US7517884B2
(en)
|
1998-03-30 |
2009-04-14 |
Kalypsys Inc. |
Sulfonyl-substituted bicyclic compounds as modulators of PPAR
|
TWI263497B
(en)
|
2002-03-29 |
2006-10-11 |
Lilly Co Eli |
Pyridinoylpiperidines as 5-HT1F agonists
|
TW200526626A
(en)
|
2003-09-13 |
2005-08-16 |
Astrazeneca Ab |
Chemical compounds
|
GB0325956D0
(en)
|
2003-11-06 |
2003-12-10 |
Addex Pharmaceuticals Sa |
Novel compounds
|
US7745630B2
(en)
*
|
2003-12-22 |
2010-06-29 |
Justin Stephen Bryans |
Triazolyl piperidine arginine vasopressin receptor modulators
|
US8207147B2
(en)
*
|
2003-12-24 |
2012-06-26 |
Prosidion Limited |
Heterocyclic derivatives as GPCR receptor agonists
|
RU2381226C2
(ru)
*
|
2004-02-18 |
2010-02-10 |
Астразенека Аб |
Полигетероциклические соединения и их применение в качестве антагонистов метаботропного рецептора глутамата
|
US7269708B2
(en)
*
|
2004-04-20 |
2007-09-11 |
Rambus Inc. |
Memory controller for non-homogenous memory system
|
MXPA06014574A
(es)
|
2004-06-24 |
2007-03-12 |
Incyte Corp |
Piperidinas n-sustituidas y su uso como farmaceuticos.
|
EA200700251A1
(ru)
*
|
2004-08-10 |
2007-08-31 |
Инсайт Корпорейшн |
Амидосоединения и их применение в качестве фармацевтических средств
|
AU2005329423A1
(en)
|
2004-09-20 |
2006-09-28 |
Xenon Pharmaceuticals Inc. |
Heterocyclic derivatives and their use as stearoyl-CoA desaturase inhibitors
|
CN101084207A
(zh)
|
2004-09-20 |
2007-12-05 |
泽农医药公司 |
杂环衍生物及其作为硬脂酰CoA去饱和酶抑制剂的用途
|
TW200626155A
(en)
|
2004-09-20 |
2006-08-01 |
Xenon Pharmaceuticals Inc |
Heterocyclic derivatives and their use as therapeutic agents
|
WO2006034279A1
(en)
|
2004-09-20 |
2006-03-30 |
Xenon Pharmaceuticals Inc. |
Heterocyclic derivatives and their use as therapeutic agents
|
BRPI0515478A
(pt)
|
2004-09-20 |
2008-07-22 |
Xenon Pharmaceuticals Inc |
derivados heterocìclicos e seu uso como mediadores de estearoil-coa-desaturase
|
TW200626154A
(en)
|
2004-09-20 |
2006-08-01 |
Xenon Pharmaceuticals Inc |
Heterocyclic derivatives and their use as therapeutic agents
|
TW200630337A
(en)
|
2004-10-14 |
2006-09-01 |
Euro Celtique Sa |
Piperidinyl compounds and the use thereof
|
AR052319A1
(es)
|
2004-10-29 |
2007-03-14 |
Kalypsys Inc |
Compuestos biciclicos sustituidos por sulfonilo en funcion de moduladores del ppar
|
ES2528674T3
(es)
|
2005-02-17 |
2015-02-11 |
Astellas Pharma Inc. |
Piperidina y carboxilatos de piperacina como inhibidores de FAAH
|
BRPI0607756A2
(pt)
|
2005-02-18 |
2010-05-18 |
Astrazeneca Ab |
composto ou um sal farmaceuticamente aceitável do mesmo, composição farmacêutica, método para inibição de dna girase bacteriana e/ou topoisomerase iv em um animal de sangue quente, uso de um composto ou um sal farmaceuticamente aceitável do mesmo, e, processo para preparar compostos ou sais farmaceuticamente aceitáveis dos mesmos
|
GB0508319D0
(en)
|
2005-04-25 |
2005-06-01 |
Novartis Ag |
Organic compounds
|
EA015813B1
(ru)
*
|
2005-05-18 |
2011-12-30 |
Аддекс Фарма Са |
Замещенные производные оксадиазола в качестве положительных аллостерических модуляторов метаботропных глутаматных рецепторов
|
GB0510142D0
(en)
*
|
2005-05-18 |
2005-06-22 |
Addex Pharmaceuticals Sa |
Novel compounds A1
|
GB0510140D0
(en)
|
2005-05-18 |
2005-06-22 |
Addex Pharmaceuticals Sa |
Novel compounds B2
|
GB0510141D0
(en)
|
2005-05-18 |
2005-06-22 |
Addex Pharmaceuticals Sa |
Novel compounds B3
|
GB0510139D0
(en)
*
|
2005-05-18 |
2005-06-22 |
Addex Pharmaceuticals Sa |
Novel compounds B1
|
BRPI0611187A2
(pt)
|
2005-06-03 |
2010-08-24 |
Xenon Pharmaceuticals Inc |
derivados aminotiazàis como inibidores da estearoil-coa desaturase humana
|
EP1907384A2
(en)
*
|
2005-06-30 |
2008-04-09 |
Prosidion Limited |
Gpcr agonists
|
US20090325924A1
(en)
*
|
2005-06-30 |
2009-12-31 |
Stuart Edward |
GPCR Agonists
|
IL169855A
(en)
*
|
2005-07-25 |
2014-05-28 |
Elta Systems Ltd |
A system and method for locating a receiver location
|
NZ565460A
(en)
|
2005-07-26 |
2011-06-30 |
Bial Portela & Ca Sa |
Nitrocatechol derivatives as COMT inhibitors
|
TW200800946A
(en)
*
|
2005-08-15 |
2008-01-01 |
Astrazeneca Ab |
Substituted piperazines as metabotropic glutamate receptor antagonists
|
HUP0500920A2
(en)
*
|
2005-10-05 |
2007-07-30 |
Richter Gedeon Nyrt |
Oxadiazole derivatives, process for their preparation and their use
|
BRPI0619282B8
(pt)
|
2005-10-25 |
2021-05-25 |
Kalypsys Inc |
sal, e composição farmacêutica
|
ES2439736T3
(es)
|
2005-11-08 |
2014-01-24 |
Vertex Pharmaceuticals Incorporated |
Moduladores heterocíclicos de transportadores de casete de unión a ATP
|
DE102005062991A1
(de)
*
|
2005-12-28 |
2007-07-05 |
Grünenthal GmbH |
Substituierte Thiazole und ihre Verwendung zur Herstellung von Arzneimitteln
|
DE102005062990A1
(de)
|
2005-12-28 |
2007-07-05 |
Grünenthal GmbH |
Substituierte Thiazole und ihre Verwendung zur Herstellung von Arzneimitteln
|
US7671221B2
(en)
|
2005-12-28 |
2010-03-02 |
Vertex Pharmaceuticals Incorporated |
Modulators of ATP-Binding Cassette transporters
|
AU2007212429A1
(en)
|
2006-02-07 |
2007-08-16 |
Wyeth |
11-beta HSD1 inhibitors
|
US7951824B2
(en)
*
|
2006-02-17 |
2011-05-31 |
Hoffman-La Roche Inc. |
4-aryl-pyridine-2-carboxyamide derivatives
|
WO2007110449A1
(en)
|
2006-03-29 |
2007-10-04 |
Euro-Celtique S.A. |
Benzenesulfonamide compounds and their use
|
MX2008012413A
(es)
|
2006-03-29 |
2008-10-07 |
Hoffmann La Roche |
Derivados de piridina y pirimidina como antagonistas del receptor metabotropico de glutamato 2 (mglur2).
|
EP1845097A1
(en)
|
2006-04-10 |
2007-10-17 |
Portela & Ca., S.A. |
Oxadiazole derivatives as COMT inhibitors
|
WO2007118853A1
(en)
|
2006-04-13 |
2007-10-25 |
Euro-Celtique S.A. |
Benzenesulfonamide compounds and their use as blockers of calcium channels
|
WO2007118854A1
(en)
|
2006-04-13 |
2007-10-25 |
Euro-Celtique S.A. |
Benzenesulfonamide compounds and the use thereof
|
TW200811156A
(en)
*
|
2006-05-05 |
2008-03-01 |
Astrazeneca Ab |
mGluR5 modulators IV
|
TW200811157A
(en)
|
2006-05-05 |
2008-03-01 |
Astrazeneca Ab |
mGluR5 modulators I
|
US7943622B2
(en)
|
2006-06-06 |
2011-05-17 |
Cornerstone Therapeutics, Inc. |
Piperazines, pharmaceutical compositions and methods of use thereof
|
FR2903405B1
(fr)
*
|
2006-07-04 |
2011-09-09 |
Pasteur Institut |
Composes a effet potentialisateur de l'activite de l'ethionamide et leurs applications
|
BRPI0719122A2
(pt)
|
2006-08-24 |
2013-12-10 |
Novartis Ag |
Compostos orgânicos
|
AU2007299870A1
(en)
|
2006-09-22 |
2008-03-27 |
Novartis Ag |
Heterocyclic organic compounds
|
KR101181194B1
(ko)
|
2006-10-18 |
2012-09-18 |
화이자 프로덕츠 인코포레이티드 |
바이아릴 에터 우레아 화합물
|
GB0622202D0
(en)
*
|
2006-11-07 |
2006-12-20 |
Addex Pharmaceuticals Sa |
Novel compounds
|
US7754739B2
(en)
|
2007-05-09 |
2010-07-13 |
Vertex Pharmaceuticals Incorporated |
Modulators of CFTR
|
CA2672776A1
(en)
|
2006-12-20 |
2008-06-26 |
Novartis Ag |
2-substituted 5-membered heterocycles as scd inhibitors
|
WO2008091863A1
(en)
|
2007-01-23 |
2008-07-31 |
Kalypsys, Inc. |
Sulfonyl-substituted bicyclic compounds as ppar modulators for the treatment of non-alcoholic steatohepatitis
|
US8524746B2
(en)
|
2007-01-31 |
2013-09-03 |
Bial-Portela & Ca., S.A. |
Dosage regimen for COMT inhibitors
|
WO2008124118A1
(en)
|
2007-04-09 |
2008-10-16 |
Purdue Pharma L.P. |
Benzenesulfonyl compounds and the use therof
|
CN104447716A
(zh)
|
2007-05-09 |
2015-03-25 |
沃泰克斯药物股份有限公司 |
Cftr调节剂
|
US8853392B2
(en)
|
2007-06-03 |
2014-10-07 |
Vanderbilt University |
Benzamide mGluR5 positive allosteric modulators and methods of making and using same
|
JP5622568B2
(ja)
*
|
2007-06-03 |
2014-11-12 |
バンダービルト ユニバーシティ |
ベンズアミドmGluR5の正のアロステリック調節因子ならびにその作製および使用方法
|
CA2697551C
(en)
|
2007-09-20 |
2013-03-12 |
Irm Llc |
Piperidine derivatives as modulators of gpr119 activity
|
EP2205073A4
(en)
|
2007-09-26 |
2013-03-06 |
Sinai School Medicine |
AZACYTIDINE ANALOGS AND USES THEREOF
|
US8765736B2
(en)
|
2007-09-28 |
2014-07-01 |
Purdue Pharma L.P. |
Benzenesulfonamide compounds and the use thereof
|
EA201070451A1
(ru)
*
|
2007-10-10 |
2010-10-29 |
Такеда Фармасьютикал Компани Лимитед |
Амидные соединения
|
PE20090982A1
(es)
|
2007-11-05 |
2009-08-13 |
Novartis Ag |
Derivados de piperidina como inhibidores de la proteina de transferencia de colesteril-ester (cetp)
|
US8759365B2
(en)
|
2007-12-03 |
2014-06-24 |
Novartis Ag |
Organic compounds
|
CN101910156B
(zh)
|
2007-12-07 |
2013-12-04 |
沃泰克斯药物股份有限公司 |
3-(6-(1-(2,2-二氟苯并[d][1,3]间二氧杂环戊烯-5-基)环丙烷甲酰氨基)-3-甲基吡啶-2-基)苯甲酸的固体形式
|
CA2989620C
(en)
|
2007-12-07 |
2022-05-03 |
Vertex Pharmaceuticals Incorporated |
Processes for producing cycloalkylcarboxamido-pyridine benzoic acids
|
GEP20125707B
(en)
*
|
2007-12-18 |
2012-12-10 |
Glenmark Pharmaceuticals Sa |
Chromane derivatives as trpv3 modulators
|
CA2715802A1
(en)
*
|
2008-02-28 |
2009-09-03 |
Bial - Portela & C.A., S.A. |
Pharmaceutical composition for poorly soluble drugs
|
EP2271622B1
(en)
|
2008-02-28 |
2017-10-04 |
Vertex Pharmaceuticals Incorporated |
Heteroaryl derivatives as CFTR Modulators
|
AR070907A1
(es)
|
2008-03-17 |
2010-05-12 |
Bial Portela & Ca Sa |
Formas cristalinas de derivado de nitrocatecol
|
UA103319C2
(xx)
|
2008-05-06 |
2013-10-10 |
Глаксосмитклайн Ллк |
Сполуки бензенсульфонамідтіазолу та -оксазолу$соединения бензенсульфонамидтиазола и -оксазола
|
MX2010011762A
(es)
*
|
2008-06-17 |
2011-02-03 |
Glenmark Pharmaceuticals Sa |
Derivados de cromano como moduladores del trpv3.
|
TWI434842B
(zh)
|
2008-07-14 |
2014-04-21 |
Astellas Pharma Inc |
Azole compounds
|
GB0813142D0
(en)
|
2008-07-17 |
2008-08-27 |
Glaxo Group Ltd |
Novel compounds
|
GB0813144D0
(en)
|
2008-07-17 |
2008-08-27 |
Glaxo Group Ltd |
Novel compounds
|
US8273900B2
(en)
|
2008-08-07 |
2012-09-25 |
Novartis Ag |
Organic compounds
|
CA2746943A1
(en)
|
2008-12-18 |
2010-07-15 |
Boehringer Ingelheim International Gmbh |
Serotonin 5-ht2b receptor inhibitors
|
CA2965223C
(en)
*
|
2008-12-22 |
2019-09-24 |
Chemocentryx, Inc. |
C5ar antagonists
|
WO2010096371A2
(en)
*
|
2009-02-18 |
2010-08-26 |
Boehringer Ingelheim International Gmbh |
Heterocyclic compounds which modulate the cb2 receptor
|
TW201035088A
(en)
|
2009-02-27 |
2010-10-01 |
Supergen Inc |
Cyclopentathiophene/cyclohexathiophene DNA methyltransferase inhibitors
|
ES2730678T3
(es)
|
2009-04-01 |
2019-11-12 |
Bial Portela & Ca Sa |
Formulaciones farmacéuticas que comprenden derivados de nitrocatecol y métodos para fabricarlas
|
ES2915698T3
(es)
*
|
2009-04-01 |
2022-06-24 |
Bial Portela & Ca Sa |
Formulaciones farmacéuticas que comprenden derivados de nitrocatecol y métodos para preparar las mismas
|
CA2757019C
(en)
*
|
2009-04-02 |
2018-05-15 |
Colucid Pharmaceuticals, Inc. |
Composition of 2,4,6-trifluoro-n-[6-(1-methyl-piperidin-4-carbonyl)-pyridin-2-yl]-benzamide
|
JP2012524798A
(ja)
*
|
2009-04-23 |
2012-10-18 |
メルク・シャープ・エンド・ドーム・コーポレイション |
2−アルキルピペリジンmglur5受容体モジュレーター
|
US8673920B2
(en)
|
2009-05-06 |
2014-03-18 |
Merck Sharp & Dohme Corp. |
Inhibitors of the renal outer medullary potassium channel
|
EP2438059A1
(en)
|
2009-06-05 |
2012-04-11 |
Link Medicine Corporation |
Aminopyrrolidinone derivatives and uses thereof
|
TW201044234A
(en)
*
|
2009-06-08 |
2010-12-16 |
Chunghwa Picture Tubes Ltd |
Method of scanning touch panel
|
US20120252792A1
(en)
*
|
2009-09-17 |
2012-10-04 |
The Regents Of The University Of Michigan |
Methods and compositions for modulating rho-mediated gene transcription
|
US8389536B2
(en)
|
2009-10-27 |
2013-03-05 |
Hoffmann-La Roche Inc. |
Positive allosteric modulators (PAM)
|
US8394858B2
(en)
|
2009-12-03 |
2013-03-12 |
Novartis Ag |
Cyclohexane derivatives and uses thereof
|
US8586581B2
(en)
|
2009-12-17 |
2013-11-19 |
Hoffmann-La Roche Inc |
Ethynyl compounds useful for treatment of CNS disorders
|
US8772301B2
(en)
|
2009-12-18 |
2014-07-08 |
Sunovion Pharmaceuticals, Inc. |
Compounds for treating disorders mediated by metabotropic glutamate receptor 5, and methods of use thereof
|
EP2523936A1
(en)
|
2010-01-15 |
2012-11-21 |
Boehringer Ingelheim International GmbH |
Compounds which modulate the cb2 receptor
|
WO2011123654A1
(en)
|
2010-04-02 |
2011-10-06 |
Colucid Pharmaceuticals, Inc. |
Compositions and methods of synthesis of pyridinoylpiperidine 5-ht1f agonists
|
DK3150198T3
(da)
|
2010-04-07 |
2021-11-01 |
Vertex Pharma |
Farmaceutiske sammensætninger af 3-(6-(1-(2,2-difluorbenzo[d][1,3]dioxol-5-yl)-cyclopropancarboxamido)-3-methylpyriodin-2-yl)benzoesyre og indgivelse deraf
|
US8420661B2
(en)
|
2010-04-13 |
2013-04-16 |
Hoffmann-La Roche Inc. |
Arylethynyl derivatives
|
US8450350B2
(en)
|
2010-05-05 |
2013-05-28 |
Infinity Pharmaceuticals, Inc. |
Triazoles as inhibitors of fatty acid synthase
|
WO2011140190A1
(en)
|
2010-05-05 |
2011-11-10 |
Infinity Pharmaceuticals |
Tetrazolones as inhibitors of fatty acid synthase
|
AU2011261375B2
(en)
|
2010-06-04 |
2016-09-22 |
Albany Molecular Research, Inc. |
Glycine transporter-1 inhibitors, methods of making them, and uses thereof
|
JP2013529647A
(ja)
|
2010-06-24 |
2013-07-22 |
ケモセントリックス,インコーポレイティド |
C5aRアンタゴニスト
|
US8846936B2
(en)
|
2010-07-22 |
2014-09-30 |
Boehringer Ingelheim International Gmbh |
Sulfonyl compounds which modulate the CB2 receptor
|
US20130210804A1
(en)
*
|
2010-10-25 |
2013-08-15 |
Neville J. Anthony |
Tricyclic mglur5 receptor modulators
|
US9073882B2
(en)
|
2010-10-27 |
2015-07-07 |
Merck Sharp & Dohme Corp. |
Inhibitors of the renal outer medullary potassium channel
|
EP2632464B1
(en)
|
2010-10-29 |
2015-04-29 |
Merck Sharp & Dohme Corp. |
Inhibitors of the renal outer medullary potassium channel
|
US20140045900A1
(en)
|
2011-02-11 |
2014-02-13 |
Bial-Portela & Ca, S.A. |
Administration regime for nitrocatechols
|
US8772300B2
(en)
|
2011-04-19 |
2014-07-08 |
Hoffmann-La Roche Inc. |
Phenyl or pyridinyl-ethynyl derivatives
|
KR101576343B1
(ko)
|
2011-04-26 |
2015-12-09 |
에프. 호프만-라 로슈 아게 |
피라졸리딘-3-온 유도체
|
CA2829170C
(en)
|
2011-04-26 |
2019-02-26 |
F. Hoffmann-La Roche Ag |
Ethynyl derivatives as positive allosteric modulators of the mglur5
|
KR20140067048A
(ko)
|
2011-08-15 |
2014-06-03 |
인터뮨, 인크. |
라이소포스파티드산 수용체 길항제
|
AU2012299227A1
(en)
|
2011-08-19 |
2014-02-20 |
Merck Sharp & Dohme Corp. |
Inhibitors of the renal outer medullary potassium channel
|
UY34305A
(es)
|
2011-09-01 |
2013-04-30 |
Novartis Ag |
Derivados de heterociclos bicíclicos para el tratamiento de la hipertensión arterial pulmonar
|
TW201317213A
(zh)
|
2011-09-16 |
2013-05-01 |
Merck Sharp & Dohme |
腎外髓質鉀通道抑制劑
|
US20130123254A1
(en)
|
2011-09-30 |
2013-05-16 |
Barbara Biemans |
Pharmaceutically acceptable mglur5 positive allosteric modulators and their methods of identification
|
US9926309B2
(en)
|
2011-10-05 |
2018-03-27 |
The Board Of Trustees Of The Leland Stanford Junior University |
Pi-kinase inhibitors with anti-infective activity
|
WO2013052845A1
(en)
|
2011-10-05 |
2013-04-11 |
The Board Of Trustees Of The Leland Stanford Junior University |
Pi-kinase inhibitors with broad spectrum anti-infective activity
|
UA110862C2
(uk)
|
2011-10-07 |
2016-02-25 |
Ф. Хоффманн-Ля Рош Аг |
Похідні етинілу як алостеричні модулятори метаботропного рецептора глутамату mglur 5
|
UA110995C2
(uk)
|
2011-10-07 |
2016-03-10 |
Ф. Хоффманн-Ля Рош Аг |
Етинільні похідні як модулятори метаботропного глутаматного рецептора
|
WO2013062892A1
(en)
|
2011-10-25 |
2013-05-02 |
Merck Sharp & Dohme Corp. |
Inhibitors of the renal outer medullary potassium channel
|
US8940898B2
(en)
|
2011-10-25 |
2015-01-27 |
Merck Sharp & Dohme Corp. |
Piperidinyl alkyne orexin receptor antagonists
|
WO2013062900A1
(en)
|
2011-10-25 |
2013-05-02 |
Merck Sharp & Dohme Corp. |
Inhibitors of the renal outer medullary potassium channel
|
WO2013066718A2
(en)
|
2011-10-31 |
2013-05-10 |
Merck Sharp & Dohme Corp. |
Inhibitors of the renal outer medullary potassium channel
|
US9139585B2
(en)
|
2011-10-31 |
2015-09-22 |
Merck Sharp & Dohme Corp. |
Inhibitors of the Renal Outer Medullary Potassium channel
|
US9108947B2
(en)
|
2011-10-31 |
2015-08-18 |
Merck Sharp & Dohme Corp. |
Inhibitors of the Renal Outer Medullary Potassium channel
|
HUE047856T2
(hu)
|
2011-12-13 |
2020-05-28 |
Bial Portela & Ca Sa |
Kémiai vegyület, amely köztitermékként használható katechol-O-metil-transzferáz inhibitor elõállításához
|
WO2013090271A1
(en)
|
2011-12-16 |
2013-06-20 |
Merck Sharp & Dohme Corp. |
Inhibitors of the renal outer medullary potassium channel
|
EA037918B1
(ru)
|
2011-12-21 |
2021-06-07 |
Новира Терапьютикс, Инк. |
Противовирусные агенты против гепатита в
|
MY170524A
(en)
|
2012-02-02 |
2019-08-09 |
Idorsia Pharmaceuticals Ltd |
4-(benzoimidazol-2-yl)-thiazole compounds and related aza derivatives
|
NZ703448A
(en)
|
2012-06-04 |
2017-07-28 |
Actelion Pharmaceuticals Ltd |
Benzimidazole-proline derivatives
|
EP2875000B1
(en)
|
2012-07-17 |
2016-09-21 |
F. Hoffmann-La Roche AG |
Arylethynyl derivatives
|
AR092031A1
(es)
|
2012-07-26 |
2015-03-18 |
Merck Sharp & Dohme |
Inhibidores del canal de potasio medular externo renal
|
UA113223C2
(xx)
|
2012-08-13 |
2016-12-26 |
|
Арилетинілпіримідини
|
UA123256C2
(uk)
|
2012-08-28 |
2021-03-10 |
ЯНССЕН САЙЄНСІЗ АЙРЛЕНД ЮСі |
Сульфамоїлариламіди та їх застосування як лікарських препаратів для лікування гепатиту b
|
KR101737245B1
(ko)
|
2012-09-27 |
2017-05-17 |
에프. 호프만-라 로슈 아게 |
아릴에틴일 유도체
|
CN104703980B
(zh)
|
2012-10-10 |
2017-09-22 |
埃科特莱茵药品有限公司 |
属于[邻双(杂)芳基]‑[2‑(间双(杂)芳基)吡咯烷‑1‑基]甲酮衍生物的食欲素受体拮抗剂
|
US9777002B2
(en)
|
2012-11-29 |
2017-10-03 |
Merck Sharp & Dohme Corp. |
Inhibitors of the renal outer medullary potassium channel
|
SG11201504516PA
(en)
|
2012-12-11 |
2015-07-30 |
Takeda Pharmaceutical |
Heterocyclic compound
|
US9573961B2
(en)
|
2012-12-19 |
2017-02-21 |
Merck Sharp & Dohme Corp. |
Inhibitors of the renal outer medullary potassium channel
|
WO2014126944A2
(en)
|
2013-02-18 |
2014-08-21 |
Merck Sharp & Dohme Corp. |
Inhibitors of the renal outer medullary potassium channel
|
HUE034820T2
(en)
|
2013-02-28 |
2018-02-28 |
Janssen Sciences Ireland Uc |
Sulphamoyl arylamides and their use as medicaments for the treatment of hepatitis B
|
US9073921B2
(en)
|
2013-03-01 |
2015-07-07 |
Novartis Ag |
Salt forms of bicyclic heterocyclic derivatives
|
EP2970241A1
(en)
|
2013-03-12 |
2016-01-20 |
Actelion Pharmaceuticals Ltd. |
Azetidine amide derivatives as orexin receptor antagonists
|
WO2014165128A2
(en)
|
2013-03-12 |
2014-10-09 |
Novira Therapeutics, Inc. |
Hepatitis b antiviral agents
|
EP2968288B1
(en)
|
2013-03-15 |
2018-07-04 |
Merck Sharp & Dohme Corp. |
Inhibitors of the renal outer medullary potassium channel
|
ES2640063T3
(es)
|
2013-04-03 |
2017-10-31 |
Janssen Sciences Ireland Uc |
Derivados de n-fenil-carboxamida y su uso como medicamentos para el tratamiento de la hepatitis B
|
EP2803668A1
(en)
|
2013-05-17 |
2014-11-19 |
Boehringer Ingelheim International Gmbh |
Novel (cyano-dimethyl-methyl)-isoxazoles and -[1,3,4]thiadiazoles
|
JO3603B1
(ar)
|
2013-05-17 |
2020-07-05 |
Janssen Sciences Ireland Uc |
مشتقات سلفامويل بيرولاميد واستخدامها كادوية لمعالجة التهاب الكبد نوع بي
|
TR201807959T4
(tr)
|
2013-07-22 |
2018-06-21 |
Idorsia Pharmaceuticals Ltd |
1-(Piperazın-1-il)-2- ([1,2,4] triazol-1-il)-etanon türevleri.
|
JP6348978B2
(ja)
|
2013-07-25 |
2018-06-27 |
ヤンセン・サイエンシズ・アイルランド・ユーシー |
グリオキサミド置換ピロールアミド誘導体およびb型肝炎を処置するための医薬品としてのその使用
|
WO2015017305A1
(en)
|
2013-07-31 |
2015-02-05 |
Merck Sharp & Dohme Corp |
Inhibitors of the renal outer medullary potassium channel
|
WO2015018027A1
(en)
|
2013-08-08 |
2015-02-12 |
Merck Sharp & Dohme Corp. |
Thiazole orexin receptor antagonists
|
KR102103256B1
(ko)
|
2013-10-14 |
2020-04-23 |
에자이 알앤드디 매니지먼트 가부시키가이샤 |
선택적으로 치환된 퀴놀린 화합물
|
KR102365952B1
(ko)
|
2013-10-14 |
2022-02-22 |
에자이 알앤드디 매니지먼트 가부시키가이샤 |
선택적으로 치환된 퀴놀린 화합물
|
ES2655518T3
(es)
|
2013-10-23 |
2018-02-20 |
Janssen Sciences Ireland Uc |
Derivados de carboxamida y su uso como medicamentos para el tratamiento de la hepatitis B
|
US10231932B2
(en)
|
2013-11-12 |
2019-03-19 |
Vertex Pharmaceuticals Incorporated |
Process of preparing pharmaceutical compositions for the treatment of CFTR mediated diseases
|
AU2014358766B2
(en)
|
2013-12-04 |
2019-01-17 |
Idorsia Pharmaceuticals Ltd |
Use of benzimidazole-proline derivatives
|
US10392349B2
(en)
|
2014-01-16 |
2019-08-27 |
Novira Therapeutics, Inc. |
Azepane derivatives and methods of treating hepatitis B infections
|
US9169212B2
(en)
|
2014-01-16 |
2015-10-27 |
Novira Therapeutics, Inc. |
Azepane derivatives and methods of treating hepatitis B infections
|
US9181288B2
(en)
|
2014-01-16 |
2015-11-10 |
Novira Therapeutics, Inc. |
Azepane derivatives and methods of treating hepatitis B infections
|
KR20160128305A
(ko)
|
2014-02-05 |
2016-11-07 |
노비라 테라퓨틱스, 인코포레이티드 |
Hbv 감염의 치료를 위한 병용 요법
|
CN110483484A
(zh)
|
2014-02-06 |
2019-11-22 |
爱尔兰詹森科学公司 |
氨磺酰基吡咯酰胺衍生物及其作为药物用于治疗乙型肝炎的用途
|
AR099789A1
(es)
|
2014-03-24 |
2016-08-17 |
Actelion Pharmaceuticals Ltd |
Derivados de 8-(piperazin-1-il)-1,2,3,4-tetrahidro-isoquinolina
|
US9400280B2
(en)
|
2014-03-27 |
2016-07-26 |
Novira Therapeutics, Inc. |
Piperidine derivatives and methods of treating hepatitis B infections
|
CA2950589A1
(en)
|
2014-06-02 |
2015-12-10 |
Children's Medical Center Corporation |
Methods and compositions for immunomodulation
|
EP3682879B1
(en)
|
2014-09-29 |
2022-08-03 |
ChemoCentryx, Inc. |
Processes and intermediates in the preparation of c5ar antagonists
|
WO2016065584A1
(en)
*
|
2014-10-30 |
2016-05-06 |
Merck Sharp & Dohme Corp. |
Piperidine oxadiazole and thiadiazole orexin receptor antagonists
|
WO2016065585A1
(en)
*
|
2014-10-30 |
2016-05-06 |
Merck Sharp & Dohme Corp. |
Piperidine isoxazole and isothiazole orexin receptor antagonists
|
WO2016065586A1
(en)
*
|
2014-10-30 |
2016-05-06 |
Merck Sharp & Dohme Corp. |
Pyrazole, triazole and tetrazole orexin receptor antagonists
|
JP6494757B2
(ja)
|
2014-11-18 |
2019-04-03 |
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 |
ハイスループット試験高速液体クロマトグラフィーを行うプロセス
|
WO2016083863A1
(en)
|
2014-11-28 |
2016-06-02 |
Bial - Portela & Ca, S.A. |
Medicaments for slowing parkinson's disease
|
NZ734542A
(en)
|
2015-01-15 |
2023-02-24 |
Idorsia Pharmaceuticals Ltd |
Hydroxyalkyl-piperazine derivatives as cxcr3 receptor modulators
|
AR103399A1
(es)
|
2015-01-15 |
2017-05-10 |
Actelion Pharmaceuticals Ltd |
Derivados de (r)-2-metil-piperazina como moduladores del receptor cxcr3
|
WO2016127358A1
(en)
|
2015-02-12 |
2016-08-18 |
Merck Sharp & Dohme Corp. |
Inhibitors of renal outer medullary potassium channel
|
US9884831B2
(en)
|
2015-03-19 |
2018-02-06 |
Novira Therapeutics, Inc. |
Azocane and azonane derivatives and methods of treating hepatitis B infections
|
KR20190038677A
(ko)
*
|
2015-04-24 |
2019-04-08 |
화이자 인코포레이티드 |
1-((2r,4r)-2-(1h-벤조[d]이미다졸-2-일)-1-메틸피페리딘-4-일)-3-(4-시아노페닐)우레아 말레에이트의 결정질 형태
|
MA42508B1
(fr)
|
2015-06-03 |
2020-05-29 |
Hoffmann La Roche |
Dérivés d'éthynyle
|
US10875876B2
(en)
|
2015-07-02 |
2020-12-29 |
Janssen Sciences Ireland Uc |
Cyclized sulfamoylarylamide derivatives and the use thereof as medicaments for the treatment of hepatitis B
|
WO2017012502A1
(en)
|
2015-07-17 |
2017-01-26 |
Sunshine Lake Pharma Co., Ltd. |
Substituted quinazoline compounds and preparation and uses thereof
|
EP3356328A1
(en)
|
2015-09-29 |
2018-08-08 |
Novira Therapeutics, Inc. |
Crystalline forms of a hepatitis b antiviral agent
|
WO2017123716A1
(en)
|
2016-01-14 |
2017-07-20 |
Chemocentryx, Inc. |
Method of treating c3 glomerulopathy
|
EP3419980A4
(en)
|
2016-02-26 |
2019-07-03 |
The Board of Trustees of the Leland Stanford Junior University |
INHIBITORS OF PI-KINASE WITH ANTI-INFECTIOUS ACTIVITY
|
KR20180129943A
(ko)
|
2016-04-15 |
2018-12-05 |
노비라 테라퓨틱스, 인코포레이티드 |
캡시드 조립 억제제를 포함하는 배합물 및 방법
|
KR20210141778A
(ko)
|
2016-06-07 |
2021-11-23 |
자코바이오 파마슈티칼스 컴퍼니 리미티드 |
Shp2 억제제로서 유용한 신규한 헤테로환형 유도체
|
EP3375778A1
(en)
*
|
2017-03-14 |
2018-09-19 |
Artax Biopharma Inc. |
Aryl-piperidine derivatives
|
KR20220113545A
(ko)
|
2017-03-23 |
2022-08-12 |
자코바이오 파마슈티칼스 컴퍼니 리미티드 |
Shp2 억제제로서 유용한 신규한 헤테로환형 유도체
|
US11440922B2
(en)
*
|
2017-06-29 |
2022-09-13 |
Recordati Industria Chimica e Farmacentica S.p.A. |
Heterocyclylmethylidene derivatives and their use as modulators of mGluR5 receptors
|
JP7258009B2
(ja)
|
2017-07-10 |
2023-04-14 |
セルジーン コーポレイション |
抗増殖化合物及びその使用方法
|
BR112020003725A2
(pt)
|
2017-10-06 |
2020-11-03 |
Forma Therapeutics, Inc. |
inibição da peptidase 30 específica de ubiquitina
|
AU2019222644B2
(en)
|
2018-02-13 |
2021-04-01 |
Gilead Sciences, Inc. |
PD-1/PD-L1 inhibitors
|
CA3090125A1
(en)
|
2018-03-14 |
2019-09-19 |
Janssen Sciences Ireland Unlimited Company |
Capsid assembly modulator dosing regimen
|
CN112041311B
(zh)
|
2018-04-19 |
2023-10-03 |
吉利德科学公司 |
Pd-1/pd-l1抑制剂
|
JP7449242B2
(ja)
|
2018-05-17 |
2024-03-13 |
フォーマ セラピューティクス,インコーポレイテッド |
ユビキチン特異的ペプチダーゼ30(usp30)阻害剤として有用な縮合二環化合物
|
EP4234030A3
(en)
|
2018-07-13 |
2023-10-18 |
Gilead Sciences, Inc. |
Pd-1/pd-l1 inhibitors
|
SI3860989T1
(sl)
|
2018-10-05 |
2023-06-30 |
Forma Therapeutics, Inc. |
Kondenzirani pirolini,ki delujejo kot zaviralci ubikvitin-specifične proteaze (usp30)
|
TWI767148B
(zh)
|
2018-10-10 |
2022-06-11 |
美商弗瑪治療公司 |
抑制脂肪酸合成酶(fasn)
|
WO2020086556A1
(en)
|
2018-10-24 |
2020-04-30 |
Gilead Sciences, Inc. |
Pd-1/pd-l1 inhibitors
|
WO2020113094A1
(en)
|
2018-11-30 |
2020-06-04 |
Nuvation Bio Inc. |
Pyrrole and pyrazole compounds and methods of use thereof
|
WO2020154431A1
(en)
*
|
2019-01-25 |
2020-07-30 |
Lynch Kevin R |
Inhibitors of spinster homolog 2 (spns2) for use in therapy
|
CN113454077A
(zh)
|
2019-02-22 |
2021-09-28 |
爱尔兰詹森科学公司 |
用于治疗hbv感染或hbv诱发的疾病的酰胺衍生物
|
BR112021021454A2
(pt)
|
2019-05-06 |
2021-12-21 |
Janssen Sciences Ireland Unlimited Co |
Derivados de amida úteis no tratamento da infecção por hbv ou doenças induzidas por hbv
|
TWI829107B
(zh)
|
2019-07-09 |
2024-01-11 |
美商美國禮來大藥廠 |
大規模製備2,4,6-三氟-n-[6-(1-甲基-哌啶-4-羰基)-吡啶-2-基]-苯甲醯胺半琥珀酸鹽的方法及中間體,以及2,4,6-三氟-n-[6-(1-甲基-哌啶-4-羰基)-吡啶-2-基]-苯甲醯胺醋酸鹽之製備
|
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
|
JP2023509452A
(ja)
|
2020-01-03 |
2023-03-08 |
バーグ エルエルシー |
がんを処置するためのube2kモジュレータとしての多環式アミド
|
US20230373937A1
(en)
*
|
2020-09-09 |
2023-11-23 |
University Of Virginia Patent Foundation |
Inhibitors of spinster homolog 2 (spns2) for use in therapy
|
WO2022069953A1
(en)
*
|
2020-09-29 |
2022-04-07 |
Ranjith Siddaraj |
Synthesis and characterization of (s)-3-(5- fluoropyridin-2-yl)-5-(piperidin-3-yl)-l,2,4-oxadiazole derivatives and their secretory phospholipase a2 (spla2) inhibitor activity
|
PE20241335A1
(es)
|
2021-06-04 |
2024-07-03 |
Vertex Pharma |
N-(hidroxialquil (hetero)aril) tetrahidrofurano carboxamidas como moduladores de canales de sodio
|
EP4370160A1
(en)
|
2021-07-15 |
2024-05-22 |
President And Fellows Of Harvard College |
Compositions and methods relating to cells with adhered particles
|