|
US6374762B1
(en)
*
|
1997-10-27 |
2002-04-23 |
Correct Craft, Inc. |
Water sport towing apparatus
|
|
WO2000027845A1
(en)
|
1998-11-10 |
2000-05-18 |
Merck & Co., Inc. |
Spiro-indolines as y5 receptor antagonists
|
|
KR20020047198A
(ko)
*
|
1999-09-30 |
2002-06-21 |
해피 페너 ; 해리 에이치. 페너 2세 |
특정 알킬렌 디아민-치환된피라졸로[1,5-a]-1,5-피리미딘 및피라졸로[1,5-a]-1,3,5-트리아진
|
|
OA12050A
(en)
|
1999-09-30 |
2006-05-02 |
Neurogen Corp |
Certain alkylene diamine-substituted heterocycles.
|
|
AU2001239731A1
(en)
*
|
2000-01-28 |
2001-08-07 |
Neurogen Corporation |
Chimeric neuropeptide y receptors
|
|
EP1347982B1
(de)
*
|
2000-12-12 |
2005-11-16 |
Neurogen Corporation |
Spiro[isobenzofuran-1,4'-piperidin]-3-one und 3h-spiroisobenzofuran-1,4'-piperidine
|
|
US6900220B2
(en)
*
|
2001-01-02 |
2005-05-31 |
Syntex (U.S.A.) Llc |
Quinazolone derivatives as alpha 1A/B adrenergic receptor antagonists
|
|
WO2002094825A1
(en)
*
|
2001-05-22 |
2002-11-28 |
Banyu Pharmaceutical Co., Ltd. |
Novel spiropiperidine derivative
|
|
US7205417B2
(en)
*
|
2001-08-07 |
2007-04-17 |
Banyu Pharmaceutical Co., Ltd. |
Spiro compounds
|
|
CA2403307A1
(en)
|
2001-10-23 |
2003-04-23 |
Neurogen Corporation |
Substituted 2-cyclohexyl-4-phenyl-1h-imidazole derivatives
|
|
AUPR975601A0
(en)
*
|
2001-12-24 |
2002-01-31 |
Fujisawa Pharmaceutical Co., Ltd. |
Quinazolinone derivatives
|
|
US7704995B2
(en)
*
|
2002-05-03 |
2010-04-27 |
Exelixis, Inc. |
Protein kinase modulators and methods of use
|
|
CA2484209C
(en)
*
|
2002-05-03 |
2013-06-11 |
Exelixis, Inc. |
Protein kinase modulators and methods of use
|
|
US7405234B2
(en)
*
|
2002-05-17 |
2008-07-29 |
Bristol-Myers Squibb Company |
Bicyclic modulators of androgen receptor function
|
|
US7105526B2
(en)
*
|
2002-06-28 |
2006-09-12 |
Banyu Pharmaceuticals Co., Ltd. |
Benzimidazole derivatives
|
|
JP4496722B2
(ja)
*
|
2002-06-28 |
2010-07-07 |
萬有製薬株式会社 |
新規ベンズイミダゾール誘導体
|
|
SE0202462D0
(sv)
*
|
2002-08-14 |
2002-08-14 |
Astrazeneca Ab |
Novel use
|
|
EP1407774A1
(de)
*
|
2002-09-10 |
2004-04-14 |
LION Bioscience AG |
2-Amino-4-chinazolinone, die an den LXR Kernrezeptor binden
|
|
EP1398032A1
(de)
*
|
2002-09-10 |
2004-03-17 |
PheneX Pharmaceuticals AG |
4-Oxochinazoline, die an den LXR Kernrezeptor binden
|
|
EP1567487A4
(de)
*
|
2002-11-15 |
2005-11-16 |
Bristol Myers Squibb Co |
Offenkettige, mit prolylharnstoff verwandtemodulatoren der androgenrezeptorfunktion
|
|
ATE433971T1
(de)
|
2002-11-29 |
2009-07-15 |
Banyu Pharma Co Ltd |
Neue azolderivate
|
|
US7772188B2
(en)
|
2003-01-28 |
2010-08-10 |
Ironwood Pharmaceuticals, Inc. |
Methods and compositions for the treatment of gastrointestinal disorders
|
|
MXPA05009245A
(es)
|
2003-03-11 |
2005-10-19 |
Pfizer Prod Inc |
Nuevos compuestos de pirazina como inhibidores del factor de crecimiento transformante (tgf).
|
|
WO2005005395A2
(en)
|
2003-07-02 |
2005-01-20 |
F. Hoffmann-La Roche Ag |
Arylamine-substituted quinazolinone compounds
|
|
JP4765627B2
(ja)
|
2003-09-22 |
2011-09-07 |
Msd株式会社 |
新規ピペリジン誘導体
|
|
WO2005030210A1
(en)
*
|
2003-09-26 |
2005-04-07 |
Pfizer Products Inc. |
Treatment of neurological disorders related to rapid eye movement (rem) sleep disturbances with npy y5 receptor antagonists
|
|
MXPA06003380A
(es)
*
|
2003-09-26 |
2006-06-08 |
Pfizer Prod Inc |
Uso de antagonista del receptor npy y5 para el tratamiento de trastornos del ritmo circadiano.
|
|
US7256208B2
(en)
*
|
2003-11-13 |
2007-08-14 |
Bristol-Myers Squibb Company |
Monocyclic N-Aryl hydantoin modulators of androgen receptor function
|
|
WO2005056036A2
(en)
*
|
2003-12-09 |
2005-06-23 |
Novo Nordisk A/S |
Regulation of food preference using glp-1 agonists
|
|
US7820702B2
(en)
|
2004-02-04 |
2010-10-26 |
Bristol-Myers Squibb Company |
Sulfonylpyrrolidine modulators of androgen receptor function and method
|
|
US20050182105A1
(en)
*
|
2004-02-04 |
2005-08-18 |
Nirschl Alexandra A. |
Method of using 3-cyano-4-arylpyridine derivatives as modulators of androgen receptor function
|
|
US7696241B2
(en)
|
2004-03-04 |
2010-04-13 |
Bristol-Myers Squibb Company |
Bicyclic compounds as modulators of androgen receptor function and method
|
|
US7388027B2
(en)
*
|
2004-03-04 |
2008-06-17 |
Bristol-Myers Squibb Company |
Bicyclic compounds as modulators of androgen receptor function and method
|
|
US7625923B2
(en)
|
2004-03-04 |
2009-12-01 |
Bristol-Myers Squibb Company |
Bicyclic modulators of androgen receptor function
|
|
US20080125403A1
(en)
|
2004-04-02 |
2008-05-29 |
Merck & Co., Inc. |
Method of Treating Men with Metabolic and Anthropometric Disorders
|
|
EA010888B1
(ru)
|
2004-05-25 |
2008-12-30 |
Пфайзер Продактс, Инк. |
Тетраазабензо[е]азуленовые производные и их аналоги
|
|
KR20070046929A
(ko)
*
|
2004-08-19 |
2007-05-03 |
버텍스 파마슈티칼스 인코포레이티드 |
무스카린 수용체 조절제
|
|
US7786141B2
(en)
*
|
2004-08-19 |
2010-08-31 |
Vertex Pharmaceuticals Incorporated |
Dihydrospiroindene modulators of muscarinic receptors
|
|
ES2325773T5
(es)
|
2004-11-01 |
2014-02-24 |
Amylin Pharmaceuticals, Llc. |
Tratamiento de la obesidad y de los trastornos relacionados
|
|
RU2007124373A
(ru)
*
|
2004-11-29 |
2009-01-10 |
Вертекс Фармасьютикалз Инкорпорейтед (Us) |
Модуляторы мускариновых рецептеров
|
|
US7538113B2
(en)
|
2005-02-18 |
2009-05-26 |
Wyeth |
4-substituted imidazo[4,5-c]pyridine antagonists of gonadotropin releasing hormone receptor
|
|
US7582634B2
(en)
|
2005-02-18 |
2009-09-01 |
Wyeth |
7-substituted imidazo[4,5-c]pyridine antagonists of gonadotropin releasing hormone receptor
|
|
US7534796B2
(en)
|
2005-02-18 |
2009-05-19 |
Wyeth |
Imidazo[4,5-b]pyridine antagonists of gonadotropin releasing hormone receptor
|
|
DE102005012874A1
(de)
*
|
2005-03-19 |
2006-09-21 |
Sanofi-Aventis Deutschland Gmbh |
Amid substituierte 8-N-Benzimidazole, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel
|
|
US7737155B2
(en)
|
2005-05-17 |
2010-06-15 |
Schering Corporation |
Nitrogen-containing heterocyclic compounds and methods of use thereof
|
|
US7531542B2
(en)
|
2005-05-18 |
2009-05-12 |
Wyeth |
Benzooxazole and benzothiazole antagonists of gonadotropin releasing hormone receptor
|
|
US7582636B2
(en)
|
2005-05-26 |
2009-09-01 |
Wyeth |
Piperazinylimidazopyridine and piperazinyltriazolopyridine antagonists of Gonadotropin Releasing Hormone receptor
|
|
US8138206B2
(en)
|
2005-05-30 |
2012-03-20 |
Msd. K.K. |
Piperidine derivative
|
|
US7825244B2
(en)
|
2005-06-10 |
2010-11-02 |
Janssen Pharmaceutica Nv |
Intermediates useful in the synthesis of alkylquinoline and alkylquinazoline kinase modulators, and related methods of synthesis
|
|
US8071768B2
(en)
|
2005-06-10 |
2011-12-06 |
Janssen Pharmaceutica, N.V. |
Alkylquinoline and alkylquinazoline kinase modulators
|
|
CA2618112A1
(en)
|
2005-08-10 |
2007-02-15 |
Banyu Pharmaceutical Co., Ltd. |
Pyridone compound
|
|
AU2006279680B2
(en)
|
2005-08-11 |
2012-12-06 |
Amylin Pharmaceuticals, Llc |
Hybrid polypeptides with selectable properties
|
|
BRPI0614649A2
(pt)
|
2005-08-11 |
2011-04-12 |
Amylin Pharmaceuticals Inc |
polipeptìdeos hìbridos com propriedades selecionáveis
|
|
WO2007024004A1
(ja)
|
2005-08-24 |
2007-03-01 |
Banyu Pharmaceutical Co., Ltd. |
フェニルピリドン誘導体
|
|
US8211919B2
(en)
*
|
2005-09-02 |
2012-07-03 |
Astellas Pharma Inc. |
Amide derivatives as rock inhibitors
|
|
AU2006288153A1
(en)
|
2005-09-07 |
2007-03-15 |
Msd K.K. |
Bicyclic aromatic substituted pyridone derivative
|
|
KR20080048502A
(ko)
*
|
2005-09-29 |
2008-06-02 |
머크 앤드 캄파니 인코포레이티드 |
멜라노코르틴-4 수용체 조절제로서의 아실화스피로피페리딘 유도체
|
|
RU2008119687A
(ru)
|
2005-10-21 |
2009-11-27 |
Новартис АГ (CH) |
Комбинации органических соединений
|
|
CA2627139A1
(en)
|
2005-10-27 |
2007-05-03 |
Banyu Pharmaceutical Co., Ltd. |
Novel benzoxathiin derivative
|
|
ES2381205T3
(es)
|
2005-11-10 |
2012-05-24 |
Msd K.K. |
Derivado espiro aza-sustituido
|
|
JP2009521483A
(ja)
*
|
2005-12-22 |
2009-06-04 |
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 |
ムスカリン受容体のモジュレーター
|
|
EP1987034B1
(de)
*
|
2006-02-22 |
2011-07-20 |
Vertex Pharmceuticals Incorporated |
Kondensierte spiropiperidine als modulatoren muskarinartiger rezeptoren
|
|
AU2007221214A1
(en)
*
|
2006-02-22 |
2007-09-07 |
Vertex Pharmaceuticals Incorporated |
Modulators of muscarinic receptors
|
|
EP1847542A1
(de)
*
|
2006-04-21 |
2007-10-24 |
Laboratorios del Dr. Esteve S.A. |
Spiro[benzopyran]- oder Spiro[benzofuran]derivative als Sigma Rezeptor Antagonisten
|
|
CN101500565A
(zh)
*
|
2006-06-29 |
2009-08-05 |
弗特克斯药品有限公司 |
毒蕈碱性受体的调节剂
|
|
FR2903985B1
(fr)
|
2006-07-24 |
2008-09-05 |
Sanofi Aventis Sa |
Derives de n-(amino-heteroaryl)-1h-indole-2-carboxamides, leur preparation et leur application en therapeutique
|
|
FR2904316B1
(fr)
|
2006-07-31 |
2008-09-05 |
Sanofi Aventis Sa |
Derives de n-(amino-heteroaryl)-1h-indole-2-carboxamides, leur preparation et leur application en therapeutique.
|
|
AU2007284548A1
(en)
*
|
2006-08-15 |
2008-02-21 |
Vertex Pharmaceuticals Incorporated |
Modulators of muscarinic receptors
|
|
EP2051715A2
(de)
|
2006-08-18 |
2009-04-29 |
Vertex Pharmceuticals Incorporated |
Modulatoren muskarinischer rezeptoren
|
|
EP2064187A2
(de)
*
|
2006-08-25 |
2009-06-03 |
Vitae Pharmaceuticals, Inc. |
11-beta-hydroxysteroid-dehydrogenase-1-hemmer
|
|
US8173629B2
(en)
|
2006-09-22 |
2012-05-08 |
Merck Sharp & Dohme Corp. |
Method of treatment using fatty acid synthesis inhibitors
|
|
WO2008047544A1
(en)
|
2006-09-28 |
2008-04-24 |
Banyu Pharmaceutical Co., Ltd. |
Diaryl ketimine derivative
|
|
US7981893B2
(en)
*
|
2006-10-19 |
2011-07-19 |
Signal Pharmaceuticals, Llc |
Heteroaryl compounds, compositions thereof, and methods of treatment therewith
|
|
CN101563323B
(zh)
*
|
2006-12-22 |
2012-07-04 |
弗·哈夫曼-拉罗切有限公司 |
螺-哌啶衍生物
|
|
FR2910473B1
(fr)
*
|
2006-12-26 |
2009-02-13 |
Sanofi Aventis Sa |
Derives de n-(amino-heteroaryl)-1h-pyrrolopyridine-2- carboxamides, leur preparation et leur application en therapeutique.
|
|
JP5319518B2
(ja)
|
2007-04-02 |
2013-10-16 |
Msd株式会社 |
インドールジオン誘導体
|
|
US8969514B2
(en)
|
2007-06-04 |
2015-03-03 |
Synergy Pharmaceuticals, Inc. |
Agonists of guanylate cyclase useful for the treatment of hypercholesterolemia, atherosclerosis, coronary heart disease, gallstone, obesity and other cardiovascular diseases
|
|
MX2009013293A
(es)
|
2007-06-04 |
2010-02-15 |
Synergy Pharmaceuticals Inc |
Agonistas de guanilato ciclasa útiles para el tratamiento de trastornos gastrointestinales, inflamación, cáncer y otros trastornos.
|
|
US7973162B2
(en)
*
|
2007-10-03 |
2011-07-05 |
Vertex Pharmaceuticals Incorporated |
Modulators of muscarinic receptors
|
|
US20090143361A1
(en)
*
|
2007-11-30 |
2009-06-04 |
Elbion Gmbh |
Pyrido[3,2-E]Pyrazines, Process For Preparing The Same, And Their Use As Inhibitors Of Phosphodiesterase 10
|
|
WO2009070584A1
(en)
*
|
2007-11-30 |
2009-06-04 |
Wyeth |
Aryl and heteroaryl fused imidazo[1,5-a]pyrazines as inhibitors of phosphodiesterase 10
|
|
WO2009108332A1
(en)
*
|
2008-02-27 |
2009-09-03 |
Vitae Pharmaceuticals, Inc. |
INHIBITORS OF 11β -HYDROXYSTEROID DEHYDROGENASE TYPE 1
|
|
JPWO2009110510A1
(ja)
|
2008-03-06 |
2011-07-14 |
Msd株式会社 |
アルキルアミノピリジン誘導体
|
|
US20110015198A1
(en)
|
2008-03-28 |
2011-01-20 |
Banyu Pharmaceutical Co., Inc. |
Diarylmethylamide derivative having melanin-concentrating hormone receptor antagonism
|
|
EP2810951B1
(de)
|
2008-06-04 |
2017-03-15 |
Synergy Pharmaceuticals Inc. |
Für die Behandlung von gastrointestinalen Erkrankungen, Entzündungen, Krebs und anderen Erkrankungen geeignete Agonisten von Guanylatcyclase
|
|
JPWO2009154132A1
(ja)
|
2008-06-19 |
2011-12-01 |
Msd株式会社 |
スピロジアミン−ジアリールケトオキシム誘導体
|
|
CA2730603C
(en)
|
2008-07-16 |
2019-09-24 |
Synergy Pharmaceuticals Inc. |
Agonists of guanylate cyclase useful for the treatment of gastrointestinal disorders, inflammation, cancer and other disorders
|
|
JPWO2010013595A1
(ja)
|
2008-07-30 |
2012-01-12 |
Msd株式会社 |
5員−5員又は5員−6員縮環シクロアルキルアミン誘導体
|
|
EP2348857B1
(de)
|
2008-10-22 |
2016-02-24 |
Merck Sharp & Dohme Corp. |
Neue cyclische benzimidazolderivate als antidiabetika
|
|
US8110578B2
(en)
|
2008-10-27 |
2012-02-07 |
Signal Pharmaceuticals, Llc |
Pyrazino[2,3-b]pyrazine mTOR kinase inhibitors for oncology indications and diseases associated with the mTOR/PI3K/Akt pathway
|
|
EP2350010B1
(de)
|
2008-10-30 |
2014-03-26 |
Merck Sharp & Dohme Corp. |
Isonikotinamide als orexinrezeptorantagonisten
|
|
JP5557845B2
(ja)
|
2008-10-31 |
2014-07-23 |
メルク・シャープ・アンド・ドーム・コーポレーション |
糖尿病用剤として有用な新規環状ベンゾイミダゾール誘導体
|
|
US20110243940A1
(en)
|
2008-12-16 |
2011-10-06 |
Schering Corporation |
Bicyclic pyranone derivatives and methods of use thereof
|
|
US20110245209A1
(en)
|
2008-12-16 |
2011-10-06 |
Schering Corporation |
Pyridopyrimidine derivatives and methods of use thereof
|
|
WO2010138833A1
(en)
|
2009-05-29 |
2010-12-02 |
Wyeth |
SUBSTITUTED IMIDAZO[1,5-a]QUINOXALINES AS INHIBITORS OF PHOSPHODIESTERASE 10
|
|
NZ618135A
(en)
|
2009-10-26 |
2015-05-29 |
Signal Pharm Llc |
Methods of synthesis and purification of heteroaryl compounds
|
|
AU2011218830B2
(en)
|
2010-02-25 |
2014-07-24 |
Merck Sharp & Dohme Corp. |
Novel cyclic benzimidazole derivatives useful anti-diabetic agents
|
|
US8680098B2
(en)
|
2010-03-05 |
2014-03-25 |
Janssen Pharmaceutica, Nv |
Substituted aza-bicyclic imidazole derivatives useful as TRPM8 receptor modulators
|
|
CA2799708A1
(en)
|
2010-05-21 |
2011-11-24 |
Pfizer Inc. |
2-phenyl benzoylamides
|
|
US9616097B2
(en)
|
2010-09-15 |
2017-04-11 |
Synergy Pharmaceuticals, Inc. |
Formulations of guanylate cyclase C agonists and methods of use
|
|
MX348131B
(es)
|
2011-02-25 |
2017-05-26 |
Merck Sharp & Dohme |
Novedosos derivados de azabencimidazol ciclico utiles como agentes antidiabeticos.
|
|
CA2828343A1
(en)
|
2011-03-04 |
2012-09-13 |
The Scripps Research Institute |
Edn3-like peptides and uses thereof
|
|
KR101978537B1
(ko)
|
2011-10-19 |
2019-05-14 |
시그날 파마소티칼 엘엘씨 |
Tor 키나제 억제제를 사용한 암의 치료
|
|
AR088352A1
(es)
|
2011-10-19 |
2014-05-28 |
Merck Sharp & Dohme |
Antagonistas del receptor de 2-piridiloxi-4-nitrilo orexina
|
|
US9403829B2
(en)
|
2011-12-02 |
2016-08-02 |
Signal Pharmaceuticals, Llc |
Pharmaceutical compositions of 7-(6-(2-hydroxypropan-2-yl)pyridin-3-yl)-1-((trans)-4-methoxycyclohexyl)-3,4-dihydropyrazino [2,3-b]pyrazin-2(1H)-one, a solid form thereof and methods of their use
|
|
JP6114317B2
(ja)
|
2012-02-24 |
2017-04-12 |
シグナル ファーマシューティカルズ,エルエルシー |
Torキナーゼ阻害剤の組合せ療法を用いて、非小細胞肺がんを処置する方法
|
|
WO2014022528A1
(en)
|
2012-08-02 |
2014-02-06 |
Merck Sharp & Dohme Corp. |
Antidiabetic tricyclic compounds
|
|
AU2013203714B2
(en)
|
2012-10-18 |
2015-12-03 |
Signal Pharmaceuticals, Llc |
Inhibition of phosphorylation of PRAS40, GSK3-beta or P70S6K1 as a marker for TOR kinase inhibitory activity
|
|
MX2015009209A
(es)
|
2013-01-16 |
2016-03-17 |
Signal Pharm Llc |
Compuestos sustituidos de pirrolopirimidina, composiciones de los mismos, y metodos de tratamiento con los mismos.
|
|
WO2014130608A1
(en)
|
2013-02-22 |
2014-08-28 |
Merck Sharp & Dohme Corp. |
Antidiabetic bicyclic compounds
|
|
WO2014139388A1
(en)
|
2013-03-14 |
2014-09-18 |
Merck Sharp & Dohme Corp. |
Novel indole derivatives useful as anti-diabetic agents
|
|
JP2016514670A
(ja)
|
2013-03-15 |
2016-05-23 |
シナジー ファーマシューティカルズ インコーポレイテッド |
他の薬物と組み合わせたグアニル酸シクラーゼ受容体アゴニスト
|
|
JP2016514671A
(ja)
|
2013-03-15 |
2016-05-23 |
シナジー ファーマシューティカルズ インコーポレイテッド |
グアニル酸シクラーゼのアゴニストおよびその使用
|
|
CA2908353C
(en)
|
2013-04-17 |
2021-11-02 |
Signal Pharmaceuticals, Llc |
Treatment of cancer with dihydropyrazino-pyrazines
|
|
US9505764B2
(en)
|
2013-04-17 |
2016-11-29 |
Signal Pharmaceuticals, Llc |
Treatment of cancer with dihydropyrazino-pyrazines
|
|
EA030726B1
(ru)
|
2013-04-17 |
2018-09-28 |
СИГНАЛ ФАРМАСЬЮТИКАЛЗ, ЭлЭлСи |
ФАРМАЦЕВТИЧЕСКИЕ СОСТАВЫ, СПОСОБЫ, ТВЕРДЫЕ ФОРМЫ И СПОСОБЫ ПРИМЕНЕНИЯ, ОТНОСЯЩИЕСЯ К 1-ЭТИЛ-7-(2-МЕТИЛ-6-(1H-1,2,4-ТРИАЗОЛ-3-ИЛ)ПИРИДИН-3-ИЛ)-3,4-ДИГИДРОПИРАЗИНО[2,3-b]ПИРАЗИН-2(1H)-ОНУ
|
|
HK1221168A1
(zh)
|
2013-04-17 |
2017-05-26 |
西格诺药品有限公司 |
用於治疗癌症的包括tor激酶抑制剂和n-(3-(5-氟-2-(4-(2-甲氧基乙氧基)苯基氨基)嘧啶-4-基氨基)苯基)丙烯醯胺的组合疗法
|
|
MX368286B
(es)
|
2013-04-17 |
2019-09-27 |
Signal Pharm Llc |
Terapia de combinacion que comprende un inhibidor de tor cinasa y un compuesto de quinazolinona 5-sustituida para tratar cancer.
|
|
AU2014254059B2
(en)
|
2013-04-17 |
2019-06-06 |
Signal Pharmaceuticals, Llc |
Combination therapy comprising a TOR kinase inhibitor and a cytidine analog for treating cancer
|
|
CA2908957C
(en)
|
2013-04-17 |
2021-05-18 |
Signal Pharmaceuticals, Llc |
Combination therapy comprising a dihydropyrazino-pyrazine compound and an androgen receptor antagonist for treating prostate cancer
|
|
HK1223286A1
(zh)
|
2013-05-29 |
2017-07-28 |
西格诺药品有限公司 |
7-(6-(2-羟基丙-2-基)吡啶-3-基)-1-((反式)-4-甲氧基环己基)-3,4-二氢吡嗪并[2,3-b]吡嗪-2(1h)-酮的药物组合物、其固体形式及它们的使用方法
|
|
EA201592263A1
(ru)
|
2013-06-05 |
2016-05-31 |
Синерджи Фармасьютикалз, Инк. |
Ультрачистые агонисты гуанилатциклазы c, способ их получения и использования
|
|
WO2015051496A1
(en)
|
2013-10-08 |
2015-04-16 |
Merck Sharp & Dohme Corp. |
Antidiabetic tricyclic compounds
|
|
EP3131552B1
(de)
|
2014-04-16 |
2020-07-15 |
Signal Pharmaceuticals, LLC |
Verfahren zur behandlung von krebs anhand einer tor-kinasehemmerkombinationstherapie
|
|
US9718824B2
(en)
|
2014-04-16 |
2017-08-01 |
Signal Pharmaceuticals, Llc |
Solid forms comprising 7-(6-(2-hydroxypropan-2-yl)pyridin-3-yl)-1-((trans)-4-methoxycyclohexyl)-3,4-dihydropyrazino[2,3-b]pyrazin-2(1H)-one, and a coformer, compositions and methods of use thereof
|
|
JP2017511367A
(ja)
|
2014-04-16 |
2017-04-20 |
シグナル ファーマシューティカルズ,エルエルシー |
1−エチル−7−(2−メチル−6−(1H−1,2,4−トリアゾール−3−イル)ピリジン−3−イル)−3,4−ジヒドロピラジノ[2,3−b]ピラジン−2(1H)−オン及び共形成物を含む固体形態、その組成物及び使用方法
|
|
NZ714742A
(en)
|
2014-04-16 |
2017-04-28 |
Signal Pharm Llc |
Solid forms of 1-ethyl-7-(2-methyl-6-(1h-1,2,4-triazol-3-yl)pyridin-3-yl)-3,4-dihydropyrazino[2,3-b]pyrazin-2(1h)-one, compositions thereof and methods of their use
|
|
EA201790189A1
(ru)
|
2014-07-14 |
2017-11-30 |
СИГНАЛ ФАРМАСЬЮТИКАЛЗ, ЭлЭлСи |
Способы лечения злокачественного новообразования с использованием замещенных пирролопиримидиновых соединений, композиции на их основе
|
|
NZ629796A
(en)
|
2014-07-14 |
2015-12-24 |
Signal Pharm Llc |
Amorphous form of 4-((4-(cyclopentyloxy)-5-(2-methylbenzo[d]oxazol-6-yl)-7h-pyrrolo[2,3-d]pyrimidin-2-yl)amino)-3-methoxy-n-methylbenzamide, compositions thereof and methods of their use
|
|
EP3186242B1
(de)
|
2014-08-29 |
2021-10-06 |
Tes Pharma S.r.l. |
Inhibitoren von alpha-amino-beta-carboxymuconsäure semialdehyd-decarboxylase
|
|
CN104387367A
(zh)
*
|
2014-11-02 |
2015-03-04 |
湖南华腾制药有限公司 |
一种2位取代苯并咪唑衍生物的制备方法
|
|
EP3480198B1
(de)
|
2016-06-30 |
2021-05-05 |
Riken |
Neuartige verbindung oder pharmazeutisch akzeptables salz davon
|
|
AU2017342083A1
(en)
|
2016-10-14 |
2019-04-11 |
Tes Pharma S.R.L. |
Inhibitors of alpha-amino-beta-carboxymuconic acid semialdehyde decarboxylase
|
|
US11072602B2
(en)
|
2016-12-06 |
2021-07-27 |
Merck Sharp & Dohme Corp. |
Antidiabetic heterocyclic compounds
|
|
EP3558298B1
(de)
|
2016-12-20 |
2026-03-11 |
Merck Sharp & Dohme LLC |
Antidiabetische spirochromanverbindungen
|
|
CN116462666B
(zh)
*
|
2017-01-10 |
2025-07-15 |
瑞士苏黎世联邦理工学院 |
细胞保护性化合物及其用途
|
|
ES2959860T3
(es)
|
2017-06-22 |
2024-02-28 |
Celgene Corp |
Tratamiento del carcinoma hepatocelular caracterizado por la infección por el virus de la hepatitis B
|
|
JP7369968B2
(ja)
*
|
2017-12-27 |
2023-10-27 |
公益財団法人がん研究会 |
抗がん剤
|
|
CA3105174A1
(en)
*
|
2018-06-27 |
2020-01-02 |
Reborna Biosciences, Inc. |
Prophylactic or therapeutic agent for spinal muscular atrophy
|
|
AR117122A1
(es)
|
2018-11-20 |
2021-07-14 |
Tes Pharma S R L |
INHIBIDORES DE LA ÁCIDO a-AMINO-b-CARBOXIMUCÓNICO SEMIALDEHÍDO DESCARBOXILASA
|
|
WO2020163689A1
(en)
|
2019-02-08 |
2020-08-13 |
University Of Pittsburgh - Of The Commonwealth System Of Higher Education |
20-hete formation inhibitors
|
|
TW202045476A
(zh)
|
2019-02-13 |
2020-12-16 |
美商默沙東藥廠 |
5-烷基吡咯啶食慾素受體促效劑
|
|
EP3923933A4
(de)
|
2019-02-13 |
2022-08-17 |
Merck Sharp & Dohme Corp. |
Pyrrolidinorexin-rezeptor-agonisten
|
|
WO2021026047A1
(en)
|
2019-08-08 |
2021-02-11 |
Merck Sharp & Dohme Corp. |
Heteroaryl pyrrolidine and piperidine orexin receptor agonists
|
|
EP3772513A1
(de)
*
|
2019-08-09 |
2021-02-10 |
C.N.C.C.S. S.c.a.r.l. Collezione Nazionale Dei Composti Chimici e Centro Screening |
Shp2-inhibitoren
|
|
MX2023001840A
(es)
|
2020-08-18 |
2023-03-13 |
Merck Sharp & Dohme Llc |
Agonistas de bicicloheptano pirrolidina de los receptores de orexina.
|
|
MX2024000271A
(es)
*
|
2021-07-09 |
2024-01-31 |
Kanaph Therapeutics Inc |
Inhibidor de shp2 y uso del mismo.
|