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
相关论文
共 32 条
[21]   AN INDUCIBLE ENDOTHELIAL-CELL SURFACE GLYCOPROTEIN MEDIATES MELANOMA ADHESION [J].
RICE, GE ;
BEVILACQUA, MP .
SCIENCE, 1989, 246 (4935) :1303-1306
[22]   TREATMENT OF INFLAMMATION WITH ANTI-ICAM-1 [J].
ROTHLEIN, R ;
MAINOLFI, EA ;
KISHIMOTO, TK .
RESEARCH IN IMMUNOLOGY, 1993, 144 (09) :735-739
[23]  
SANDERS SK, 1994, J CELL BIOCH A S, V18, pE516
[24]   ACYL-COENZYME A-CHOLESTEROL-ACYLTRANSFERASE (ACAT) INHIBITORS MODULATE MONOCYTE ADHESION TO AORTIC ENDOTHELIAL-CELLS [J].
SAXENA, U ;
FERGUSON, E ;
NEWTON, RS .
ATHEROSCLEROSIS, 1995, 112 (01) :7-17
[25]   THE PHARMACOLOGICAL EFFECTS OF 5-[3,5-BIS(1,1-DIMETHYLETHYL)-4-HYDROXYPHENYL]-1,3,4-THIADIAZOLE-2(3H)-THIONE, CHOLINE SALT (CI-986), A NOVEL INHIBITOR OF ARACHIDONIC-ACID METABOLISM IN MODELS OF INFLAMMATION, ANALGESIA AND GASTRIC IRRITATION [J].
SCHRIER, DJ ;
BARAGI, VM ;
CONNOR, DT ;
DYER, RD ;
JORDAN, JH ;
IMRE, KM ;
LESCH, ME ;
MULLICAN, MD ;
OKONKWO, GCN ;
CONROY, MC .
PROSTAGLANDINS, 1994, 47 (01) :17-30
[26]  
SCHRIER DJ, 1994, J CELL BIOCHEMSUP A, V18, pE517
[27]   TRAFFIC SIGNALS FOR LYMPHOCYTE RECIRCULATION AND LEUKOCYTE EMIGRATION - THE MULTISTEP PARADIGM [J].
SPRINGER, TA .
CELL, 1994, 76 (02) :301-314
[28]  
Stelmach H., 1970, J AM CHEM SOC, V92, P863
[29]   NOVEL INDOLECARBOXAMIDOTETRAZOLES AS POTENTIAL ANTIALLERGY AGENTS [J].
UNANGST, PC ;
CONNOR, DT ;
STABLER, SR ;
WEIKERT, RJ ;
CARETHERS, ME ;
KENNEDY, JA ;
THUESON, DO ;
CHESTNUT, JC ;
ADOLPHSON, RL ;
CONROY, MC .
JOURNAL OF MEDICINAL CHEMISTRY, 1989, 32 (06) :1360-1366
[30]   SYNTHESIS OF NOVEL 1-PHENYL-1H-INDOLE-2-CARBOXYLIC ACIDS .1. UTILIZATION OF ULLMANN AND DIECKMANN REACTIONS FOR THE PREPARATION OF 3-HYDROXY, 3-ALKOXY, AND 3-ALKYL DERIVATIVES [J].
UNANGST, PC ;
CONNOR, DT ;
STABLER, SR ;
WEIKERT, RJ .
JOURNAL OF HETEROCYCLIC CHEMISTRY, 1987, 24 (03) :811-815