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Antitrypanosomal activity of purine nucleosides can be enhanced by their conversion to O-acetylated derivatives
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Published in: | Antimicrobial Agents and Chemotherapy 1996-11, Vol.40 (11), p.2567-2572 |
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container_end_page | 2572 |
container_issue | 11 |
container_start_page | 2567 |
container_title | Antimicrobial Agents and Chemotherapy |
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creator | Sufrin, J R Rattendi, D Spiess, A J Lane, S Marasco, Jr, C J Bacchi, C J |
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doi_str_mv | 10.1128/AAC.40.11.2567 |
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</description><subject>Acetylation</subject><subject>Animals</subject><subject>Mice</subject><subject>Purine Nucleosides</subject><subject>Purine Nucleosides - chemistry</subject><subject>Purine Nucleosides - pharmacology</subject><subject>Research Support, Non-U.S. Gov't</subject><subject>Structure-Activity Relationship</subject><subject>Trypanocidal Agents</subject><subject>Trypanocidal Agents - pharmacology</subject><subject>Trypanosoma brucei</subject><subject>Trypanosoma brucei brucei</subject><subject>Trypanosoma brucei brucei - drug effects</subject><subject>Trypanosoma brucei rhodesiense</subject><subject>Trypanosoma brucei rhodesiense - drug effects</subject><subject>Trypanosomiasis, African - drug therapy</subject><subject>Trypanosomiasis, African - parasitology</subject><issn>0066-4804</issn><issn>1098-6596</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><recordid>eNqFkc-L1DAUx4Mo67h69SYED16kY5K2aXvwMAz-goW96Dm8pK_bLG0yJuks_e_NMMOyHsRTXvh-vx9e8iXkLWdbzkX7abfbb6vTvBW1bJ6RDWddW8i6k8_JhjEpi6pl1UvyKsZ7lu91x67IVdvxspJyQ_zOJZvCegDno59homCSPdq0Uj_QwxKsQ-oWM6GPtsdIDTiqkaIbwRnsqV5pGtEGarw7YojWO5o8vS3AYFonSNnTY7BHyFiMr8mLAaaIby7nNfn19cvP_ffi5vbbj_3upoCqaVOBWmpTa6FRG9HVjRkabZCVvSmroe90iQKFYQgAJdOag-l5KUwOSN6Wui6vyecz97DoGXuDLgWY1CHYGcKqPFj1t-LsqO78UXFZ1k2T8x8u-eB_LxiTmm00OE3g0C9RNW0teNWJ_xp5prVVx7Jxezaa4GMMODwuw5k6Valylao6zepUZQ58PAcgzkLd-yW4_GP_dr97-uBH-KXprL8_66O9Gx9sQJWxCsA8hfwBO2a3JA</recordid><startdate>19961101</startdate><enddate>19961101</enddate><creator>Sufrin, J R</creator><creator>Rattendi, D</creator><creator>Spiess, A J</creator><creator>Lane, S</creator><creator>Marasco, Jr, C J</creator><creator>Bacchi, C J</creator><general>American Society for Microbiology</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>M7N</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19961101</creationdate><title>Antitrypanosomal activity of purine nucleosides can be enhanced by their conversion to O-acetylated derivatives</title><author>Sufrin, J R ; Rattendi, D ; Spiess, A J ; Lane, S ; Marasco, Jr, C J ; Bacchi, C J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a478t-eb6bc5b2bebc2957cf7bce03dc34fd9b3e2e2c0eaaa30bb1acd132cb2b6183b53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Acetylation</topic><topic>Animals</topic><topic>Mice</topic><topic>Purine Nucleosides</topic><topic>Purine Nucleosides - chemistry</topic><topic>Purine Nucleosides - pharmacology</topic><topic>Research Support, Non-U.S. Gov't</topic><topic>Structure-Activity Relationship</topic><topic>Trypanocidal Agents</topic><topic>Trypanocidal Agents - pharmacology</topic><topic>Trypanosoma brucei</topic><topic>Trypanosoma brucei brucei</topic><topic>Trypanosoma brucei brucei - drug effects</topic><topic>Trypanosoma brucei rhodesiense</topic><topic>Trypanosoma brucei rhodesiense - drug effects</topic><topic>Trypanosomiasis, African - drug therapy</topic><topic>Trypanosomiasis, African - parasitology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sufrin, J R</creatorcontrib><creatorcontrib>Rattendi, D</creatorcontrib><creatorcontrib>Spiess, A J</creatorcontrib><creatorcontrib>Lane, S</creatorcontrib><creatorcontrib>Marasco, Jr, C J</creatorcontrib><creatorcontrib>Bacchi, C J</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Antimicrobial Agents and Chemotherapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sufrin, J R</au><au>Rattendi, D</au><au>Spiess, A J</au><au>Lane, S</au><au>Marasco, Jr, C J</au><au>Bacchi, C J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Antitrypanosomal activity of purine nucleosides can be enhanced by their conversion to O-acetylated derivatives</atitle><jtitle>Antimicrobial Agents and Chemotherapy</jtitle><stitle>Antimicrob Agents Chemother</stitle><addtitle>Antimicrob Agents Chemother</addtitle><date>1996-11-01</date><risdate>1996</risdate><volume>40</volume><issue>11</issue><spage>2567</spage><epage>2572</epage><pages>2567-2572</pages><issn>0066-4804</issn><eissn>1098-6596</eissn><abstract>Services
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</abstract><cop>United States</cop><pub>American Society for Microbiology</pub><pmid>8913466</pmid><doi>10.1128/AAC.40.11.2567</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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source | American Society for Microbiology Journals; PubMed Central |
subjects | Acetylation Animals Mice Purine Nucleosides Purine Nucleosides - chemistry Purine Nucleosides - pharmacology Research Support, Non-U.S. Gov't Structure-Activity Relationship Trypanocidal Agents Trypanocidal Agents - pharmacology Trypanosoma brucei Trypanosoma brucei brucei Trypanosoma brucei brucei - drug effects Trypanosoma brucei rhodesiense Trypanosoma brucei rhodesiense - drug effects Trypanosomiasis, African - drug therapy Trypanosomiasis, African - parasitology |
title | Antitrypanosomal activity of purine nucleosides can be enhanced by their conversion to O-acetylated derivatives |
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