US5354768A
(en)
*
|
1988-07-26 |
1994-10-11 |
Sankyo Company, Limited |
Use of imidazopyrazole derivatives as analgesics and anti-inflammatory agents
|
US6277969B1
(en)
*
|
1991-03-18 |
2001-08-21 |
New York University |
Anti-TNF antibodies and peptides of human tumor necrosis factor
|
US5356897A
(en)
*
|
1991-09-09 |
1994-10-18 |
Fujisawa Pharmaceutical Co., Ltd. |
3-(heteroaryl)-pyrazololi[1,5-a]pyrimidines
|
GB9303993D0
(en)
*
|
1993-02-26 |
1993-04-14 |
Fujisawa Pharmaceutical Co |
New heterocyclic derivatives
|
TW256831B
(zh)
*
|
1993-04-22 |
1995-09-11 |
Senju Pharma Co |
|
KR100228949B1
(ko)
*
|
1993-07-06 |
1999-11-01 |
디. 제이. 우드, 스피겔 알렌 제이 |
이환상 테트라하이드로 피라졸로피리딘
|
US6642268B2
(en)
|
1994-09-13 |
2003-11-04 |
G.D. Searle & Co. |
Combination therapy employing ileal bile acid transport inhibiting benzothipines and HMG Co-A reductase inhibitors
|
US6262277B1
(en)
|
1994-09-13 |
2001-07-17 |
G.D. Searle And Company |
Intermediates and processes for the preparation of benzothiepines having activity as inhibitors of ileal bile acid transport and taurocholate uptake
|
US6268392B1
(en)
|
1994-09-13 |
2001-07-31 |
G. D. Searle & Co. |
Combination therapy employing ileal bile acid transport inhibiting benzothiepines and HMG Co-A reductase inhibitors
|
US6228871B1
(en)
|
1995-07-10 |
2001-05-08 |
Merck & Co., Inc. |
Angiogenesis inhibitors
|
CA2252536C
(en)
|
1996-04-25 |
2010-04-06 |
Nissan Chemical Industries, Ltd. |
Ethylene derivatives and pesticides containing said derivatives
|
FR2750048B1
(fr)
*
|
1996-06-21 |
1998-08-14 |
Oreal |
Compositions de teinture des fibres keratiniques contenant des derives pyrazolo-(1, 5-a)-pyrimidine, procede de teinture, nouveaux derives pyrazolo-(1, 5-a)-pyrimidine et leur procede de preparation
|
EP0912548A1
(en)
|
1996-07-11 |
1999-05-06 |
Pfizer Inc. |
Pyridylpyrrole compounds useful as interleukin- and tnf antagonists
|
US6313124B1
(en)
|
1997-07-23 |
2001-11-06 |
Dupont Pharmaceuticals Company |
Tetrazine bicyclic compounds
|
US6191131B1
(en)
|
1997-07-23 |
2001-02-20 |
Dupont Pharmaceuticals Company |
Azolo triazines and pyrimidines
|
US7094782B1
(en)
|
1996-07-24 |
2006-08-22 |
Bristol-Myers Squibb Company |
Azolo triazines and pyrimidines
|
US6124289A
(en)
*
|
1996-07-24 |
2000-09-26 |
Dupont Pharmaceuticals Co. |
Azolo triazines and pyrimidines
|
HU229024B1
(en)
*
|
1996-07-24 |
2013-07-29 |
Bristol Myers Squibb Pharma Co |
Azolo-pyridimidines, pharmaceutical compositions containing the same and use thereof
|
US6060478A
(en)
*
|
1996-07-24 |
2000-05-09 |
Dupont Pharmaceuticals |
Azolo triazines and pyrimidines
|
CA2259583C
(en)
*
|
1996-07-24 |
2009-11-17 |
Du Pont Pharmaceuticals Company |
Azolo triazines and pyrimidines
|
US6087496A
(en)
*
|
1998-05-22 |
2000-07-11 |
G. D. Searle & Co. |
Substituted pyrazoles suitable as p38 kinase inhibitors
|
EP0983260A2
(en)
*
|
1997-05-22 |
2000-03-08 |
G.D. Searle & Co. |
3(5)-HETEROARYL SUBSTITUTED PYRAZOLES AS p38 KINASE INHIBITORS
|
AU7726898A
(en)
|
1997-05-22 |
1998-12-11 |
G.D. Searle & Co. |
Pyrazole derivatives as p38 kinase inhibitors
|
US6514977B1
(en)
|
1997-05-22 |
2003-02-04 |
G.D. Searle & Company |
Substituted pyrazoles as p38 kinase inhibitors
|
US6979686B1
(en)
|
2001-12-07 |
2005-12-27 |
Pharmacia Corporation |
Substituted pyrazoles as p38 kinase inhibitors
|
US6235741B1
(en)
*
|
1997-05-30 |
2001-05-22 |
Merck & Co., Inc. |
Angiogenesis inhibitors
|
JP2001521934A
(ja)
*
|
1997-11-03 |
2001-11-13 |
ベーリンガー インゲルハイム ファーマシューティカルズ インコーポレイテッド |
抗炎症薬としての芳香族ヘテロ環式化合物
|
EP1473292A1
(en)
*
|
1997-11-03 |
2004-11-03 |
Boehringer Ingelheim Pharmaceuticals, Inc. |
Aromatic heterocyclic compounds as anti-inflammatory agents
|
US6380203B1
(en)
*
|
1998-01-14 |
2002-04-30 |
Merck & Co., Inc. |
Angiogenesis inhibitors
|
WO2000038721A1
(en)
|
1998-12-23 |
2000-07-06 |
G.D. Searle Llc |
Combinations of cholesteryl ester transfer protein inhibitors and nicotinic acid derivatives for cardiovascular indications
|
US6569905B1
(en)
|
1998-12-23 |
2003-05-27 |
G.D. Searle, Llc |
Combinations of cholesteryl ester transfer protein inhibitors and bile acid sequestering agents for cardiovascular indications
|
DE69907960T2
(de)
|
1998-12-23 |
2004-02-26 |
G.D. Searle Llc, Chicago |
Kombinationen von ileumgallensäuretransports inhibitoren und fibronsäure derivaten für kardiovaskuläre indikationen
|
JP2002533414A
(ja)
|
1998-12-23 |
2002-10-08 |
ジー.ディー.サール エルエルシー |
心臓血管に適用するための回腸胆汁酸輸送阻害剤および胆汁酸隔離剤の組み合わせ
|
AU2157400A
(en)
|
1998-12-23 |
2000-07-31 |
G.D. Searle & Co. |
Combinations of cholesteryl ester transfer protein inhibitors and hmg coa reductase inhibitors for cardiovascular indications
|
ES2200587T3
(es)
|
1998-12-23 |
2004-03-01 |
G.D. Searle Llc |
Combinaciones de inhibidors del transporte de acidos biliares del ileon e inhibidores de la proteina de transferencia de colesteril ester para indicaciones cardiovasculares.
|
EA009466B1
(ru)
|
1998-12-23 |
2007-12-28 |
Джи.Ди. Сирл Ллс |
Ингибитор белка, переносящего эфир холестерила
|
AU4331500A
(en)
|
1999-04-06 |
2000-10-23 |
Du Pont Pharmaceuticals Company |
Pyrazolotriazines as crf antagonists
|
WO2000059908A2
(en)
|
1999-04-06 |
2000-10-12 |
Du Pont Pharmaceuticals Company |
Pyrazolopyrimidines as crf antagonists
|
CN1222520C
(zh)
*
|
1999-08-12 |
2005-10-12 |
沃泰克斯药物股份有限公司 |
c-JUN N-末端激酶(JNK)和其它蛋白激酶的抑制剂
|
AU2006203676B2
(en)
*
|
1999-08-13 |
2010-04-22 |
Vertex Pharmaceuticals Incorporated |
Inhibitors of c-JUN N-Terminal Kinases (JNK) and Other Protein Kinases
|
CA2379421A1
(en)
*
|
1999-08-27 |
2001-03-08 |
Abbott Laboratories |
Sulfonylphenylpyrazole compounds useful as cox-2 inhibitors
|
US6472416B1
(en)
|
1999-08-27 |
2002-10-29 |
Abbott Laboratories |
Sulfonylphenylpyrazole compounds useful as COX-2 inhibitors
|
EP1208748A4
(en)
*
|
1999-08-31 |
2002-11-20 |
Fujisawa Pharmaceutical Co |
PRESERVATIVES FOR ORGANS
|
IL148905A0
(en)
*
|
1999-09-30 |
2002-09-12 |
Neurogen Corp Pfizer Inc |
Certain alkylene diamine-substituted pyrazolo{1,5,-a}-1,5-pyrimidines and pyrazolo{1,5,-a}-1,3,5-triazines
|
EP1286984A2
(en)
|
2000-03-10 |
2003-03-05 |
Pharmacia Corporation |
Method for the preparation of tetrahydrobenzothiepines
|
US6630476B2
(en)
|
2000-07-07 |
2003-10-07 |
Bristol-Myers Squibb Pharma Company |
Pyrrolo [3,4-d] pyrimidines as corticotropin releasing factor (CRF) antagonists
|
DE10153344A1
(de)
*
|
2001-10-29 |
2003-05-15 |
Gruenenthal Gmbh |
Verwendung von substituierten Pyrazolopyrimidinen als Liganden von Nucleosid-Transport-Proteinen und/oder von Purinorezeptoren
|
DE60221392T2
(de)
*
|
2001-05-24 |
2008-04-17 |
Eli Lilly And Co., Indianapolis |
Neue pyrrolderivate als pharmazeutische mittel
|
WO2003004497A1
(fr)
*
|
2001-07-05 |
2003-01-16 |
Sumitomo Pharmaceuticals Company, Limited |
Compose heterocyclique
|
US6740663B2
(en)
|
2001-11-02 |
2004-05-25 |
G.D. Searle, Llc |
Mono- and di-fluorinated benzothiepine compounds as inhibitors of apical sodium co-dependent bile acid transport (ASBT) and taurocholate uptake
|
WO2003053976A1
(en)
*
|
2001-12-20 |
2003-07-03 |
Biovitrum Ab |
PIPAZOLO [1,5-a] PYRIMIDINE DERIVATIVES AS MODULATORS OF PPAR
|
US6852753B2
(en)
|
2002-01-17 |
2005-02-08 |
Pharmacia Corporation |
Alkyl/aryl hydroxy or keto thiepine compounds as inhibitors of apical sodium co-dependent bile acid transport (ASBT) and taurocholate uptake
|
WO2003095455A2
(en)
*
|
2002-05-10 |
2003-11-20 |
Smithkline Beecham Corporation |
Substituted pyrazolopyrimidines
|
CZ293015B6
(cs)
*
|
2002-10-25 |
2004-01-14 |
Léčiva, A.S. |
Způsob výroby N-ethyl-N-[3-(3-methyl-pyrazolo[1,5-a]pyrimidin-7-yl)-fenyl]-acetamidu (zaleplonu)
|
JP2006522735A
(ja)
*
|
2002-11-21 |
2006-10-05 |
イーライ リリー アンド カンパニー |
ミックス系統キナーゼモジュレータ
|
UA80571C2
(en)
*
|
2002-11-22 |
2007-10-10 |
Lilly Co Eli |
Quinolinyl-pyrrolopyrazoles
|
WO2004110454A1
(ja)
*
|
2003-06-13 |
2004-12-23 |
Ishihara Sangyo Kaisha, Ltd. |
アデノシンA2a受容体アゴニストの投与が必要な疾患を治療又は予防するための組成物
|
DE10332487A1
(de)
*
|
2003-07-16 |
2005-02-10 |
Boehringer Ingelheim Pharma Gmbh & Co. Kg |
Ambroxol für die Behandlung von chronisch nozizeptiven Schmerzen
|
US7511065B2
(en)
|
2003-11-12 |
2009-03-31 |
Eli Lilly And Company |
Mixed lineage kinase modulators
|
US20110104186A1
(en)
|
2004-06-24 |
2011-05-05 |
Nicholas Valiante |
Small molecule immunopotentiators and assays for their detection
|
TW200639163A
(en)
|
2005-02-04 |
2006-11-16 |
Genentech Inc |
RAF inhibitor compounds and methods
|
JP5178515B2
(ja)
|
2005-08-12 |
2013-04-10 |
シンタ ファーマシューティカルズ コーポレーション |
Hsp90活性を調節するピラゾール化合物
|
EP1919919A1
(en)
*
|
2005-09-01 |
2008-05-14 |
Astellas Pharma Inc. |
Pyridazinone derivatives used for the treatment of pain
|
WO2007129195A2
(en)
*
|
2006-05-04 |
2007-11-15 |
Pfizer Products Inc. |
4-pyrimidine-5-amino-pyrazole compounds
|
TW200800260A
(en)
*
|
2006-05-25 |
2008-01-01 |
Synta Pharmaceuticals Corp |
Method for treating proliferative disorders associated with protooncogene products
|
JP2010540451A
(ja)
*
|
2007-09-20 |
2010-12-24 |
ワイス・エルエルシー |
ピラゾロ[5,1−c][1,2,4]トリアジン、その調製法および使用法
|
JP2011506465A
(ja)
*
|
2007-12-12 |
2011-03-03 |
イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー |
殺菌性二環式ピラゾール
|
US8809344B2
(en)
|
2008-10-29 |
2014-08-19 |
Apath, Llc |
Compounds, compositions, and methods for control of hepatitis C viral infections
|
ES2540867T3
(es)
*
|
2010-02-26 |
2015-07-14 |
Mitsubishi Tanabe Pharma Corporation |
Compuestos de pirazolopirimidina y su uso como inhibidores de PDE10
|
US9205086B2
(en)
|
2010-04-19 |
2015-12-08 |
Synta Pharmaceuticals Corp. |
Cancer therapy using a combination of a Hsp90 inhibitory compounds and a EGFR inhibitor
|
EP2402345A1
(en)
*
|
2010-06-29 |
2012-01-04 |
Basf Se |
Pyrazole fused bicyclic compounds
|
EP2402344A1
(en)
*
|
2010-06-29 |
2012-01-04 |
Basf Se |
Pyrazole fused bicyclic compounds
|
EP2402339A1
(en)
*
|
2010-06-29 |
2012-01-04 |
Basf Se |
Pyrazolopyridine compounds
|
MX355016B
(es)
|
2011-10-06 |
2018-04-02 |
Bayer Ip Gmbh |
Heterociclilpiri(mi)dinilpirazoles como fungicidas.
|
AU2012332421A1
(en)
|
2011-11-02 |
2014-06-05 |
Synta Pharmaceuticals Corp. |
Cancer therapy using a combination of Hsp90 inhibitors with topoisomerase I inhibitors
|
WO2013067165A1
(en)
|
2011-11-02 |
2013-05-10 |
Synta Pharmaceuticals Corp. |
Combination therapy of hsp90 inhibitors with platinum-containing agents
|
WO2013074594A1
(en)
|
2011-11-14 |
2013-05-23 |
Synta Pharmaceuticals Corp. |
Combination therapy of hsp90 inhibitors with braf inhibitors
|
JO3407B1
(ar)
|
2012-05-31 |
2019-10-20 |
Eisai R&D Man Co Ltd |
مركبات رباعي هيدرو بيرازولو بيريميدين
|
JP6449845B2
(ja)
|
2013-03-15 |
2019-01-09 |
クロモセル コーポレイション |
疼痛の処置のためのナトリウムチャネルモジュレーター
|
US9505767B2
(en)
|
2013-09-05 |
2016-11-29 |
Genentech, Inc. |
Pyrazolo[1,5-A]pyrimidin-7(4H)-onehistone demethylase inhibitors
|
KR20160054570A
(ko)
|
2013-09-10 |
2016-05-16 |
크로모셀 코포레이션 |
통증과 당뇨병의 치료를 위한 나트륨 통로 조절인자
|
CN106132967B
(zh)
*
|
2014-03-27 |
2019-05-28 |
詹森药业有限公司 |
作为ros1抑制剂的化合物
|
MX367914B
(es)
|
2014-03-27 |
2019-09-11 |
Janssen Pharmaceutica Nv |
Derivados de 4,5,6,7-tetrahidro-pirazolo[1,5-a]pirazina sustituidos y derivados de 5,6,7,8-tetrahidro-4h-pirazolo[1,5-a][1 ,4]diazepina como inhibidores de ros1.
|
CN104140427A
(zh)
*
|
2014-07-05 |
2014-11-12 |
湖南华腾制药有限公司 |
一种四氢吡唑并[1,5-a]嘧啶的制备方法
|
EP3193610A4
(en)
*
|
2014-09-09 |
2018-04-04 |
Chromocell Corporation |
Selective nav1.7 inhibitors for the treatment of diabetes
|
KR102384652B1
(ko)
*
|
2015-02-03 |
2022-04-27 |
솔루스첨단소재 주식회사 |
유기 화합물 및 이를 포함하는 유기 전계 발광 소자
|
WO2018045071A1
(en)
|
2016-08-31 |
2018-03-08 |
Agios Pharmaceuticals, Inc. |
Inhibitors of cellular metabolic processes
|
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
|
MX2023001688A
(es)
|
2020-08-12 |
2023-02-22 |
Spruce Biosciences Inc |
Metodos y composiciones para tratar el sindrome de ovario poliquistico.
|
PE20241335A1
(es)
|
2021-06-04 |
2024-07-03 |
Vertex Pharma |
N-(hidroxialquil (hetero)aril) tetrahidrofurano carboxamidas como moduladores de canales de sodio
|