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Syntheses and platelet aggregation inhibitory and antithrombotic properties of (2-(( omega -Aminoalkoxy) phenyl) ethyl) benzenes
A series of (2-(( omega -aminoalkoxy)phenyl)ethyl) benzene derivatives were synthesized and evaluated for their ability to inhibit collagen-induced platelet aggregation in vitro and to protect experimental thrombosis in mice. The results showed that the compounds were in vitro inhibitors of collagen...
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Published in: | Journal of medicinal chemistry 1990-01, Vol.33 (6), p.1818-1823 |
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container_issue | 6 |
container_start_page | 1818 |
container_title | Journal of medicinal chemistry |
container_volume | 33 |
creator | Kikumoto, R Hara, H Ninomiya, K Osakabe, M Sugano, M Fukami, H Tamao, Y |
description | A series of (2-(( omega -aminoalkoxy)phenyl)ethyl) benzene derivatives were synthesized and evaluated for their ability to inhibit collagen-induced platelet aggregation in vitro and to protect experimental thrombosis in mice. The results showed that the compounds were in vitro inhibitors of collagen-induced platelet aggregation. Most of them were also effective in the mouse antithrombotic assay. The compounds were found to be potent antagonists to S sub(2) serotonergic receptors, and good correlation (r = 0.85) between their S sub(2) serotonergic receptor antagonism and their potency as platelet, antiaggregatory drugs was observed. Among the compounds studied mono(2-(dimethylamino)-1-((2-(2-(3-methoxyphenyl)ethyl)phenoxy)met hyl)ethyl) succinate hydrochloride (12b, MCI-9042) was selected for further pharmacological and toxicological evaluation. |
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The results showed that the compounds were in vitro inhibitors of collagen-induced platelet aggregation. Most of them were also effective in the mouse antithrombotic assay. The compounds were found to be potent antagonists to S sub(2) serotonergic receptors, and good correlation (r = 0.85) between their S sub(2) serotonergic receptor antagonism and their potency as platelet, antiaggregatory drugs was observed. 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The results showed that the compounds were in vitro inhibitors of collagen-induced platelet aggregation. Most of them were also effective in the mouse antithrombotic assay. The compounds were found to be potent antagonists to S sub(2) serotonergic receptors, and good correlation (r = 0.85) between their S sub(2) serotonergic receptor antagonism and their potency as platelet, antiaggregatory drugs was observed. Among the compounds studied mono(2-(dimethylamino)-1-((2-(2-(3-methoxyphenyl)ethyl)phenoxy)met hyl)ethyl) succinate hydrochloride (12b, MCI-9042) was selected for further pharmacological and toxicological evaluation.</description><subject>benzene</subject><issn>0022-2623</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1990</creationdate><recordtype>article</recordtype><recordid>eNqNjLtOw0AQAK8AKeHxD1shp7B0OSuGFiEQPfTROdn4Npx3ze1GwlR8OgbxAVTTzMyZW3ofQh3a0CzcherRe9-sQ7N0Xy8TW0JFhch7GHM0zGgQ-75gH42EgThRRyZl-nUiG1kqMnRitIOxyIjFaD7IAapQVxXIMLdQ3w_EEvObfEwrGBPylFeAln7QIX8io16580PMitd_vHQ3T4-vD8_1_H0_odp2IN1hzpFRTrpdb27b1m_umn-L37ptUzI</recordid><startdate>19900101</startdate><enddate>19900101</enddate><creator>Kikumoto, R</creator><creator>Hara, H</creator><creator>Ninomiya, K</creator><creator>Osakabe, M</creator><creator>Sugano, M</creator><creator>Fukami, H</creator><creator>Tamao, Y</creator><scope>8FD</scope><scope>FR3</scope><scope>M7Z</scope><scope>P64</scope></search><sort><creationdate>19900101</creationdate><title>Syntheses and platelet aggregation inhibitory and antithrombotic properties of (2-(( omega -Aminoalkoxy) phenyl) ethyl) benzenes</title><author>Kikumoto, R ; Hara, H ; Ninomiya, K ; Osakabe, M ; Sugano, M ; Fukami, H ; Tamao, Y</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_miscellaneous_157660583</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1990</creationdate><topic>benzene</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kikumoto, R</creatorcontrib><creatorcontrib>Hara, H</creatorcontrib><creatorcontrib>Ninomiya, K</creatorcontrib><creatorcontrib>Osakabe, M</creatorcontrib><creatorcontrib>Sugano, M</creatorcontrib><creatorcontrib>Fukami, H</creatorcontrib><creatorcontrib>Tamao, Y</creatorcontrib><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biochemistry Abstracts 1</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Journal of medicinal chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kikumoto, R</au><au>Hara, H</au><au>Ninomiya, K</au><au>Osakabe, M</au><au>Sugano, M</au><au>Fukami, H</au><au>Tamao, Y</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Syntheses and platelet aggregation inhibitory and antithrombotic properties of (2-(( omega -Aminoalkoxy) phenyl) ethyl) benzenes</atitle><jtitle>Journal of medicinal chemistry</jtitle><date>1990-01-01</date><risdate>1990</risdate><volume>33</volume><issue>6</issue><spage>1818</spage><epage>1823</epage><pages>1818-1823</pages><issn>0022-2623</issn><abstract>A series of (2-(( omega -aminoalkoxy)phenyl)ethyl) benzene derivatives were synthesized and evaluated for their ability to inhibit collagen-induced platelet aggregation in vitro and to protect experimental thrombosis in mice. The results showed that the compounds were in vitro inhibitors of collagen-induced platelet aggregation. Most of them were also effective in the mouse antithrombotic assay. The compounds were found to be potent antagonists to S sub(2) serotonergic receptors, and good correlation (r = 0.85) between their S sub(2) serotonergic receptor antagonism and their potency as platelet, antiaggregatory drugs was observed. Among the compounds studied mono(2-(dimethylamino)-1-((2-(2-(3-methoxyphenyl)ethyl)phenoxy)met hyl)ethyl) succinate hydrochloride (12b, MCI-9042) was selected for further pharmacological and toxicological evaluation.</abstract></addata></record> |
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ispartof | Journal of medicinal chemistry, 1990-01, Vol.33 (6), p.1818-1823 |
issn | 0022-2623 |
language | eng |
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source | American Chemical Society |
subjects | benzene |
title | Syntheses and platelet aggregation inhibitory and antithrombotic properties of (2-(( omega -Aminoalkoxy) phenyl) ethyl) benzenes |
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