US5420297A
(en)
*
|
1990-10-24 |
1995-05-30 |
Fujisawa Pharmaceutical Co., Ltd. |
Peptides having substance P antagonistic activity
|
US5610140A
(en)
*
|
1991-04-01 |
1997-03-11 |
Cortech, Inc. |
Bradykinin receptor antagonists with neurokinin receptor blocking activity
|
CA2110514A1
(en)
*
|
1991-07-05 |
1993-01-21 |
Raymond Baker |
Aromatic compounds, pharmaceutical compositions containing them and their use in therapy
|
US5654400A
(en)
*
|
1991-10-04 |
1997-08-05 |
Fujisawa Pharmaceutical Co., Ltd. |
Process for making peptide compounds having tachykinin antagonistic activity
|
AU2681392A
(en)
*
|
1991-11-12 |
1993-06-15 |
Pfizer Inc. |
Acyclic ethylenediamine derivatives as substance p receptor antagonists
|
GB9200535D0
(en)
*
|
1992-01-10 |
1992-02-26 |
Fujisawa Pharmaceutical Co |
New compound
|
JP3507494B2
(ja)
*
|
1992-08-13 |
2004-03-15 |
ワーナー−ランバート・コンパニー |
タキキニン拮抗薬
|
DE4243496A1
(de)
*
|
1992-09-03 |
1994-03-10 |
Boehringer Ingelheim Kg |
Neue Dipeptidderivate, Verfahren zu ihrer Herstellung und diese Verbindungen enthaltende pharmazeutische Zusammensetzungen
|
DK0610487T3
(da)
*
|
1992-09-03 |
2000-05-15 |
Boehringer Ingelheim Pharma |
Nye aminosyrederivater, fremgangsmåde til deres fremstilling og farmaceutiske præparater indeholdende disse forbindelser
|
FR2700472B1
(fr)
|
1993-01-19 |
1995-02-17 |
Rhone Poulenc Rorer Sa |
Association synergisante ayant un effet antagoniste des récepteurs NK1 et NK2.
|
WO1994020126A1
(en)
*
|
1993-03-03 |
1994-09-15 |
Fujisawa Pharmaceutical Co., Ltd. |
Use of peptides for the manufacture of a medicament
|
WO1995000536A1
(en)
*
|
1993-06-22 |
1995-01-05 |
Fujisawa Pharmaceutical Co., Ltd. |
Peptide compounds
|
KR960703621A
(ko)
*
|
1993-08-10 |
1996-08-31 |
후지야마 아키라 |
경피흡수 제제(Percutaneously absorbable preparation)
|
AU696167B2
(en)
*
|
1993-10-29 |
1998-09-03 |
Trustees Of Boston University |
Physiologically stable compositions of butyric acid, and butyric acid salts and derivatives as anti-neoplastic agents
|
US6403577B1
(en)
|
1993-11-17 |
2002-06-11 |
Eli Lilly And Company |
Hexamethyleneiminyl tachykinin receptor antagonists
|
ITFI940009A1
(it)
*
|
1994-01-19 |
1995-07-19 |
Menarini Farma Ind |
Antagonisti delle tachichinine, loro preparazione e formulazioni farmaceutiche che li contengono.
|
KR100344607B1
(ko)
*
|
1994-03-17 |
2002-11-20 |
후지레비오 가부시끼가이샤 |
아자펩티드유도체
|
FR2719312B1
(fr)
*
|
1994-04-28 |
1996-06-14 |
Adir |
Nouveau pseudopeptides dérivés de neurokinines, leur procédé de préparation et les compositions pharmaceutiques qui les contiennent.
|
EE9600186A
(et)
*
|
1994-05-07 |
1997-08-15 |
Boehringer Ingelheim Kg |
Neurokiniini (tahhüülkiniini) antagonistid
|
FR2728169A1
(fr)
|
1994-12-19 |
1996-06-21 |
Oreal |
Utilisation d'un antagoniste de substance p pour le traitement des prurits et des dysesthesies oculaires ou palpebrales
|
FR2728166A1
(fr)
|
1994-12-19 |
1996-06-21 |
Oreal |
Composition topique contenant un antagoniste de substance p
|
FR2728165A1
(fr)
|
1994-12-19 |
1996-06-21 |
Oreal |
Utilisation d'un antagoniste de substance p pour le traitement des rougeurs cutanees d'origine neurogene
|
US5966295A
(en)
*
|
1994-12-27 |
1999-10-12 |
Autonics Corporation |
Convertible flush or exposure type terminal board of control device
|
FR2741262B1
(fr)
|
1995-11-20 |
1999-03-05 |
Oreal |
Utilisation d'un antagoniste de tnf-alpha pour le traitement des rougeurs cutanees d'origine neurogene
|
GB9700597D0
(en)
*
|
1997-01-14 |
1997-03-05 |
Sandoz Pharma Uk |
Organic compounds
|
CA2287487A1
(en)
*
|
1997-04-24 |
1998-10-29 |
Merck Sharp & Dohme Limited |
Use of nk-1 receptor antagonists for treating eating disorders
|
US6903075B1
(en)
|
1997-05-29 |
2005-06-07 |
Merck & Co., Inc. |
Heterocyclic amide compounds as cell adhesion inhibitors
|
JP2002512625A
(ja)
*
|
1997-05-29 |
2002-04-23 |
メルク エンド カンパニー インコーポレーテッド |
細胞接着阻害薬としての複素環アミド化合物
|
GB9716457D0
(en)
*
|
1997-08-04 |
1997-10-08 |
Merck Sharp & Dohme |
Therapeutic agents
|
CA2298779A1
(en)
*
|
1997-08-04 |
1999-02-18 |
Merck Sharp & Dohme Limited |
Use of nk-1 receptor antagonists for treating aggressive behaviour disorders
|
GB9716463D0
(en)
*
|
1997-08-04 |
1997-10-08 |
Merck Sharp & Dohme |
Therapeutic agents
|
CA2298777A1
(en)
*
|
1997-08-04 |
1999-02-18 |
Merck Sharp & Dohme Limited |
Use of nk-1 receptor antagonists for treating mania
|
US6441131B1
(en)
*
|
1997-12-22 |
2002-08-27 |
Ono Pharmaceutical Co., Ltd. |
Peptides, method for assaying human pepsinogen II or human pepsin II, and assaying kit
|
CA2324426A1
(en)
*
|
1998-02-11 |
1999-08-19 |
Douglas V. Faller |
Compositions and methods for the treatment of cystic fibrosis
|
AU8059598A
(en)
*
|
1998-06-11 |
1999-12-30 |
Merck & Co., Inc. |
Heterocyclic amide compounds as cell adhesion inhibitors
|
GB9816897D0
(en)
*
|
1998-08-04 |
1998-09-30 |
Merck Sharp & Dohme |
Therapeutic use
|
US6307049B1
(en)
|
1998-09-30 |
2001-10-23 |
The Procter & Gamble Co. |
Heterocyclic 2-substituted ketoamides
|
US6300341B1
(en)
|
1998-09-30 |
2001-10-09 |
The Procter & Gamble Co. |
2-substituted heterocyclic sulfonamides
|
US6472418B1
(en)
|
1998-12-18 |
2002-10-29 |
Warner-Lambert Company |
Non-peptide NK1 receptors antagonists
|
KR100699404B1
(ko)
|
1999-02-18 |
2007-03-23 |
가켄 세야쿠 가부시키가이샤 |
성장 호르몬 분비촉진제로서의 신규 아미드 유도체
|
ATE387429T1
(de)
|
1999-11-03 |
2008-03-15 |
Amr Technology Inc |
Arly- und heteroaryl-substituierte tetrahydroisoquinoline und ihre verwendung als hemmer der wiederaufnahme von norepinephrin, dopamin und serotonin
|
US7163949B1
(en)
|
1999-11-03 |
2007-01-16 |
Amr Technology, Inc. |
4-phenyl substituted tetrahydroisoquinolines and use thereof
|
EP1299393A2
(en)
|
2000-07-11 |
2003-04-09 |
Bristol-Myers Squibb Pharma Company |
4-phenyl substituted tetrahydroisoquinolines and therapeutic use thereof
|
KR100960802B1
(ko)
|
2003-03-08 |
2010-06-01 |
주식회사유한양행 |
씨형 간염바이러스 감염 치료용 엔에스3 프로테아제 억제제
|
WO2005073195A2
(en)
|
2004-01-30 |
2005-08-11 |
Medivir Ab |
Hcv ns-3 serine protease inhibitors
|
CA2573271C
(en)
|
2004-07-15 |
2015-10-06 |
Amr Technology, Inc. |
Aryl-and heteroaryl-substituted tetrahydroisoquinolines and use thereof to block reuptake of norepinephrine, dopamine, and serotonin
|
WO2006123182A2
(en)
|
2005-05-17 |
2006-11-23 |
Merck Sharp & Dohme Limited |
Cyclohexyl sulphones for treatment of cancer
|
BRPI0613403A2
(pt)
|
2005-07-15 |
2009-02-10 |
Amr Technology Inc |
tetrahidrobenzodiazepinas aril- e heteroarila-substituÍdas e uso das mesmas para bloquear a recaptaÇço de norepinefrina, dopamina e serotonina
|
PE20070211A1
(es)
|
2005-07-29 |
2007-05-12 |
Medivir Ab |
Compuestos macrociclicos como inhibidores del virus de hepatitis c
|
GB0603041D0
(en)
|
2006-02-15 |
2006-03-29 |
Angeletti P Ist Richerche Bio |
Therapeutic compounds
|
US20110218176A1
(en)
|
2006-11-01 |
2011-09-08 |
Barbara Brooke Jennings-Spring |
Compounds, methods, and treatments for abnormal signaling pathways for prenatal and postnatal development
|
EP2336120B1
(en)
|
2007-01-10 |
2014-07-16 |
MSD Italia S.r.l. |
Combinations containing amide substituted indazoles as poly(adp-ribose)polymerase (parp) inhibitors
|
BRPI0807972A2
(pt)
|
2007-01-24 |
2014-06-10 |
Glaxo Group Ltd |
Composições farmacêuticas compreendendo 3,5-diamino-6-(2,3-diclofenil)-l,2,4-triazina ou r(-)-2,4-diamino-5-(2,3-diclorofenil)-6-fluorometilpirim idina e uma nk1
|
US8389553B2
(en)
|
2007-06-27 |
2013-03-05 |
Merck Sharp & Dohme Corp. |
4-carboxybenzylamino derivatives as histone deacetylase inhibitors
|
AR071997A1
(es)
|
2008-06-04 |
2010-07-28 |
Bristol Myers Squibb Co |
Forma cristalina de 6-((4s)-2-metil-4-(2-naftil)-1,2,3,4-tetrahidroisoquinolin-7-il)piridazin-3-amina
|
US9156812B2
(en)
|
2008-06-04 |
2015-10-13 |
Bristol-Myers Squibb Company |
Crystalline form of 6-[(4S)-2-methyl-4-(2-naphthyl)-1,2,3,4-tetrahydroisoquinolin-7-yl]pyridazin-3-amine
|
UA105182C2
(ru)
|
2008-07-03 |
2014-04-25 |
Ньюрексон, Інк. |
Бензоксазины, бензотиазины и родственные соединения, которые имеют ингибирующую nos активность
|
WO2010105112A1
(en)
*
|
2009-03-11 |
2010-09-16 |
Hemaquest Pharmaceuticals, Inc. |
Detection of short-chain fatty acids in biological samples
|
SG174389A1
(en)
|
2009-03-17 |
2011-10-28 |
Daiichi Sankyo Co Ltd |
Amide derivative
|
US8691825B2
(en)
|
2009-04-01 |
2014-04-08 |
Merck Sharp & Dohme Corp. |
Inhibitors of AKT activity
|
ES2662072T3
(es)
|
2009-05-12 |
2018-04-05 |
Albany Molecular Research, Inc. |
7-([1,2,4]triazolo[1,5-a]piridin-6-il)-4-(3,4-diclorofenil)-1,2,3,4-tetrahidroisoquinolina y uso de la misma
|
EP2429295B1
(en)
|
2009-05-12 |
2013-12-25 |
Albany Molecular Research, Inc. |
Aryl, heteroaryl, and heterocycle substituted tetrahydroisoquinolines and use thereof
|
JP5739415B2
(ja)
|
2009-05-12 |
2015-06-24 |
ブリストル−マイヤーズ スクウィブ カンパニー |
(S)−7−([1,2,4]トリアゾロ[1,5−a]ピリジン−6−イル)−4−(3,4−ジクロロフェニル)−1,2,3,4−テトラヒドロイソキノリンの結晶形態およびその使用
|
WO2011038224A1
(en)
|
2009-09-24 |
2011-03-31 |
Trustees Of Boston University |
Methods for treating viral disorders
|
KR101485645B1
(ko)
|
2009-10-14 |
2015-01-22 |
머크 샤프 앤드 돔 코포레이션 |
p53 활성을 증가시키는 치환된 피페리딘 및 그의 용도
|
EP2509418A4
(en)
|
2009-12-08 |
2013-03-20 |
Hemaquest Pharmaceuticals Inc |
METHODS AND REGIMES AT LOW DOSE FOR TREATING RED GLOBULAR DISORDERS
|
WO2011113013A2
(en)
|
2010-03-11 |
2011-09-15 |
Hemaquest Pharmaceuticals, Inc. |
Methods and compositions for treating viral or virally-induced conditions
|
CN107090456B
(zh)
|
2010-08-02 |
2022-01-18 |
瑟纳治疗公司 |
使用短干扰核酸的RNA干扰介导的联蛋白(钙粘蛋白关联蛋白质),β1基因表达的抑制
|
EP4079856A1
(en)
|
2010-08-17 |
2022-10-26 |
Sirna Therapeutics, Inc. |
Rna interference mediated inhibition of hepatitis b virus (hbv) gene expression using short interfering nucleic acid (sina)
|
EP2608669B1
(en)
|
2010-08-23 |
2016-06-22 |
Merck Sharp & Dohme Corp. |
NOVEL PYRAZOLO[1,5-a]PYRIMIDINE DERIVATIVES AS mTOR INHIBITORS
|
WO2012030685A2
(en)
|
2010-09-01 |
2012-03-08 |
Schering Corporation |
Indazole derivatives useful as erk inhibitors
|
EP2615916B1
(en)
|
2010-09-16 |
2017-01-04 |
Merck Sharp & Dohme Corp. |
Fused pyrazole derivatives as novel erk inhibitors
|
WO2012058210A1
(en)
|
2010-10-29 |
2012-05-03 |
Merck Sharp & Dohme Corp. |
RNA INTERFERENCE MEDIATED INHIBITION OF GENE EXPRESSION USING SHORT INTERFERING NUCLEIC ACIDS (siNA)
|
EP2654748B1
(en)
|
2010-12-21 |
2016-07-27 |
Merck Sharp & Dohme Corp. |
Indazole derivatives useful as erk inhibitors
|
US20140045847A1
(en)
|
2011-04-21 |
2014-02-13 |
Piramal Enterprises Limited |
Crystalline form of a salt of a morpholino sulfonyl indole derivative and a process for its preparation
|
EP2770987B1
(en)
|
2011-10-27 |
2018-04-04 |
Merck Sharp & Dohme Corp. |
Novel compounds that are erk inhibitors
|
EP2844261B1
(en)
|
2012-05-02 |
2018-10-17 |
Sirna Therapeutics, Inc. |
SHORT INTERFERING NUCLEIC ACID (siNA) COMPOSITIONS
|
EP2900241B1
(en)
|
2012-09-28 |
2018-08-08 |
Merck Sharp & Dohme Corp. |
Novel compounds that are erk inhibitors
|
SI2925888T1
(en)
|
2012-11-28 |
2018-02-28 |
Merck Sharp & Dohme Corp. |
Compounds and methods for the treatment of cancer
|
RU2690663C2
(ru)
|
2012-12-20 |
2019-06-05 |
Мерк Шарп И Доум Корп. |
Замещенные имидазопиридины в качестве ингибиторов hdm2
|
US9540377B2
(en)
|
2013-01-30 |
2017-01-10 |
Merck Sharp & Dohme Corp. |
2,6,7,8 substituted purines as HDM2 inhibitors
|
EP3041938A1
(en)
|
2013-09-03 |
2016-07-13 |
Moderna Therapeutics, Inc. |
Circular polynucleotides
|
US10947234B2
(en)
|
2017-11-08 |
2021-03-16 |
Merck Sharp & Dohme Corp. |
PRMT5 inhibitors
|
EP3833668A4
(en)
|
2018-08-07 |
2022-05-11 |
Merck Sharp & Dohme Corp. |
PRMT5 INHIBITORS
|
US11981701B2
(en)
|
2018-08-07 |
2024-05-14 |
Merck Sharp & Dohme Llc |
PRMT5 inhibitors
|
EP3976198A4
(en)
|
2019-05-31 |
2023-07-19 |
Viracta Subsidiary, Inc. |
METHODS OF TREATMENT OF VIRAL ASSOCIATED CANCER WITH HISTONE DEACETYLASE INHIBITORS
|