期刊
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
卷 20, 期 13, 页码 3893-3896出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.bmcl.2010.05.024
关键词
Antifungal; beta-1,6-Glucan; Cell wall; Pyridobenzimidazole; Candida glabrata
Based on the HTS hit compound 1a, an inhibitor of beta-1,6-glucan synthesis, we synthesized novel pyridobenzimidazole derivatives and evaluated their antifungal activity. Among the compounds synthesized, we identified the potent compound 15e, which exhibits excellent activity superior to fluconazole against both Candida glabrata and Candida krusei. From the SAR study, we revealed essential moieties for antifungal activity. (c) 2010 Elsevier Ltd. All rights reserved.
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