US4844732A
(en)
|
1985-10-24 |
1989-07-04 |
Daicel Chemical Industries Ltd. |
Pyridine-3-carboxamide derivatives
|
JPH075555B2
(ja)
|
1986-02-25 |
1995-01-25 |
ダイセル化学工業株式会社 |
ピリドン−3−カルボキサミドの製法
|
JPH075554B2
(ja)
|
1986-02-25 |
1995-01-25 |
ダイセル化学工業株式会社 |
5−ブロモピリドン−3−カルボキサミド化合物の製法
|
KR920701167A
(ko)
|
1989-07-07 |
1992-08-11 |
에릭 에스. 딕커 |
약제학적 활성 화합물
|
US5304121A
(en)
|
1990-12-28 |
1994-04-19 |
Boston Scientific Corporation |
Drug delivery system making use of a hydrogel polymer coating
|
MY106399A
(en)
|
1990-07-24 |
1995-05-30 |
Pfizer |
Cephalosporins and homologeus, preparation and pharmaceutical composition
|
FR2665440B1
(fr)
|
1990-07-31 |
1994-02-04 |
Lipha |
Nouveaux cycloalkylsulfonamides substitues, procedes de preparation et medicaments les contenant.
|
JPH05107574A
(ja)
|
1991-03-12 |
1993-04-30 |
Mitsui Petrochem Ind Ltd |
有機非線形光学材料
|
PT100639A
(pt)
|
1991-06-27 |
1993-09-30 |
Univ Virginia Commonwealth |
Metodo para o tratamento terapeutico com compostos que sao ligandos ao receptor sigma e compostos ai utilizados, nomeadamente derivados fenilalquil-amina, aminotetralina,piperazina e piperidina
|
US5356897A
(en)
|
1991-09-09 |
1994-10-18 |
Fujisawa Pharmaceutical Co., Ltd. |
3-(heteroaryl)-pyrazololi[1,5-a]pyrimidines
|
IT1254134B
(it)
|
1992-01-16 |
1995-09-08 |
Angeletti P Ist Richerche Bio |
Oligonucleotidi antisenso chimicamente modificati.
|
HRP930210A2
(en)
|
1992-02-25 |
1995-06-30 |
Recordati Chem Pharm |
Heterobicyclic compounds and pharmaceutical preparations containing them
|
IT1254469B
(it)
|
1992-02-25 |
1995-09-25 |
Recordati Chem Pharm |
Derivati benzopiranici e benzotiopiranici
|
EP0664792B1
(en)
|
1992-10-14 |
2000-01-05 |
Merck & Co. Inc. |
Fibrinogen receptor antagonists
|
US5716981A
(en)
|
1993-07-19 |
1998-02-10 |
Angiogenesis Technologies, Inc. |
Anti-angiogenic compositions and methods of use
|
US6099562A
(en)
|
1996-06-13 |
2000-08-08 |
Schneider (Usa) Inc. |
Drug coating with topcoat
|
GB2300856A
(en)
|
1995-05-16 |
1996-11-20 |
Pfizer Ltd |
Beta-lactam preparation
|
JP3964478B2
(ja)
|
1995-06-30 |
2007-08-22 |
エーザイ・アール・アンド・ディー・マネジメント株式会社 |
ヘテロ環含有カルボン酸誘導体及びそれを含有する医薬
|
WO1997014419A1
(en)
|
1995-10-20 |
1997-04-24 |
Flora Inc. |
Transdermal delivery of alpha adrenoceptor blocking agents
|
AU703203B2
(en)
|
1996-01-30 |
1999-03-18 |
Merck & Co., Inc. |
Inhibitors of farnesyl-protein transferase
|
US5968965A
(en)
|
1996-01-30 |
1999-10-19 |
Merck & Co., Inc. |
Inhibitors of farnesyl-protein transferase
|
FR2746309B1
(fr)
|
1996-03-22 |
1998-04-17 |
Oreal |
Composition de teinture des fibres keratiniques contenant des pyrazolopyrimidineoxo ; leur utilisation pour la teinture comme coupleurs, procedes de teinture
|
SK284054B6
(sk)
|
1996-10-16 |
2004-08-03 |
Icn Pharmaceuticals, Inc. |
Substituované triazolové nukleozidy, farmaceutický prostriedok s ich obsahom a ich použitie
|
ES2212814T3
(es)
|
1996-10-31 |
2004-08-01 |
Harbor Branch Oceanographic Institution, Inc. |
Uso de compuestos y composiciones antiinflamatorias neurogenicas.
|
JPH10213820A
(ja)
|
1997-01-31 |
1998-08-11 |
Canon Inc |
液晶素子及び液晶装置
|
US5942508A
(en)
|
1997-02-04 |
1999-08-24 |
Senju Pharmaceutical Co., Ltd. |
Method for solubilizing pyridonecarboxylic acid solubilizer thereof and aqueous solution containing solubilized pyridonecarboxylic acid
|
US6355669B1
(en)
|
1997-10-22 |
2002-03-12 |
Eisai Co., Ltd. |
Retinoic acid agonists as preventive and therapeutic agents for nephritis
|
US6150379A
(en)
|
1997-11-26 |
2000-11-21 |
Axys Pharmaceuticals, Inc. |
Compounds and compositions as anticoagulants
|
AU6060099A
(en)
|
1998-09-30 |
2000-04-17 |
Procter & Gamble Company, The |
2-substituted ketoamides
|
WO2000025789A1
(en)
|
1998-10-29 |
2000-05-11 |
Merck & Co., Inc. |
A method of treating endometriosis
|
JP2002543065A
(ja)
|
1999-04-28 |
2002-12-17 |
アベンティス・ファーマ・ドイチユラント・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツング |
Ppap受容体リガンドとしてのトリアリール酸誘導体
|
WO2001012183A1
(en)
|
1999-08-16 |
2001-02-22 |
Merck & Co., Inc. |
Heterocycle amides as cell adhesion inhibitors
|
WO2001019788A2
(en)
|
1999-09-17 |
2001-03-22 |
Cor Therapeutics, Inc. |
BENZAMIDES AND RELATED INHIBITORS OF FACTOR Xa
|
NZ517828A
(en)
|
1999-09-17 |
2003-10-31 |
Millennium Pharm Inc |
Inhibitors having activity against mammalian factor Xa
|
IL148577A0
(en)
|
1999-10-29 |
2002-09-12 |
Pfizer Prod Inc |
Hygromycin derivatives
|
ATE318809T1
(de)
|
1999-11-05 |
2006-03-15 |
Sod Conseils Rech Applic |
Heterocyclische verbindungen und ihre verwendung als medikamente
|
TWI284639B
(en)
|
2000-01-24 |
2007-08-01 |
Shionogi & Co |
A compound having thrombopoietin receptor agonistic effect
|
EP1259485B1
(en)
|
2000-02-29 |
2005-11-30 |
Millennium Pharmaceuticals, Inc. |
BENZAMIDES AND RELATED INHIBITORS OF FACTOR Xa
|
NZ521225A
(en)
|
2000-03-09 |
2004-08-27 |
Aventis Pharma Gmbh |
Therapeutic uses of PPAR mediators
|
WO2002008748A2
(en)
|
2000-07-10 |
2002-01-31 |
Aurora Biosciences Corporation |
Ion channel assay methods
|
WO2002020492A1
(en)
|
2000-09-06 |
2002-03-14 |
Neurogen Corporation |
Aryl substituted tetrahydroindazoles and their use as ligands for the gaba-a receptor
|
WO2002060905A2
(en)
|
2000-10-24 |
2002-08-08 |
Glaxo Group Ltd |
METHOD FOR PREPARING HIV PROTEASE INHIBITOR INTERMEDIATES
|
WO2002036553A2
(en)
|
2000-11-04 |
2002-05-10 |
Aventis Pharma Limited |
Substituted alkanoic acids
|
EP1217000A1
(en)
|
2000-12-23 |
2002-06-26 |
Aventis Pharma Deutschland GmbH |
Inhibitors of factor Xa and factor VIIa
|
IL156595A0
(en)
|
2001-01-16 |
2004-01-04 |
Astrazeneca Ab |
Therapeutic heterocyclic compounds
|
WO2002070483A1
(en)
|
2001-03-05 |
2002-09-12 |
E. I. Du Pont De Nemours And Company |
Heterocyclic diamide invertebrate pest control agents
|
EP1381592A1
(en)
|
2001-04-13 |
2004-01-21 |
Boehringer Ingelheim Pharmaceuticals Inc. |
1,4-disubstituted benzo-fused compounds
|
JP2003034671A
(ja)
|
2001-05-17 |
2003-02-07 |
Nippon Nohyaku Co Ltd |
ベンズアミド誘導体及び農園芸用薬剤並びにその使用方法
|
WO2003070912A2
(en)
|
2001-06-06 |
2003-08-28 |
Sirna Therapeutics, Inc. |
RNA INTERFERENCE MEDIATED INHIBITION OF EPIDERMAL GROWTH FACTOR RECEPTOR GENE EXPRESSION USING SHORT INTERFERING NUCLEIC ACID (siNA)
|
US20030175950A1
(en)
|
2001-05-29 |
2003-09-18 |
Mcswiggen James A. |
RNA interference mediated inhibition of HIV gene expression using short interfering RNA
|
US20050080112A1
(en)
|
2001-06-22 |
2005-04-14 |
Madsen Lars Siim |
Compounds for use in disorders associated with mast cell or basophil acitvity
|
PL204263B1
(pl)
|
2001-09-21 |
2009-12-31 |
Bristol Myers Squibb Co |
Pochodna 1H-pirazolo[3,4-c]pirydyny i jej zastosowanie oraz kompozycja farmaceutyczna i jej zastosowanie
|
FR2831536A1
(fr)
|
2001-10-26 |
2003-05-02 |
Aventis Pharma Sa |
Nouveaux derives de benzimidazoles, leur procede de preparation, leur application a titre de medicament, compositions pharmaceutiques et nouvelle utilisation notamment comme inhibiteurs de kdr
|
SE0103648D0
(sv)
|
2001-11-01 |
2001-11-01 |
Astrazeneca Ab |
Therapeutic quinolone compounds
|
WO2003048135A1
(en)
|
2001-11-14 |
2003-06-12 |
Teva Pharmaceutical Industries Ltd. |
Amorphous and crystalline forms of losartan potassium and process for their preparation
|
US20050038035A1
(en)
|
2001-11-28 |
2005-02-17 |
Hisashi Takasugi |
Heterocyclic amide compounds as apolipoprotein b inhibitors
|
WO2003048081A2
(en)
|
2001-12-04 |
2003-06-12 |
Bristol-Myers Squibb Company |
Glycinamides as factor xa inhibitors
|
JP2005516037A
(ja)
|
2002-01-22 |
2005-06-02 |
イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー |
ジアミド無脊椎有害生物防除剤
|
EP1336602A1
(en)
|
2002-02-13 |
2003-08-20 |
Giovanni Scaramuzzino |
Nitrate prodrugs able to release nitric oxide in a controlled and selective way and their use for prevention and treatment of inflammatory, ischemic and proliferative diseases
|
OA12771A
(en)
|
2002-02-14 |
2006-07-04 |
Pharmacia Corp |
Substituted pyridinones as modulators of P38 map kinase.
|
JP2005523292A
(ja)
|
2002-02-21 |
2005-08-04 |
イーライ・リリー・アンド・カンパニー |
ペルオキシソーム増殖因子活性化受容体モジュレーター
|
JP2005525358A
(ja)
|
2002-02-28 |
2005-08-25 |
ビオタ インコーポレーティッド |
ヌクレオチド模倣体およびそのプロドラッグ
|
WO2004041277A1
(en)
|
2002-11-01 |
2004-05-21 |
Merck & Co., Inc. |
Carbonylamino-benzimidazole derivatives as androgen receptor modulators
|
US7189716B2
(en)
|
2003-01-03 |
2007-03-13 |
Bristol-Myers Squibb Company |
Tyrosine kinase inhibitors
|
KR101145252B1
(ko)
|
2003-01-08 |
2012-05-24 |
유니버시티 오브 워싱톤 |
항균제
|
US7122557B2
(en)
|
2003-03-18 |
2006-10-17 |
Bristol-Myers Squibb Company |
Sulfonyl-amidino-containing and tetrahydropyrimidino-containing compounds as factor Xa inhibitors
|
EP1616034A4
(en)
|
2003-04-01 |
2008-12-03 |
Activx Biosciences Inc |
ACYL PHOSPHATE AND PHOSPHONATE EASTS AND PROCESSES FOR THEIR SYNTHESIS AND USE IN PROTEAM ANALYSIS
|
EP1613261A4
(en)
|
2003-04-09 |
2011-01-26 |
Novo Nordisk As |
INTRA-CELLULAR FORMATION OF PEPTIDE CONJUGATES
|
US20040229839A1
(en)
|
2003-05-14 |
2004-11-18 |
Biocryst Pharmaceuticals, Inc. |
Substituted nucleosides, preparation thereof and use as inhibitors of RNA viral polymerases
|
US7652044B2
(en)
|
2003-06-03 |
2010-01-26 |
Novartis A.G. |
P-38 inhibitors
|
WO2005000309A2
(en)
|
2003-06-27 |
2005-01-06 |
Ionix Pharmaceuticals Limited |
Chemical compounds
|
GB0315111D0
(en)
|
2003-06-27 |
2003-07-30 |
Cancer Rec Tech Ltd |
Substituted 5-membered ring compounds and their use
|
EP2332912A1
(en)
|
2003-08-08 |
2011-06-15 |
Vertex Pharmaceuticals Incorporated |
Heteroarylaminosulfonylphenylderivates for use as sodium or calcium channel blockers in the treatment of pain
|
JP2007502778A
(ja)
|
2003-08-21 |
2007-02-15 |
グリフィス ユニバーシティ |
新規スルフェンアミドオキシド
|
JP2007502779A
(ja)
|
2003-08-21 |
2007-02-15 |
グリフィス ユニバーシティ |
新規スルフェンアミド
|
WO2005021568A2
(en)
|
2003-08-27 |
2005-03-10 |
Biota, Inc. |
Novel tricyclic nucleosides or nucleotides as therapeutic agents
|
WO2005033079A1
(ja)
|
2003-09-30 |
2005-04-14 |
Eisai Co., Ltd. |
ヘテロ環化合物を含有する新規な抗真菌剤
|
GB0325956D0
(en)
|
2003-11-06 |
2003-12-10 |
Addex Pharmaceuticals Sa |
Novel compounds
|
JP4526801B2
(ja)
|
2003-11-13 |
2010-08-18 |
新日鐵化学株式会社 |
複素環化合物の製造方法
|
EP1532980A1
(en)
|
2003-11-24 |
2005-05-25 |
Novo Nordisk A/S |
N-heteroaryl indole carboxamides and analogues thereof, for use as glucokinase activators in the treatment of diabetes
|
WO2005051393A1
(en)
|
2003-11-25 |
2005-06-09 |
Pfizer Products Inc. |
Method of treatment of atherosclerosis
|
US7649004B2
(en)
|
2004-07-23 |
2010-01-19 |
Pfizer, Inc. |
Pyridine derivatives
|
US7915255B2
(en)
|
2004-08-16 |
2011-03-29 |
Verva Pharmaceuticals Pty Ltd |
Metabolism-modulating agents and uses therefor
|
NZ589252A
(en)
|
2004-09-02 |
2012-06-29 |
Vertex Pharma |
Quinazolines useful as inhibitors of voltage-gated sodium channels
|
AU2006222563A1
(en)
|
2005-03-08 |
2006-09-14 |
Biota Scientific Management Pty Ltd. |
Bicyclic nucleosides and nucleotides as therapeutic agents
|
US8461128B2
(en)
|
2005-04-15 |
2013-06-11 |
Sloan-Kettering Institute For Cancer Research |
Anti-microbial agents and uses thereof
|
US7544810B2
(en)
|
2005-05-09 |
2009-06-09 |
Vertex Pharmaceuticals Incorporated |
Processes for preparing biaryl ureas and analogs thereof
|
WO2006124780A2
(en)
|
2005-05-12 |
2006-11-23 |
Kalypsys, Inc. |
Ih-benzo [d] imidazole compounds as inhibitors of b-raf kinase
|
GB0510141D0
(en)
|
2005-05-18 |
2005-06-22 |
Addex Pharmaceuticals Sa |
Novel compounds B3
|
EP1891039A1
(en)
|
2005-05-20 |
2008-02-27 |
Vertex Pharmaceuticals Incorporated |
Quinoline derivatives useful as modulators of ion channels
|
JP5388574B2
(ja)
|
2005-05-31 |
2014-01-15 |
バーテックス ファーマシューティカルズ インコーポレイテッド |
イオンチャネルのモジュレーターとして有用なヘテロ環式類
|
JP2007056213A
(ja)
|
2005-08-26 |
2007-03-08 |
Fujifilm Corp |
焼結含油軸受油用組成物、並びにそれを用いた軸受け装置及び摺動部材
|
WO2007052843A1
(ja)
|
2005-11-04 |
2007-05-10 |
Takeda Pharmaceutical Company Limited |
複素環アミド化合物およびその用途
|
WO2007081966A2
(en)
|
2006-01-09 |
2007-07-19 |
University Of Southern California |
Small molecules for treating cancer and abnormal cell proliferation disorders
|
PE20071025A1
(es)
|
2006-01-31 |
2007-10-17 |
Mitsubishi Tanabe Pharma Corp |
Compuesto amina trisustituido
|
WO2007095187A2
(en)
|
2006-02-13 |
2007-08-23 |
Trustees Of Boston University |
Compositions and methods for antibiotic potentiation and drug discovery
|
TW200808723A
(en)
|
2006-03-13 |
2008-02-16 |
Univ California |
Conformationally restricted urea inhibitors of soluble epoxide hydrolase
|
US7480400B2
(en)
|
2006-03-16 |
2009-01-20 |
Siemens Medical Solutions Usa, Inc. |
Detection of fiber pathways
|
MX2008013194A
(es)
|
2006-04-11 |
2008-12-01 |
Vertex Pharma |
Composiciones utiles como inhibidores de canales de sodio regulados por voltaje.
|
AU2007257959A1
(en)
|
2006-06-09 |
2007-12-21 |
Kemia, Inc. |
Therapy using cytokine inhibitors
|
EP2035395A2
(en)
|
2006-06-27 |
2009-03-18 |
Glenmark Pharmaceuticals S.A. |
Novel processes for the preparation of dpp iv inhibitors
|
US7842672B2
(en)
|
2006-07-07 |
2010-11-30 |
Gilead Sciences, Inc. |
Phosphonate inhibitors of HCV
|
PE20080948A1
(es)
|
2006-07-25 |
2008-09-10 |
Irm Llc |
Derivados de imidazol como moduladores de la senda de hedgehog
|
EP1882475A1
(en)
|
2006-07-26 |
2008-01-30 |
Novartis AG |
Method of treating disorders mediated by the fibroblast growth factor receptor
|
ME02789B
(me)
|
2006-08-08 |
2011-06-30 |
Millennium Pharm Inc |
Jedinjenja heteroarila korisna kao inhibitori e1 aktivirajućih enzima
|
JP5244596B2
(ja)
|
2006-08-09 |
2013-07-24 |
株式会社アイエスティー |
タンパク質の検出方法及びそれに用いる蛍光色素
|
AU2007296740B2
(en)
|
2006-09-11 |
2012-09-27 |
Curis, Inc. |
Substituted 2-indolinone as PTK inhibitors containing a zinc binding moiety
|
AU2007296743B2
(en)
|
2006-09-11 |
2012-02-16 |
Curis, Inc. |
Tyrosine kinase inhibitors containing a zinc binding moiety
|
EP2073806B1
(en)
|
2006-10-12 |
2012-02-15 |
Xenon Pharmaceuticals Inc. |
Use of spiro-oxindole compounds as therapeutic agents
|
CN101541759A
(zh)
|
2006-11-27 |
2009-09-23 |
诺瓦提斯公司 |
取代的二氢咪唑类及其在治疗肿瘤中的用途
|
PT2101760E
(pt)
|
2006-12-08 |
2013-05-07 |
Millennium Pharm Inc |
Formulações de dose unitária e métodos de tratamento da trombose com um inibidor oral do fator xa
|
WO2008133753A2
(en)
|
2006-12-20 |
2008-11-06 |
Abbott Laboratories |
Anti-viral compounds
|
FR2911139A1
(fr)
|
2007-01-05 |
2008-07-11 |
Sanofi Aventis Sa |
Nouveaux derives de phenyl-(4-phenyl-pyrimidin-2-yl)amines, leur preparation a titre de medicaments, compositions pharmaceutiques et notamment comme inhibiteurs de ikk
|
FR2911138B1
(fr)
|
2007-01-05 |
2009-02-20 |
Sanofi Aventis Sa |
Nouveaux derives de n, n'-2,4-dianilinopyrimidines, leur preparation a titre de medicaments, compositions pharmaceutiques et notamment comme inhibiteurs de ikk
|
FR2911140B1
(fr)
|
2007-01-05 |
2009-02-20 |
Sanofi Aventis Sa |
Nouveaux derives de 2-anilino 4-heteroaryle pyrimides, leur preparation a titre de medicaments, compositions pharmaceutiques et notamment comme inhibiteurs de ikk
|
WO2008094507A2
(en)
|
2007-01-26 |
2008-08-07 |
Cellicon Biotechnologies, Inc. |
Novel fusion compounds
|
WO2008115262A2
(en)
|
2007-03-20 |
2008-09-25 |
Curis, Inc. |
Hsp90 inhibitors containing a zinc binding moiety
|
CA2680398A1
(en)
|
2007-03-20 |
2008-09-25 |
Curis, Inc. |
Raf kinase inhibitors containing a zinc binding moiety
|
JP4657384B2
(ja)
|
2007-05-03 |
2011-03-23 |
ファイザー・リミテッド |
ナトリウムチャンネルモジュレーターとしての2−ピリジンカルボキサミド誘導体
|
WO2008156783A2
(en)
|
2007-06-18 |
2008-12-24 |
University Of Louisville Research Foundation, Inc. |
Family of pfkfb3 inhibitors with anti-neoplastic activities
|
MX2009013753A
(es)
|
2007-06-26 |
2010-01-26 |
Sanofi Aventis |
Una sintesis regioselectiva catalizada por cobre de bencimidazoles y azabencimidazoles.
|
PT2178865E
(pt)
|
2007-07-19 |
2015-11-16 |
Lundbeck & Co As H |
Amidas heterocíclicas com 5 membros e compostos relacionados
|
JP4834699B2
(ja)
|
2007-07-30 |
2011-12-14 |
田辺三菱製薬株式会社 |
医薬組成物
|
JP4846769B2
(ja)
|
2007-07-30 |
2011-12-28 |
田辺三菱製薬株式会社 |
医薬組成物
|
FR2919869B1
(fr)
|
2007-08-09 |
2009-09-25 |
Sanofi Aventis Sa |
Nouveaux derives de n, n'-2,4-dianilinopyrimidines, leur preparation a titre de medicaments, compositions pharmaceutiques et notamment comme inhibiteurs de ikk
|
TW200920357A
(en)
|
2007-09-10 |
2009-05-16 |
Curis Inc |
HSP90 inhibitors containing a zinc binding moiety
|
WO2009036066A1
(en)
|
2007-09-10 |
2009-03-19 |
Curis, Inc. |
Vegfr inhibitors containing a zinc binding moiety
|
WO2009036051A1
(en)
|
2007-09-10 |
2009-03-19 |
Curis, Inc. |
Bcl-2 inhibitors containing a zinc binding moiety
|
JP5564947B2
(ja)
|
2007-09-26 |
2014-08-06 |
アステラス製薬株式会社 |
キノロン誘導体
|
AU2008310519B2
(en)
|
2007-10-08 |
2013-05-02 |
Advinus Therapeutics Private Limited |
Acetamide derivatives as glucokinase activators, their process and medicinal applications
|
US8389734B2
(en)
|
2007-10-11 |
2013-03-05 |
Vertex Pharmaceuticals Incorporated |
Amides useful as inhibitors of voltage-gated sodium channels
|
CA2701946A1
(en)
|
2007-10-11 |
2009-04-16 |
Vertex Pharmaceuticals Incorporated |
Heteroaryl amides useful as inhibitors of voltage-gated sodium channels
|
CA2702101A1
(en)
|
2007-10-11 |
2009-04-16 |
Vertex Pharmaceuticals Incorporated |
Aryl amides useful as inhibitors of voltage-gated sodium channels
|
WO2009069132A2
(en)
|
2007-11-29 |
2009-06-04 |
Ramot At Tel Aviv University Ltd. |
Novel reverse transcriptase inhibitors
|
JP5637859B2
(ja)
|
2007-12-13 |
2014-12-10 |
バーテックス ファーマシューティカルズ インコーポレイテッドVertex Pharmaceuticals Incorporated |
嚢胞性線維症膜コンダクタンスレギュレーターのモジュレーター
|
WO2009086303A2
(en)
|
2007-12-21 |
2009-07-09 |
University Of Rochester |
Method for altering the lifespan of eukaryotic organisms
|
WO2009091941A1
(en)
|
2008-01-17 |
2009-07-23 |
Purdue Research Foundation |
Small molecule inhibitors of hiv proteases
|
WO2009114470A2
(en)
|
2008-03-10 |
2009-09-17 |
Curis, Inc. |
Tetrahydroindole and tetrahdyroindazole as hsp90 inhibitors containing a zinc binding moiety
|
JP5219583B2
(ja)
|
2008-03-31 |
2013-06-26 |
住友化学株式会社 |
組成物、光学フィルムとその製造方法、光学部材及び表示装置
|
TW201000107A
(en)
|
2008-04-09 |
2010-01-01 |
Infinity Pharmaceuticals Inc |
Inhibitors of fatty acid amide hydrolase
|
PT2959900T
(pt)
|
2008-06-16 |
2017-06-22 |
Univ Tennessee Res Found |
Composto para tratamento do cancro
|
KR20110036602A
(ko)
|
2008-07-03 |
2011-04-07 |
서트리스 파마슈티컬즈, 인코포레이티드 |
시르투인 조절제로서의 벤즈이미다졸 및 관련 유사체
|
JP5443720B2
(ja)
|
2008-09-05 |
2014-03-19 |
住友化学株式会社 |
組成物、光学フィルム及びその製造方法、光学部材ならびに表示装置
|
US8309707B2
(en)
|
2008-09-06 |
2012-11-13 |
Chemgenes Corporation |
RNA synthesis-phosphoramidites for synthetic RNA in the reverse direction, and application in convenient introduction of ligands, chromophores and modifications of synthetic RNA at the 3′-end
|
US8541569B2
(en)
|
2008-09-06 |
2013-09-24 |
Chemgenes Corporation |
Phosphoramidites for synthetic RNA in the reverse direction, efficient RNA synthesis and convenient introduction of 3'-end ligands, chromophores and modifications of synthetic RNA
|
US8354444B2
(en)
|
2008-09-18 |
2013-01-15 |
Hoffmann-La Roche Inc. |
Substituted pyrrolidine-2-carboxamides
|
PT2340021E
(pt)
|
2008-09-18 |
2013-01-25 |
Hoffmann La Roche |
Pirrolidino-2-carboxamidas substituídas
|
AU2009295948B2
(en)
|
2008-09-29 |
2013-12-05 |
GlaxoSmithKline, LLC |
Quinazolinone, quinolone and related analogs as sirtuin modulators
|
WO2010048149A2
(en)
|
2008-10-20 |
2010-04-29 |
Kalypsys, Inc. |
Heterocyclic modulators of gpr119 for treatment of disease
|
EP2184273A1
(de)
|
2008-11-05 |
2010-05-12 |
Bayer CropScience AG |
Halogen-substituierte Verbindungen als Pestizide
|
AR074231A1
(es)
|
2008-11-27 |
2010-12-29 |
Boehringer Ingelheim Int |
Derivados de 6, 7, 8, 9-tetrahidro-5h-1, 4, 7, 10a-tetraaza-ciclohept[f]indeno, composiciones farmacéuticas que contienen estos compuestos, su uso en el agonismo del receptor 5-ht2c y procesos para prepararlos.
|
GB0821913D0
(en)
|
2008-12-02 |
2009-01-07 |
Price & Co |
Antibacterial compounds
|
US20110237622A1
(en)
|
2008-12-10 |
2011-09-29 |
Merck Frosst Canada Ltd. |
Renin inhibitors
|
US20120040916A1
(en)
|
2008-12-22 |
2012-02-16 |
Massachusetts Institute Of Technology |
Molecular inhibitors of the wnt/beta-catenin pathway
|
KR101370185B1
(ko)
|
2008-12-23 |
2014-03-05 |
에프. 호프만-라 로슈 아게 |
P2x7 조절제로서의 디히드로피리돈 아미드
|
US8471038B2
(en)
|
2008-12-26 |
2013-06-25 |
Dainippon Sumitomo Pharma Co., Ltd. |
Bicyclic heterocyclic compound
|
KR20100087540A
(ko)
|
2009-01-28 |
2010-08-05 |
삼성전자주식회사 |
잉크젯 기록용 잉크 조성물
|
WO2010107739A2
(en)
|
2009-03-18 |
2010-09-23 |
The Board Of Trustees Of The Leland Stanford Junior University |
Methods and compositions of treating a flaviviridae family viral infection
|
SG10201401169QA
(en)
|
2009-04-02 |
2014-05-29 |
Merck Serono Sa |
Dihydroorotate dehydrogenase inhibitors
|
TWI638807B
(zh)
|
2009-04-28 |
2018-10-21 |
環球展覽公司 |
具有甲基-d3取代之銥錯合物
|
WO2010129864A2
(en)
|
2009-05-07 |
2010-11-11 |
The Board Of Trustees Of The Leland Stanford Junior University |
Methods and compositions for studying, imaging, and treating pain
|
CN102459265A
(zh)
|
2009-05-27 |
2012-05-16 |
雅培制药有限公司 |
激酶活性的嘧啶抑制剂
|
ES2520991T3
(es)
|
2009-05-27 |
2014-11-12 |
Abbvie Inc. |
Inhibidores de pirimidina de la actividad cinasa
|
CA2761639C
(en)
|
2009-05-29 |
2016-06-07 |
Raqualia Pharma Inc. |
Aryl substituted carboxamide derivatives as calcium or sodium channel blockers
|
TW201103904A
(en)
|
2009-06-11 |
2011-02-01 |
Hoffmann La Roche |
Janus kinase inhibitor compounds and methods
|
AR077252A1
(es)
|
2009-06-29 |
2011-08-10 |
Xenon Pharmaceuticals Inc |
Enantiomeros de compuestos de espirooxindol y sus usos como agentes terapeuticos
|
US8927513B2
(en)
|
2009-07-07 |
2015-01-06 |
Alnylam Pharmaceuticals, Inc. |
5′ phosphate mimics
|
US8629149B2
(en)
|
2009-09-04 |
2014-01-14 |
Zalicus Pharmaceuticals Ltd. |
Oxopiperazine derivatives for the treatment of pain and epilepsy
|
CA2773561A1
(en)
|
2009-09-14 |
2011-03-17 |
Phusis Therapeutics Inc. |
Pharmaceutical compositions and formulations including inhibitors of the pleckstrin homology domain and methods for using same
|
US20110124597A1
(en)
|
2009-09-25 |
2011-05-26 |
Anacor Pharmaceuticals, Inc. |
Boron containing small molecules
|
CN102712657A
(zh)
|
2009-10-16 |
2012-10-03 |
Rib-X制药公司 |
抗微生物化合物和其制备和使用方法
|
US11084811B2
(en)
|
2010-03-01 |
2021-08-10 |
Oncternal Therapeutics, Inc. |
Compounds for treatment of cancer
|
CN102883607B
(zh)
|
2010-03-01 |
2015-07-22 |
Gtx公司 |
用于治疗癌的化合物
|
HUE028983T2
(en)
|
2010-05-06 |
2017-01-30 |
Vertex Pharma |
Heterocyclic chromene-spirocyclic piperidine amides as ion channel modulators
|
WO2011141909A2
(en)
|
2010-05-10 |
2011-11-17 |
Radikal Therapeutics Inc. |
Lipoic acid and nitroxide derivatives and uses thereof
|
WO2011151619A1
(en)
|
2010-06-01 |
2011-12-08 |
Summit Corporation Plc |
Compounds for the treatment of clostridium difficile associated disease
|
US20120010235A1
(en)
|
2010-07-12 |
2012-01-12 |
Xin-Jie Chu |
N-substituted pyrrolidines
|
WO2012016133A2
(en)
|
2010-07-29 |
2012-02-02 |
President And Fellows Of Harvard College |
Ros1 kinase inhibitors for the treatment of glioblastoma and other p53-deficient cancers
|
US9290485B2
(en)
|
2010-08-04 |
2016-03-22 |
Novartis Ag |
N-((6-amino-pyridin-3-yl)methyl)-heteroaryl-carboxamides
|
WO2012020725A1
(ja)
|
2010-08-10 |
2012-02-16 |
塩野義製薬株式会社 |
Npy y5受容体拮抗作用を有するヘテロ環誘導体
|
MX2013003913A
(es)
|
2010-10-08 |
2013-09-26 |
Abbvie Inc |
Compuestos de furo [3, 2-d] pirimidina.
|
GB201017315D0
(en)
|
2010-10-13 |
2010-11-24 |
Antoxis Ltd |
Compound
|
US9394290B2
(en)
|
2010-10-21 |
2016-07-19 |
Universitaet Des Saarlandes Campus Saarbruecken |
Selective CYP11B1 inhibitors for the treatment of cortisol dependent diseases
|
FI20106119A0
(fi)
|
2010-10-27 |
2010-10-27 |
Sirtuin Valley Oy |
Energia-aineenvaihduntaan vaikuttava koostumus
|
GB201020076D0
(en)
|
2010-11-26 |
2011-01-12 |
Liverpool School Tropical Medicine |
Antimalarial compounds
|
AU2011336209B2
(en)
|
2010-11-29 |
2015-03-19 |
Pfizer Inc. |
Monobactams
|
CA2818903C
(en)
|
2010-12-14 |
2021-03-23 |
Electrophoretics Limited |
5-(1,3-benzoxazol-2-yl)-4-(pyridin-4-yl)pyrimidin-2-amine and its use as a casein kinase 1delta inhibitor
|
TWI574687B
(zh)
|
2011-01-03 |
2017-03-21 |
古利斯股份有限公司 |
具有鋅結合部份之刺蝟拮抗劑
|
WO2012097330A2
(en)
|
2011-01-14 |
2012-07-19 |
University Of Washington |
Compositions and methods for treating degenerative muscle conditions
|
EP3056495A1
(en)
|
2011-02-02 |
2016-08-17 |
Vertex Pharmaceuticals Inc. |
Pyrrolopyrazine-spirocyclic piperidine amides as modulators of ion channels
|
WO2012106534A2
(en)
|
2011-02-02 |
2012-08-09 |
The Regents Of The University Of California |
Hiv integrase inhibitors
|
JP2012167027A
(ja)
|
2011-02-10 |
2012-09-06 |
Shionogi & Co Ltd |
Npyy5受容体拮抗作用を有する縮合ヘテロ環誘導体
|
US10385070B2
(en)
|
2011-02-18 |
2019-08-20 |
Vertex Pharmaceuticals Incorporated |
Chroman-spirocyclic piperidine amides as modulators of ion channels
|
EP2681200A4
(en)
|
2011-03-03 |
2015-05-27 |
Zalicus Pharmaceuticals Ltd |
INHIBITORS OF BENZIMIDAZOLE TYPE OF SODIUM CHANNEL
|
WO2012125613A1
(en)
|
2011-03-14 |
2012-09-20 |
Vertex Pharmaceuticals Incorporated |
Morpholine-spirocyclic piperidine amides as modulators of ion channels
|
CA2830234A1
(en)
|
2011-03-15 |
2012-09-20 |
Abbvie Inc. |
Nuclear hormone receptor modulators
|
US9464065B2
(en)
|
2011-03-24 |
2016-10-11 |
The Scripps Research Institute |
Compounds and methods for inducing chondrogenesis
|
JP5866100B2
(ja)
|
2011-04-13 |
2016-02-17 |
住友化学株式会社 |
レジスト組成物及びレジストパターンの製造方法
|
SG194873A1
(en)
|
2011-05-11 |
2013-12-30 |
Sanofi Sa |
Spiro-oxindole mdm2 antagonists
|
US9278910B2
(en)
|
2011-05-31 |
2016-03-08 |
Receptos, Inc. |
GLP-1 receptor stabilizers and modulators
|
US20140094465A1
(en)
|
2011-06-10 |
2014-04-03 |
N30 Pharmaceuticals, Inc. |
Compounds as S-Nitrosoglutathione Reductase Inhibitors
|
JP2014520161A
(ja)
|
2011-06-22 |
2014-08-21 |
バーテックス ファーマシューティカルズ インコーポレイテッド |
Atrキナーゼ阻害剤として有用な化合物
|
WO2013005057A1
(en)
|
2011-07-07 |
2013-01-10 |
Centro Nacional De Investigaciones Oncológicas (Cnio) |
New compounds
|
GB201111705D0
(en)
|
2011-07-07 |
2011-08-24 |
Takeda Pharmaceutical |
Compounds and their use
|
WO2013022740A2
(en)
|
2011-08-05 |
2013-02-14 |
Corning Incorporated |
Gpr35 ligands and the uses thereof
|
CN104080782B
(zh)
|
2011-09-12 |
2016-06-01 |
默克专利有限公司 |
用作激酶活性调节剂的咪唑胺
|
WO2013049725A2
(en)
|
2011-09-30 |
2013-04-04 |
Tufts University |
Methods of using adenosine a1 receptor activation for treating depression
|
PE20141682A1
(es)
|
2011-10-26 |
2014-11-14 |
Pfizer Ltd |
Derivados de (4-fenilimidazol-2-il) etilamina utiles como moduladores de canal de sodio
|
EP2788332A1
(en)
|
2011-12-07 |
2014-10-15 |
Amgen, Inc. |
Bicyclic aryl and heteroaryl sodium channel inhibitors
|
CN103159738B
(zh)
|
2011-12-19 |
2016-09-07 |
上海泓博智源医药股份有限公司 |
炔基桥连的杂芳香化合物及其应用
|
US9403839B2
(en)
|
2012-01-16 |
2016-08-02 |
Vertex Pharmaceuticals Incorporated |
Pyran-spirocyclic piperidine amides as modulators of ion channels
|
FR2985916B1
(fr)
|
2012-01-25 |
2015-12-04 |
Univ Bordeaux Segalen |
Decontamination par hydrogels d'echantillons aqueux contenant des nanoparticules
|
CA2861439C
(en)
|
2012-02-03 |
2016-07-12 |
Pfizer Inc. |
Benzimidazole and imidazopyridine derivatives as sodium channel modulators
|
EP2812346A1
(en)
|
2012-02-08 |
2014-12-17 |
Graffinity Pharmaceuticals GmbH |
Ligands for antibody and fc-fusion protein purification by affinity chromotography iv
|
KR102251706B1
(ko)
|
2012-02-22 |
2021-05-14 |
메르크 파텐트 게엠베하 |
액정 매질
|
WO2013131018A1
(en)
|
2012-03-02 |
2013-09-06 |
Zalicus Pharmaceuticals Ltd. |
Biaryl inhibitors of the sodium channel
|
LT2822953T
(lt)
|
2012-03-06 |
2017-04-10 |
Pfizer Inc. |
Makrocikliniai dariniai, skirti proliferacinių ligų gydymui
|
JP5798066B2
(ja)
|
2012-03-08 |
2015-10-21 |
富士フイルム株式会社 |
化合物、液晶組成物、高分子材料およびフィルム
|
WO2013134518A1
(en)
|
2012-03-09 |
2013-09-12 |
Amgen Inc. |
Sulfamide sodium channel inhibitors
|
JP5804991B2
(ja)
|
2012-03-19 |
2015-11-04 |
富士フイルム株式会社 |
光反射フィルム、自動車用フロントガラス、建材用ガラス
|
US20150057243A1
(en)
|
2012-04-02 |
2015-02-26 |
Northern University |
Compositions and Methods for the Inhibition of Methyltransferases
|
AU2013269798A1
(en)
|
2012-05-30 |
2014-10-02 |
F. Hoffmann-La Roche Ag |
Substituted pyrrolidine-2-carboxamides
|
JP5867298B2
(ja)
|
2012-06-06 |
2016-02-24 |
Jsr株式会社 |
フォトレジスト組成物及びレジストパターン形成方法
|
WO2013188881A1
(en)
|
2012-06-15 |
2013-12-19 |
President And Fellows Of Harvard College |
Compounds, compositions and methods for treating or preventing neurodegenerative disorders
|
US20140005181A1
(en)
|
2012-06-21 |
2014-01-02 |
Sanford-Burnham Medical Research Institute |
Small molecule antagonists of the apelin receptor for the treatment of disease
|
WO2014003153A1
(ja)
|
2012-06-28 |
2014-01-03 |
協和発酵キリン株式会社 |
置換アミド化合物
|
US9682970B2
(en)
|
2012-06-29 |
2017-06-20 |
Biotium, Inc. |
Fluorescent compounds and uses thereof
|
US9040498B2
(en)
|
2012-07-06 |
2015-05-26 |
Research Foundation Of The City University Of New York |
1,2,3-Triazolyl purine derivatives
|
JP6256467B2
(ja)
|
2012-07-17 |
2018-01-10 |
ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング |
ロイコトリエン生成を阻害するピラゾール誘導体
|
AU2013291098A1
(en)
|
2012-07-19 |
2015-02-05 |
Sumitomo Dainippon Pharma Co., Ltd. |
1-(cycloalkyl-carbonyl)proline derivative
|
JP6324380B2
(ja)
|
2012-07-27 |
2018-05-16 |
バイオジェン・エムエイ・インコーポレイテッドBiogen MA Inc. |
S1p調節剤および/またはatx調節剤である化合物
|
WO2014015523A1
(en)
|
2012-07-27 |
2014-01-30 |
Hutchison Medipharma Limited |
Novel heteroaryl and heterocycle compounds, compositions and methods
|
WO2014020152A1
(en)
|
2012-08-02 |
2014-02-06 |
Graffinity Pharmaceuticals Gmbh |
Ligands for apheresis and immunoabsorption
|
US9428511B2
(en)
|
2012-09-06 |
2016-08-30 |
Bristol-Myers Squibb Company |
Imidazopyridazine JAK3 inhibitors and their use for the treatment of inflammatory and autoimmune diseases
|
CN104812382A
(zh)
|
2012-09-20 |
2015-07-29 |
坦普尔大学 |
取代的烷基二芳基衍生物、制备方法和用途
|
UA110688C2
(uk)
|
2012-09-21 |
2016-01-25 |
Пфайзер Інк. |
Біциклічні піридинони
|
FR2997851B1
(fr)
|
2012-11-09 |
2014-11-28 |
Oreal |
Composition comprenant un derive dicarbonyle et procede de lissage des cheveux a partir de cette composition
|
EP2919770A4
(en)
|
2012-11-14 |
2017-03-08 |
The Board of Regents of The University of Texas System |
Inhibition of hif-2 heterodimerization with hif1 (arnt)
|
MX2015006192A
(es)
|
2012-11-16 |
2015-08-10 |
Merck Sharp & Dohme |
Inhibidores de purina de fosfatidilinositol 3-quinasa delta humana.
|
RU2015126856A
(ru)
|
2012-12-06 |
2017-01-13 |
Мерк Шарп И Доум Корп. |
Дисульфидные маскированные пролекарственные композиции и способы
|
CA2894452A1
(en)
|
2013-01-08 |
2014-07-17 |
European Molecular Biology Laboratory |
Pyridone derivatives and their use in the treatment, amelioration or prevention of a viral disease
|
US20140200215A1
(en)
|
2013-01-15 |
2014-07-17 |
Intermune, Inc. |
Lysophosphatidic acid receptor antagonists
|
SI2951172T1
(sl)
|
2013-01-29 |
2017-08-31 |
Redx Pharma Plc |
Piridin derivati kot inhibitorji mehkih kamnov
|
UY35288A
(es)
|
2013-01-31 |
2014-08-29 |
Vertex Pharma |
Piridonamidas como moduladores de canales de sodio
|
SG11201505954RA
(en)
|
2013-01-31 |
2015-08-28 |
Vertex Pharma |
Amides as modulators of sodium channels
|
TWI606048B
(zh)
|
2013-01-31 |
2017-11-21 |
帝人製藥股份有限公司 |
唑苯衍生物
|
ES2620379T3
(es)
|
2013-01-31 |
2017-06-28 |
Vertex Pharmaceuticals Inc. |
Quinolina y quinoxalina amidas como moduladores de canales de sodio
|
WO2014130856A2
(en)
|
2013-02-21 |
2014-08-28 |
Wayne Rothbaum |
Treatment of skeletal-related disorders
|
US9580400B2
(en)
|
2013-02-26 |
2017-02-28 |
Northeastern University |
Cannabinergic nitrate esters and related analogs
|
WO2014151958A1
(en)
|
2013-03-14 |
2014-09-25 |
VenatoRx Pharmaceuticals, Inc. |
Beta-lactamase inhibitors
|
US9357781B2
(en)
|
2013-05-03 |
2016-06-07 |
Inscent, Inc. |
Honeybee repellents and uses thereof
|
JP2014232188A
(ja)
|
2013-05-29 |
2014-12-11 |
コニカミノルタ株式会社 |
セルロースアシレートフィルム、円偏光板及び画像表示装置
|
US9776995B2
(en)
|
2013-06-12 |
2017-10-03 |
Amgen Inc. |
Bicyclic sulfonamide compounds as sodium channel inhibitors
|
TWI637949B
(zh)
|
2013-06-14 |
2018-10-11 |
塩野義製藥股份有限公司 |
胺基三衍生物及含有其等之醫藥組合物
|
AR096654A1
(es)
|
2013-06-20 |
2016-01-27 |
Ab Science |
Derivados de benzimidazol como inhibidores selectivos de proteína quinasa
|
WO2015003991A1
(en)
|
2013-07-12 |
2015-01-15 |
Syngenta Participations Ag |
Novel microbiocides
|
US20160145304A1
(en)
|
2013-07-12 |
2016-05-26 |
Helmholtz-Zentrum für Infektionsforschung GmbH |
Cystobactamides
|
WO2015003723A1
(en)
|
2013-07-12 |
2015-01-15 |
Københavns Universitet |
Substituted 4-proline derivatives as iglur antagonists
|
CA2918365C
(en)
|
2013-07-19 |
2021-09-07 |
Vertex Pharmaceuticals Incorporated |
Sulfonamides as modulators of sodium channels
|
JP2016529241A
(ja)
|
2013-07-25 |
2016-09-23 |
フォンダッツィオーネ・テレソン |
Fapp2阻害剤及びそれらの使用
|
US9789096B2
(en)
|
2013-09-04 |
2017-10-17 |
Board Of Regents Of The University Of Texas System |
Methods and compositions for selective and targeted cancer therapy
|
HRP20220911T1
(hr)
|
2013-09-11 |
2022-10-28 |
Emory University |
Sastav nukleotida i nukleozida i njihova uporaba
|
KR101628288B1
(ko)
|
2013-09-30 |
2016-06-08 |
주식회사 엘지화학 |
음성 광학 분산도를 갖는 광학 소자 제조용 조성물 및 이로부터 제조된 광학 이방체
|
KR20160060660A
(ko)
|
2013-10-01 |
2016-05-30 |
글락소스미스클라인 인털렉츄얼 프로퍼티 디벨로프먼트 리미티드 |
친화성 크로마토그래피를 위한 및 치료제의 반감기를 연장시키기 위한 화합물
|
US20160264614A1
(en)
|
2013-10-02 |
2016-09-15 |
Moderna Therapeutics, Inc. |
Polynucleotide molecules and uses thereof
|
WO2015054337A1
(en)
|
2013-10-09 |
2015-04-16 |
Emory University |
Heterocyclic coupling catalysts and methods related thereto
|
CN106414403B
(zh)
|
2013-12-03 |
2019-08-30 |
Fmc公司 |
吡咯烷酮除草剂
|
WO2015085238A1
(en)
|
2013-12-05 |
2015-06-11 |
The Regents Of The University Of California, A California Corporation |
Inhibitors of lpxc
|
SG11201604477SA
(en)
|
2013-12-13 |
2016-07-28 |
Vertex Pharma |
Prodrugs of pyridone amides useful as modulators of sodium channels
|
US20150167017A1
(en)
|
2013-12-13 |
2015-06-18 |
Moderna Therapeutics, Inc. |
Alternative nucleic acid molecules and uses thereof
|
KR20150070027A
(ko)
|
2013-12-16 |
2015-06-24 |
메르크 파텐트 게엠베하 |
액정 매질
|
US9611252B2
(en)
|
2013-12-30 |
2017-04-04 |
Lifesci Pharmaceuticals, Inc. |
Therapeutic inhibitory compounds
|
JP6759100B2
(ja)
|
2013-12-30 |
2020-09-23 |
ライフサイ ファーマシューティカルズ,インク. |
治療用阻害化合物
|
EP3129381B1
(en)
|
2014-04-09 |
2020-11-04 |
Siteone Therapeutics Inc. |
10',11'-modified saxitoxins useful for the treatment of pain
|
WO2015162244A1
(en)
|
2014-04-25 |
2015-10-29 |
Basf Se |
N-acylamidine compounds
|
JP6295992B2
(ja)
|
2014-05-09 |
2018-03-20 |
信越化学工業株式会社 |
単量体の製造方法
|
US9701627B2
(en)
|
2014-06-16 |
2017-07-11 |
University Of Maryland, Baltimore |
LRRK2 GTP binding inhibitors for treatment of Parkinson's disease and neuroinflammatory disorders
|
EP3157572A4
(en)
|
2014-06-19 |
2018-02-14 |
Moderna Therapeutics, Inc. |
Alternative nucleic acid molecules and uses thereof
|
US20170136132A1
(en)
|
2014-06-19 |
2017-05-18 |
Moderna Therapeutics, Inc. |
Alternative nucleic acid molecules and uses thereof
|
EP3157573A4
(en)
|
2014-06-19 |
2018-02-21 |
Moderna Therapeutics, Inc. |
Alternative nucleic acid molecules and uses thereof
|
EP3164406A4
(en)
|
2014-07-01 |
2018-04-04 |
Rempex Pharmaceuticals, Inc. |
Boronic acid derivatives and therapeutic uses thereof
|
WO2016007837A1
(en)
|
2014-07-11 |
2016-01-14 |
Spero Therapeutics, Inc. |
Carbonyl linked bicyclic heteroaryl antibiotic tolerance inhibitors
|
JP6951970B2
(ja)
|
2014-07-16 |
2021-10-20 |
ライフサイ ファーマシューティカルズ,インク. |
治療用阻害化合物
|
EP2977374A1
(en)
|
2014-07-21 |
2016-01-27 |
Université de Strasbourg |
Molecules presenting dual emission properties
|
EP2985334B1
(en)
|
2014-08-15 |
2018-06-20 |
Merck Patent GmbH |
Liquid-crystalline medium
|
WO2016029146A1
(en)
|
2014-08-22 |
2016-02-25 |
University Of Washington |
Specific inhibitors of methionyl-trna synthetase
|
SG10201901192TA
(en)
|
2014-09-10 |
2019-03-28 |
Epizyme Inc |
Smyd inhibitors
|
WO2016040449A1
(en)
|
2014-09-10 |
2016-03-17 |
Raze Therapeutics, Inc. |
3-phosphoglycerate dehydrogenase inhibitors and uses thereof
|
JP2016079098A
(ja)
|
2014-10-10 |
2016-05-16 |
塩野義製薬株式会社 |
セフェム化合物
|
EP3215152A4
(en)
|
2014-11-05 |
2018-06-13 |
The University of Kansas |
SMALL MOLECULE INHIBITORS OF THE MITOCHONDRIAL PERMEABILITY TRANSITION PORE (mtPTP)
|
WO2016094690A1
(en)
|
2014-12-10 |
2016-06-16 |
Mars, Incorporated |
Flavor compositions and pet food products containing the same
|
FR3030242B1
(fr)
|
2014-12-18 |
2018-01-26 |
L'oreal |
Emulsion contenant un tensioactif gemine ayant deux groupements amide gras et un filtre uv organique hydrosoluble
|
CN105985330A
(zh)
|
2015-02-04 |
2016-10-05 |
苏州旺山旺水生物医药有限公司 |
一类杂环化合物、其制备方法和用途
|
JP6394430B2
(ja)
|
2015-02-13 |
2018-09-26 |
信越化学工業株式会社 |
化合物、高分子化合物、レジスト材料及びパターン形成方法
|
TN2017000376A1
(en)
|
2015-03-02 |
2019-01-16 |
Amgen Inc |
Bicyclic ketone sulfonamide compounds
|
WO2016145142A1
(en)
|
2015-03-10 |
2016-09-15 |
Emory University |
Nucleotide and nucleoside therapeutics compositions and uses related thereto
|
EP3085360A1
(en)
|
2015-04-20 |
2016-10-26 |
Universite De Bordeaux |
Lipid based nanocarrier compositions loaded with metal nanoparticles and therapeutic agent
|
WO2016172631A2
(en)
|
2015-04-24 |
2016-10-27 |
President And Fellows Of Harvard College |
Substrate selective inhibitors of insulin-degrading enzyme (ide) and uses thereof
|
WO2016186967A1
(en)
|
2015-05-15 |
2016-11-24 |
Gilead Sciences, Inc. |
Benzimidazole and imadazopyridine carboximidamide compounds having activity as inhibitors of indoleamine 2,3-dioxygenase
|
EP3303321A1
(en)
|
2015-06-02 |
2018-04-11 |
E. I. du Pont de Nemours and Company |
Substituted cyclic amides and their use as herbicides
|
WO2016198908A1
(en)
|
2015-06-09 |
2016-12-15 |
Abbvie Inc. |
Ror nuclear receptor modulators
|
ES2744775T3
(es)
|
2015-07-06 |
2020-02-26 |
Bayer Cropscience Ag |
Heterociclos que contienen nitrógeno como pesticidas
|
JP2018526430A
(ja)
|
2015-07-10 |
2018-09-13 |
アルヴィナス・インコーポレイテッド |
タンパク質分解のmdm2系修飾因子および関連の使用方法
|
CN106518766A
(zh)
|
2015-09-11 |
2017-03-22 |
中国人民解放军军事医学科学院毒物药物研究所 |
新型二芳基脲类化合物,其制备方法及其医药用途
|
CN106518767A
(zh)
|
2015-09-11 |
2017-03-22 |
中国人民解放军军事医学科学院毒物药物研究所 |
取代苯并吡唑二芳基脲类化合物,其制备方法及其医药用途
|
WO2017051319A1
(en)
|
2015-09-21 |
2017-03-30 |
Glenmark Pharmaceuticals S.A. |
Aryl and heteroaryl ether compounds as ror gamma modulators
|
WO2017059385A1
(en)
|
2015-09-30 |
2017-04-06 |
Siteone Therapeutics, Inc. |
11,13-modified saxitoxins for the treatment of pain
|
US10874686B2
(en)
|
2015-10-01 |
2020-12-29 |
Memorial Sloan-Kettering Cancer Center |
Anthranilyl-adenosinemonosulfamate analogs and uses thereof
|
US11413278B2
(en)
|
2015-10-08 |
2022-08-16 |
The Regents Of The University Of California |
Compounds and methods for promoting stress resistance
|
US20180305334A1
(en)
|
2015-10-14 |
2018-10-25 |
Aquinnah Pharmaceuticals, Inc. |
Compounds, compositions and methods of use against stress granules
|
ES2914225T3
(es)
|
2015-10-16 |
2022-06-08 |
Modernatx Inc |
Análogos de cap de ARNm con enlace de fosfato modificado
|
WO2017066782A1
(en)
|
2015-10-16 |
2017-04-20 |
Modernatx, Inc. |
Hydrophobic mrna cap analogs
|
WO2017066791A1
(en)
|
2015-10-16 |
2017-04-20 |
Modernatx, Inc. |
Sugar substituted mrna cap analogs
|
WO2017090743A1
(ja)
|
2015-11-27 |
2017-06-01 |
田辺三菱製薬株式会社 |
新規イミダゾール化合物およびメラノコルチン受容体作動薬としての用途
|
GB201522232D0
(en)
|
2015-12-16 |
2016-01-27 |
Liverpool School Tropical Medicine |
Combination product
|
KR102606339B1
(ko)
|
2016-03-02 |
2023-11-24 |
삼성전자주식회사 |
유기금속 화합물 및 이를 포함한 유기 발광 소자
|
MX2018011105A
(es)
|
2016-03-16 |
2018-11-22 |
Kura Oncology Inc |
Inhibidores sustituidos de menina-mll y metodos de uso.
|
GB201604638D0
(en)
|
2016-03-18 |
2016-05-04 |
Mission Therapeutics Ltd |
Novel compounds
|
PL3436446T3
(pl)
|
2016-03-31 |
2023-09-11 |
Vertex Pharmaceuticals Incorporated |
Modulatory mukowiscydozowego przezbłonowego regulatora przewodnictwa
|
CN105906591A
(zh)
|
2016-04-22 |
2016-08-31 |
中国药科大学 |
2-氨基-γ-丁内酯类盐酸盐的合成
|
WO2017223260A1
(en)
|
2016-06-23 |
2017-12-28 |
Albert Einstein College Of Medicine, Inc. |
Pu.1 inhibitors
|
CN106220667B
(zh)
|
2016-07-21 |
2018-10-30 |
北京航空航天大学 |
螺环有机硅化合物及其应用
|
WO2018045106A1
(en)
|
2016-08-30 |
2018-03-08 |
Ohio State Innovation Foundation |
Anti-fungal treatment
|
WO2018055235A1
(en)
|
2016-09-21 |
2018-03-29 |
University Of Helsinki |
Isoxazole-amides for treating cardiac diseases
|
KR20190063473A
(ko)
|
2016-09-28 |
2019-06-07 |
블레이드 테라퓨틱스, 인크. |
칼페인 조정자 및 그 치료학적 용도
|
EP3519533B1
(en)
|
2016-09-28 |
2020-12-16 |
Merck Patent GmbH |
Polymerisable liquid crystal material and polymerised liquid crystal film
|
US11179708B2
(en)
|
2016-10-04 |
2021-11-23 |
Massachusetts Institute Of Technology |
Compositions and methods for selective carbonylation of heterocyclic compounds
|
EP3553065A4
(en)
|
2016-12-12 |
2020-07-01 |
Hangzhou Innogate Pharma Co., Ltd. |
HETEROCYCLIC CONNECTION AS A SYK INHIBITOR AND / OR SYK-HDAC DOUBLE INHIBITOR
|
EP3573608A1
(en)
|
2017-01-30 |
2019-12-04 |
Université de Liège |
Perk and ire-1a inhibitors against neurodevelopmental disorders
|
WO2018161033A1
(en)
|
2017-03-02 |
2018-09-07 |
Wright, Adrian |
Small molecule ire1-alpha inhibitors
|
CN108658972A
(zh)
|
2017-03-28 |
2018-10-16 |
中国海洋大学 |
一种取代内酰胺类化合物及其制备方法和用途
|
CN108658974A
(zh)
|
2017-03-28 |
2018-10-16 |
中国海洋大学 |
一种内酰胺类化合物及其制备方法和用途
|
US11279706B2
(en)
|
2017-03-29 |
2022-03-22 |
Siteone Therapeutics, Inc. |
11,13-modified saxitoxins for the treatment of pain
|
CA3058214A1
(en)
|
2017-03-29 |
2018-10-04 |
Siteone Therapeutics, Inc. |
11,13-modified saxitoxins for the treatment of pain
|
US20200113901A1
(en)
|
2017-03-31 |
2020-04-16 |
Epizyme, Inc. |
Methods of using ehmt2 inhibitors
|
JP2020100564A
(ja)
|
2017-04-03 |
2020-07-02 |
京都薬品工業株式会社 |
リードスルー誘導剤およびその医薬用途
|
US11339144B2
(en)
|
2017-04-10 |
2022-05-24 |
Navitor Pharmaceuticals, Inc. |
Heteroaryl Rheb inhibitors and uses thereof
|
CN108689942B
(zh)
|
2017-04-11 |
2023-06-09 |
广东东阳光药业有限公司 |
含氮双环化合物及其制备方法和用途
|
WO2018195439A2
(en)
|
2017-04-20 |
2018-10-25 |
The Regents Of The University Of California |
K-ras modulators
|
AU2018254577B2
(en)
|
2017-04-21 |
2024-06-13 |
Epizyme, Inc. |
Combination therapies with EHMT2 inhibitors
|
WO2018213426A1
(en)
|
2017-05-16 |
2018-11-22 |
Vertex Pharmaceuticals Incorporated |
Deuterated pyridone amides and prodrugs thereof as modulators of sodium channels
|
CN107033149B
(zh)
|
2017-06-12 |
2020-01-03 |
上海交通大学 |
一种dpp-4酶抑制剂及其制备和应用
|
EP3642182A4
(en)
|
2017-06-21 |
2020-12-09 |
Wave Life Sciences Ltd. |
COMPOUNDS, COMPOSITIONS AND SYNTHESIS METHODS
|
JOP20200001A1
(ar)
|
2017-07-11 |
2022-10-30 |
Vertex Pharma |
كاربوكسأميدات بوصفها معدلات لقنوات الصوديوم
|
CN109320509B
(zh)
|
2017-07-31 |
2022-02-08 |
轩竹生物科技股份有限公司 |
Fxr受体激动剂
|
CN109384712B
(zh)
|
2017-08-14 |
2021-05-07 |
北京宽厚医药科技有限公司 |
靶向nk1受体拮抗剂及其在化疗所致恶心、呕吐治疗中的应用
|
WO2019036657A1
(en)
|
2017-08-17 |
2019-02-21 |
Kyn Therapeutics |
AHR INHIBITORS AND USES THEREOF
|
WO2019036562A1
(en)
|
2017-08-18 |
2019-02-21 |
Saint Louis University |
ERR INVERSE AGONISTS
|
CN109553608B
(zh)
|
2017-09-26 |
2020-12-08 |
北京大学 |
一类五元六元杂环化合物及其制备方法和治疗肿瘤的用途
|
EA202090955A1
(ru)
|
2017-10-18 |
2020-11-27 |
Эпизайм, Инк. |
Способы применения ингибиторов ehmt2 в лечении или предупреждении нарушений со стороны крови
|
EP3697400A4
(en)
|
2017-10-18 |
2021-08-11 |
Epizyme, Inc. |
METHODS FOR THE USE OF EHMT2 INHIBITORS IN THE TREATMENT OR PREVENTION OF BLOOD DISORDERS
|
EP3700527A4
(en)
|
2017-10-25 |
2021-03-10 |
Children's Medical Center Corporation |
PAPD5 INHIBITORS AND THEIR METHODS OF USE
|
EP3479843A1
(en)
|
2017-11-01 |
2019-05-08 |
GenKyoTex Suisse SA |
Use of nox inhibitors for treatment of cancer
|
TW201922690A
(zh)
|
2017-11-10 |
2019-06-16 |
中央研究院 |
環-amp反應元素結合蛋白的抑制劑
|
WO2019097515A1
(en)
|
2017-11-15 |
2019-05-23 |
Metabomed Ltd |
Acss2 inhibitors and methods of use thereof
|
EP3502684A1
(en)
|
2017-12-22 |
2019-06-26 |
Universite De Bordeaux |
Method for metal ion detection in aqueous solutions using nucleolipid compounds
|
KR20190076339A
(ko)
|
2017-12-22 |
2019-07-02 |
한미약품 주식회사 |
신규한 2,6-나프티리딘 2-옥시드 유도체 화합물 및 이의 용도
|
WO2019137201A1
(zh)
|
2018-01-09 |
2019-07-18 |
四川科伦博泰生物医药股份有限公司 |
杂芳基并四氢吡啶类化合物、其制备方法、药物组合物及应用
|
EP3749649A1
(en)
|
2018-02-08 |
2020-12-16 |
ENYO Pharma |
Non-fused thiophene derivatives and their uses
|
EP3752152A1
(en)
|
2018-02-12 |
2020-12-23 |
Vertex Pharmaceuticals Incorporated |
A method of treating pain
|
EP3749195B1
(en)
|
2018-04-05 |
2023-10-18 |
St. Jude Medical, Cardiology Division, Inc. |
High density electrode mapping catheter
|
CN112041413A
(zh)
|
2018-04-27 |
2020-12-04 |
默克专利股份有限公司 |
可聚合的液晶材料和聚合的液晶膜
|
WO2019207081A1
(en)
|
2018-04-27 |
2019-10-31 |
Merck Patent Gmbh |
Polymerisable liquid crystal material and polymerised liquid crystal film
|
TW202003450A
(zh)
|
2018-05-16 |
2020-01-16 |
美商貝利特生物有限公司 |
脂肪酸類似物及使用方法
|
TWI812739B
(zh)
|
2018-06-21 |
2023-08-21 |
景凱生物科技股份有限公司 |
Nadph氧化酶抑制劑、含其的醫藥組合物、及其應用
|
EP3820866A4
(en)
|
2018-07-09 |
2022-04-06 |
Lieber Institute, Inc. |
PYRIDINE CARBOXAMIDE COMPOUNDS TO INHIBIT NAV1.8
|
JP2021531256A
(ja)
|
2018-07-09 |
2021-11-18 |
リーバー インスティチュート インコーポレイテッドLieber Institute, Inc. |
NaV1.8を阻害するピリダジン化合物
|
EP3831823A4
(en)
|
2018-08-01 |
2022-04-27 |
Shanghai Ennovabio Pharmaceuticals Co., Ltd. |
PREPARATION AND USE OF AN AROMATIC COMPOUND WITH IMMUNEGULATORY FUNCTION
|
US11945803B2
(en)
|
2018-08-07 |
2024-04-02 |
Tosk, Inc. |
Modulators of RAS GTPase
|
WO2020034058A1
(en)
|
2018-08-13 |
2020-02-20 |
Rhodia Operations |
PROCESS FOR REDUCTIVE AMINATION OF α,β-UNSATURATED CARBONYL COMPOUND
|
WO2020034062A1
(en)
|
2018-08-13 |
2020-02-20 |
Rhodia Operations |
Process for the reductive amination of a carbonyl compound
|
SG11202102208WA
(en)
|
2018-09-04 |
2021-04-29 |
Magenta Therapeutics Inc |
Aryl hydrocarbon receptor antagonists and methods of use
|
MX2021003559A
(es)
|
2018-09-28 |
2021-08-24 |
Acucela Inc |
Inhibidores de vap-1.
|
KR102092838B1
(ko)
|
2018-10-02 |
2020-03-24 |
성균관대학교산학협력단 |
신규 퓨란계 폴리카보네이트 및 이의 제조 방법
|
EP3860714B1
(en)
|
2018-10-03 |
2023-09-06 |
Siteone Therapeutics, Inc. |
11,13-modified saxitoxins for the treatment of pain
|
TW202028183A
(zh)
|
2018-10-10 |
2020-08-01 |
大陸商江蘇豪森藥業集團有限公司 |
含氮雜芳類衍生物調節劑、其製備方法和應用
|
WO2020081572A1
(en)
|
2018-10-15 |
2020-04-23 |
Dana-Farber Cancer Institute, Inc. |
Transcriptional enhanced associate domain (tead) transcription factor inhibitors and uses thereof
|
BR112021008524A8
(pt)
|
2018-11-02 |
2023-02-07 |
Merck Sharp & Dohme |
2-amino-n-heteroaril-nicotinamidas como inibidores de nav 1.8
|
EP3873468A4
(en)
|
2018-11-02 |
2022-10-26 |
Merck Sharp & Dohme LLC |
2-AMINO-N-PHENYL-NICOTINAMIDE USED AS NAV1.8 INHIBITORS
|
KR102151855B1
(ko)
|
2018-11-30 |
2020-09-03 |
롯데케미칼 주식회사 |
공액 디엔계 및 방향족 비닐계 공중합체의 제조 방법 및 이로부터 제조된 공액 디엔계 및 방향족 비닐계의 공중합체를 포함하는 타이어
|
EP3891157A4
(en)
|
2018-12-05 |
2022-08-31 |
Merck Sharp & Dohme Corp. |
4-AMINO- OR 4-ALKOXY-SUBSTITUTED ARYLSULFONAMIDE COMPOUNDS WITH SELECTIVE ACTIVITY IN VOLTAGE-GATE SODIUM CHANNELS
|
US20220023270A1
(en)
|
2018-12-06 |
2022-01-27 |
The Children's Medical Center Corporation |
Antibacterial compounds and uses thereof
|
EP3894392A4
(en)
|
2018-12-11 |
2022-08-24 |
Duke University |
COMPOSITIONS AND METHODS FOR THE TREATMENT OF CANCER
|
WO2020140959A1
(zh)
|
2019-01-04 |
2020-07-09 |
江苏恒瑞医药股份有限公司 |
6-氧代-1,6-二氢哒嗪类衍生物、其制备方法及其在医药上的应用
|
US20220110923A1
(en)
|
2019-01-10 |
2022-04-14 |
Vertex Pharmaceuticals Incorporated |
Esters and carbamates as modulators of sodium channels
|
WO2020146682A1
(en)
|
2019-01-10 |
2020-07-16 |
Vertex Pharmaceuticals Incorporated |
Carboxamides as modulators of sodium channels
|
CN111434655A
(zh)
|
2019-01-15 |
2020-07-21 |
武汉朗来科技发展有限公司 |
溶血磷脂酸受体拮抗剂及其制备方法
|
EP3914669B1
(en)
|
2019-01-22 |
2024-10-02 |
Merck Patent GmbH |
Method for the preparation of a liquid crystal polymer film
|
TW202043200A
(zh)
|
2019-01-25 |
2020-12-01 |
大陸商江蘇恆瑞醫藥股份有限公司 |
2-側氧基-1,2-二氫吡啶類衍生物、其製備方法及其在醫藥上的應用
|
JP7473565B2
(ja)
|
2019-01-28 |
2024-04-23 |
ミトコンドリア エモーション, インク. |
マイトフュージン活性化物質及びその使用方法
|
WO2020160225A1
(en)
|
2019-01-30 |
2020-08-06 |
Ohio State Innovation Foundation |
ESTROGEN RECEPTOR BETA (ERβ) AGONISTS FOR THE TREATMENT OF FIBROTIC CONDITIONS
|
WO2020191227A1
(en)
|
2019-03-20 |
2020-09-24 |
Cornell University |
Methods for controlling prostaglandin-mediated biological processes
|
WO2020191501A1
(en)
|
2019-03-27 |
2020-10-01 |
Algernon Pharmaceuticals Inc. |
Methods and uses of bemithyl and derivatives for treating lung disease, fatty liver disease, and kidney disorders
|
WO2020221677A1
(en)
|
2019-04-30 |
2020-11-05 |
Merck Patent Gmbh |
Reactive mesogens
|
KR20220007681A
(ko)
|
2019-05-10 |
2022-01-18 |
와커 헤미 아게 |
양이온성 게르마늄(ii) 화합물, 그의 제조 방법, 및 히드로실릴화에서의 촉매로서의 그의 용도
|
MX2021013839A
(es)
|
2019-05-14 |
2022-01-18 |
Metabomed Ltd |
Inhibidores de acss2 y metodos de uso de los mismos.
|
WO2020251974A1
(en)
|
2019-06-10 |
2020-12-17 |
Kymera Therapeutics, Inc. |
Smarca inhibitors and uses thereof
|
BR112021025317A2
(pt)
|
2019-06-21 |
2022-03-15 |
Bayer Ag |
Tienilhidroxiisoxazolinas e derivados das mesmas
|
WO2020261114A1
(en)
|
2019-06-27 |
2020-12-30 |
Glaxosmithkline Intellectual Property Development Limited |
2,3-dihydroquinazolin compounds as nav1.8 inhibitors
|
WO2021001739A1
(en)
|
2019-07-02 |
2021-01-07 |
Effector Therapeutics, Inc. |
Translational enhancers and related methods
|
CN112300069A
(zh)
|
2019-07-31 |
2021-02-02 |
明慧医药(上海)有限公司 |
一种选择性钠通道调节剂及其制备和应用
|
CN112300051A
(zh)
|
2019-07-31 |
2021-02-02 |
明慧医药(上海)有限公司 |
一种选择性钠通道调节剂及其制备和应用
|
WO2021032074A1
(zh)
|
2019-08-19 |
2021-02-25 |
江苏恒瑞医药股份有限公司 |
苯甲酰胺稠芳环类衍生物、其制备方法及其在医药上的应用
|
CN112390745B
(zh)
|
2019-08-19 |
2022-10-21 |
江苏恒瑞医药股份有限公司 |
吡啶烟酰胺类衍生物、其制备方法及其在医药上的应用
|
CN112409331B
(zh)
|
2019-08-21 |
2024-02-20 |
上海翰森生物医药科技有限公司 |
杂环类衍生物抑制剂、其制备方法和应用
|
CN112441969A
(zh)
|
2019-08-30 |
2021-03-05 |
明慧医药(上海)有限公司 |
一种选择性钠通道调节剂及其制备和应用
|
CN118146148A
(zh)
|
2019-09-12 |
2024-06-07 |
上海济煜医药科技有限公司 |
吡啶氮氧化合物及其制备方法和用途
|
CA3150673A1
(en)
|
2019-10-17 |
2021-04-22 |
Enyo Pharma |
THIOPHENE DERIVATIVES FOR USE IN THE TREATMENT OF PORTAL INFLAMMATION AND FIBROSIS
|
TW202128675A
(zh)
|
2019-12-06 |
2021-08-01 |
美商維泰克斯製藥公司 |
作為鈉通道調節劑之經取代四氫呋喃
|
CN111217776A
(zh)
|
2020-01-19 |
2020-06-02 |
中国人民解放军军事科学院军事医学研究院 |
含苯并杂环结构的酰胺衍生物、组合物和应用
|
EP4157888A4
(en)
|
2020-05-28 |
2024-07-10 |
Cullgen Shanghai Inc |
MODIFIED PROTEINS AND PROTEIN DEGRADERS
|
JP2021195368A
(ja)
|
2020-06-10 |
2021-12-27 |
アムジエン・インコーポレーテツド |
シクロブチルジヒドロキノリンスルホンアミド化合物
|
JP2021195367A
(ja)
|
2020-06-10 |
2021-12-27 |
アムジエン・インコーポレーテツド |
シクロプロピルジヒドロキノリンスルホンアミド化合物
|
US20230227442A1
(en)
|
2020-06-10 |
2023-07-20 |
Amgen Inc. |
Heteroalkyl dihydroquinoline sulfonamide compounds
|
AU2021292061A1
(en)
|
2020-06-17 |
2023-01-19 |
Merck Sharp & Dohme Llc |
2-oxo-oxazolidine-5-carboxamides as Nav1.8 inhibitors
|
JP7323723B2
(ja)
|
2020-06-17 |
2023-08-08 |
メルク・シャープ・アンド・ドーム・エルエルシー |
Nav1.8阻害剤としての2-オキソイミダゾリジン-4-カルボキサミド
|
MX2022015580A
(es)
|
2020-06-17 |
2023-01-24 |
Merck Sharp & Dohme Llc |
5-oxopirrolidin-3-carboxamidas como inhibidores de nav1.8.
|
GB202011996D0
(en)
|
2020-07-31 |
2020-09-16 |
Adorx Therapeutics Ltd |
Antagonist compounds
|
CA3188924A1
(en)
|
2020-08-14 |
2022-02-17 |
Hassan Pajouhesh |
Non-hydrated ketone inhibitors of nav1.7 for the treatment of pain
|
TW202220962A
(zh)
|
2020-08-19 |
2022-06-01 |
大陸商江蘇恒瑞醫藥股份有限公司 |
選擇性NaV抑制劑的結晶形式及其製備方法
|
TW202214259A
(zh)
|
2020-08-19 |
2022-04-16 |
大陸商江蘇恆瑞醫藥股份有限公司 |
一種選擇性NaV抑制劑的前藥及其晶型
|
CN111808019B
(zh)
|
2020-09-08 |
2020-11-27 |
上海济煜医药科技有限公司 |
一种并环化合物及其应用
|
WO2022063902A1
(en)
|
2020-09-24 |
2022-03-31 |
Merck Patent Gmbh |
Polymerizable liquid crystal material and polymerized liquid crystal film
|
WO2022070048A1
(en)
|
2020-09-29 |
2022-04-07 |
Cadila Healthcare Limited |
Novel amide derivatives
|
EP4232020A4
(en)
|
2020-10-21 |
2024-08-07 |
Kura Oncology Inc |
TREATMENT OF HEMATOLOGICAL MALIGNANTS WITH MENIN INHIBITORS
|
CN112225695B
(zh)
|
2020-12-15 |
2021-03-02 |
上海济煜医药科技有限公司 |
一种氮氧化合物及其制备方法和用途
|
CN112457294B
(zh)
|
2021-01-27 |
2021-06-04 |
上海济煜医药科技有限公司 |
一种作为NaV1.8阻滞剂的化合物及其制备方法和用途
|