388341A1
(en)
*
|
2002-08-07 |
2004-02-11 |
Aventis Pharma Deutschland GmbH |
Acylamino-substituted heteroaromatic compounds and their use as pharmaceuticals
|
DE60329030D1
(de)
|
2002-12-04 |
2009-10-08 |
Ore Pharmaceuticals Inc |
Melanocortin-rezeptormodulatoren
|
US7696225B2
(en)
|
2003-01-06 |
2010-04-13 |
Osi Pharmaceuticals, Inc. |
(2-carboxamido)(3-Amino) thiophene compounds
|
TWI299664B
(en)
|
2003-01-06 |
2008-08-11 |
Osi Pharm Inc |
(2-carboxamido)(3-amino)thiophene compounds
|
US7087761B2
(en)
|
2003-01-07 |
2006-08-08 |
Hoffmann-La Roche Inc. |
Cyclization process for substituted benzothiazole derivatives
|
ATE551324T1
(de)
*
|
2003-02-03 |
2012-04-15 |
Janssen Pharmaceutica Nv |
Chinolin-amid-derivate als modulatoren von vanilloid-vr1-rezeptoren
|
ES2337254T3
(es)
|
2003-02-14 |
2010-04-22 |
Glaxo Group Limited |
Derivados de carboxamida.
|
TWI422583B
(zh)
|
2003-03-07 |
2014-01-11 |
參天製藥股份有限公司 |
具有以4-吡啶烷硫基為取代基之新穎化合物
|
CL2004001120A1
(es)
|
2003-05-19 |
2005-04-15 |
Irm Llc |
Compuestos derivados de amina sustituidas con heterociclos, inmunosupresores; composicion farmaceutica; y uso para tratar enfermedades mediadas por interacciones de linfocito, tales como enfermedades autoinmunes, inflamatorias, infecciosas, cancer.
|
MY150088A
(en)
|
2003-05-19 |
2013-11-29 |
Irm Llc |
Immunosuppressant compounds and compositions
|
US20050004133A1
(en)
*
|
2003-06-05 |
2005-01-06 |
Makings Lewis R. |
Modulators of VR1 receptor
|
US7202260B2
(en)
|
2003-06-13 |
2007-04-10 |
Schering Ag |
VEGFR-2 and VEGFR-3 inhibitory anthranilamide pyridones
|
DE10327719A1
(de)
*
|
2003-06-13 |
2005-01-20 |
Schering Ag |
VEGFR-2 und VEGFR-3 Inhibitorische Anthranylamidpyridone
|
US8309562B2
(en)
|
2003-07-03 |
2012-11-13 |
Myrexis, Inc. |
Compounds and therapeutical use thereof
|
WO2006074147A2
(en)
|
2005-01-03 |
2006-07-13 |
Myriad Genetics, Inc. |
Nitrogen containing bicyclic compounds and therapeutical use thereof
|
ES2380201T3
(es)
|
2003-07-11 |
2012-05-09 |
Merck Patent Gmbh |
Derivados de benzimidazol
|
GB0326601D0
(en)
*
|
2003-11-14 |
2003-12-17 |
Novartis Ag |
Organic compounds
|
UA89035C2
(ru)
|
2003-12-03 |
2009-12-25 |
Лео Фарма А/С |
Эфиры гидроксамовых кислот и их фармацевтическое применение
|
US7544703B2
(en)
|
2004-02-17 |
2009-06-09 |
Santen Pharmaceutical Co., Ltd. |
Cyclic compound having 4-pyridylalkylthio group having substituted or unsubstituted amino group introduced therein
|
EP1568368A1
(en)
*
|
2004-02-26 |
2005-08-31 |
Schering Aktiengesellschaft |
Pharmaceutical combination comprising a CDK inhibitor and a VEGF receptor inhibitor
|
DE102004009238A1
(de)
*
|
2004-02-26 |
2005-09-08 |
Merck Patent Gmbh |
Arylamid-Derivate
|
WO2005085188A2
(en)
*
|
2004-03-02 |
2005-09-15 |
Compass Pharmaceuticals Llc |
Compounds and methods for anti-tumor therapy
|
DE102004011720B4
(de)
*
|
2004-03-10 |
2008-04-03 |
Bayer Schering Pharma Aktiengesellschaft |
Radiohalogenierte Benzamidderivate und deren Verwendung in der Tumordiagnostik und Tumortherapie
|
US7427390B2
(en)
*
|
2004-03-10 |
2008-09-23 |
Schering Ag |
Radiohalogenated benzamide derivatives and their use in tumor diagnosis and tumor therapy
|
EA011279B1
(ru)
|
2004-05-24 |
2009-02-27 |
Ф. Хоффманн-Ля Рош Аг |
(4-метокси-7-морфолин-4-илбензотиазол-2-ил)-амид 4-гидрокси-4-метилпиперидин-1-карбоновой кислоты
|
DE102004039876A1
(de)
*
|
2004-06-23 |
2006-01-26 |
Lanxess Deutschland Gmbh |
Herstellung von fluorierten 1,3-Benzodioxanen
|
GB0512324D0
(en)
|
2005-06-16 |
2005-07-27 |
Novartis Ag |
Organic compounds
|
SG155941A1
(en)
|
2004-09-22 |
2009-10-29 |
Janssen Pharmaceutica Nv |
Inhibitors of the interaction between mdm2 and p53
|
US7906533B2
(en)
*
|
2004-11-03 |
2011-03-15 |
Bayer Schering Pharma Ag |
Nicotinamide pyridinureas as vascular endothelial growth factor (VEGF) receptor kinase inhibitors
|
EP1657241A1
(en)
|
2004-11-03 |
2006-05-17 |
Schering Aktiengesellschaft |
Novel anthranilamide pyridinureas as VEGF receptor kinase inhibitors
|
EP1655297A1
(en)
*
|
2004-11-03 |
2006-05-10 |
Schering Aktiengesellschaft |
Nicotinamide pyridinureas as vascular endothelial growth factor (VEGF) receptor kinase inhibitors
|
EP1655295A1
(en)
*
|
2004-11-03 |
2006-05-10 |
Schering Aktiengesellschaft |
Anthranilamide pyridinureas as VEGF receptor kinase inhibitors
|
CN101056857B
(zh)
|
2004-11-05 |
2010-12-01 |
弗·哈夫曼-拉罗切有限公司 |
异烟酸衍生物的制备方法
|
US8258145B2
(en)
|
2005-01-03 |
2012-09-04 |
Myrexis, Inc. |
Method of treating brain cancer
|
DE602006016564D1
(de)
|
2005-03-03 |
2010-10-14 |
Santen Pharmaceutical Co Ltd |
Neue cyclische verbindung mit chinolylalkylthiogruppe
|
BRPI0609719B8
(pt)
|
2005-03-23 |
2021-05-25 |
Hoffmann La Roche |
derivados de acetilenil-pirazol-pirimidina como antagonistas de mgbur2
|
ES2548729T3
(es)
|
2005-03-31 |
2015-10-20 |
Santen Pharmaceutical Co., Ltd. |
Nuevo compuesto cíclico que tiene grupo pirimidinilalquiltio
|
GB0510390D0
(en)
|
2005-05-20 |
2005-06-29 |
Novartis Ag |
Organic compounds
|
ATE463495T1
(de)
|
2005-09-27 |
2010-04-15 |
Hoffmann La Roche |
Oxadiazolylpyrazolopyrimidine als mglur2- antagonisten
|
RU2008116314A
(ru)
|
2005-09-27 |
2009-11-10 |
Новартис АГ (CH) |
Соединения карбоксамина и их применение для лечения hdac-зависимых заболеваний
|
US8247556B2
(en)
*
|
2005-10-21 |
2012-08-21 |
Amgen Inc. |
Method for preparing 6-substituted-7-aza-indoles
|
PT2275103E
(pt)
|
2005-11-21 |
2014-07-24 |
Novartis Ag |
Inibidores de mtor para o tratamento de tumores endócrinos
|
US8106190B2
(en)
*
|
2005-11-30 |
2012-01-31 |
Astellas Pharma Inc. |
2-aminobenzamide derivatives
|
AU2007228784B2
(en)
|
2006-03-22 |
2012-03-08 |
Janssen Pharmaceutica N.V. |
Cyclic-alkylaminederivatives as inhibitors of the interaction between MDM2 and p53
|
US8232298B2
(en)
|
2006-03-22 |
2012-07-31 |
Janssen Pharmaceutica N.V. |
Inhibitors of the interaction between MDM2 and P53
|
US20090098137A1
(en)
|
2006-04-05 |
2009-04-16 |
Novartis Ag |
Combinations of therapeutic agents for treating cancer
|
CN101443002B
(zh)
|
2006-05-09 |
2012-03-21 |
诺瓦提斯公司 |
包含铁螯合剂和抗肿瘤药的组合及其用途
|
GB0612721D0
(en)
|
2006-06-27 |
2006-08-09 |
Novartis Ag |
Organic compounds
|
CA2664378A1
(en)
|
2006-09-29 |
2008-04-03 |
Novartis Ag |
Pyrazolopyrimidines as pi3k lipid kinase inhibitors
|
WO2008077809A1
(en)
*
|
2006-12-22 |
2008-07-03 |
F. Hoffmann-La Roche Ag |
Process for the manufacture of 7-oxa-bicyclo derivatives
|
JP2008266295A
(ja)
|
2007-01-29 |
2008-11-06 |
Santen Pharmaceut Co Ltd |
キナーセ゛阻害活性を有する新規チアシ゛アソ゛ール誘導体
|
EP2120900A2
(en)
|
2007-02-15 |
2009-11-25 |
Novartis AG |
Combination of lbh589 with other therapeutic agents for treating cancer
|
EP1975166A1
(en)
*
|
2007-03-30 |
2008-10-01 |
Bayer Schering Pharma AG |
Synthesis of anthranilamides
|
US8853406B2
(en)
*
|
2007-08-06 |
2014-10-07 |
Janssen Pharmaceutica Nv |
Substituted phenylenediamines as inhibitors of the interaction between MDM2 and P53
|
EP2628726A1
(en)
|
2008-03-26 |
2013-08-21 |
Novartis AG |
Hydroxamate-based inhibitors of deacetylases b
|
NZ591820A
(en)
|
2008-08-27 |
2012-12-21 |
Leo Pharma As |
Pyridine derivatives as vegfr-2 receptor and protein tyrosine kinase inhibitors
|
ES2704986T3
(es)
|
2008-10-16 |
2019-03-21 |
Celator Pharmaceuticals Inc |
Combinaciones de una camptotecina liposomal soluble en agua con cetuximab o bevacizumab
|
UY32330A
(es)
|
2008-12-18 |
2010-07-30 |
Novartis Ag |
Novedosa forma de sal de ácido 1-(4-{1-[e-4-ciclohexil-3-trifluoro-metil-benciloxi-imino]-etil}-2-etil-bencil)-azetidin-3-carboxílico, formas polimórficas, composiciones farmacéuticas conteniéndolas, procesos de preparación y aplicaciones
|
CN103204794A
(zh)
|
2008-12-18 |
2013-07-17 |
诺瓦提斯公司 |
新的盐
|
RU2011129230A
(ru)
|
2008-12-18 |
2013-01-27 |
Новартис Аг |
Новая полиморфная форма 1-[4-[1-(4-циклогексил-3-трифторметилбензилоксиимино)этил]-2-этилбензил]азетидин-3-карбоновой кислоты
|
TW201031406A
(en)
|
2009-01-29 |
2010-09-01 |
Novartis Ag |
Substituted benzimidazoles for the treatment of astrocytomas
|
MX2011008195A
(es)
|
2009-02-04 |
2011-09-06 |
Janssen Pharmaceutica Nv |
Derivados de indol como agentes anticancer.
|
UA105794C2
(uk)
|
2009-06-26 |
2014-06-25 |
Новартіс Аг |
1,3-ДИЗАМІЩЕНІ ПОХІДНІ ІМІДАЗОЛІДИН-2-ОНУ ЯК ІНГІБІТОРИ Cyp17
|
US8389526B2
(en)
|
2009-08-07 |
2013-03-05 |
Novartis Ag |
3-heteroarylmethyl-imidazo[1,2-b]pyridazin-6-yl derivatives
|
AU2010283806A1
(en)
|
2009-08-12 |
2012-03-01 |
Novartis Ag |
Heterocyclic hydrazone compounds and their uses to treat cancer and inflammation
|
MX2012002066A
(es)
|
2009-08-17 |
2012-03-29 |
Intellikine Inc |
Compuestos heterociclicos y usos de los mismos.
|
JP5775871B2
(ja)
|
2009-08-20 |
2015-09-09 |
ノバルティス アーゲー |
ヘテロ環式オキシム化合物
|
EP2470502A1
(en)
|
2009-08-26 |
2012-07-04 |
Novartis AG |
Tetra-substituted heteroaryl compounds and their use as mdm2 and/or mdm4 modulators
|
IN2012DN02139A
(US07122547-20061017-C00125.png)
|
2009-09-10 |
2015-08-07 |
Novartis Ag |
|
AU2010317167B2
(en)
|
2009-11-04 |
2012-11-29 |
Novartis Ag |
Heterocyclic sulfonamide derivatives useful as MEK inhibitors
|
US20120289501A1
(en)
|
2009-11-25 |
2012-11-15 |
Novartis Ag |
Benzene-fused 6-membered oxygen-containing heterocyclic derivatives of bicyclic heteroaryls
|
EP2509964B1
(en)
|
2009-12-08 |
2014-04-30 |
Novartis AG |
Heterocyclic sulfonamide derivatives
|
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
|
EP2582680A1
(en)
|
2010-06-17 |
2013-04-24 |
Novartis AG |
Biphenyl substituted 1,3-dihydro-benzoimidazol-2-ylideneamine derivatives
|
JP2013532149A
(ja)
|
2010-06-17 |
2013-08-15 |
ノバルティス アーゲー |
ピペリジニル置換1,3−ジヒドロ−ベンゾイミダゾール−2−イリデンアミン誘導体
|
US20130102477A1
(en)
|
2010-06-23 |
2013-04-25 |
Ryan D. Morin |
Biomarkers for non-hodgkin lymphomas and uses thereof
|
US9175331B2
(en)
|
2010-09-10 |
2015-11-03 |
Epizyme, Inc. |
Inhibitors of human EZH2, and methods of use thereof
|
RU2618475C2
(ru)
|
2010-09-10 |
2017-05-03 |
Эпизайм, Инк. |
Ингибиторы ezh2 человека и способы их применения
|
US8946260B2
(en)
|
2010-09-16 |
2015-02-03 |
Novartis Ag |
17α-hydroxylase/C17,20-lyase inhibitors
|
US20130324526A1
(en)
|
2011-02-10 |
2013-12-05 |
Novartis Ag |
[1,2,4] triazolo [4,3-b] pyridazine compounds as inhibitors of the c-met tyrosine kinase
|
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
|
EP3323820B1
(en)
|
2011-02-28 |
2023-05-10 |
Epizyme, Inc. |
Substituted 6,5-fused bicyclic heteroaryl compounds
|
WO2012120469A1
(en)
|
2011-03-08 |
2012-09-13 |
Novartis Ag |
Fluorophenyl bicyclic heteroaryl compounds
|
TW201733984A
(zh)
|
2011-04-13 |
2017-10-01 |
雅酶股份有限公司 |
經取代之苯化合物
|
JO3438B1
(ar)
|
2011-04-13 |
2019-10-20 |
Epizyme Inc |
مركبات بنزين مستبدلة بأريل أو أريل غير متجانس
|
KR20140025492A
(ko)
|
2011-04-28 |
2014-03-04 |
노파르티스 아게 |
17α-히드록실라제/C17,20-리아제 억제제
|
EA201391820A1
(ru)
|
2011-06-09 |
2014-12-30 |
Новартис Аг |
Гетероциклические сульфонамидные производные
|
US8859535B2
(en)
|
2011-06-20 |
2014-10-14 |
Novartis Ag |
Hydroxy substituted isoquinolinone derivatives
|
US8859586B2
(en)
|
2011-06-20 |
2014-10-14 |
Novartis Ag |
Cyclohexyl isoquinolinone compounds
|
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
|
US8969341B2
(en)
|
2011-11-29 |
2015-03-03 |
Novartis Ag |
Pyrazolopyrrolidine compounds
|
BR112014015308A2
(pt)
|
2011-12-23 |
2017-06-13 |
Novartis Ag |
compostos para inibição da interação de bcl2 com contrapartes de ligação
|
CA2859869A1
(en)
|
2011-12-23 |
2013-06-27 |
Novartis Ag |
Compounds for inhibiting the interaction of bcl2 with binding partners
|
WO2013096051A1
(en)
|
2011-12-23 |
2013-06-27 |
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
|
BR112014015274A8
(pt)
|
2011-12-23 |
2017-06-13 |
Novartis Ag |
compostos e composições para inibição da interação de bcl2 com parceiros de ligação
|
CN102603729A
(zh)
*
|
2012-01-12 |
2012-07-25 |
贵州大学 |
N-(2-(取代苯并噻唑-2-氨基甲酰基)-取代苯基)吡啶甲酰胺类衍生物
|
UY34591A
(es)
|
2012-01-26 |
2013-09-02 |
Novartis Ag |
Compuestos de imidazopirrolidinona
|
WO2013138753A1
(en)
|
2012-03-16 |
2013-09-19 |
Fox Chase Chemical Diversity Center, Inc. |
Prodrugs of riluzole and their method of use
|
CN104245701A
(zh)
|
2012-04-03 |
2014-12-24 |
诺华有限公司 |
有酪氨酸激酶抑制剂的组合产品和其应用
|
DK2836491T3
(en)
|
2012-04-13 |
2017-03-06 |
Epizyme Inc |
SALT FORM OF A HUMAN HISTONMETHYL TRANSFERASE EZH2 INHIBITOR
|
US9365576B2
(en)
|
2012-05-24 |
2016-06-14 |
Novartis Ag |
Pyrrolopyrrolidinone compounds
|
KR102057365B1
(ko)
|
2012-10-15 |
2019-12-18 |
에피자임, 인코포레이티드 |
치환된 벤젠 화합물
|
EP2948451B1
(en)
|
2013-01-22 |
2017-07-12 |
Novartis AG |
Substituted purinone compounds
|
WO2014115080A1
(en)
|
2013-01-22 |
2014-07-31 |
Novartis Ag |
Pyrazolo[3,4-d]pyrimidinone compounds as inhibitors of the p53/mdm2 interaction
|
CN105246482A
(zh)
|
2013-03-15 |
2016-01-13 |
因特利凯有限责任公司 |
激酶抑制剂的组合及其用途
|
CN103130696B
(zh)
*
|
2013-03-21 |
2014-06-11 |
山东大学 |
邻氨基苯甲酰胺类化合物及其制备方法与应用
|
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
|
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
|
WO2015022664A1
(en)
|
2013-08-14 |
2015-02-19 |
Novartis Ag |
Compounds and compositions as inhibitors of mek
|
CN103405434A
(zh)
*
|
2013-08-22 |
2013-11-27 |
中国药科大学 |
Vegfr-2抑制剂及其用途
|
FI3057962T3
(fi)
|
2013-10-16 |
2023-11-03 |
Epizyme Inc |
Hydrokloridisuolamuoto ezh2-estoon
|
CN104163794A
(zh)
*
|
2013-10-17 |
2014-11-26 |
中国药科大学 |
2-氨基芳环类血管内皮生长因子受体(vegfr)抑制剂及其制备方法和用途
|
WO2015084804A1
(en)
|
2013-12-03 |
2015-06-11 |
Novartis Ag |
Combination of mdm2 inhibitor and braf inhibitor and their use
|
JP6526789B2
(ja)
|
2014-07-31 |
2019-06-05 |
ノバルティス アーゲー |
組み合わせ療法
|
WO2019077037A1
(en)
|
2017-10-18 |
2019-04-25 |
Chemotherapeutisches Forschungsinstitut Georg-Speyer-Haus |
METHODS AND COMPOUNDS FOR ENHANCED IMMUNE CELL THERAPY
|
EP3730483B1
(en)
|
2017-12-21 |
2023-08-30 |
Hefei Institutes of Physical Science, Chinese Academy of Sciences |
Class of pyrimidine derivative kinase inhibitors
|
US20220395553A1
(en)
|
2019-11-14 |
2022-12-15 |
Cohbar, Inc. |
Cxcr4 antagonist peptides
|
JP2023509452A
(ja)
|
2020-01-03 |
2023-03-08 |
バーグ エルエルシー |
がんを処置するためのube2kモジュレータとしての多環式アミド
|
WO2022222890A1
(en)
*
|
2021-04-19 |
2022-10-27 |
Shanghai Yao Yuan Biotechnology Co., Ltd. |
Benzothiazole and quinoline derivatives for use in treating kawasaki disease
|