SYNTHESIS AND BETA-BLOCKING ACTIVITY OF (E)-IMINOETHERS AND (Z)-IMINOETHERS OF 1,8-NAPHTHYRIDINE - POTENTIAL ANTIHYPERTENSIVE AGENTS .4.

被引:19
作者
FERRARINI, PL [1 ]
MORI, C [1 ]
PRIMOFIORE, G [1 ]
DASETTIMO, A [1 ]
BRESCHI, MC [1 ]
MARTINOTTI, E [1 ]
NIERI, P [1 ]
CIUCCI, MA [1 ]
机构
[1] UNIV PISA,IST POLICATTEDRA DISCIPLINE BIOL,I-56100 PISA,ITALY
关键词
1,8-naphthyridine derivatives; iminoethers; β-blockers;
D O I
10.1016/0223-5234(90)90143-Q
中图分类号
R914 [药物化学];
学科分类号
100701 [药物化学];
摘要
A series of substituted (E)-and (Z)-iminoethers of 1,8-naphthyridine was synthesized from corresponding ketones. The pharmacological activity of these compounds was evaluated on isolated preparations to assess the eventual interaction with α and β adrenoceptors. All the compounds exhibited β2 stimulating and β1 blocking properties, while on α receptors neither stimulating nor blocking activity was observed. © 1990.
引用
收藏
页码:489 / 496
页数:8
相关论文
共 19 条
[1]
AMLAIKY N, 1984, EUR J MED CHEM, V19, P341
[2]
ARIENS EJ, 1954, ARCH INT PHARMACOD T, V99, P32
[3]
ARIENS EJ, 1957, ARCH INT PHARMACOD T, V110, P275
[4]
SOME QUANTITATIVE USES OF DRUG ANTAGONISTS [J].
ARUNLAKSHANA, O ;
SCHILD, HO .
BRITISH JOURNAL OF PHARMACOLOGY AND CHEMOTHERAPY, 1959, 14 (01) :48-58
[5]
USE OF (S)-(TRIFLOXYMETHYL)OXIRANE IN THE SYNTHESIS OF A CHIRAL BETA-ADRENOCEPTOR ANTAGONIST, (R) AND (S)-9-[[3-(TERT-BUTYLAMINO)-2-HYDROXYPROPYL]OXIMINO]FLUORENE [J].
BALDWIN, JJ ;
MCCLURE, DE ;
GROSS, DM ;
WILLIAMS, M .
JOURNAL OF MEDICINAL CHEMISTRY, 1982, 25 (08) :931-936
[6]
BOUZOUBAA M, 1984, J MED CHEM, V27, P1291, DOI 10.1021/jm00376a011
[7]
CARBONI S, 1982, EUR J MED CHEM, V17, P159
[8]
CARBONI S, 1975, FARMACO-ED SCI, V30, P237
[9]
DASETTIMO A, 1978, FARMACO-ED SCI, V33, P770
[10]
DASETTIMO A, 1980, J HETEROCYCLIC CHEM, V7, P1225