|
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
|
|
KR100685192B1
(ko)
*
|
1998-12-17 |
2007-02-22 |
에프. 호프만-라 로슈 아게 |
4,5-아졸로-옥신돌
|
|
US6153634A
(en)
|
1998-12-17 |
2000-11-28 |
Hoffmann-La Roche Inc. |
4,5-azolo-oxindoles
|
|
BR9916327A
(pt)
*
|
1998-12-17 |
2001-09-18 |
Hoffmann La Roche |
Oxindóis de 4-alquenila (e alquinila) como inibidores de cinases dependentes de ciclina, em particular, cdk2
|
|
CN1136217C
(zh)
|
1998-12-17 |
2004-01-28 |
霍夫曼-拉罗奇有限公司 |
作为jnk蛋白质激酶抑制剂的4-芳基羟吲哚
|
|
CN1158283C
(zh)
|
1998-12-17 |
2004-07-21 |
霍夫曼-拉罗奇有限公司 |
作为蛋白激酶抑制剂的4-和5-吡嗪基羟吲哚
|
|
CA2360581A1
(en)
|
1999-01-13 |
2000-07-20 |
The Research Foundation Of State University Of New York |
A novel method for designing protein kinase inhibitors
|
|
GB9904930D0
(en)
*
|
1999-03-04 |
1999-04-28 |
Glaxo Group Ltd |
Thiazoloindolinone compounds
|
|
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
|
|
US6492398B1
(en)
*
|
1999-03-04 |
2002-12-10 |
Smithkline Beechman Corporation |
Thiazoloindolinone 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
|
|
US6423699B1
(en)
|
1999-05-04 |
2002-07-23 |
American Home Products Corporation |
Combination therapies using benzimidazolones
|
|
US6498154B1
(en)
|
1999-05-04 |
2002-12-24 |
Wyeth |
Cyclic regimens using quinazolinone and benzoxazine derivatives
|
|
US6391907B1
(en)
*
|
1999-05-04 |
2002-05-21 |
American Home Products Corporation |
Indoline derivatives
|
|
US6399593B1
(en)
|
1999-05-04 |
2002-06-04 |
Wyeth |
Cyclic regimens using cyclic urea and cyclic amide derivatives
|
|
US6358948B1
(en)
|
1999-05-04 |
2002-03-19 |
American Home Products Corporation |
Quinazolinone and benzoxazine derivatives as progesterone receptor modulators
|
|
US6444668B1
(en)
|
1999-05-04 |
2002-09-03 |
Wyeth |
Combination regimens using progesterone receptor modulators
|
|
US6462032B1
(en)
|
1999-05-04 |
2002-10-08 |
Wyeth |
Cyclic regimens utilizing indoline derivatives
|
|
US6407101B1
(en)
|
1999-05-04 |
2002-06-18 |
American Home Products Corporation |
Cyanopyrroles
|
|
US6339098B1
(en)
|
1999-05-04 |
2002-01-15 |
American Home Products Corporation |
2,1-benzisothiazoline 2,2-dioxides
|
|
US6319912B1
(en)
|
1999-05-04 |
2001-11-20 |
American Home Products Corporation |
Cyclic regimens using 2,1-benzisothiazoline 2,2-dioxides
|
|
US6358947B1
(en)
|
1999-05-04 |
2002-03-19 |
American Home Products Corporation |
Tetracyclic progesterone receptor modulator compounds and methods
|
|
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
|
|
US6509334B1
(en)
|
1999-05-04 |
2003-01-21 |
American Home Products Corporation |
Cyclocarbamate derivatives as progesterone receptor modulators
|
|
US6369056B1
(en)
|
1999-05-04 |
2002-04-09 |
American Home Products Corporation |
Cyclic urea and cyclic amide derivatives
|
|
US6355648B1
(en)
|
1999-05-04 |
2002-03-12 |
American Home Products Corporation |
Thio-oxindole derivatives
|
|
US6380178B1
(en)
|
1999-05-04 |
2002-04-30 |
American Home Products Corporation |
Cyclic regimens using cyclocarbamate and cyclic amide derivatives
|
|
US6329416B1
(en)
|
1999-05-04 |
2001-12-11 |
American Home Products Corporation |
Combination regimens using 3,3-substituted indoline derivatives
|
|
US6417214B1
(en)
|
1999-05-04 |
2002-07-09 |
Wyeth |
3,3-substituted indoline 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
|
|
US6552008B1
(en)
*
|
1999-09-24 |
2003-04-22 |
Smithkline Beecham Corporation |
Thrombopoietin mimetics
|
|
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
|
|
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
|
|
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
|
|
CA2369502A1
(en)
|
2000-02-05 |
2001-08-09 |
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
|
|
EP1274706A1
(en)
|
2000-04-18 |
2003-01-15 |
Agouron Pharmaceuticals, Inc. |
Pyrazoles for inhibiting protein kinases
|
|
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
|
|
CA2411928A1
(en)
|
2000-08-09 |
2002-02-14 |
Agouron Pharmaceuticals, Inc. |
Pyrazole-thiazole compounds, pharmaceutical compositions containing them, and methods of their use for inhibiting cyclindependent kinases
|
|
MXPA03001452A
(es)
|
2000-08-18 |
2004-05-04 |
Agouron Pharma |
Hidroximino-fluorenos heterociclicos y su uso para la inhibicion de las proteinas cinasas.
|
|
AU8664701A
(en)
*
|
2000-09-01 |
2002-03-22 |
Glaxo Group Ltd |
Oxindole derivatives
|
|
AU2001288374A1
(en)
|
2000-09-01 |
2002-03-22 |
Glaxo Group Limited |
Substituted oxindole derivatives as tyrosine kinase inhibitors
|
|
DE60106947T2
(de)
|
2000-09-01 |
2005-11-10 |
Glaxo Group Ltd., Greenford |
Oxindolderivate
|
|
EP1201765A3
(en)
*
|
2000-10-16 |
2003-08-27 |
Axxima Pharmaceuticals Aktiengesellschaft |
Cellular kinases involved in cytomegalovirus infection and their inhibition
|
|
US6638965B2
(en)
|
2000-11-01 |
2003-10-28 |
Boehringer Ingelheim Pharma Kg |
Substituted indolinones, preparation thereof and their use as pharmaceutical compositions
|
|
DE10054019A1
(de)
*
|
2000-11-01 |
2002-05-23 |
Boehringer Ingelheim Pharma |
Neue 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
|
|
DE10117204A1
(de)
*
|
2001-04-06 |
2002-10-10 |
Boehringer Ingelheim Pharma |
In 6-Stellung substituierte Indolinone, ihre Herstellung und ihre Verwendung als Arzneimittel
|
|
EP1396490A1
(en)
*
|
2001-05-24 |
2004-03-10 |
Yamanouchi Pharmaceutical Co. Ltd. |
3-quinoline-2-(1h)-ylideneindolin-2-one derivatives
|
|
WO2003003006A2
(en)
|
2001-06-29 |
2003-01-09 |
Ab Science |
New potent, selective and non toxic c-kit inhibitors
|
|
ATE343415T1
(de)
|
2001-06-29 |
2006-11-15 |
Ab Science |
Die verwendung von c-kit hemmer zur behandlung von entzündlichen darmerkrankungen
|
|
PT1401415E
(pt)
|
2001-06-29 |
2006-09-29 |
Ab Science |
Utilizacao de derivados de n-fenil-2-pirimidino-amina para o tratamento de doencas inflamatorias
|
|
US20040241226A1
(en)
*
|
2001-09-20 |
2004-12-02 |
Alain Moussy |
Use of potent, selective and non-toxic c-kit inhibitors for treating bacterial infections
|
|
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
|
|
AU2002341881B2
(en)
*
|
2001-09-27 |
2008-05-08 |
Allergan, Inc. |
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
|
|
WO2003035621A1
(en)
*
|
2001-10-22 |
2003-05-01 |
The Research Foundation Of State University Of New York |
Protein kinase and phosphatase inhibitors, methods for designing them, and methods of using them
|
|
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
|
|
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
|
|
WO2003051883A1
(en)
*
|
2001-12-18 |
2003-06-26 |
Kyowa Hakko Kogyo Co., Ltd. |
Indole derivative
|
|
AU2002351412B2
(en)
|
2001-12-21 |
2010-05-20 |
Exelixis Patent Company Llc |
Modulators of LXR
|
|
US7482366B2
(en)
*
|
2001-12-21 |
2009-01-27 |
X-Ceptor Therapeutics, Inc. |
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
|
|
JP2005523928A
(ja)
*
|
2002-04-30 |
2005-08-11 |
アルコン,インコーポレイテッド |
眼内圧の低下および緑内障性網膜症/眼神経障害の処置の両方のための独特の手段としての、結合組織増殖因子(ctgf)の活性および/または発現を調節するか、阻害するか、または調整する薬剤
|
|
AR040083A1
(es)
|
2002-05-22 |
2005-03-16 |
Smithkline Beecham Corp |
Compuesto bis-(monoetanolamina) del acido 3'-[(2z)-[1-(3,4-dimetilfenil) -1,5-dihidro-3-metil-5-oxo-4h-pirazol-4-iliden] hidrazino] -2'-hidroxi-[1,1'-bifenil]-3-carboxilico, procedimiento para prepararlo, composicion farmaceutica que lo comprende, procedimiento para preparar dicha composicion farmac
|
|
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
|
|
WO2004014854A1
(en)
*
|
2002-08-07 |
2004-02-19 |
Synaptic Pharmaceutical Corporation |
3-imino-2-indolones for the treatment of depression and/or anxiety
|
|
US20040082615A1
(en)
*
|
2002-08-07 |
2004-04-29 |
Michael Konkel |
3-Imino-2-indolones for the treatement of depression and/or anxiety
|
|
GB0225873D0
(en)
*
|
2002-11-06 |
2002-12-11 |
Cyclacel Ltd |
Combination
|
|
WO2004048366A1
(ja)
*
|
2002-11-22 |
2004-06-10 |
Yamanouchi Pharmaceutical Co., Ltd. |
2−オキソインドリン誘導体
|
|
DE60311879T2
(de)
|
2002-12-23 |
2007-12-20 |
Astex Therapeutics Ltd., Cambridge |
Synthese und screening von liganden mit hilfe von röntgenkristallographie
|
|
US7122542B2
(en)
|
2003-07-30 |
2006-10-17 |
Rigel Pharmaceuticals, Inc. |
Methods of treating or preventing autoimmune diseases with 2,4-pyrimidinediamine compounds
|
|
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
|
|
JP4728340B2
(ja)
*
|
2004-10-25 |
2011-07-20 |
リガンド・ファーマシューティカルズ・インコーポレイテッド |
トロンボポエチン活性を変調する化合物および変調方法
|
|
GT200500321A
(es)
*
|
2004-11-09 |
2006-09-04 |
|
Compuestos y composiciones como inhibidores de proteina kinase.
|
|
US20080125432A1
(en)
|
2004-12-01 |
2008-05-29 |
Devgen Nv |
5-Carboxamido Substituted Thiazole Derivatives that Interact With Ion Channels, In Particular With Ion Channels From the Kv Family
|
|
WO2006063848A1
(en)
*
|
2004-12-17 |
2006-06-22 |
Devgen N.V. |
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
|
|
SG137989A1
(en)
|
2005-06-08 |
2008-01-28 |
Rigel Pharmaceuticals Inc |
Compositions and methods for inhibition of the JAK pathway
|
|
US20070203161A1
(en)
|
2006-02-24 |
2007-08-30 |
Rigel Pharmaceuticals, Inc. |
Compositions and methods for inhibition of the jak pathway
|
|
US7749530B2
(en)
|
2005-07-13 |
2010-07-06 |
Allergan, Inc. |
Kinase inhibitors
|
|
CA2602389A1
(en)
|
2005-07-13 |
2007-01-18 |
Allergan, Inc. |
Kinase inhibitors
|
|
WO2007008985A2
(en)
*
|
2005-07-13 |
2007-01-18 |
Allergan, Inc. |
Kinase inhibitors
|
|
GB0523041D0
(en)
*
|
2005-11-11 |
2005-12-21 |
Cyclacel Ltd |
Combination
|
|
JP2009528295A
(ja)
|
2006-02-24 |
2009-08-06 |
ライジェル ファーマシューティカルズ, インコーポレイテッド |
Jak経路の阻害のための組成物および方法
|
|
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
|
|
CA2664147A1
(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
|
|
BRPI0807626B1
(pt)
*
|
2007-02-13 |
2022-03-03 |
Ab Science |
Processo para a síntese de compostos de 2-aminotiazol como inibidores de quinase
|
|
US20100143440A1
(en)
*
|
2007-04-30 |
2010-06-10 |
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
|
|
MX2010008926A
(es)
|
2008-02-15 |
2011-02-23 |
Rigel Pharmaceuticals Inc |
Compuestos de pirimidin-2-amina y su uso como inhibidores de jak cinasas.
|
|
US20110092452A1
(en)
*
|
2008-03-05 |
2011-04-21 |
The Regents Of The University Of Michigan |
Compositions and methods for diagnosing and treating pancreatic cancer
|
|
US8138339B2
(en)
|
2008-04-16 |
2012-03-20 |
Portola Pharmaceuticals, Inc. |
Inhibitors of protein kinases
|
|
US8063058B2
(en)
|
2008-04-16 |
2011-11-22 |
Portola Pharmaceuticals, Inc. |
Inhibitors of syk and JAK protein kinases
|
|
EP2116236A1
(en)
|
2008-04-21 |
2009-11-11 |
Université de Mons-Hainaut |
Bisbenzamidine derivatives for use as antioxidant
|
|
CN102066338A
(zh)
|
2008-04-22 |
2011-05-18 |
波托拉医药品公司 |
蛋白激酶抑制剂
|
|
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
|
|
NZ589719A
(en)
|
2008-06-09 |
2012-08-31 |
Cyclacel Ltd |
Combinations of sapacitabine or cndac with dna methyltransferase inhibitors such as decitabine and procaine
|
|
AU2009298367A1
(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
|
|
JP2012526850A
(ja)
|
2009-05-13 |
2012-11-01 |
ザ ユニバーシティ オブ ノース カロライナ アット チャペル ヒル |
サイクリン依存性キナーゼ阻害剤及びその用法
|
|
SG176088A1
(en)
|
2009-05-29 |
2011-12-29 |
Glaxosmithkline Llc |
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.
|
|
CA2774998A1
(en)
|
2009-09-30 |
2011-04-07 |
President And Fellows Of Harvard College |
Methods for modulation of autophagy through the modulation of autophagy-inhibiting gene products
|
|
US8652534B2
(en)
|
2009-10-14 |
2014-02-18 |
Berry Pharmaceuticals, LLC |
Compositions and methods for treatment of mammalian skin
|
|
EP2493895B1
(en)
*
|
2009-10-29 |
2017-04-26 |
Vectura Limited |
N-containing heteroaryl derivatives as jak3 kinase inhibitors
|
|
US20120328568A1
(en)
|
2010-02-12 |
2012-12-27 |
Emory University |
Compositions and uses of lectins
|
|
WO2011107608A1
(en)
|
2010-03-02 |
2011-09-09 |
Amakem Nv |
Heterocyclic amides as rock inhibitors
|
|
CA2803697A1
(en)
|
2010-06-25 |
2011-12-29 |
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
|
|
EP3187197B1
(en)
|
2010-08-18 |
2020-01-01 |
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
|
|
RS55135B1
(sr)
|
2010-10-25 |
2016-12-30 |
G1 Therapeutics Inc |
Cdk inhibitori
|
|
EP2886120B1
(en)
|
2010-10-29 |
2019-06-19 |
Emory University |
Quinazoline derivatives, compositions and uses related thereto
|
|
WO2012061428A2
(en)
|
2010-11-01 |
2012-05-10 |
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
|
|
EP2640394A4
(en)
|
2010-11-17 |
2015-02-25 |
Univ North Carolina |
PROTECTION OF KIDNEY TISSUE FROM ISCHEMIA BY THE INHIBITION OF PROLEVERATIVE KINASES CDK4 AND CDK6
|
|
EP3153510B1
(en)
|
2010-12-03 |
2020-05-06 |
Emory University |
Fused azines as chemokine cxcr4 receptor modulators and uses related thereto
|
|
US8691777B2
(en)
|
2011-01-27 |
2014-04-08 |
Emory University |
Combination therapy
|
|
EP2678050B1
(en)
|
2011-02-24 |
2020-10-14 |
Emory University |
Noggin blocking compositions for ossification and methods related thereto
|
|
WO2012116137A2
(en)
|
2011-02-24 |
2012-08-30 |
Emory University |
Jab1 blocking compositions for ossification and methods related thereto
|
|
EP2691095B1
(en)
|
2011-03-31 |
2017-07-05 |
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
|
|
EP2699539B1
(en)
|
2011-04-21 |
2019-03-06 |
Emory University |
Cyclopropyl derivatives and methods of use
|
|
GB201107223D0
(en)
|
2011-04-29 |
2011-06-15 |
Amakem Nv |
Novel rock inhibitors
|
|
EP2707034A1
(en)
|
2011-05-09 |
2014-03-19 |
Universiteit Antwerpen |
Activity-based probes for the urokinase plasminogen activator
|
|
GB201108225D0
(en)
|
2011-05-17 |
2011-06-29 |
Amakem Nv |
Novel KBC inhibitors
|
|
CA2839956A1
(en)
|
2011-06-20 |
2012-12-27 |
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
|
|
US9040567B2
(en)
|
2011-08-19 |
2015-05-26 |
Emory University |
BAX agonist, compositions, and methods related thereto
|
|
GB201114854D0
(en)
|
2011-08-29 |
2011-10-12 |
Amakem Nv |
Novel rock inhibitors
|
|
MX2014002395A
(es)
|
2011-08-31 |
2014-06-05 |
Amakem Nv |
Inhibidores de rock suaves, novedosos.
|
|
CA2849999A1
(en)
|
2011-09-30 |
2013-04-04 |
Oncodesign S.A. |
Macrocyclic flt3 kinase inhibitors
|
|
AU2012314035B2
(en)
|
2011-09-30 |
2016-12-15 |
Oncodesign S.A. |
Macrocyclic LRRK2 kinase inhibitors
|
|
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
|
|
AU2012340555B2
(en)
|
2011-11-23 |
2016-10-20 |
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
|
|
CA2868966C
(en)
|
2012-03-29 |
2021-01-26 |
Francis Xavier Tavares |
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
|
|
US9676756B2
(en)
|
2012-10-08 |
2017-06-13 |
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
|
|
JP6479670B2
(ja)
|
2012-11-05 |
2019-03-06 |
エモリー ユニバーシティー |
7,8−ジヒドロキシフラボンおよび7,8−置換フラボン誘導体、組成物、およびそれらに関連する方法
|
|
WO2014072419A1
(en)
|
2012-11-08 |
2014-05-15 |
Universiteit Antwerpen |
Novel anti-hiv compounds
|
|
MX367818B
(es)
|
2013-01-29 |
2019-09-09 |
Redx Pharma Plc |
Derivados de piridina como inhibidores de serina/treonina rock y uso de los mismos en el tratamiento de enfermedades autoinmunitarias, inflamatorias, cardiovasculares, etc.
|
|
JP2016510797A
(ja)
|
2013-03-15 |
2016-04-11 |
オンコデザイン エス.ア. |
大環状塩誘導性キナーゼ阻害剤
|
|
CA2906157C
(en)
|
2013-03-15 |
2022-05-17 |
G1 Therapeutics, Inc. |
Highly active anti-neoplastic and anti-proliferative agents
|
|
US9572815B2
(en)
|
2013-03-15 |
2017-02-21 |
St. Jude Children's Research Hospital |
Methods and compositions of p27KIP1 transcriptional modulators
|
|
SMT201900681T1
(it)
|
2013-03-15 |
2020-01-14 |
G1 Therapeutics Inc |
Protezione transitoria di cellule normali durante la chemioterapia
|
|
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
|
|
PL3043803T3
(pl)
|
2013-09-11 |
2022-11-07 |
Emory University |
Kompozycje nukleotydowe i nukleozydowe oraz ich zastosowanie
|
|
EP3057619A1
(en)
|
2013-10-16 |
2016-08-24 |
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
|
|
PL3068888T3
(pl)
|
2013-11-12 |
2018-07-31 |
Vrije Universiteit Brussel |
Wektor transkrypcyjny rna oraz jego zastosowania
|
|
EP4592275A3
(en)
|
2013-11-27 |
2025-10-29 |
Redwood Bioscience, Inc. |
Hydrazinyl-pyrrolo compounds and methods for producing a conjugate
|
|
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
|
|
WO2015150337A1
(en)
|
2014-04-01 |
2015-10-08 |
Amakem Nv |
Lim kinase inhibitors
|
|
US20170165240A1
(en)
|
2014-04-01 |
2017-06-15 |
Université Libre de Bruxelles |
New strategies for treating melanoma
|
|
WO2015161287A1
(en)
|
2014-04-17 |
2015-10-22 |
G1 Therapeutics, Inc. |
Tricyclic lactams for use in the protection of normal cells during chemotherapy
|
|
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
|
|
EA032838B1
(ru)
|
2014-09-17 |
2019-07-31 |
Онкодизайн С.А. |
Макроциклические ингибиторы lrrk2-киназы
|
|
US10676486B2
(en)
|
2014-09-17 |
2020-06-09 |
Oncodesign S.A. |
Macrocyclic RIP2 kinase inhibitors
|
|
WO2016083490A1
(en)
|
2014-11-27 |
2016-06-02 |
Remynd Nv |
Compounds for the treatment of amyloid-associated diseases
|
|
US10683319B2
(en)
|
2014-12-15 |
2020-06-16 |
Emory University |
Phosphoramidates for the treatment of hepatitis B virus
|
|
ES2892123T3
(es)
|
2014-12-26 |
2022-02-02 |
Univ Emory |
Derivados antivíricos de N4-hidroxicitidina
|
|
WO2016146651A1
(en)
|
2015-03-16 |
2016-09-22 |
Oncodesign Sa |
Macrocyclic activin-like receptor kinase inhibitors
|
|
JP7193232B2
(ja)
|
2015-04-28 |
2022-12-20 |
ニューサウス イノベーションズ ピーティーワイ リミテッド |
化学療法及び放射線療法誘発性認知機能障害、神経障害及び不活動を治療するためのnad+の標的化
|
|
EP3804706B1
(en)
|
2015-05-29 |
2023-08-23 |
Emory University |
2-amino-n'-benzylideneacetohydrazides and derivatives for the management of cftr protein mediated diseases
|
|
JP6902025B2
(ja)
*
|
2015-06-18 |
2021-07-14 |
ティン セラピューティックス エルエルシー |
聴覚損失の予防および治療のための方法および組成物
|
|
MX2018005785A
(es)
|
2015-11-09 |
2019-04-04 |
Scherer Technologies Llc R P |
Conjugados de anticuerpo anti-cd22-maytansina y metodos de uso de los mismos.
|
|
WO2017148925A1
(en)
|
2016-02-29 |
2017-09-08 |
Oncodesign Sa |
Radiolabeled macrocyclic egfr inhibitor
|
|
WO2017157882A1
(en)
|
2016-03-14 |
2017-09-21 |
Université Catholique de Louvain |
Serine biosynthetic pathway inhibitors
|
|
US11077110B2
(en)
|
2016-03-18 |
2021-08-03 |
Tufts Medical Center |
Compositions and methods for treating and preventing metabolic disorders
|
|
EA201892448A1
(ru)
|
2016-04-28 |
2019-06-28 |
Эмори Юниверсити |
Алкинсодержащие нуклеотидные и нуклеозидные терапевтические композиции и связанные с ними способы применения
|
|
WO2017198753A1
(en)
|
2016-05-19 |
2017-11-23 |
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
|
|
WO2018071911A1
(en)
|
2016-10-14 |
2018-04-19 |
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
|
|
AU2017377993A1
(en)
|
2016-12-13 |
2019-07-04 |
Emory University |
Polypeptides for managing viral infections
|
|
EA201991622A1
(ru)
|
2017-01-06 |
2020-01-23 |
Г1 Терапьютикс, Инк. |
Комплексная терапия для лечения рака
|
|
EP3656382A1
(en)
|
2017-01-30 |
2020-05-27 |
Université de Liège |
Perk and ire-1a inhibitors against neurodevelopmental disorders
|
|
IL309069A
(en)
|
2017-02-21 |
2024-02-01 |
Univ Emory |
CXCR4 cytokine receptor modulators and related uses
|
|
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
|
|
KR102659211B1
(ko)
|
2017-06-29 |
2024-04-18 |
쥐원 쎄라퓨틱스, 인크. |
G1t38의 형체 형태 및 그의 제조 방법
|
|
ES2995458T3
(en)
|
2017-12-07 |
2025-02-10 |
Univ Emory |
N4-hydroxycytidine derivative and anti-viral uses related thereto
|
|
CA3135420A1
(en)
|
2018-04-05 |
2019-10-10 |
Universiteit Hasselt |
Selective pde4d inhibitors against demyelinating diseases
|
|
ES2965834T3
(es)
|
2018-06-29 |
2024-04-17 |
Rejuvenate Biomed |
Combinación farmacéutica que comprende una biguanida y un inhibidor de la acetilcolinesterasa para usar en enfermedades relacionadas con la edad y/o degenerativas
|
|
PL3833343T3
(pl)
|
2018-08-07 |
2024-06-24 |
Emory University |
Heterocykliczne pochodne flawonu, kompozycje, i sposoby z nimi związane
|
|
CN112839657B
(zh)
|
2018-08-24 |
2025-07-25 |
法码科思莫斯控股有限公司 |
1,4-二氮杂螺[5.5]十一烷-3-酮改进的合成
|
|
CA3110661A1
(en)
|
2018-08-29 |
2020-03-05 |
University Of Massachusetts |
Inhibition of protein kinases to treat friedreich ataxia
|
|
SG11202103459WA
(en)
*
|
2018-10-05 |
2021-05-28 |
Ichnos Sciences S A |
Indolinone compounds for use as map4k1 inhibitors
|
|
US12240829B2
(en)
|
2019-03-20 |
2025-03-04 |
Emory University |
Prostaglandin receptor EP2 antagonists, derivatives, and uses related thereto
|
|
ES2966719T3
(es)
|
2019-05-14 |
2024-04-23 |
Suzhou Four Health Pharmaceuticals Co Ltd |
Derivados de quinazolina-2,4-diona como inhibidores de PARP
|
|
JP7614169B2
(ja)
*
|
2019-07-22 |
2025-01-15 |
ラジウス ファーマシューティカルズ,インコーポレイテッド |
エストロゲン受容体調節化合物
|
|
EP4110777A1
(en)
|
2020-02-24 |
2023-01-04 |
Katholieke Universiteit Leuven, K.U.Leuven R&D |
Pyrrolopyridine and imidazopyridine antiviral compounds
|
|
GB202003240D0
(en)
|
2020-03-05 |
2020-04-22 |
Ecosynth Nv |
Antiviral treatment
|
|
EP4121121A4
(en)
|
2020-03-16 |
2024-09-25 |
Emory University |
RADIONUCLIDE TRACERS OF 1-AMINO-3,4-DIFLUOROCYCLOPENTAN-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
|
|
US20240350492A1
(en)
|
2020-07-10 |
2024-10-24 |
Ting Therapeutics Llc |
Methods for the Prevention and Treatment of Hearing Loss
|
|
WO2022157381A1
(en)
|
2021-01-25 |
2022-07-28 |
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Phloretin for use in the treatment of neurodegenerative and demyelinating diseases
|
|
KR20220128285A
(ko)
*
|
2021-03-12 |
2022-09-20 |
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|
|
MX2024001266A
(es)
|
2021-07-26 |
2024-04-16 |
Celcuity Inc |
1-(4-{[4-(dimetilamino)piperidin-1-il]carbonil}fenil)-3-[4-(4,6-d imorfolin-4-il-1,3,5-triazin-2-il)fenil]urea (gedatolisib) y sus combinaciones para usarse en el tratamiento de cancer.
|
|
AU2022318349A1
(en)
|
2021-07-30 |
2024-02-15 |
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
|
|
US20250144125A1
(en)
|
2021-08-18 |
2025-05-08 |
Katholieke Universiteit Leuven |
6-substituted- and 6,7-disubstituted-7-deazapurine ribonucleoside analogues
|
|
US20250066365A1
(en)
|
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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
|
|
US11760722B2
(en)
|
2022-01-18 |
2023-09-19 |
Ascletis Bioscience Co., Ltd. |
Inhibitors of cysteine proteases and methods of use thereof
|
|
WO2023139402A1
(en)
|
2022-01-18 |
2023-07-27 |
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 |
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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
|
|
CN116514783A
(zh)
|
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2023-08-01 |
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)
|
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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
|