Abstract
It was previously reported that 3-alkoxybenzo[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 1, including benzofurans, indoles, and napthalenes. 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.
MeSH terms
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Administration, Oral
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Amides / chemical synthesis
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Amides / pharmacology*
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Animals
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Anti-Inflammatory Agents, Non-Steroidal / chemistry
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Anti-Inflammatory Agents, Non-Steroidal / pharmacology*
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Benzofurans / chemical synthesis
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Benzofurans / pharmacology
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Cell Adhesion / drug effects*
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Cell Adhesion Molecules / pharmacology*
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Cells, Cultured
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E-Selectin / pharmacology
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Endothelium, Vascular / cytology
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Humans
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Indoles / chemical synthesis
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Indoles / pharmacology
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Intercellular Adhesion Molecule-1 / pharmacology
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Magnetic Resonance Spectroscopy
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Mice
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Naphthalenes / chemical synthesis
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Naphthalenes / pharmacology
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Neutrophils / cytology
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Thiophenes / chemical synthesis
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Thiophenes / pharmacology
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Tumor Necrosis Factor-alpha / pharmacology
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Vascular Cell Adhesion Molecule-1 / pharmacology
Substances
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Amides
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Anti-Inflammatory Agents, Non-Steroidal
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Benzofurans
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Cell Adhesion Molecules
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E-Selectin
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Indoles
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Naphthalenes
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Thiophenes
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Tumor Necrosis Factor-alpha
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Vascular Cell Adhesion Molecule-1
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Intercellular Adhesion Molecule-1
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PD 144795