JP2006504738A5 - - Google Patents

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Publication number
JP2006504738A5
JP2006504738A5 JP2004543386A JP2004543386A JP2006504738A5 JP 2006504738 A5 JP2006504738 A5 JP 2006504738A5 JP 2004543386 A JP2004543386 A JP 2004543386A JP 2004543386 A JP2004543386 A JP 2004543386A JP 2006504738 A5 JP2006504738 A5 JP 2006504738A5
Authority
JP
Japan
Prior art keywords
alkyl
alkynyl
alkenyl
compound
compound according
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP2004543386A
Other languages
English (en)
Japanese (ja)
Other versions
JP2006504738A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2003/031592 external-priority patent/WO2004033444A1/en
Publication of JP2006504738A publication Critical patent/JP2006504738A/ja
Publication of JP2006504738A5 publication Critical patent/JP2006504738A5/ja
Pending legal-status Critical Current

Links

JP2004543386A 2002-10-07 2003-10-07 L型カルシウムチャンネルを遮断し、かつホスホジエステラーゼ3型活性を阻害する同時能力を有するジヒドロピリジン化合物 Pending JP2006504738A (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US41625402P 2002-10-07 2002-10-07
PCT/US2003/031592 WO2004033444A1 (en) 2002-10-07 2003-10-07 Dihydropyridine compounds having simultaneous ability to block l-type calcium channels and to inhibit phosphodiesterase type 3 activity

Publications (2)

Publication Number Publication Date
JP2006504738A JP2006504738A (ja) 2006-02-09
JP2006504738A5 true JP2006504738A5 (enExample) 2006-11-24

Family

ID=32093831

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2004543386A Pending JP2006504738A (ja) 2002-10-07 2003-10-07 L型カルシウムチャンネルを遮断し、かつホスホジエステラーゼ3型活性を阻害する同時能力を有するジヒドロピリジン化合物

Country Status (14)

Country Link
US (1) US7098211B2 (enExample)
EP (1) EP1554267A1 (enExample)
JP (1) JP2006504738A (enExample)
KR (1) KR20050070036A (enExample)
CN (1) CN1720243A (enExample)
AU (1) AU2003275450A1 (enExample)
BR (1) BR0315103A (enExample)
CA (1) CA2501534A1 (enExample)
MX (1) MXPA05003640A (enExample)
NO (1) NO20052169L (enExample)
PL (1) PL376405A1 (enExample)
RU (1) RU2005110062A (enExample)
WO (1) WO2004033444A1 (enExample)
ZA (1) ZA200502711B (enExample)

Families Citing this family (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7094806B2 (en) * 2000-07-07 2006-08-22 Trustees Of Tufts College 7, 8 and 9-substituted tetracycline compounds
WO2005016885A2 (en) * 2003-08-14 2005-02-24 Artesian Therapeutics, Inc. COMPOUNDS WITH COMBINED CALCIUM CHANNEL BLOCKER AND β-ADRENERGIC ANTAGONIST OR PARTIAL AGONIST ACTIVITIES FOR TREATMENT OF HEART DISEASE
WO2005035505A2 (en) * 2003-09-30 2005-04-21 Artesian Therapeutics, Inc. Compounds with phosphodiesterase inhibiting and calcium channel blocking activities
DE102004011512B4 (de) 2004-03-08 2022-01-13 Boehringer Ingelheim Vetmedica Gmbh Pharmazeutische Zubereitung enthaltend Pimobendan
EP1579862A1 (en) 2004-03-25 2005-09-28 Boehringer Ingelheim Vetmedica Gmbh Use of PDE III inhibitors for the reduction of heart size in mammals suffering from heart failure
US8980894B2 (en) 2004-03-25 2015-03-17 Boehringer Ingelheim Vetmedica Gmbh Use of PDE III inhibitors for the treatment of asymptomatic (occult) heart failure
KR20070087602A (ko) * 2004-12-13 2007-08-28 아이알엠 엘엘씨 화합물 및 스테로이드성 수용체 및 칼슘 채널 활성의조절제로서의 조성물
NL1028564C2 (nl) * 2005-03-17 2006-09-20 Rademaker Holding B V Toepassing van een coumarine-groep omvattende derivaten voor de bereiding van een antiviraal middel, coumarine-group omvattende derivaten, een werkwijze voor de bereiding daarvan, en farmaceutische preparaten die deze bevatten.
EP1920785A1 (en) 2006-11-07 2008-05-14 Boehringer Ingelheim Vetmedica Gmbh Liquid preparation comprising a complex of pimobendan and cyclodextrin
CN101215258A (zh) * 2008-01-21 2008-07-09 中国药科大学 二氢吡啶类钙拮抗剂化合物及其制备方法与医药用途
EP2294062B1 (en) 2008-06-09 2013-08-21 Bayer Intellectual Property GmbH Substituted 4- (indazolyl) -1,4-dihydropyridines and methods of use thereof
US8664252B2 (en) * 2008-11-25 2014-03-04 Boehringer Ingelheim Vetmedica Gmbh Phosphodiesterase type III (PDE III) inhibitors or CA2+-sensitizing agents for the treatment of hypertrophic cardiomyopathy
EP2509596B1 (en) 2009-12-08 2019-08-28 Case Western Reserve University Gamma aminoacids for treating ocular disorders
GB201017783D0 (en) * 2010-10-21 2010-12-01 Shire Llc Process for the preparation of anagrelide and analogues thereof
ES2924478T3 (es) 2012-03-15 2022-10-07 Boehringer Ingelheim Vetmedica Gmbh Formulación de comprimidos farmacéuticos para el sector médico veterinario, método de producción y uso de los mismos
PL3021832T3 (pl) 2013-07-19 2021-08-23 Boehringer Ingelheim Vetmedica Gmbh Konserwowana ciekła wodna kompozycja farmaceutyczna zawierająca eteryfikowane pochodne cyklodekstryny
BR122019024673B1 (pt) 2013-12-04 2023-04-11 Boehringer Ingelheim Vetmedica Gmbh Composições farmacêuticas aprimoradas de pimobendan
US10537570B2 (en) 2016-04-06 2020-01-21 Boehringer Ingelheim Vetmedica Gmbh Use of pimobendan for the reduction of heart size and/or the delay of onset of clinical symptoms in patients with asymptomatic heart failure due to mitral valve disease
TWI903299B (zh) 2018-03-08 2025-11-01 美商英塞特公司 作為PI3K-γ抑制劑之胺基吡嗪二醇化合物
WO2020010003A1 (en) 2018-07-02 2020-01-09 Incyte Corporation AMINOPYRAZINE DERIVATIVES AS PI3K-γ INHIBITORS
CN115838351B (zh) * 2022-12-06 2025-01-28 昆明理工大学 4-烷基-1,4-二氢吡啶化合物及其制备方法和应用
CN116693454A (zh) * 2023-06-06 2023-09-05 中山大学 一种取代氰基喹啉酮类化合物及其制备方法与应用

Family Cites Families (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57200386A (en) * 1981-06-04 1982-12-08 Yoshitomi Pharmaceut Ind Ltd Novel 1,4-dihydropyridine-3,5-dicarboxylic ester derivative and its salts
CH655110A5 (de) * 1982-09-03 1986-03-27 Otsuka Pharma Co Ltd Carbostyrilderivate, verfahren zu deren herstellung und arzneimittel, welche diese enthalten.
PT77842B (en) * 1982-12-21 1986-05-05 Pfizer Process for preparing dihydropyridines
GB8306666D0 (en) * 1983-03-10 1983-04-13 Pfizer Ltd Therapeutic agents
US4568677A (en) * 1983-07-23 1986-02-04 Pfizer Inc. 2-(4-Pyrimidone alkoxyalkyl) dihydropyridine anti-ischaemic and antihypertensive agents
DE3445852A1 (de) 1984-12-15 1986-06-19 Bayer Ag, 5090 Leverkusen Dihydropyridin-carbonsaeureamide, verfahren zu ihrer herstellung und ihre verwendung in arzneimitteln
GB8501395D0 (en) 1985-01-19 1985-02-20 Pfizer Ltd Dihydropyridine anti-ischaemic & anti-hypertensive agents
US4723014A (en) * 1986-11-19 1988-02-02 Warner-Lambert Company Process for the preparation of 2-substituted-1,4-dihydropyridines
US4820842A (en) * 1986-11-19 1989-04-11 Warner-Lambert Company 2-substituted-1,4-dihydropyridines
DE3712369A1 (de) 1987-04-11 1988-10-27 Bayer Ag Substituierte 5-nitro-1,4-dihydropyridine, verfahren zur herstellung und ihre verwendung
DE3712371A1 (de) 1987-04-11 1988-10-27 Bayer Ag Substituierte 1,4-dihydropyridine, verfahren zu ihrer herstellung und ihre verwendung
DE3716652A1 (de) 1987-05-19 1988-12-08 Bayer Ag Dioxyalkylenaryl-dihydropyridine, zwischenprodukte zu ihrer herstellung, verfahren zu ihrer herstellung und ihre verwendung
DE3724909A1 (de) 1987-07-28 1989-02-09 Bayer Ag Neue substituierte nitro-dihydropyridine, verfahren zu ihrer herstellung und ihre verwendung
US5096904A (en) * 1989-09-01 1992-03-17 Glaxo Inc. Pyridazinones having cardiotonic and beta blocking activities
WO1992006087A1 (en) 1990-10-02 1992-04-16 Kaken Pharmaceutical Co., Ltd. Pyridazinone-substituted ethynylphenyl derivative and remedy for circulatory organ disease containing the same as active ingredient
US5100892A (en) * 1990-11-13 1992-03-31 Glaxo Inc. Dihydropyridine vasodilator agents
US5258519A (en) * 1990-11-13 1993-11-02 Glaxo Inc. Dihydropyridine vasodilators agents
PL359416A1 (en) 2000-07-18 2004-08-23 Yamanouchi Pharmaceutical Co, Ltd. Medicine comprising dicyanopyridine derivative
DE10110747A1 (de) 2001-03-07 2002-09-12 Bayer Ag Substituierte 2,6-Diamino-3,5-dicyano-4-aryl-pyridine und ihre Verwendung

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