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Title:
EGFおよび/又はPDGF受容体チロシンキナーゼを阻害するビスモノ−および二環式アリールおよびヘテロアリール化合物
Document Type and Number:
Japanese Patent JP3507071
Kind Code:
B2
Abstract:
PCT No. PCT/US92/03736 Sec. 371 Date Nov. 8, 1993 Sec. 102(e) Date Nov. 8, 1993 PCT Filed May 6, 1992 PCT Pub. No. WO92/20642 PCT Pub. Date Nov. 26, 1992.This invention relates to bis mono- and/or bicyclic aryl and/or heteroaryl compounds exhibiting protein tyrosine kinase inhibition activity. More specifically, it relates to the method of inhibiting abnormal cell proliferation in a patient suffering from a disorder characterized by such proliferation comprising the administration thereto of an EGF and/or PDGF receptor inhibiting effective amount of said bis mono- and/or bicyclic aryl and/or heteroaryl compound and to the preparation of said compounds and their use in pharmaceutical compositions used in this method.

Inventors:
スパダ アルフレッド ピー
パーソンズ ポール イー
マイアーズ マイケル アール
マグワイアー マーティン ピー
Application Number:
JP50006893A
Publication Date:
March 15, 2004
Filing Date:
May 06, 1992
Export Citation:
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Assignee:
アヴェンティス ファーマシューティカルズ インコーポレイテッド
International Classes:
A61K31/047; A61K31/40; A61K31/403; A61K31/404; A61K31/425; A61K31/428; A61K31/435; A61K31/4375; A61K31/44; A61K31/4402; A61K31/4406; A61K31/4409; A61K31/4412; A61K31/4418; A61K31/4427; A61K31/443; A61K31/4433; A61K31/47; A61K31/4709; A61K31/472; A61K31/4725; A61K31/495; A61K31/498; A61K31/505; A61K31/085; A61K31/517; A61K31/535; A61K31/536; A61P9/10; A61P33/00; A61P35/00; A61P35/02; C07C43/205; C07C43/225; C07C43/23; C07D209/04; C07D213/30; C07D213/64; C07D215/14; C07D215/18; C07D215/20; C07D215/22; C07D215/233; C07D215/38; C07D215/50; C07D217/24; C07D239/74; C07D239/88; C07D239/91; C07D239/93; C07D239/94; C07D241/42; C07D241/52; C07D265/22; C07D277/64; C07D401/04; C07D401/06; C07D401/12; C07D403/04; C07D403/06; C07D403/12; C07D405/04; C07D405/12; C07D409/04; C07D409/06; C07D409/12; C07D417/04; C07D471/04; C07D521/00; C12N9/99; (IPC1-7): C07C43/23; A61K31/47; A61K31/495; A61P9/10; A61P33/00; A61P35/00; A61P35/02; C07D215/14; C07D215/22; C07D215/38; C07D217/24; C07D241/42; C07D401/04; C07D401/06; C07D401/12; C07D403/06; C07D403/12; C07D405/04; C07D409/04; C07D409/06; C07D409/12; C07D417/04; C12N9/99
Other References:
Ali A.H.Saeed,Canadian Journal of Spectroscopy,1986,vol.31,No.2,p.40−43
BASS R.J.,Chem.Ind.(London),1973,No.17,p.849
BREIDING−MACK S.et al.,J.Antibiotics,1987,Vol.40,No.7,p.953−960
Chemical Abstracts,Vol.108,No.55860,1988
Chemical Abstracts,Vol.87,No.53052,1977
LIVINGSTONE D.B.et al.,Chem.Ind.(London),1973,No.17,p.848−849
LORIGA M.et al.,Eur.J.Med.Chem.,1990,Vol.25,p.527−532
Thomas Kauffmann and Rolf Otter,Chem.Ber.,1983,116,p.980−991
VAGNEUR B.et al.,Can.J.Chem.,1989,Vol.67,p.2116−2118
Attorney, Agent or Firm:
中村 稔 (外6名)