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Syntheses and complement inhibitory activities of 4-(2-phenyl-1H-indol-3-yl)cyclohexane-1-carboxylic acids
The syntheses of 4-(2-phenyl-1H-indol-3-yl)cyclohexane-1-carboxylic acids are described. These compounds express potent in vitro inhibition of the human classical complement pathway, and qualitative SAR have been determined. Several of the in vitro active compounds also suppressed the complement dep...
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Published in: | Journal of medicinal chemistry 1985-02, Vol.28 (2), p.160-164 |
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container_end_page | 164 |
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container_title | Journal of medicinal chemistry |
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creator | Bailey, Denis M DeGrazia, George D Alexander, E. John Powles, Ronald G Johnson, Robert E Patrick, Richard A Heerdt, Barbara G Fairbain, Margo E Pruden, Donald J |
description | The syntheses of 4-(2-phenyl-1H-indol-3-yl)cyclohexane-1-carboxylic acids are described. These compounds express potent in vitro inhibition of the human classical complement pathway, and qualitative SAR have been determined. Several of the in vitro active compounds also suppressed the complement dependent reverse passive Arthus reaction (RPAR) in guinea pigs. |
doi_str_mv | 10.1021/jm00380a002 |
format | article |
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John</au><au>Powles, Ronald G</au><au>Johnson, Robert E</au><au>Patrick, Richard A</au><au>Heerdt, Barbara G</au><au>Fairbain, Margo E</au><au>Pruden, Donald J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Syntheses and complement inhibitory activities of 4-(2-phenyl-1H-indol-3-yl)cyclohexane-1-carboxylic acids</atitle><jtitle>Journal of medicinal chemistry</jtitle><addtitle>J. Med. Chem</addtitle><date>1985-02</date><risdate>1985</risdate><volume>28</volume><issue>2</issue><spage>160</spage><epage>164</epage><pages>160-164</pages><issn>0022-2623</issn><eissn>1520-4804</eissn><coden>JMCMAR</coden><abstract>The syntheses of 4-(2-phenyl-1H-indol-3-yl)cyclohexane-1-carboxylic acids are described. These compounds express potent in vitro inhibition of the human classical complement pathway, and qualitative SAR have been determined. Several of the in vitro active compounds also suppressed the complement dependent reverse passive Arthus reaction (RPAR) in guinea pigs.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>3155799</pmid><doi>10.1021/jm00380a002</doi><tpages>5</tpages></addata></record> |
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subjects | Animals Arthus Reaction Chemistry Complement Inactivator Proteins - chemical synthesis Complement Pathway, Classical - drug effects Cyclohexanecarboxylic Acids - chemical synthesis Cyclohexanecarboxylic Acids - pharmacology Exact sciences and technology Guinea Pigs Hemolysis Heterocyclic compounds Heterocyclic compounds with only one n hetero atom and condensed derivatives Humans Male Organic chemistry Preparations and properties Stereoisomerism |
title | Syntheses and complement inhibitory activities of 4-(2-phenyl-1H-indol-3-yl)cyclohexane-1-carboxylic acids |
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