Synthesis and Evaluation of Hydroquinone Derivatives as Inhibitors of Isocitrate Lyase
Isocitrate lyase (ICL) is envisaged as an attractive drug target for the development of antimicrobial agents. We have prepared a series of hydroquinone derivatives on the basis of the structure of halisulfates, a naturally occurring inhibitor of ICL. The obtained derivatives were evaluated against I...
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Published in | Archives of pharmacal research Vol. 30; no. 8; pp. 955 - 961 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | Korean |
Published |
2007
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Subjects | |
Online Access | Get full text |
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Summary: | Isocitrate lyase (ICL) is envisaged as an attractive drug target for the development of antimicrobial agents. We have prepared a series of hydroquinone derivatives on the basis of the structure of halisulfates, a naturally occurring inhibitor of ICL. The obtained derivatives were evaluated against ICL of C. albicans. The preliminary structure-activity relationships and the minimal structural requirements for potency were established through structural modifications. |
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Bibliography: | KISTI1.1003/JNL.JAKO200736038098961 |
ISSN: | 0253-6269 1976-3786 |