Semi-synthetic puwainaphycin/minutissamide cyclic lipopeptides with improved antifungal activity and limited cytotoxicity
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Both the substitution of free hydroxyl substituents and extending/branching of the fatty acid moiety improved the antifungal potency and limits the cytotoxicity of cyanobacterial cyclic lipopeptides puwainaphycin/minutissamides.
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2003 ◽
Vol 278
(15)
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pp. 12946-12954
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2014 ◽
Vol 11
(3)
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pp. 304-315
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1959 ◽
Vol 37
(1)
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pp. 17-23
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2009 ◽
Vol 42
(7)
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pp. 599-605
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