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
|
WO1991000858A1
(en)
|
1989-07-07 |
1991-01-24 |
Schering Corporation |
Pharmaceutically active compounds
|
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
|
CA2111957A1
(en)
|
1991-06-27 |
1993-01-07 |
Richard A. Glennon |
Sigma receptor ligands and the use thereof
|
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.
|
IT1254469B
(it)
|
1992-02-25 |
1995-09-25 |
Recordati Chem Pharm |
Derivati benzopiranici e benzotiopiranici
|
SG65570A1
(en)
|
1992-02-25 |
1999-06-22 |
Recordati Chem Pharm |
Heterobicyclic compounds
|
CA2144763A1
(en)
|
1992-10-14 |
1994-04-28 |
George D. Hartman |
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
|
EP0944387A1
(en)
|
1996-01-30 |
1999-09-29 |
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
|
NZ334915A
(en)
|
1996-10-16 |
2000-11-24 |
Icn Pharmaceuticals |
Monocyclic L-nucleosides, analogs thereof and their use in the modulation of Th1 and Th2 activities
|
DE69727305T2
(de)
|
1996-10-31 |
2004-06-24 |
Harbor Branch Oceanographic Institution, Inc., Fort Pierce |
Verwendung neurogen-entzuendungshemmender verbindungen und zusammensetzungen
|
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
|
CN1332722A
(zh)
|
1998-09-30 |
2002-01-23 |
宝洁公司 |
2-取代的酮酰胺
|
AU1230100A
(en)
|
1998-10-29 |
2000-05-22 |
Merck & Co., Inc. |
A method of treating endometriosis
|
KR100693771B1
(ko)
|
1999-04-28 |
2007-03-12 |
사노피-아벤티스 도이칠란트 게엠베하 |
Ppar 수용체 리간드로서의 트리아릴 산 유도체 및 이를 포함하는 약제학적 조성물
|
AU6903200A
(en)
|
1999-08-16 |
2001-03-13 |
Merck & Co., Inc. |
Heterocycle amides as cell adhesion inhibitors
|
CN1272316C
(zh)
|
1999-09-17 |
2006-08-30 |
千禧药品公司 |
苯甲酰胺和相关的因子Xa抑制剂
|
JP2003509412A
(ja)
|
1999-09-17 |
2003-03-11 |
シーオーアール セラピューティクス インコーポレイテッド |
Xa因子阻害剤
|
WO2001030795A1
(en)
|
1999-10-29 |
2001-05-03 |
Pfizer Products Inc. |
Hygromycin derivatives
|
EP1233962B1
(fr)
|
1999-11-05 |
2006-03-01 |
Societe De Conseils De Recherches Et D'applications Scientifiques (S.C.R.A.S.) |
Composes heterocycliques et leur application a titre de medicaments
|
TWI284639B
(en)
|
2000-01-24 |
2007-08-01 |
Shionogi & Co |
A compound having thrombopoietin receptor agonistic effect
|
WO2001064643A2
(en)
|
2000-02-29 |
2001-09-07 |
Cor Therapeutics, Inc. |
BENZAMIDES AND RELATED INHIBITORS OF FACTOR Xa
|
KR20020081424A
(ko)
|
2000-03-09 |
2002-10-26 |
아벤티스 파마 도이칠란트 게엠베하 |
Ppar 매개인자의 치료학적 용도
|
AU7588101A
(en)
|
2000-07-10 |
2002-02-05 |
Aurora Biosciences Corp |
Ion channel assay methods
|
BR0113697A
(pt)
|
2000-09-06 |
2003-07-22 |
Neurogen Corp |
Composto ou um sal farmaceuticamente aceitável do mesmo, composição farmacêutica, uso de um composto ou sal, embalagem e métodos para, para alterar a atividade transdutora de sinal dos receptores de gabaa, para tratar ansiedade, depressão, um distúrbio do sono, ou demência de alzheimer, para demonstrar a presença dos receptores de gabaa em células ou amostras de tecido e para preparar um composto
|
JP2004519473A
(ja)
|
2000-10-24 |
2004-07-02 |
グラクソ グループ リミテッド |
Hivプロテアーゼ阻害剤の中間体の製造方法
|
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
|
JP4280067B2
(ja)
|
2001-01-16 |
2009-06-17 |
アストラゼネカ・アクチエボラーグ |
治療用ヘテロ環式化合物
|
KR100874324B1
(ko)
|
2001-03-05 |
2008-12-18 |
이 아이 듀폰 디 네모아 앤드 캄파니 |
헤테로시클릭 디아미드 무척추 해충 방제제
|
CA2443697A1
(en)
|
2001-04-13 |
2002-10-24 |
Pier F. Cirillo |
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
|
US20030175950A1
(en)
|
2001-05-29 |
2003-09-18 |
Mcswiggen James A. |
RNA interference mediated inhibition of HIV gene expression using short interfering RNA
|
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)
|
WO2003000245A1
(en)
|
2001-06-22 |
2003-01-03 |
Poseidon Pharmaceuticals A/S |
Compounds for use in disorders associated with mast cell or basophil activity
|
KR100909141B1
(ko)
|
2001-09-21 |
2009-07-23 |
브리스톨-마이어스스퀴브컴파니 |
인자 Xa 억제제로서의 락탐-함유 화합물 및 그의 유도체
|
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
|
JP2005510564A
(ja)
|
2001-11-28 |
2005-04-21 |
藤沢薬品工業株式会社 |
アポリポタンパク質b阻害剤としての複素環式アミド化合物
|
AU2002350217A1
(en)
|
2001-12-04 |
2003-06-17 |
Bristol-Myers Squibb Company |
Glycinamides as factor xa inhibitors
|
WO2003062221A1
(en)
|
2002-01-22 |
2003-07-31 |
E.I. Du Pont De Nemours And Company |
Diamide invertebrate pest control agents
|
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
|
EA008008B1
(ru)
|
2002-02-14 |
2007-02-27 |
Фармация Корпорейшн |
Замещённые пиридиноны в качестве модуляторов мар-киназы р38
|
US20050250831A1
(en)
|
2002-02-21 |
2005-11-10 |
Gibson Tracey A |
Peroxisome proliferator activated receptor modulators
|
CA2477741A1
(en)
|
2002-02-28 |
2003-09-04 |
Biota, Inc. |
Nucleotide mimics and their prodrugs
|
AU2003286757B2
(en)
|
2002-11-01 |
2009-06-04 |
Merck Sharp & Dohme Corp. |
Carbonylamino-benzimidazole derivatives as androgen receptor modulators
|
US7189716B2
(en)
|
2003-01-03 |
2007-03-13 |
Bristol-Myers Squibb Company |
Tyrosine kinase inhibitors
|
US20040229955A1
(en)
|
2003-01-08 |
2004-11-18 |
Andersen Niels H. |
Antibacterial agents
|
US7122557B2
(en)
|
2003-03-18 |
2006-10-17 |
Bristol-Myers Squibb Company |
Sulfonyl-amidino-containing and tetrahydropyrimidino-containing compounds as factor Xa inhibitors
|
JP4742029B2
(ja)
|
2003-04-01 |
2011-08-10 |
アクティブクス バイオサイエンシズ、インコーポレイテッド |
アシル−リン酸及びホスホン酸プローブ並びにその合成方法並びにプロテオーム分析における使用
|
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
|
PL1635824T3
(pl)
|
2003-06-03 |
2010-01-29 |
Novartis Ag |
5-Członowe heterocykliczne inhibitory P-38
|
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
|
US8202861B2
(en)
|
2003-08-08 |
2012-06-19 |
Vertex Pharmaceuticals Incorporated |
Compositions useful as inhibitors of voltage-gated sodium channels
|
RU2006108577A
(ru)
|
2003-08-21 |
2007-09-27 |
Гриффит Юниверсити (Au) |
Новые сульфенамиды
|
BRPI0413684A
(pt)
|
2003-08-21 |
2006-10-24 |
Univ Griffith |
compostos, composição farmacêutica e respectivos métodos de preparação, de tratamento de infecção microbiana e de extermìnio de microrganismo e usos
|
EP1660511B1
(en)
|
2003-08-27 |
2010-11-03 |
Biota Scientific Management Pty. Ltd. |
Novel tricyclic nucleosides or nucleotides as therapeutic agents
|
US7932272B2
(en)
|
2003-09-30 |
2011-04-26 |
Eisai R&D Management Co., Ltd. |
Antifungal agent containing heterocyclic compound
|
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
|
EP1689407A1
(en)
|
2003-11-25 |
2006-08-16 |
Pfizer Products Inc. |
Method of treatment of atherosclerosis
|
EA200700099A1
(ru)
|
2004-07-23 |
2007-08-31 |
Пфайзер Инк. |
Производные пиридина
|
CA2577169A1
(en)
|
2004-08-16 |
2006-02-23 |
The University Of Queensland |
Metabolism-modulating agents and uses therefor
|
EP1784393B1
(en)
|
2004-09-02 |
2009-07-01 |
Vertex Pharmaceuticals Incorporated |
Quinazolines useful as modulators of ion 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
|
JP2008543742A
(ja)
|
2005-05-09 |
2008-12-04 |
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 |
ビアリール尿素およびそのアナログの調製プロセス
|
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
|
US7683066B2
(en)
|
2005-05-20 |
2010-03-23 |
Vertex Pharmaceuticals Incorporated |
Isoquinolines useful as modulators of ion channels
|
EP1904491A2
(en)
|
2005-05-31 |
2008-04-02 |
Vertex Pharmaceuticals Incorporated |
Heterocycles useful as modulators of ion channels
|
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
|
DK1954697T3
(da)
|
2005-10-21 |
2010-06-14 |
Glaxo Group Ltd |
Peri-kondenserede tricykliske forbindelser, der er anvendelige som antibakterielle midler
|
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
|
US20070203224A1
(en)
|
2006-01-09 |
2007-08-30 |
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
|
EP2004596A2
(en)
|
2006-04-11 |
2008-12-24 |
Vertex Pharmaceuticals Incorporated |
Compositions useful as inhibitors of voltage-gated sodium channels
|
EP2035005A4
(en)
|
2006-06-09 |
2011-07-06 |
Kemia Inc |
THERAPY BASED ON CYTOKINE INHIBITORS
|
EP2035395A2
(en)
|
2006-06-27 |
2009-03-18 |
Glenmark Pharmaceuticals S.A. |
Novel processes for the preparation of dpp iv inhibitors
|
WO2008005542A2
(en)
|
2006-07-07 |
2008-01-10 |
Gilead Sciences, Inc., |
Antiviral phosphinate compounds
|
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
|
NZ574513A
(en)
|
2006-08-08 |
2012-02-24 |
Millennium Pharm Inc |
Heteroaryl compounds useful as inhibitors of e1 activating enzymes
|
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
|
CA2662580C
(en)
|
2006-09-11 |
2013-05-21 |
Curis, Inc. |
Tyrosine kinase inhibitors containing a zinc binding moiety
|
EP2061758A4
(en)
|
2006-09-11 |
2011-11-30 |
Curis Inc |
A ZINC BINDING GROUP CONTAINING SUBSTITUTED 2-INDOLINONE AS PTK INHIBITORS
|
CN101631546A
(zh)
|
2006-10-12 |
2010-01-20 |
泽农医药公司 |
螺-吲哚酮化合物作为治疗剂的用途
|
EP2097386A2
(en)
|
2006-11-27 |
2009-09-09 |
Novartis AG |
Substituted dihydroimidazoles and their use in the treatment of tumors
|
EP2101760B1
(en)
|
2006-12-08 |
2013-02-27 |
Millennium Pharmaceuticals, Inc. |
Unit dose formulations and methods of treating thrombosis with an oral factor xa inhibitor
|
CA2672737A1
(en)
|
2006-12-20 |
2008-11-06 |
Abbott Laboratories |
Anti-viral compounds
|
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
|
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
|
WO2008094507A2
(en)
|
2007-01-26 |
2008-08-07 |
Cellicon Biotechnologies, Inc. |
Novel fusion compounds
|
US20080234297A1
(en)
|
2007-03-20 |
2008-09-25 |
Changgeng Qian |
HSP90 Inhibitors Containing a Zinc Binding Moiety
|
CN101674833A
(zh)
|
2007-03-20 |
2010-03-17 |
柯瑞斯公司 |
含有锌结合半族的Raf激酶抑制剂
|
KR20100007956A
(ko)
|
2007-05-03 |
2010-01-22 |
화이자 리미티드 |
나트륨 채널 조절제로서의 2-피리딘 카복스아마이드 유도체
|
US8088385B2
(en)
|
2007-06-18 |
2012-01-03 |
University Of Louisville Research Foundation Inc. |
PFKB3 inhibitor for the treatment of a proliferative cancer
|
AU2008267444A1
(en)
|
2007-06-26 |
2008-12-31 |
Sanofi-Aventis |
A regioselective copper catalyzed synthesis of benzimidazoles and azabenzimidazoles
|
SI2178865T1
(sl)
|
2007-07-19 |
2015-11-30 |
Lundbeck, H., A/S |
5-členski heterociklični amidi in sorodne spojine
|
JP4846769B2
(ja)
|
2007-07-30 |
2011-12-28 |
田辺三菱製薬株式会社 |
医薬組成物
|
JP4834699B2
(ja)
|
2007-07-30 |
2011-12-14 |
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
|
CN101801933A
(zh)
|
2007-09-26 |
2010-08-11 |
安斯泰来制药株式会社 |
喹诺酮衍生物
|
BRPI0818501A2
(pt)
|
2007-10-08 |
2015-04-22 |
Advinus Therapeutics Private Ltd |
Derivados de acetamida como ativadores de glicoquinase, seu processo e aplicações medicinais
|
US8779197B2
(en)
|
2007-10-11 |
2014-07-15 |
Vertex Pharmaceuticals Incorporated |
Aryl amides useful as inhibitors of voltage-gated sodium channels
|
AU2008310660A1
(en)
|
2007-10-11 |
2009-04-16 |
Vertex Pharmaceuticals Incorporated |
Heteroaryl amides useful as inhibitors of voltage-gated sodium channels
|
WO2009049181A1
(en)
|
2007-10-11 |
2009-04-16 |
Vertex Pharmaceuticals Incorporated |
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
|
EP2231671B1
(en)
|
2007-12-13 |
2013-04-24 |
Vertex Pharmaceuticals Incorporated |
Modulators of cystic fibrosis transmembrane conductance regulator
|
CA2709784A1
(en)
|
2007-12-21 |
2009-07-09 |
University Of Rochester |
Method for altering the lifespan of eukaryotic organisms
|
EP2244571A4
(en)
|
2008-01-17 |
2014-02-19 |
Purdue Research Foundation |
SMALL INHIBITORY MOLECULES OF HIV PROTEASES
|
US20120108630A1
(en)
|
2008-02-12 |
2012-05-03 |
The Board Of Trustees Of The Leland Stanford Junior University |
Hedgehog Pathway Antagonists and Methods of Use
|
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
|
AU2009233711B2
(en)
|
2008-04-09 |
2015-02-12 |
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
|
US9029408B2
(en)
|
2008-06-16 |
2015-05-12 |
Gtx, Inc. |
Compounds for treatment of cancer
|
CN102143957B
(zh)
|
2008-07-03 |
2014-08-20 |
西特里斯药业公司 |
作为沉默调节蛋白调节剂的苯并咪唑类和相关的类似物
|
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
|
AU2009288632B2
(en)
|
2008-09-06 |
2015-08-13 |
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
|
CA2734363C
(en)
|
2008-09-18 |
2016-10-25 |
F. Hoffmann-La Roche Ag |
Substituted pyrrolidine-2-carboxamides
|
US8354444B2
(en)
|
2008-09-18 |
2013-01-15 |
Hoffmann-La Roche Inc. |
Substituted pyrrolidine-2-carboxamides
|
CN102227417B
(zh)
|
2008-09-29 |
2015-09-16 |
西特里斯药业公司 |
作为沉默调节蛋白调节剂的色烯酮类似物
|
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
|
EP2384328B1
(en)
|
2008-11-27 |
2013-02-13 |
Boehringer Ingelheim International GmbH |
6,7,8,9-tetrahydro-5h-1,4,7,10a-tetraaza-cyclohept[f]indene derivatives, pharmaceutical compositions containing these compounds, their use and process for preparing them
|
GB0821913D0
(en)
|
2008-12-02 |
2009-01-07 |
Price & Co |
Antibacterial compounds
|
EP2376473A4
(en)
|
2008-12-10 |
2012-05-02 |
Merck Canada Inc |
3,4-SUBSTITUTED PIPERIDINE DERIVATIVES AS RENIN INHIBITORS
|
WO2010075282A1
(en)
|
2008-12-22 |
2010-07-01 |
University Of Washington |
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
|
CN104030987B
(zh)
|
2009-04-02 |
2017-04-12 |
默克雪兰诺有限公司 |
二氢乳清酸脱氢酶抑制剂
|
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
|
CN102459273A
(zh)
|
2009-05-07 |
2012-05-16 |
里兰斯坦福初级大学理事会 |
用于研究、成像以及治疗疼痛的方法和组合物
|
WO2010138576A1
(en)
|
2009-05-27 |
2010-12-02 |
Abbott Laboratories |
Pyrimidine inhibitors of kinase activity
|
MX2011012629A
(es)
|
2009-05-27 |
2012-03-06 |
Abbott Lab |
Inhibidores de actividad de cinasa tipo pirimidina.
|
EP3632899A1
(en)
|
2009-05-29 |
2020-04-08 |
RaQualia Pharma Inc. |
Aryl substituted carboxamide derivatives as calcium or sodium channel blockers
|
AR077033A1
(es)
|
2009-06-11 |
2011-07-27 |
Hoffmann La Roche |
Compuestos inhibidores de las quinasas de janus y su uso en el tratamiento de enfermedades inmunologicas
|
AR077252A1
(es)
|
2009-06-29 |
2011-08-10 |
Xenon Pharmaceuticals Inc |
Enantiomeros de compuestos de espirooxindol y sus usos como agentes terapeuticos
|
WO2011005860A2
(en)
|
2009-07-07 |
2011-01-13 |
Alnylam Pharmaceuticals, Inc. |
5' phosphate mimics
|
CA2771472A1
(en)
|
2009-09-04 |
2011-03-10 |
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
|
WO2011037731A1
(en)
|
2009-09-25 |
2011-03-31 |
Anacor Pharmaceuticals, Inc. |
Boron containing small molecules
|
EA201270568A1
(ru)
|
2009-10-16 |
2012-11-30 |
Риб-Экс Фармасьютикалз, Инк. |
Антимикробные композиции и способы их получения и применения
|
US11084811B2
(en)
|
2010-03-01 |
2021-08-10 |
Oncternal Therapeutics, Inc. |
Compounds for treatment of cancer
|
AU2010347233B2
(en)
|
2010-03-01 |
2015-06-18 |
Oncternal Therapeutics, Inc. |
Compounds for treatment of cancer
|
HUE028983T2
(en)
|
2010-05-06 |
2017-01-30 |
Vertex Pharma |
Heterocyclic chromene-spirocyclic piperidine amides as ion channel modulators
|
US20130116284A1
(en)
|
2010-05-10 |
2013-05-09 |
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
|
AU2011311867A1
(en)
|
2010-10-08 |
2013-04-18 |
Abbvie Inc. |
Furo(3,2-d)pyrimidine compounds
|
GB201017315D0
(en)
|
2010-10-13 |
2010-11-24 |
Antoxis Ltd |
Compound
|
JP2013540145A
(ja)
|
2010-10-21 |
2013-10-31 |
ウニベルシテート デス ザールランデス |
コルチゾール依存性疾患の治療用の選択的cyp11b1阻害剤
|
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
|
CA2815821C
(en)
|
2010-11-29 |
2015-07-07 |
Pfizer Inc. |
Monobactams useful for treating bacterial infections
|
US20120150063A1
(en)
|
2010-12-13 |
2012-06-14 |
Neural Pathways, Llc |
Handheld emg stimulator device with adjustable shaft length
|
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
|
WO2012106534A2
(en)
|
2011-02-02 |
2012-08-09 |
The Regents Of The University Of California |
Hiv integrase inhibitors
|
US8916565B2
(en)
|
2011-02-02 |
2014-12-23 |
Vertex Pharmaceuticals Incorporated |
Pyrrolopyrazine-spirocyclic piperidine amides as modulators of ion channels
|
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
|
WO2012112743A1
(en)
|
2011-02-18 |
2012-08-23 |
Vertex Pharmaceuticals Incorporated |
Chroman - spirocyclic piperidine amides as modulators of ion channels
|
WO2012116440A1
(en)
|
2011-03-03 |
2012-09-07 |
Zalicus Pharmaceuticals Ltd. |
Benzimidazole inhibitors of the sodium channel
|
JP6088443B2
(ja)
|
2011-03-14 |
2017-03-01 |
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 |
イオンチャネルのモジュレーターとしてのモルホリン−スピロ環式ピペリジンアミド
|
AR085412A1
(es)
|
2011-03-15 |
2013-10-02 |
Abbott Lab |
Moduladores de los receptores de hormonas nucleares
|
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
|
EP2707372B1
(en)
|
2011-05-11 |
2016-12-21 |
The Regents Of The University Of Michigan |
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
|
WO2012178123A1
(en)
|
2011-06-22 |
2012-12-27 |
Vertex Pharmaceuticals Incorporated |
Compounds useful as inhibitors of atr kinase
|
GB201111705D0
(en)
|
2011-07-07 |
2011-08-24 |
Takeda Pharmaceutical |
Compounds and their use
|
WO2013005057A1
(en)
|
2011-07-07 |
2013-01-10 |
Centro Nacional De Investigaciones Oncológicas (Cnio) |
New compounds
|
WO2013022740A2
(en)
|
2011-08-05 |
2013-02-14 |
Corning Incorporated |
Gpr35 ligands and the uses thereof
|
EP2755965B1
(en)
|
2011-09-12 |
2017-07-26 |
Merck Patent GmbH |
Novel imidazole amines as modulators of kinase activity
|
WO2013049725A2
(en)
|
2011-09-30 |
2013-04-04 |
Tufts University |
Methods of using adenosine a1 receptor activation for treating depression
|
KR101586966B1
(ko)
|
2011-10-26 |
2016-01-19 |
화이자 리미티드 |
나트륨 채널 조절제로서 유용한 (4-페닐이미다졸-2-일) 에틸아민 유도체
|
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
|
MX2014008591A
(es)
|
2012-01-16 |
2014-08-22 |
Vertex Pharma |
Piperidinamidas piranoespirociclicas como moduladores de canales de iones.
|
FR2985916B1
(fr)
|
2012-01-25 |
2015-12-04 |
Univ Bordeaux Segalen |
Decontamination par hydrogels d'echantillons aqueux contenant des nanoparticules
|
WO2013114250A1
(en)
|
2012-02-03 |
2013-08-08 |
Pfizer Inc. |
Benziimidazole and imidazopyridine derivatives as sodium channel modulators
|
BR112014019773A8
(pt)
|
2012-02-08 |
2017-07-11 |
Graffinity Pharmaceuticals Gmbh |
Ligantes para anticorpo e proteína de fusão fc para cromatografia de afinidade
|
CN107057719A
(zh)
|
2012-02-22 |
2017-08-18 |
默克专利股份有限公司 |
液晶介质
|
WO2013131018A1
(en)
|
2012-03-02 |
2013-09-06 |
Zalicus Pharmaceuticals Ltd. |
Biaryl inhibitors of the sodium channel
|
EP2822953B9
(en)
|
2012-03-06 |
2017-06-21 |
Pfizer Inc |
Macrocyclic derivatives for the treatment of proliferative diseases
|
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
|
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
|
WO2013151975A1
(en)
|
2012-04-02 |
2013-10-10 |
Northeastern University |
Compositions and methods for the inhibition of methyltransferases
|
MX2014014229A
(es)
|
2012-05-30 |
2015-02-17 |
Hoffmann La Roche |
Pirrolidina-2-carboxamidas sustituidas.
|
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
|
WO2014005125A2
(en)
|
2012-06-29 |
2014-01-03 |
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
|
TW201416354A
(zh)
|
2012-07-17 |
2014-05-01 |
Boehringer Ingelheim Int |
白三烯生成抑制劑
|
TW201416362A
(zh)
|
2012-07-19 |
2014-05-01 |
Dainippon Sumitomo Pharma Co |
1-(環烷基羰基)脯胺酸衍生物
|
WO2014015523A1
(en)
|
2012-07-27 |
2014-01-30 |
Hutchison Medipharma Limited |
Novel heteroaryl and heterocycle compounds, compositions and methods
|
US9550798B2
(en)
|
2012-07-27 |
2017-01-24 |
Biogen Ma Inc. |
Compounds that are S1P modulating agents and/or ATX modulating agents
|
WO2014020152A1
(en)
|
2012-08-02 |
2014-02-06 |
Graffinity Pharmaceuticals Gmbh |
Ligands for apheresis and immunoabsorption
|
ES2666353T3
(es)
|
2012-09-06 |
2018-05-04 |
Bristol-Myers Squibb Company |
Inhibidores de JAK3 de imidazopiridazina y su uso para el tratamiento de enfermedades inflamatorias y autoinmunitarias
|
CA2885217C
(en)
|
2012-09-20 |
2019-10-08 |
Temple University - Of The Commonwealth System Of Higher Education |
Substituted alkyl diaryl derivatives, methods of preparation and uses
|
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
|
CA2890897A1
(en)
|
2012-11-14 |
2014-05-22 |
The Board Of Regents Of The University Of Texas System |
Inhibition of hif-2.alpha. heterodimerization with hif 1.beta. (arnt)
|
AU2013347539B2
(en)
|
2012-11-16 |
2017-06-15 |
Merck Sharp & Dohme Corp. |
Purine inhibitors of human phosphatidylinositol 3-kinase delta
|
WO2014088920A1
(en)
|
2012-12-06 |
2014-06-12 |
Merck Sharp & Dohme Corp. |
Disulfide masked prodrug compositions and methods
|
CN104903294A
(zh)
|
2013-01-08 |
2015-09-09 |
萨维拉制药有限公司 |
吡啶酮衍生物及其在治疗、改善或预防病毒疾病中的用途
|
US20140200215A1
(en)
|
2013-01-15 |
2014-07-17 |
Intermune, Inc. |
Lysophosphatidic acid receptor antagonists
|
EP2951172B8
(en)
|
2013-01-29 |
2017-08-02 |
Redx Pharma Plc |
Pyridine derivatives as soft rock inhibitors
|
SG11201505954RA
(en)
|
2013-01-31 |
2015-08-28 |
Vertex Pharma |
Amides as modulators of sodium channels
|
DK3239134T3
(da)
|
2013-01-31 |
2021-02-22 |
Vertex Pharma |
Pyridonamider som modulatorer af natriumkanaler
|
TWI606048B
(zh)
|
2013-01-31 |
2017-11-21 |
帝人製藥股份有限公司 |
唑苯衍生物
|
JP6362623B2
(ja)
|
2013-01-31 |
2018-07-25 |
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 |
ナトリウムチャネルの調節剤としてのキノリンおよびキノキサリンアミド
|
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
|
WO2014179785A1
(en)
|
2013-05-03 |
2014-11-06 |
Inscent, Inc. |
Improved 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
|
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
|
WO2015003723A1
(en)
|
2013-07-12 |
2015-01-15 |
Københavns Universitet |
Substituted 4-proline derivatives as iglur antagonists
|
JP6730183B2
(ja)
|
2013-07-12 |
2020-07-29 |
ヘルムホルツ−ツェントルム フュア インフェクツィオンスフォルシュンク ゲーエムベーハー |
シストバクトアミド(Cystobactamides)
|
UA119147C2
(uk)
|
2013-07-19 |
2019-05-10 |
Вертекс Фармасьютікалз Інкорпорейтед |
Сульфонаміди як модулятори натрієвих каналів
|
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
|
WO2015035051A1
(en)
|
2013-09-04 |
2015-03-12 |
Board Of Regents Of The University Of Texas System |
Methods and compositions for selective and targeted cancer therapy
|
EP4094767A1
(en)
|
2013-09-11 |
2022-11-30 |
Emory University |
Nucleotide and nucleoside therapeutic compositions and uses related thereto
|
KR101628288B1
(ko)
|
2013-09-30 |
2016-06-08 |
주식회사 엘지화학 |
음성 광학 분산도를 갖는 광학 소자 제조용 조성물 및 이로부터 제조된 광학 이방체
|
AU2014330781B2
(en)
|
2013-10-01 |
2017-05-04 |
Glaxosmithkline Intellectual Property Development Limited |
Compounds for affinity chromatography and for extending the half-life of a therapeutic agent
|
US20160264614A1
(en)
|
2013-10-02 |
2016-09-15 |
Moderna Therapeutics, Inc. |
Polynucleotide molecules and uses thereof
|
US9700881B2
(en)
|
2013-10-09 |
2017-07-11 |
Emory University |
Heterocyclic coupling catalysts and methods related thereto
|
EP3077374B1
(en)
|
2013-12-03 |
2020-02-05 |
FMC Corporation |
Pyrrolidinones as herbicides
|
WO2015085238A1
(en)
|
2013-12-05 |
2015-06-11 |
The Regents Of The University Of California, A California Corporation |
Inhibitors of lpxc
|
TWI668226B
(zh)
|
2013-12-13 |
2019-08-11 |
美商維泰克斯製藥公司 |
作為納通道調節劑之吡啶酮醯胺之前藥
|
US20150167017A1
(en)
|
2013-12-13 |
2015-06-18 |
Moderna Therapeutics, Inc. |
Alternative nucleic acid molecules and uses thereof
|
EP2883934B1
(en)
|
2013-12-16 |
2019-11-13 |
Merck Patent GmbH |
Liquid-crystalline medium
|
US9611252B2
(en)
|
2013-12-30 |
2017-04-04 |
Lifesci Pharmaceuticals, Inc. |
Therapeutic inhibitory compounds
|
MX2016008688A
(es)
|
2013-12-30 |
2017-01-12 |
Lifesci Pharmaceuticals Inc |
Compuestos terapéuticos inhibidores.
|
CA2944549A1
(en)
|
2014-04-09 |
2015-10-15 |
Siteone Therapeutics, Inc. |
10',11'-modified saxitoxin 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
|
EP3157573A4
(en)
|
2014-06-19 |
2018-02-21 |
Moderna Therapeutics, Inc. |
Alternative nucleic acid molecules and uses thereof
|
WO2015196118A1
(en)
|
2014-06-19 |
2015-12-23 |
Moderna Therapeutics, Inc. |
Alternative nucleic acid molecules and uses thereof
|
EP3157572A4
(en)
|
2014-06-19 |
2018-02-14 |
Moderna Therapeutics, Inc. |
Alternative nucleic acid molecules and uses thereof
|
JP6700203B2
(ja)
|
2014-07-01 |
2020-05-27 |
レンペックス・ファーマシューティカルズ・インコーポレイテッド |
ボロン酸誘導体およびその治療的使用
|
WO2016007837A1
(en)
|
2014-07-11 |
2016-01-14 |
Spero Therapeutics, Inc. |
Carbonyl linked bicyclic heteroaryl antibiotic tolerance inhibitors
|
KR102286305B1
(ko)
|
2014-07-16 |
2021-08-09 |
라이프에스씨아이 파마슈티컬스, 인크. |
치료적 억제 화합물
|
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
|
US10913736B2
(en)
|
2014-08-22 |
2021-02-09 |
University Of Washington |
Specific inhibitors of methionyl-tRNA synthetase
|
AU2015315174B2
(en)
|
2014-09-10 |
2019-12-12 |
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
|
JP2017538676A
(ja)
|
2014-11-05 |
2017-12-28 |
ザ ユニバーシティ オブ カンザス |
ミトコンドリア透過性遷移孔(mtPTP)の小分子阻害剤
|
JP6813485B2
(ja)
|
2014-12-10 |
2021-01-13 |
マース インコーポレーテッドMars Incorporated |
香味組成物およびそれを含有するペットフード製品
|
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
|
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
|
BR112017024331A2
(pt)
|
2015-05-15 |
2018-07-24 |
Gilead Sciences, Inc. |
composto, composição farmacêutica, método de tratamento de um humano, métodos para inibir a atividade de uma proteína ido1, o crescimento ou a proliferação de células cancerosas, e a imunossupressão em um paciente, e de tratamento de uma doença, e, uso de um composto
|
AU2016271374B2
(en)
|
2015-06-02 |
2020-11-26 |
Fmc Corporation |
Substituted cyclic amides and their use as herbicides
|
WO2016198908A1
(en)
|
2015-06-09 |
2016-12-15 |
Abbvie Inc. |
Ror nuclear receptor modulators
|
CN107848975A
(zh)
|
2015-07-06 |
2018-03-27 |
拜耳作物科学股份公司 |
作为杀虫剂的含氮杂环
|
WO2017011371A1
(en)
|
2015-07-10 |
2017-01-19 |
Arvinas, Inc |
Mdm2-based modulators of proteolysis and associated methods of use
|
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
|
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
|
WO2017051319A1
(en)
|
2015-09-21 |
2017-03-30 |
Glenmark Pharmaceuticals S.A. |
Aryl and heteroaryl ether compounds as ror gamma modulators
|
ES2895155T3
(es)
|
2015-09-30 |
2022-02-17 |
Siteone Therapeutics Inc |
Saxitoxinas modificadas en 11,13 para el tratamiento del dolor
|
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
|
WO2017066791A1
(en)
|
2015-10-16 |
2017-04-20 |
Modernatx, Inc. |
Sugar substituted mrna cap analogs
|
WO2017066782A1
(en)
|
2015-10-16 |
2017-04-20 |
Modernatx, Inc. |
Hydrophobic mrna cap analogs
|
EP3362461B1
(en)
|
2015-10-16 |
2022-03-16 |
Modernatx, Inc. |
Mrna cap analogs with modified phosphate linkage
|
EP3381913B1
(en)
|
2015-11-27 |
2021-03-31 |
Mitsubishi Tanabe Pharma Corporation |
2-(((pyrrolidin-3-yl)carbonyl)amino)-1h-imidazole derivatives as melanocortin receptor 1 (mcr1) agonists for treating rheumatoid arthritis
|
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
|
PT3429591T
(pt)
|
2016-03-16 |
2023-06-21 |
Univ Michigan Regents |
Derivados de tieno[2,3-d]pirimidina substituídos como inibidores de menina-llm e métodos de utilização
|
GB201604638D0
(en)
|
2016-03-18 |
2016-05-04 |
Mission Therapeutics Ltd |
Novel compounds
|
WO2017173274A1
(en)
|
2016-03-31 |
2017-10-05 |
Vertex Pharmaceuticals Incorporated |
Modulators of cystic fibrosis transmembrane conductance regulator
|
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
|
CN109790468B
(zh)
|
2016-09-28 |
2023-06-13 |
默克专利股份有限公司 |
可聚合的液晶材料及经聚合的液晶膜
|
AU2017336523B2
(en)
|
2016-09-28 |
2022-07-21 |
Blade Therapeutics, Inc. |
Calpain modulators and therapeutic uses thereof
|
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
|
EP3656382A1
(en)
|
2017-01-30 |
2020-05-27 |
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
|
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
|
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
|
US11236097B2
(en)
|
2017-03-29 |
2022-02-01 |
Siteone Therapeutics, Inc. |
11,13-modified saxitoxins for the treatment of pain
|
WO2018183782A1
(en)
|
2017-03-29 |
2018-10-04 |
Siteone Therapeutics, Inc. |
11,13-modified saxitoxins for the treatment of pain
|
JP2020512861A
(ja)
|
2017-03-30 |
2020-04-30 |
ショー インダストリーズ グループ インコーポレイテッド |
カーペットタイル及びシステムとその製造方法
|
AU2018243749A1
(en)
|
2017-03-31 |
2019-11-21 |
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
|
TW201900638A
(zh)
|
2017-04-20 |
2019-01-01 |
加州大學董事會 |
K-ras調節劑
|
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
|
SG11202000230VA
(en)
|
2017-07-11 |
2020-02-27 |
Vertex Pharma |
Carboxamides as modulators of sodium channels
|
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
|
AU2018319016B2
(en)
|
2017-08-17 |
2023-08-31 |
Ikena Oncology, Inc. |
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
|
MA50417A
(fr)
|
2017-10-18 |
2020-08-26 |
Epizyme Inc |
Procédés d'utilisation d'inhibiteurs de l'ehmt2 dans le traitement ou la prévention de troubles du sang
|
EA202090955A1
(ru)
|
2017-10-18 |
2020-11-27 |
Эпизайм, Инк. |
Способы применения ингибиторов ehmt2 в лечении или предупреждении нарушений со стороны крови
|
WO2019084271A1
(en)
|
2017-10-25 |
2019-05-02 |
Children's Medical Center Corporation |
PAPD5 INHIBITORS AND METHODS OF USE
|
EP3479843A1
(en)
|
2017-11-01 |
2019-05-08 |
GenKyoTex Suisse SA |
Use of nox inhibitors for treatment of cancer
|
WO2019094732A1
(en)
|
2017-11-10 |
2019-05-16 |
Academia Sinica |
Inhibitors of cyclic-amp response element-binding protein
|
MX2020004994A
(es)
|
2017-11-15 |
2020-10-12 |
Metabomed Ltd |
Inhibidores de acss2 y metodos de uso de los mismos.
|
KR20190076339A
(ko)
|
2017-12-22 |
2019-07-02 |
한미약품 주식회사 |
신규한 2,6-나프티리딘 2-옥시드 유도체 화합물 및 이의 용도
|
EP3502684A1
(en)
|
2017-12-22 |
2019-06-26 |
Universite De Bordeaux |
Method for metal ion detection in aqueous solutions using nucleolipid compounds
|
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
|
KR20200141026A
(ko)
|
2018-02-08 |
2020-12-17 |
엔요 파마 |
비-융합된 티오펜 유도체 및 이의 용도
|
JP2021512935A
(ja)
|
2018-02-12 |
2021-05-20 |
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 |
疼痛を処置する方法
|
CN112040861B
(zh)
|
2018-04-05 |
2024-09-17 |
圣犹达医疗用品心脏病学部门有限公司 |
高密度电极标测导管
|
CN112041414B
(zh)
|
2018-04-27 |
2024-07-19 |
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
|
EP3784753B1
(en)
|
2018-04-27 |
2022-06-08 |
Merck Patent GmbH |
Polymerisable liquid crystal material and polymerised liquid crystal film
|
WO2019222414A1
(en)
|
2018-05-16 |
2019-11-21 |
Belite Bio, Llc |
Fatty acid analogues and methods of use
|
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
|
KR20210019119A
(ko)
|
2018-07-09 |
2021-02-19 |
리버 인스티튜트, 아이엔씨 |
Nav1.8을 억제하기 위한 피리다진(PYRIDAZINE) 화합물
|
WO2020014246A1
(en)
|
2018-07-09 |
2020-01-16 |
Lieber Institute, Inc. |
Pyridine carboxamide compounds for inhibiting nav1.8
|
EP3831823A4
(en)
|
2018-08-01 |
2022-04-27 |
Shanghai Ennovabio Pharmaceuticals Co., Ltd. |
PREPARATION AND USE OF AN AROMATIC COMPOUND WITH IMMUNEGULATORY FUNCTION
|
WO2020033413A2
(en)
|
2018-08-07 |
2020-02-13 |
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
|
CA3111392A1
(en)
|
2018-09-04 |
2020-03-12 |
Magenta Therapeutics, Inc. |
Aryl hydrocarbon receptor antagonists and methods of use
|
CA3114208A1
(en)
|
2018-09-28 |
2020-04-02 |
Acucela Inc. |
Inhibitors of vap-1
|
KR102092838B1
(ko)
|
2018-10-02 |
2020-03-24 |
성균관대학교산학협력단 |
신규 퓨란계 폴리카보네이트 및 이의 제조 방법
|
US20220009938A1
(en)
|
2018-10-03 |
2022-01-13 |
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
|
AU2019362788A1
(en)
|
2018-10-15 |
2021-04-15 |
Dana-Farber Cancer Institute, Inc. |
Transcriptional enhanced associate domain (TEAD) transcription factor inhibitors and uses thereof
|
US20210387966A1
(en)
|
2018-11-02 |
2021-12-16 |
Merck Sharp & Dohme Corp. |
2-amino-n-heteroaryl-nicotinamides as nav1.8 inhibitors
|
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
|
WO2020118036A1
(en)
|
2018-12-06 |
2020-06-11 |
The Children's Medical Center Corporation |
Antibacterial compounds and uses thereof
|
US12098117B2
(en)
|
2018-12-11 |
2024-09-24 |
Duke University |
Compositions and methods for the treatment of cancer
|
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
|
WO2020159576A1
(en)
|
2019-01-28 |
2020-08-06 |
Mitochondria Emotion, Inc. |
Mitofusin activators and methods of use thereof
|
WO2020160225A1
(en)
|
2019-01-30 |
2020-08-06 |
Ohio State Innovation Foundation |
ESTROGEN RECEPTOR BETA (ERβ) AGONISTS FOR THE TREATMENT OF FIBROTIC CONDITIONS
|
US20220160705A1
(en)
|
2019-03-20 |
2022-05-26 |
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
|
EP3963026A1
(en)
|
2019-04-30 |
2022-03-09 |
Merck Patent GmbH |
Reactive mesogens
|
WO2020228922A1
(de)
|
2019-05-10 |
2020-11-19 |
Wacker Chemie Ag |
Kationische germanium(ii)-verbindungen, verfahren zu deren herstellung und deren verwendung als katalysator in der hydrosilylierung
|
KR20220024027A
(ko)
|
2019-05-14 |
2022-03-03 |
메타보메드 리미티드 |
Acss2 저해제 및 이의 사용 방법
|
US20220324880A1
(en)
|
2019-06-10 |
2022-10-13 |
Kymara Therapeutics, Inc. |
Smarca inhibitors and uses thereof
|
EP3986888A1
(en)
|
2019-06-21 |
2022-04-27 |
Bayer Aktiengesellschaft |
Thienylhydroxyisoxazolines and derivatives thereof
|
WO2021001739A1
(en)
|
2019-07-02 |
2021-01-07 |
Effector Therapeutics, Inc. |
Translational enhancers and related methods
|
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
|
US20240156778A1
(en)
|
2019-10-17 |
2024-05-16 |
Enyo Pharma |
Thiophene derivatives for use in treating portal inflammation and fibrosis
|
MX2022006865A
(es)
|
2019-12-06 |
2022-07-11 |
Vertex Pharma |
Tetrahidrofuranos sustituidos como moduladores de canales de sodio.
|
KR102512868B1
(ko)
|
2019-12-20 |
2023-03-22 |
주식회사 삼양홀딩스 |
올라파립의 용해도 및 생체이용율이 개선된 조성물
|
EP4157888A4
(en)
|
2020-05-28 |
2024-07-10 |
Cullgen Shanghai Inc |
MODIFIED PROTEINS AND PROTEIN DEGRADERS
|
GB202011996D0
(en)
|
2020-07-31 |
2020-09-16 |
Adorx Therapeutics Ltd |
Antagonist compounds
|
EP4217442A1
(en)
|
2020-09-24 |
2023-08-02 |
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
|
WO2022256622A1
(en)
|
2021-06-04 |
2022-12-08 |
Vertex Pharmaceuticals Incorporated |
N-(hydroxyalkyl (hetero)aryl) tetrahydrofuran carboxamides as modulators of sodium channels
|