|
US6407132B1
(en)
*
|
1997-07-25 |
2002-06-18 |
James Black Foundation Limited |
Substituted imidazole derivatives and their use as histamine H3 receptor ligands
|
|
GB9718913D0
(en)
*
|
1997-09-05 |
1997-11-12 |
Glaxo Group Ltd |
Substituted oxindole derivatives
|
|
DE19816624A1
(de)
*
|
1998-04-15 |
1999-10-21 |
Boehringer Ingelheim Pharma |
Neue substituierte Indolinone, ihre Herstellung und ihre Verwendung als Arzneimittel
|
|
DE19824922A1
(de)
*
|
1998-06-04 |
1999-12-09 |
Boehringer Ingelheim Pharma |
Neue substituierte Indolinone, ihre Herstellung und ihre Verwendung als Arzneimittel
|
|
US6319918B1
(en)
|
1998-06-04 |
2001-11-20 |
Boehringer Ingelheim Pharma Kg |
Substituted indolinones with kinase inhibitory activity
|
|
KR20010101266A
(ko)
|
1998-12-17 |
2001-11-14 |
프리돌린 클라우스너, 롤란드 비. 보레르 |
Jnk 단백질 키나제의 억제제로서의 4-아릴옥신돌
|
|
ES2192878T3
(es)
*
|
1998-12-17 |
2003-10-16 |
Hoffmann La Roche |
4,5-azolo-oxindoles.
|
|
DE69906152T2
(de)
|
1998-12-17 |
2004-02-12 |
F. Hoffmann-La Roche Ag |
4-alkenyl (und alkinyl)oxoindole als inhibitoren cyclinabhängiger kinasen, insbesondere cdk2
|
|
ES2301255T3
(es)
*
|
1998-12-17 |
2008-06-16 |
F. Hoffmann-La Roche Ag |
4,5-pirazinaxindoles como inhibidores de proteinoquinasas.
|
|
US6153634A
(en)
|
1998-12-17 |
2000-11-28 |
Hoffmann-La Roche Inc. |
4,5-azolo-oxindoles
|
|
EP1147214B1
(en)
|
1999-01-13 |
2011-01-05 |
The Research Foundation Of State University Of New York |
A novel method for designing protein kinase inhibitors
|
|
US6624171B1
(en)
|
1999-03-04 |
2003-09-23 |
Smithkline Beecham Corporation |
Substituted aza-oxindole derivatives
|
|
GB9904933D0
(en)
*
|
1999-03-04 |
1999-04-28 |
Glaxo Group Ltd |
Compounds
|
|
GB9904932D0
(en)
*
|
1999-03-04 |
1999-04-28 |
Glaxo Group Ltd |
Composition and method for preventing/reducing the severity of side effects of chemotherapy and/or radiation therapy
|
|
GB9904930D0
(en)
*
|
1999-03-04 |
1999-04-28 |
Glaxo Group Ltd |
Thiazoloindolinone compounds
|
|
US6492398B1
(en)
*
|
1999-03-04 |
2002-12-10 |
Smithkline Beechman Corporation |
Thiazoloindolinone compounds
|
|
US6306851B1
(en)
|
1999-05-04 |
2001-10-23 |
American Home Products Corporation |
Cyclocarbamate and cyclic amide derivatives
|
|
US6380235B1
(en)
|
1999-05-04 |
2002-04-30 |
American Home Products Corporation |
Benzimidazolones and analogues
|
|
US6358947B1
(en)
|
1999-05-04 |
2002-03-19 |
American Home Products Corporation |
Tetracyclic progesterone receptor modulator compounds and methods
|
|
US6329416B1
(en)
|
1999-05-04 |
2001-12-11 |
American Home Products Corporation |
Combination regimens using 3,3-substituted indoline derivatives
|
|
US6462032B1
(en)
|
1999-05-04 |
2002-10-08 |
Wyeth |
Cyclic regimens utilizing indoline derivatives
|
|
US6399593B1
(en)
|
1999-05-04 |
2002-06-04 |
Wyeth |
Cyclic regimens using cyclic urea and cyclic amide derivatives
|
|
US6391907B1
(en)
*
|
1999-05-04 |
2002-05-21 |
American Home Products Corporation |
Indoline derivatives
|
|
US6355648B1
(en)
|
1999-05-04 |
2002-03-12 |
American Home Products Corporation |
Thio-oxindole derivatives
|
|
US6319912B1
(en)
|
1999-05-04 |
2001-11-20 |
American Home Products Corporation |
Cyclic regimens using 2,1-benzisothiazoline 2,2-dioxides
|
|
US6509334B1
(en)
|
1999-05-04 |
2003-01-21 |
American Home Products Corporation |
Cyclocarbamate derivatives as progesterone receptor modulators
|
|
US6339098B1
(en)
|
1999-05-04 |
2002-01-15 |
American Home Products Corporation |
2,1-benzisothiazoline 2,2-dioxides
|
|
US6369056B1
(en)
|
1999-05-04 |
2002-04-09 |
American Home Products Corporation |
Cyclic urea and cyclic amide derivatives
|
|
US6444668B1
(en)
|
1999-05-04 |
2002-09-03 |
Wyeth |
Combination regimens using progesterone receptor modulators
|
|
US6423699B1
(en)
|
1999-05-04 |
2002-07-23 |
American Home Products Corporation |
Combination therapies using benzimidazolones
|
|
US6417214B1
(en)
|
1999-05-04 |
2002-07-09 |
Wyeth |
3,3-substituted indoline derivatives
|
|
US6380178B1
(en)
|
1999-05-04 |
2002-04-30 |
American Home Products Corporation |
Cyclic regimens using cyclocarbamate and cyclic amide derivatives
|
|
US6407101B1
(en)
|
1999-05-04 |
2002-06-18 |
American Home Products Corporation |
Cyanopyrroles
|
|
US6358948B1
(en)
|
1999-05-04 |
2002-03-19 |
American Home Products Corporation |
Quinazolinone and benzoxazine derivatives as progesterone receptor modulators
|
|
US6498154B1
(en)
|
1999-05-04 |
2002-12-24 |
Wyeth |
Cyclic regimens using quinazolinone and benzoxazine derivatives
|
|
GB9911053D0
(en)
*
|
1999-05-12 |
1999-07-14 |
Pharmacia & Upjohn Spa |
4,5,6,7-tetrahydroindazole derivatives process for their preparation and their use as antitumour agents
|
|
DE19924401A1
(de)
*
|
1999-05-27 |
2000-11-30 |
Boehringer Ingelheim Pharma |
Neue substituierte Indolinone, ihre Herstellung und ihre Verwendung als Arzneimittel
|
|
WO2001016130A1
(de)
*
|
1999-08-27 |
2001-03-08 |
Boehringer Ingelheim Pharma Kg |
Substituierte indolinone als tyrosinkinase inhibitoren
|
|
AU771460B2
(en)
*
|
1999-09-24 |
2004-03-25 |
Smithkline Beecham Corporation |
Thrombopoietin mimetics
|
|
UA75054C2
(uk)
*
|
1999-10-13 |
2006-03-15 |
Бьорінгер Інгельхайм Фарма Гмбх & Ко. Кг |
Заміщені в положенні 6 індолінони, їх одержання та їх застосування як лікарського засобу
|
|
DE19949209A1
(de)
*
|
1999-10-13 |
2001-04-19 |
Boehringer Ingelheim Pharma |
In 5-Stellung substituierte Indolinone, ihre Herstellung und ihre Verwendung als Arzneimittel
|
|
US6762180B1
(en)
|
1999-10-13 |
2004-07-13 |
Boehringer Ingelheim Pharma Kg |
Substituted indolines which inhibit receptor tyrosine kinases
|
|
US6313310B1
(en)
|
1999-12-15 |
2001-11-06 |
Hoffmann-La Roche Inc. |
4-and 5-alkynyloxindoles and 4-and 5-alkenyloxindoles
|
|
YU54202A
(sh)
*
|
2000-01-18 |
2006-01-16 |
Agouron Pharmaceuticals Inc. |
Jedinjenja indazola, farmaceutske smeše i postupci za stimulisanje i inhibiranje ćelijske proliferacije
|
|
HN2001000008A
(es)
|
2000-01-21 |
2003-12-11 |
Inc Agouron Pharmaceuticals |
Compuesto de amida y composiciones farmaceuticas para inhibir proteinquinasas, y su modo de empleo
|
|
EP1207864A2
(en)
|
2000-02-05 |
2002-05-29 |
Vertex Pharmaceuticals Incorporated |
Compositions useful as inhibitors of erk
|
|
US6620818B1
(en)
|
2000-03-01 |
2003-09-16 |
Smithkline Beecham Corporation |
Method for reducing the severity of side effects of chemotherapy and/or radiation therapy
|
|
BR0110302A
(pt)
|
2000-04-18 |
2003-01-14 |
Agouron Pharma |
Compostos de pirazol para inibição de proteìnas cinase, sal e pró-droga farmaceuticamente aceitável, metabólito farmaceuticamente ativo ou sal farmaceuticamente aceitável de metabólito, composição farmacêutica, método de tratamento de condição doentia em mamìferos mediada pela atividade de proteìna cinase, método de modulação ou inibição da atividade de um receptor de proteìna cinase
|
|
UA73119C2
(en)
|
2000-04-19 |
2005-06-15 |
American Home Products Corpoir |
Derivatives of cyclic thiocarbamates, pharmaceutical composition including noted derivatives of cyclic thiocarbamates and active ingredients of medicines as modulators of progesterone receptors
|
|
US6534531B2
(en)
*
|
2000-04-27 |
2003-03-18 |
Bristol-Myers Squibb Company |
Methods for preventing and treating alopecia induced by chemotherapy or radiotherapy
|
|
WO2001082967A1
(fr)
*
|
2000-04-28 |
2001-11-08 |
Yamanouchi Pharmaceutical Co., Ltd. |
Compositions medicinales destinees a supprimer la production de ?-amyloide
|
|
CY2010012I2
(el)
|
2000-05-25 |
2020-05-29 |
Novartis Ag |
Μιμητικα θρομβοποιητινης
|
|
GB0016454D0
(en)
|
2000-07-04 |
2000-08-23 |
Hoffmann La Roche |
Thienopyrrolidinones
|
|
BR0113139A
(pt)
|
2000-08-09 |
2003-06-24 |
Agouron Pharma |
Compostos, seus sais, formas multiméricas, pró-drogas ou metabólitos, composições farmacêuticas, método de tratamento de uma doença ou disfunção mediana através da inibição de cdk4 ou um complexo de cdk4/ciclina, método de tratamento de condição doentia em mamìferos mediada pela atividade de proteìna cinase e método de modulação ou inibição da atividade de um receptor de proteìna cinase
|
|
MXPA03001452A
(es)
|
2000-08-18 |
2004-05-04 |
Agouron Pharma |
Hidroximino-fluorenos heterociclicos y su uso para la inhibicion de las proteinas cinasas.
|
|
ES2230337T3
(es)
|
2000-09-01 |
2005-05-01 |
Glaxo Group Limited |
Derivados de oxindol.
|
|
WO2002020513A1
(en)
*
|
2000-09-01 |
2002-03-14 |
Glaxo Group Limited |
Oxindole derivatives
|
|
US7071217B2
(en)
|
2000-09-01 |
2006-07-04 |
Smithkline Beecham Corporation |
Substituted oxindole derivatives as tyrosine kinase inhibitors
|
|
EP1201765A3
(en)
*
|
2000-10-16 |
2003-08-27 |
Axxima Pharmaceuticals Aktiengesellschaft |
Cellular kinases involved in cytomegalovirus infection and their inhibition
|
|
DE10054019A1
(de)
*
|
2000-11-01 |
2002-05-23 |
Boehringer Ingelheim Pharma |
Neue substituierte Indolinone, ihre Herstellung und ihre Verwendung als Arzneimittel
|
|
US6638965B2
(en)
|
2000-11-01 |
2003-10-28 |
Boehringer Ingelheim Pharma Kg |
Substituted indolinones, preparation thereof and their use as pharmaceutical compositions
|
|
DE10117204A1
(de)
*
|
2001-04-06 |
2002-10-10 |
Boehringer Ingelheim Pharma |
In 6-Stellung substituierte Indolinone, ihre Herstellung und ihre Verwendung als Arzneimittel
|
|
SE0101230L
(sv)
*
|
2001-04-06 |
2002-10-07 |
Innoventus Project Ab |
Ny användning av en tyrosinkinasinhibitor
|
|
KR20040000507A
(ko)
*
|
2001-05-24 |
2004-01-03 |
야마노우치세이야쿠 가부시키가이샤 |
3-퀴놀린-2(1h)-일리덴인돌린-2-온 유도체
|
|
WO2003003006A2
(en)
|
2001-06-29 |
2003-01-09 |
Ab Science |
New potent, selective and non toxic c-kit inhibitors
|
|
PT1401416E
(pt)
|
2001-06-29 |
2007-02-28 |
Ab Science |
Utilização de inibidores de c-kit para tratar doenças inflamatórias intestinais (dii)
|
|
ATE330608T1
(de)
|
2001-06-29 |
2006-07-15 |
Ab Science |
Die verwendung von n-phenyl-2-pyrimidine-amine derivaten zur behandlung von entzündlichen erkrankungen
|
|
DE60225590T2
(de)
*
|
2001-09-20 |
2008-09-25 |
Ab Science |
C-kithemmer zur behandlung von bakteriellen infektionen
|
|
EP1461032B1
(en)
*
|
2001-09-20 |
2008-07-16 |
AB Science |
Use of c-kit inhibitors for promoting hair growth
|
|
WO2003027109A1
(en)
*
|
2001-09-27 |
2003-04-03 |
Allergan, Inc. |
3-(heteroarylamino)methylene-1, 3-dihydro-2h-indol-2-ones as kinase inhibitors
|
|
US20030225152A1
(en)
*
|
2001-09-27 |
2003-12-04 |
Andrews Steven W. |
3-(Arylamino)methylene-1, 3-dihydro-2h-indol-2-ones as kinase inhibitors
|
|
WO2003033491A1
(en)
*
|
2001-10-16 |
2003-04-24 |
Nippon Kayaku Kabushiki Kaisha |
Medicinal composition for prevention or alleviation of side effect of antitumor and medicinal antitumor composition
|
|
US7005445B2
(en)
|
2001-10-22 |
2006-02-28 |
The Research Foundation Of State University Of New York |
Protein kinase and phosphatase inhibitors and methods for designing them
|
|
JP4623962B2
(ja)
*
|
2001-10-22 |
2011-02-02 |
ザ・リサーチ・ファウンデーション・オブ・ステイト・ユニバーシティ・オブ・ニューヨーク |
タンパク質キナーゼおよびホスファターゼ阻害剤、それらを設計する方法、ならびにそれらを使用する方法
|
|
US20030187026A1
(en)
|
2001-12-13 |
2003-10-02 |
Qun Li |
Kinase inhibitors
|
|
US6797825B2
(en)
|
2001-12-13 |
2004-09-28 |
Abbott Laboratories |
Protein kinase inhibitors
|
|
EP1464645A1
(en)
*
|
2001-12-18 |
2004-10-06 |
Kyowa Hakko Kogyo Co., Ltd. |
Indole derivative
|
|
US7482366B2
(en)
*
|
2001-12-21 |
2009-01-27 |
X-Ceptor Therapeutics, Inc. |
Modulators of LXR
|
|
US7998986B2
(en)
|
2001-12-21 |
2011-08-16 |
Exelixis Patent Company Llc |
Modulators of LXR
|
|
TWI329105B
(en)
|
2002-02-01 |
2010-08-21 |
Rigel Pharmaceuticals Inc |
2,4-pyrimidinediamine compounds and their uses
|
|
FR2836914B1
(fr)
|
2002-03-11 |
2008-03-14 |
Aventis Pharma Sa |
Indazoles substitues, compositions les contenant, procede de fabrication et utilisation
|
|
EP1497420A4
(en)
*
|
2002-04-30 |
2005-04-27 |
Alcon Inc |
AGENTS THAT REGULATE, RESTRICT OR MODULATE THE ACTIVITY AND / OR EXPRESSION OF BIND WEAVE GROWTH FACTOR (CTGF) AS UNIQUE MEDICAMENTS BOTH TO REDUCE EYESPRINTS AND TREAT GLACCOMPETOSIS RETINOPATHIES / OPTIC NEUROPATHIES
|
|
MY142390A
(en)
|
2002-05-22 |
2010-11-30 |
Glaxosmithkline Llc |
3' - [(2z)-[1-(3,4-dimethylphenyl)-1,5- dihydro-3- methyl-5-0xo-4h-pyrazol-4- ylidene]hydrazino]-2' -hydroxy -[1,1' -biphenyl]-3-carboxylic acid bis-(monoethanolamine)
|
|
US7514468B2
(en)
|
2002-07-23 |
2009-04-07 |
Boehringer Ingelheim Pharma Gmbh & Co. Kg |
Indolinone derivatives substituted in the 6 position, the preparation thereof and their use as pharmaceutical compositions
|
|
US7169936B2
(en)
|
2002-07-23 |
2007-01-30 |
Boehringer Ingelheim Pharma Gmbh & Co. Kg |
Indolinone derivatives substituted in the 6-position, their preparation and their use as medicaments
|
|
DE10233500A1
(de)
*
|
2002-07-24 |
2004-02-19 |
Boehringer Ingelheim Pharma Gmbh & Co. Kg |
3-Z-[1-(4-(N-((4-Methyl-piperazin-1-yl)-methylcarbonyl)-N-methyl-amino)-anilino)-1-phenyl-methylen]-6-methoxycarbonyl-2-indolinon-Monoethansulfonat und dessen Verwendung als Arzneimittel
|
|
US20040082615A1
(en)
*
|
2002-08-07 |
2004-04-29 |
Michael Konkel |
3-Imino-2-indolones for the treatement of depression and/or anxiety
|
|
WO2004014854A1
(en)
*
|
2002-08-07 |
2004-02-19 |
Synaptic Pharmaceutical Corporation |
3-imino-2-indolones for the treatment of depression and/or anxiety
|
|
GB0225873D0
(en)
*
|
2002-11-06 |
2002-12-11 |
Cyclacel Ltd |
Combination
|
|
AU2003284572A1
(en)
*
|
2002-11-22 |
2004-06-18 |
Yamanouchi Pharmaceutical Co., Ltd. |
2-oxoindoline derivatives
|
|
WO2004057340A1
(en)
|
2002-12-23 |
2004-07-08 |
Astex Technology Limited |
Synthesis and screening of ligands using x-ray crystallography
|
|
ES2421139T3
(es)
|
2003-07-30 |
2013-08-29 |
Rigel Pharmaceuticals, Inc. |
Compuestos de 2,4-pirimidindiamina para su uso en el tratamiento o la prevención de enfermedades autoinmunitarias
|
|
TW200526638A
(en)
|
2003-10-22 |
2005-08-16 |
Smithkline Beecham Corp |
2-(3,4-dimethylphenyl)-4-{[2-hydroxy-3'-(1H-tetrazol-5-yl)biphenyl-3-yl]-hydrazono}-5-methyl-2,4-dihydropyrazol-3-one choline
|
|
GB0328180D0
(en)
*
|
2003-12-04 |
2004-01-07 |
Cyclacel Ltd |
Combination
|
|
DE102004012069A1
(de)
*
|
2004-03-12 |
2005-09-29 |
Boehringer Ingelheim Pharma Gmbh & Co. Kg |
Neue aryl-haltige 5-Acylindolinone, deren Herstellung und deren Verwendung als Arzneimittel
|
|
WO2005118551A2
(en)
*
|
2004-05-28 |
2005-12-15 |
Ligand Pharmaceuticals Inc. |
Thrombopoietin activity modulating compounds and methods
|
|
DE602005024599D1
(de)
*
|
2004-10-25 |
2010-12-16 |
Ligand Pharm Inc |
Verbindungen modulierende thrombopoietinaktivität und verfahren
|
|
GT200500321A
(es)
*
|
2004-11-09 |
2006-09-04 |
|
Compuestos y composiciones como inhibidores de proteina kinase.
|
|
BRPI0516915A
(pt)
|
2004-12-01 |
2008-03-11 |
Devgen Nv |
derivados de tiazol substituìdos por 5-carboxamido que interagem com canais de ìons, particularmante com canais de ìons da famìlia kv
|
|
EP1969940A3
(en)
|
2004-12-17 |
2008-12-10 |
Devgen NV |
Nematicidal compositions
|
|
PE20060777A1
(es)
*
|
2004-12-24 |
2006-10-06 |
Boehringer Ingelheim Int |
Derivados de indolinona para el tratamiento o la prevencion de enfermedades fibroticas
|
|
WO2006101937A1
(en)
*
|
2005-03-18 |
2006-09-28 |
Janssen Pharmaceutica N.V. |
Acylhydrazones as kinase modulators
|
|
WO2006119660A1
(en)
*
|
2005-05-11 |
2006-11-16 |
Givaudan Sa |
Encapsulation method
|
|
US20070203161A1
(en)
|
2006-02-24 |
2007-08-30 |
Rigel Pharmaceuticals, Inc. |
Compositions and methods for inhibition of the jak pathway
|
|
WO2006133426A2
(en)
|
2005-06-08 |
2006-12-14 |
Rigel Pharmaceuticals, Inc. |
Compositions and methods for inhibition of the jak pathway
|
|
CA2602389A1
(en)
|
2005-07-13 |
2007-01-18 |
Allergan, Inc. |
Kinase inhibitors
|
|
EP1902024B1
(en)
|
2005-07-13 |
2013-04-17 |
Allergan, Inc. |
Kinase inhibitors
|
|
US7749530B2
(en)
|
2005-07-13 |
2010-07-06 |
Allergan, Inc. |
Kinase inhibitors
|
|
GB0523041D0
(en)
*
|
2005-11-11 |
2005-12-21 |
Cyclacel Ltd |
Combination
|
|
WO2007098507A2
(en)
|
2006-02-24 |
2007-08-30 |
Rigel Pharmaceuticals, Inc. |
Compositions and methods for inhibition of the jak pathway
|
|
US8987474B2
(en)
*
|
2006-04-07 |
2015-03-24 |
University Of South Florida |
Inhibition of Shp2/PTPN11 protein tyrosine phosphatase by NSC-87877, NSC-117199 and their analogs
|
|
US7838542B2
(en)
|
2006-06-29 |
2010-11-23 |
Kinex Pharmaceuticals, Llc |
Bicyclic compositions and methods for modulating a kinase cascade
|
|
US8217177B2
(en)
*
|
2006-07-14 |
2012-07-10 |
Amgen Inc. |
Fused heterocyclic derivatives and methods of use
|
|
US8036664B2
(en)
*
|
2006-09-22 |
2011-10-11 |
Kineto Wireless, Inc. |
Method and apparatus for determining rove-out
|
|
WO2008045627A2
(en)
*
|
2006-10-06 |
2008-04-17 |
Irm Llc |
Protein kinase inhibitors and methods for using thereof
|
|
GB0625283D0
(en)
*
|
2006-12-19 |
2007-01-24 |
Cyclacel Ltd |
Combination
|
|
HRP20110709T1
(hr)
*
|
2007-02-13 |
2011-11-30 |
Ab Science |
Postupak sinteze spojeva 2-aminotioazola kao inhibitora kinaza
|
|
WO2008134124A1
(en)
*
|
2007-04-30 |
2008-11-06 |
The Uab Research Foundation |
Ul97 inhibitors for treatment of proliferative disorders
|
|
ECSP077628A
(es)
|
2007-05-03 |
2008-12-30 |
Smithkline Beechman Corp |
Nueva composición farmacéutica
|
|
US7863315B2
(en)
*
|
2008-01-15 |
2011-01-04 |
Shenzhen Chipscreen Biosciences, Ltd. |
2-indolinone derivatives as selective histone deacetylase inhibitors
|
|
HRP20170317T1
(hr)
|
2008-02-15 |
2017-04-21 |
Rigel Pharmaceuticals, Inc. |
Spojevi pirimidin-2-amina i njihova uporaba kao inhibitora jak kinaza
|
|
WO2009111644A2
(en)
*
|
2008-03-05 |
2009-09-11 |
The Regents Of The University Of Michigan |
Compositions and methods for diagnosing and treating pancreatic cancer
|
|
US8063058B2
(en)
|
2008-04-16 |
2011-11-22 |
Portola Pharmaceuticals, Inc. |
Inhibitors of syk and JAK protein kinases
|
|
US8138339B2
(en)
|
2008-04-16 |
2012-03-20 |
Portola Pharmaceuticals, Inc. |
Inhibitors of protein kinases
|
|
EP2116236A1
(en)
|
2008-04-21 |
2009-11-11 |
Université de Mons-Hainaut |
Bisbenzamidine derivatives for use as antioxidant
|
|
BRPI0910668A2
(pt)
|
2008-04-22 |
2019-09-24 |
Portola Pharmaceutiacals Inc |
inibidores de proteína quinases
|
|
WO2009135000A2
(en)
*
|
2008-04-30 |
2009-11-05 |
H. Lee Moffitt Cancer Center And Research Institute, Inc. |
Inhibition of shp2/ptpn11 protein tyrosine phosphatase by nsc-117199 and analogs
|
|
WO2009139834A1
(en)
*
|
2008-05-13 |
2009-11-19 |
Poniard Pharmaceuticals, Inc. |
Bioactive compounds for treatment of cancer and neurodegenerative diseases
|
|
PL2307002T3
(pl)
*
|
2008-06-09 |
2013-05-31 |
Cyclacel Ltd |
Kombinacje sapacytabiny lub cndac z inhibitorami metylotransferazy dna, takimi jak decytabina i prokaina
|
|
WO2010039997A2
(en)
*
|
2008-10-01 |
2010-04-08 |
The University Of North Carolina At Chapel Hill |
Hematopoietic protection against chemotherapeutic compounds using selective cyclin-dependent kinase 4/6 inhibitors
|
|
AU2009310352A1
(en)
*
|
2008-10-01 |
2010-05-06 |
The University Of North Carolina At Chapel Hill |
Hematopoietic protection against ionizing radiation using selective cyclin-dependent kinase 4/6 inhibitors
|
|
WO2010121212A2
(en)
|
2009-04-17 |
2010-10-21 |
H. Lee Moffit Cancer Center And Research Institute, Inc. |
Indoline scaffold shp-2 inhibitors and method of treating cancer
|
|
EP3025724B1
(en)
|
2009-05-13 |
2018-07-11 |
The University of North Carolina At Chapel Hill |
Cyclin dependent kinase inhibitors and methods of use
|
|
EP2434894B1
(en)
|
2009-05-29 |
2016-08-31 |
Novartis AG |
Methods of administration of thrombopoietin agonist compounds
|
|
MX337849B
(es)
*
|
2009-07-28 |
2016-03-09 |
Rigel Pharmaceuticals Inc |
Composiciones y metodos para inhibicion de la via jak.
|
|
CN102639700A
(zh)
|
2009-09-30 |
2012-08-15 |
哈佛大学校长及研究员协会 |
通过调节自噬增强基因产物调节自噬的方法
|
|
US8652534B2
(en)
|
2009-10-14 |
2014-02-18 |
Berry Pharmaceuticals, LLC |
Compositions and methods for treatment of mammalian skin
|
|
JP5759471B2
(ja)
*
|
2009-10-29 |
2015-08-05 |
ヴェクチュラ リミテッド |
Jak3キナーゼ阻害剤としての窒素含有ヘテロアリール誘導体
|
|
EP2533793B1
(en)
|
2010-02-12 |
2015-12-09 |
Emory University |
GAL-4 for use in the treatment of infectious diseases
|
|
NZ602191A
(en)
|
2010-03-02 |
2014-07-25 |
Amakem Nv |
Heterocyclic amides as rock inhibitors
|
|
US9168247B2
(en)
|
2010-06-25 |
2015-10-27 |
Facultes Universitaires Notre Dame De La Paix |
Beta carboline derivatives useful in the treatment of proliferative disorders
|
|
US8785648B1
(en)
|
2010-08-10 |
2014-07-22 |
The Regents Of The University Of California |
PKC-epsilon inhibitors
|
|
CA2808655C
(en)
|
2010-08-18 |
2019-11-26 |
Emory University |
Compounds and compositions for ossification and methods related thereto
|
|
WO2012022780A1
(en)
|
2010-08-19 |
2012-02-23 |
Université Libre de Bruxelles |
18-beta-glycyrrhetinic acid derivatives with anti-tumor activity
|
|
US8691830B2
(en)
|
2010-10-25 |
2014-04-08 |
G1 Therapeutics, Inc. |
CDK inhibitors
|
|
KR102186969B1
(ko)
|
2010-10-25 |
2020-12-04 |
쥐원 쎄라퓨틱스, 인크. |
Cdk 억제제
|
|
WO2012058211A2
(en)
|
2010-10-29 |
2012-05-03 |
Emory University |
Quinazoline derivatives, compositions, and uses related thereto
|
|
EP2975027A1
(en)
|
2010-11-01 |
2016-01-20 |
Portola Pharmaceuticals, Inc. |
Nicotinamides as jak kinase modulators
|
|
GB201019043D0
(en)
|
2010-11-10 |
2010-12-22 |
Protea Biopharma N V |
Use of 2',5'-oligoadenylate derivative compounds
|
|
WO2012068381A2
(en)
|
2010-11-17 |
2012-05-24 |
The University Of North Carolina At Chapel Hill |
Protection of renal tissues from schema through inhibition of the proliferative kisses cdk4 and cdk6
|
|
AU2011336397B2
(en)
|
2010-12-03 |
2016-12-15 |
Emory University |
Chemokine CXCR4 receptor modulators and uses related thereto
|
|
US8691777B2
(en)
|
2011-01-27 |
2014-04-08 |
Emory University |
Combination therapy
|
|
US9295754B2
(en)
|
2011-02-24 |
2016-03-29 |
Emory University |
Noggin inhibitory compositions for ossification and methods related thereto
|
|
US11179500B2
(en)
|
2011-02-24 |
2021-11-23 |
Emory University |
JAB1 inhibitory compositions for ossification and methods related thereto
|
|
US9365523B2
(en)
|
2011-03-31 |
2016-06-14 |
Emory University |
Imidazolyl amide compounds and uses related thereto
|
|
PL2696878T3
(pl)
|
2011-04-14 |
2020-01-31 |
Cyclacel Limited |
Schemat dawkowania dla sapacytabiny i decytabiny w kombinacji do leczenia ostrej białaczki szpikowej
|
|
WO2012145234A2
(en)
|
2011-04-21 |
2012-10-26 |
Emory University |
Cyclopropyl derivatives and methods of use
|
|
GB201107223D0
(en)
|
2011-04-29 |
2011-06-15 |
Amakem Nv |
Novel rock inhibitors
|
|
US20140079632A1
(en)
|
2011-05-09 |
2014-03-20 |
Universiteit Antwerpen |
Activity-based probes for the urokinase plasminogen activator
|
|
GB201108225D0
(en)
|
2011-05-17 |
2011-06-29 |
Amakem Nv |
Novel KBC inhibitors
|
|
EP2721011B1
(en)
|
2011-06-20 |
2017-09-06 |
Emory University |
Prostaglandin receptor ep2 antagonists, derivatives, compositions, and uses related thereto
|
|
GB201113689D0
(en)
|
2011-08-09 |
2011-09-21 |
Amakem Nv |
Novel PDE4 inhibitors
|
|
WO2013028543A1
(en)
|
2011-08-19 |
2013-02-28 |
Emory University |
Bax agonist, compositions, and methods related thereto
|
|
GB201114854D0
(en)
|
2011-08-29 |
2011-10-12 |
Amakem Nv |
Novel rock inhibitors
|
|
EP2751079A1
(en)
|
2011-08-31 |
2014-07-09 |
Amakem NV |
Biphenylcarboxamides as rock kinase inhibitors
|
|
PT2760453T
(pt)
|
2011-09-30 |
2016-08-02 |
Ipsen Pharma Sas |
Inibidores macrocíclicos da cinase lrrk2
|
|
MX347765B
(es)
|
2011-09-30 |
2017-05-12 |
Oncodesign Sa |
Inhibidores macrociclicos de la quinasa flt3.
|
|
GB201119358D0
(en)
|
2011-11-10 |
2011-12-21 |
Lewi Paulus J |
Disubstituted triazine dimers for treatment and/or prevention of infectious diseases
|
|
DE102011119127A1
(de)
*
|
2011-11-22 |
2013-05-23 |
Merck Patent Gmbh |
3-Cyanaryl-1H-pyrrolo[2.3-b]pyridin-Derivate
|
|
EP2782579B1
(en)
|
2011-11-23 |
2019-01-02 |
Portola Pharmaceuticals, Inc. |
Pyrazine kinase inhibitors
|
|
EP2810198B1
(en)
|
2012-01-30 |
2023-07-12 |
Universiteit Gent |
Anti-invasive compounds
|
|
GB201204756D0
(en)
|
2012-03-19 |
2012-05-02 |
Lewi Paulus J |
Triazines with suitable spacers for treatment and/or prevention of HIV infections
|
|
EP3216792B1
(en)
|
2012-03-29 |
2020-05-27 |
G1 Therapeutics, Inc. |
Lactam kinase inhibitors
|
|
WO2013181135A1
(en)
|
2012-05-31 |
2013-12-05 |
Emory University |
Quinazoline derivatives, compositions, and uses related thereto
|
|
CN104487429B
(zh)
|
2012-07-27 |
2017-07-14 |
爱默蕾大学 |
杂环黄酮衍生物、组合物及与其相关的方法
|
|
WO2014058921A2
(en)
|
2012-10-08 |
2014-04-17 |
Portola Pharmaceuticals, Inc. |
Substituted pyrimidinyl kinase inhibitors
|
|
WO2014059034A2
(en)
|
2012-10-09 |
2014-04-17 |
President And Fellows Of Harvard College |
Nad biosynthesis and precursors for the treatment and prevention of cancer and proliferation
|
|
EP3369730B1
(en)
|
2012-11-05 |
2020-08-05 |
Emory University |
7,8-dihydoxyflavone and 7,8-substituted flavone derivatives, compositions, and methods related thereto
|
|
WO2014072419A1
(en)
|
2012-11-08 |
2014-05-15 |
Universiteit Antwerpen |
Novel anti-hiv compounds
|
|
HUE033962T2
(en)
|
2013-01-29 |
2018-01-29 |
Redx Pharma Plc |
Pyridine derivatives as soft rock (RHO kinase) inhibitors
|
|
CA2906262A1
(en)
|
2013-03-15 |
2014-09-18 |
Oncodesign S.A. |
Macrocyclic salt-inducible kinase inhibitors
|
|
JP6430483B2
(ja)
|
2013-03-15 |
2018-11-28 |
ジー1、セラピューティクス、インコーポレイテッドG1 Therapeutics, Inc. |
化学療法の間の正常細胞の一時的な保護
|
|
CA2906157C
(en)
|
2013-03-15 |
2022-05-17 |
G1 Therapeutics, Inc. |
Highly active anti-neoplastic and anti-proliferative agents
|
|
WO2014145205A2
(en)
|
2013-03-15 |
2014-09-18 |
St. Jude Children's Research Hospital |
Methods and compositions of p27kip1 transcription modulators
|
|
KR101548803B1
(ko)
*
|
2013-09-09 |
2015-09-01 |
경북대학교병원 |
3(6(4(트리플루오로메톡시)페닐아미노)피리미딘4일)벤자미드 또는 이의 약학적으로 허용 가능한 염을 유효성분으로 함유하는 당뇨병의 예방 또는 치료용 약학적 조성물
|
|
TW201542581A
(zh)
|
2013-09-11 |
2015-11-16 |
艾默理大學 |
核苷酸與核苷治療組成物及其相關用途
|
|
WO2015055796A1
(en)
|
2013-10-16 |
2015-04-23 |
Université Libre de Bruxelles |
Formulations useful in the treatment of proliferative diseases affecting the respiratory tract
|
|
CN103588758A
(zh)
*
|
2013-11-04 |
2014-02-19 |
南京大学 |
一类含1,4-苯并二噁烷骨架的硝基咪唑衍生物的合成、制备及其在抗癌药物中的应用
|
|
WO2015071295A1
(en)
|
2013-11-12 |
2015-05-21 |
Vrije Universiteit Brussel |
Rna transcription vector and uses thereof
|
|
CN115504924A
(zh)
|
2013-11-27 |
2022-12-23 |
雷德伍德生物科技股份有限公司 |
肼基-吡咯并化合物及用于生成缀合物的方法
|
|
KR101602203B1
(ko)
*
|
2014-03-11 |
2016-03-11 |
경북대학교병원 |
N(2하이드록시에틸)3(6(4(트리플루오로메톡시)페닐아미노)피리미딘-4-일)벤자미드 또는 이의 약학적으로 허용 가능한 염을 유효성분으로 함유하는 당뇨병의 예방 또는 치료용 약학적 조성물
|
|
WO2015150472A2
(en)
|
2014-04-01 |
2015-10-08 |
Université Libre de Bruxelles |
New strategies for treating melanoma
|
|
WO2015150337A1
(en)
|
2014-04-01 |
2015-10-08 |
Amakem Nv |
Lim kinase inhibitors
|
|
WO2015161283A1
(en)
|
2014-04-17 |
2015-10-22 |
G1 Therapeutics, Inc. |
Tricyclic lactams for use in hspc-sparing treatments for rb-positive abnormal cellular proliferation
|
|
CN106458821B
(zh)
|
2014-05-05 |
2019-12-31 |
爱默蕾大学 |
Bh4拮抗剂及其相关方法
|
|
WO2015175855A1
(en)
|
2014-05-16 |
2015-11-19 |
Emory University |
Chemokine cxcr4 and ccr5 receptor modulators and used related thereto
|
|
WO2016003450A1
(en)
|
2014-07-01 |
2016-01-07 |
The Regents Of The University Of California |
Pkc-epsilon inhibitors
|
|
WO2016005340A1
(en)
|
2014-07-08 |
2016-01-14 |
Universiteit Gent |
Hamamelitannin analogues and uses thereof
|
|
EP3191098A4
(en)
|
2014-09-12 |
2018-04-25 |
G1 Therapeutics, Inc. |
Combinations and dosing regimes to treat rb-positive tumors
|
|
WO2016040848A1
(en)
|
2014-09-12 |
2016-03-17 |
G1 Therapeutics, Inc. |
Treatment of rb-negative tumors using topoisomerase inhibitors in combination with cyclin dependent kinase 4/6 inhibitors
|
|
AU2015316799B2
(en)
|
2014-09-17 |
2019-07-11 |
Oncodesign Precision Medicine (OPM) |
Macrocyclic RIP2 kinase inhibitors
|
|
ES2717510T3
(es)
|
2014-09-17 |
2019-06-21 |
Oncodesign Sa |
Inhibidores macrocíclicos de cinasa LRRK2
|
|
WO2016083490A1
(en)
|
2014-11-27 |
2016-06-02 |
Remynd Nv |
Compounds for the treatment of amyloid-associated diseases
|
|
WO2016099982A2
(en)
|
2014-12-15 |
2016-06-23 |
Emory University |
Phosphoramidates for the treatment of hepatitis b virus
|
|
WO2016106050A1
(en)
|
2014-12-26 |
2016-06-30 |
Emory University |
N4-hydroxycytidine and derivatives and anti-viral uses related thereto
|
|
WO2016146651A1
(en)
|
2015-03-16 |
2016-09-22 |
Oncodesign Sa |
Macrocyclic activin-like receptor kinase inhibitors
|
|
CA2984379C
(en)
|
2015-04-28 |
2024-06-11 |
Newsouth Innovations Pty Limited |
Targeting nad+ to treat chemotherapy and radiotherapy induced cognitive impairment, neuropathies, and inactivity
|
|
EP3288384A4
(en)
|
2015-05-01 |
2019-01-23 |
Georgia State University Research Foundation |
BENZHYDROL DERIVATIVES FOR ADMINISTERING CONDITIONS RELATED TO HYPOXIC INDUCIBLE FACTORS
|
|
EP3804706B1
(en)
|
2015-05-29 |
2023-08-23 |
Emory University |
2-amino-n'-benzylideneacetohydrazides and derivatives for the management of cftr protein mediated diseases
|
|
CN108137595B
(zh)
*
|
2015-06-18 |
2021-04-20 |
听治疗有限责任公司 |
预防和治疗听力损失的方法和组合物
|
|
WO2017083306A1
(en)
|
2015-11-09 |
2017-05-18 |
R.P. Scherer Technologies, Llc |
Anti-cd22 antibody-maytansine conjugates and methods of use thereof
|
|
US10716869B2
(en)
|
2016-02-29 |
2020-07-21 |
Oncodesign Sa |
Radiolabeled macrocyclic EGFR inhibitor
|
|
WO2017157882A1
(en)
|
2016-03-14 |
2017-09-21 |
Université Catholique de Louvain |
Serine biosynthetic pathway inhibitors
|
|
WO2017161253A1
(en)
*
|
2016-03-18 |
2017-09-21 |
Tufts Medical Center |
Compositions and methods for treating and preventing metabolic disorders
|
|
JP7129703B2
(ja)
|
2016-04-28 |
2022-09-02 |
エモリー ユニバーシティー |
アルキン含有ヌクレオチド及びヌクレオシド治療組成物並びにそれらに関連した使用
|
|
US11166967B2
(en)
|
2016-05-19 |
2021-11-09 |
Universiteit Antwerpen |
Bis(acetamidophenyl) guanidinophenylethylphosphonates for use in the prevention and/or treatment of PAR-related diseases
|
|
BE1023757B1
(nl)
|
2016-06-30 |
2017-07-12 |
Yun NV |
Bewaring van micro-organismen
|
|
WO2018065387A1
(en)
|
2016-10-04 |
2018-04-12 |
Universiteit Gent |
Novel hamamelitannin analogues and uses thereof
|
|
US20190256573A1
(en)
|
2016-10-14 |
2019-08-22 |
Emory University |
Nanoparticles Having Molecules That Bind or Block PD-L1 and Uses In Treating Cancer
|
|
EP3532289B1
(en)
|
2016-10-26 |
2024-03-06 |
Emory University |
Polyoxometalate complexes and uses in managing cancer
|
|
WO2018096088A1
(en)
|
2016-11-24 |
2018-05-31 |
Universiteit Antwerpen |
Halogenated benzotropolones as atg4b inhibitors
|
|
CA3046927A1
(en)
|
2016-12-13 |
2018-06-21 |
Emory University |
Polypeptides for managing viral infections
|
|
JP7229162B2
(ja)
|
2017-01-06 |
2023-02-27 |
ジー1 セラピューティクス, インコーポレイテッド |
癌の治療に対する併用療法
|
|
WO2018138358A1
(en)
|
2017-01-30 |
2018-08-02 |
Université de Liège |
Perk and ire-1a inhibitors against neurodevelopmental disorders
|
|
US11497744B2
(en)
|
2017-02-21 |
2022-11-15 |
Emory University |
Chemokine CXCR4 receptor modulators and uses related thereto
|
|
WO2018160967A1
(en)
*
|
2017-03-02 |
2018-09-07 |
Board Of Regents, The University Of Texas System |
Indolinone derivatives as inhibitors of maternal embryonic leucine zipper kinase
|
|
CN106977508A
(zh)
*
|
2017-05-05 |
2017-07-25 |
遵义医学院 |
具有靛红结构的吡唑衍生物用于防治肿瘤的药物及其制法
|
|
US12178805B2
(en)
|
2017-05-11 |
2024-12-31 |
Remynd N.V. |
Inhibitors of PDE6Delta for use in the prevention and/or treatment of epilepsy and/or neurodegenerative disorders
|
|
PL3621963T3
(pl)
|
2017-05-11 |
2024-05-20 |
Remynd N.V. |
Związki do leczenia epilepsji, zaburzeń neurodegeneracyjnych i innych zaburzeń oun
|
|
US11661581B2
(en)
*
|
2017-05-25 |
2023-05-30 |
University Of Massachusetts |
Use of CDK inhibitors to enhance growth and self-renewal of progenitor cells
|
|
EP3645001B1
(en)
|
2017-06-29 |
2024-07-03 |
G1 Therapeutics, Inc. |
Morphic forms of git38 and methods of manufacture thereof
|
|
RU2020116571A
(ru)
|
2017-12-07 |
2021-11-22 |
Эмори Юниверсити |
N4-гидроксицитидин и производные и связанные с этим противовирусные применения
|
|
CA3135420A1
(en)
|
2018-04-05 |
2019-10-10 |
Universiteit Hasselt |
Selective pde4d inhibitors against demyelinating diseases
|
|
CA3104397C
(en)
|
2018-06-29 |
2023-08-01 |
Rejuvenate Biomed |
Pharmaceutical combination for use in age-related and/or degenerative diseases
|
|
ES2974972T3
(es)
|
2018-08-07 |
2024-07-02 |
Univ Emory |
Derivados heterocíclicos de flavona, composiciones y métodos relacionados con los mismos
|
|
KR102962306B1
(ko)
|
2018-08-24 |
2026-05-08 |
쥐원 쎄라퓨틱스, 인크. |
1,4-디아자스피로[5.5]운데칸-3-온의 개선된 합성
|
|
CA3110661A1
(en)
|
2018-08-29 |
2020-03-05 |
University Of Massachusetts |
Inhibition of protein kinases to treat friedreich ataxia
|
|
US20230009626A1
(en)
*
|
2018-10-05 |
2023-01-12 |
Ichnos Sciences S.A. |
Indolinone compounds for use as map4k1 inhibitors
|
|
WO2020191208A1
(en)
|
2019-03-20 |
2020-09-24 |
Emory University |
Prostaglandin receptor ep2 antagonists, derivatives, and uses related thereto
|
|
AU2020274407B2
(en)
|
2019-05-14 |
2023-09-28 |
Suzhou Four Health Pharmaceuticals Co., Ltd |
Quinazoline-2,4-dione derivatives as PARP inhibitors
|
|
WO2020242933A1
(en)
|
2019-05-24 |
2020-12-03 |
Emory University |
Asparagine endopeptidase (aep) inhibitors, compositions, and uses related thereto
|
|
WO2021016254A1
(en)
*
|
2019-07-22 |
2021-01-28 |
Radius Pharmaceuticals, Inc. |
Estrogen receptor-modulating compounds
|
|
US12577242B2
(en)
|
2020-02-24 |
2026-03-17 |
Katholieke Universiteit Leuven |
Pyrrolopyridine and imidazopyridine antiviral compounds
|
|
GB202003240D0
(en)
|
2020-03-05 |
2020-04-22 |
Ecosynth Nv |
Antiviral treatment
|
|
US20230158178A1
(en)
|
2020-03-16 |
2023-05-25 |
Emory University |
Radionuclide Tracers of 1-Amino-3,4-Difluorocyclopentane-1-Carboxylic Acid, Derivatives, and Uses Thereof
|
|
US10988479B1
(en)
|
2020-06-15 |
2021-04-27 |
G1 Therapeutics, Inc. |
Morphic forms of trilaciclib and methods of manufacture thereof
|
|
WO2022020114A2
(en)
|
2020-07-10 |
2022-01-27 |
Ting Therapeutics Llc |
Methods for the prevention and treatment of hearing loss
|
|
WO2022157381A1
(en)
|
2021-01-25 |
2022-07-28 |
Universiteit Hasselt |
Phloretin for use in the treatment of neurodegenerative and demyelinating diseases
|
|
US20240325363A1
(en)
*
|
2021-03-12 |
2024-10-03 |
Oncocross Co.,Ltd. |
Composition for treatment of anticancer agent-resistant cancer
|
|
KR20240040768A
(ko)
|
2021-07-26 |
2024-03-28 |
셀퀴티 인크. |
암의 치료에 사용하기 위한 1-(4-{[4-(디메틸아미노)피페리딘-1-일]카르보닐}페닐)-3-[4-(4,6-디모르폴린-4-일-1,3,5-트리아진-2-일)페닐]우레아 (게다톨리십) 및 그의 조합물
|
|
AU2022318349B2
(en)
|
2021-07-30 |
2025-12-18 |
Confo Therapeutics N.V. |
Compounds for the treatment of pain, in particular neuropathic pain, and/or other diseases or disorders that are associated with at2r and/or at2r mediated signaling
|
|
EP4387629A1
(en)
|
2021-08-18 |
2024-06-26 |
Katholieke Universiteit Leuven KU Leuven Research & Development |
6-substituted- and 6,7-disubstituted-7-deazapurine ribonucleoside analogues
|
|
US20250066365A1
(en)
|
2021-09-23 |
2025-02-27 |
Katholieke Universiteit Leuven |
Ribonucleoside Analogues Against -Sars-Cov-2
|
|
WO2023105283A1
(en)
|
2021-12-08 |
2023-06-15 |
Fundacio Privada Institut De Recerca De La Sida - Caixa |
Nucleoside reverse transcriptase inhibitors for use in down syndrome and alzheimer`s disease therapy
|
|
US11541071B1
(en)
|
2021-12-16 |
2023-01-03 |
Ascletis BioScience Co., Ltd |
Nucleoside derivatives and methods of use thereof
|
|
WO2023111683A1
(en)
|
2021-12-16 |
2023-06-22 |
Ascletis Bioscience Co., Ltd. |
N4-hydroxycytidine derivatives and use thereof as antiviral agent
|
|
WO2023139402A1
(en)
|
2022-01-18 |
2023-07-27 |
Ascletis Bioscience Co., Ltd. |
Inhibitors of cysteine proteases and methods of use thereof
|
|
US11760722B2
(en)
|
2022-01-18 |
2023-09-19 |
Ascletis Bioscience Co., Ltd. |
Inhibitors of cysteine proteases and methods of use thereof
|
|
WO2023180567A1
(en)
|
2022-03-24 |
2023-09-28 |
Fundacion Privada Institut De Recerca De La Sida-Caixa |
Cyclodextrins for use in coronavirus infection therapy
|
|
WO2023241799A1
(en)
|
2022-06-15 |
2023-12-21 |
Université Libre de Bruxelles |
Flavanols for use in the treatment of retroviral infections
|
|
US20240025885A1
(en)
|
2022-07-08 |
2024-01-25 |
Ascletis BioScience Co., Ltd |
Triazine derivatives and methods of use thereof
|
|
CN117700397A
(zh)
*
|
2022-11-02 |
2024-03-15 |
徐诺药业(南京)有限公司 |
2-氧代吲哚啉类衍生物及其制备方法和应用
|
|
CN115504968B
(zh)
|
2022-11-21 |
2023-04-18 |
歌礼生物科技(杭州)有限公司 |
三嗪衍生物
|
|
WO2024193451A1
(en)
|
2023-03-17 |
2024-09-26 |
Ascletis BioScience Co., Ltd |
Triazine derivatives, method of making and method of using thereof
|
|
WO2025104221A1
(en)
|
2023-11-15 |
2025-05-22 |
Université Libre de Bruxelles |
Uses of protein tyrosine phosphatase receptor kappa inhibitors
|
|
WO2025155711A1
(en)
*
|
2024-01-17 |
2025-07-24 |
The Board Of Trustees Of The Leland Stanford Junior University |
Lrrk2 inhibitors and compositions and uses thereof
|
|
WO2026013165A1
(en)
|
2024-07-10 |
2026-01-15 |
Université Libre de Bruxelles |
Combination of ship2 inhibitor and plk1 inhibitor for use in the treatment of cancer
|
|
WO2026024674A1
(en)
|
2024-07-22 |
2026-01-29 |
Genesis Therapeutics, Inc. |
Methods of treating skp2-associated cancers
|
|
US20260053814A1
(en)
|
2024-08-21 |
2026-02-26 |
Celcuity Inc. |
Treatment regimens for gedatolisib in hormonally-driven disorders
|