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Synthesis and antibacterial activity of novel 6-O-substituted erythromycin A derivatives
A series of novel 6-O-substituted erythromycin A derivatives has been synthesized. Good in vitro antibacterial activity has been demonstrated for analogues incorporating a variety of structural features. The methodology disclosed is expected to find application in the design of future macrolide anti...
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Published in: | Bioorganic & medicinal chemistry letters 2000-04, Vol.10 (8), p.815-819 |
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Main Authors: | , , , , , , , , , , |
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cites | cdi_FETCH-LOGICAL-c266t-cfca278f3e1fb68dd7b0c685179481c8734ecb871d57c1e046b2877b362c2bd33 |
container_end_page | 819 |
container_issue | 8 |
container_start_page | 815 |
container_title | Bioorganic & medicinal chemistry letters |
container_volume | 10 |
creator | CLARK, R. F ZHENKUN MA YAT SUN OR SANYI WANG GRIESGRABER, G TUFANO, M HONG YONG LEPING LI XIAOLIN ZHANG NILIUS, A. M CHU, D. T. W |
description | A series of novel 6-O-substituted erythromycin A derivatives has been synthesized. Good in vitro antibacterial activity has been demonstrated for analogues incorporating a variety of structural features. The methodology disclosed is expected to find application in the design of future macrolide antibiotics that target the prevalent bacterial resistance problem. |
doi_str_mv | 10.1016/S0960-894X(00)00106-2 |
format | article |
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F</au><au>ZHENKUN MA</au><au>YAT SUN OR</au><au>SANYI WANG</au><au>GRIESGRABER, G</au><au>TUFANO, M</au><au>HONG YONG</au><au>LEPING LI</au><au>XIAOLIN ZHANG</au><au>NILIUS, A. M</au><au>CHU, D. T. W</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis and antibacterial activity of novel 6-O-substituted erythromycin A derivatives</atitle><jtitle>Bioorganic & medicinal chemistry letters</jtitle><addtitle>Bioorg Med Chem Lett</addtitle><date>2000-04-17</date><risdate>2000</risdate><volume>10</volume><issue>8</issue><spage>815</spage><epage>819</epage><pages>815-819</pages><issn>0960-894X</issn><eissn>1464-3405</eissn><abstract>A series of novel 6-O-substituted erythromycin A derivatives has been synthesized. Good in vitro antibacterial activity has been demonstrated for analogues incorporating a variety of structural features. The methodology disclosed is expected to find application in the design of future macrolide antibiotics that target the prevalent bacterial resistance problem.</abstract><cop>Oxford</cop><pub>Elsevier</pub><pmid>10782693</pmid><doi>10.1016/S0960-894X(00)00106-2</doi><tpages>5</tpages></addata></record> |
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subjects | Anti-Infective Agents - chemical synthesis Anti-Infective Agents - pharmacology Antibacterial agents Antibiotics. Antiinfectious agents. Antiparasitic agents Biological and medical sciences Erythromycin - analogs & derivatives Erythromycin - chemical synthesis Erythromycin - pharmacology Medical sciences Microbial Sensitivity Tests Pharmacology. Drug treatments Structure-Activity Relationship |
title | Synthesis and antibacterial activity of novel 6-O-substituted erythromycin A derivatives |
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