INHIBITION OF E-SELECTIN-MEDIATED, ICAM-1-MEDIATED, AND VCAM-1-MEDIATED CELL-ADHESION BY BENZO[B]THIOPHENE-CARBOXAMIDES, BENZOFURAN-CARBOXAMIDES, INDOLE-, AND NAPHTHALENE-2-CARBOXAMIDES - IDENTIFICATION OF PD-144795 AS AN ANTIINFLAMMATORY AGENT

被引:63
作者
BOSCHELLI, DH
KRAMER, JB
KHATANA, SS
SORENSON, RJ
CONNOR, DT
FERIN, MA
WRIGHT, CD
LESCH, ME
IMRE, K
OKONKWO, GC
SCHRIER, DJ
CONROY, MC
FERGUSON, E
WOELLE, J
SAXENA, U
机构
[1] PARKE DAVIS PHARMACEUT RES, DEPT IMMUNOPATHOL, ANN ARBOR, MI 48105 USA
[2] PARKE DAVIS PHARMACEUT RES, DEPT ATHEROSCLEROSIS, ANN ARBOR, MI 48105 USA
关键词
D O I
10.1021/jm00022a026
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
It was previously reported that 3-alkoxybenzol[b]thiophene-2-carboxamides exemplified by 1, 5-methoxy-3-(1-methylethoxy)benzo[b]thiophene-2-carboxamide, decreased the adherence of neutrophils to activated endothelial cells by inhibiting the upregulation of the adhesion molecules E-selectin and ICAM-1 on the surface of the endothelium. This finding is extended here to a series of 3-thiobenzo[b]thiophene-2-carboxamides and also heterocyclic analogs of I, including benzofurans, indoles, and naphthalenes. The compounds that inhibited the expression of E-selectin and ICAM-1 had the same effect on the expression of VCAM-1. PD 144795, 5-methoxy-3-(1-methylethoxy)benzo[b]thiophene-2-carboxamide 1-oxide (44), the sulfoxide analog of 1, was orally active in several models of inflammation. The in vitro and in vivo activity of PD 144795 resided predominately in the S-enantiomer.
引用
收藏
页码:4597 / 4614
页数:18
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