Anticandidal properties of N super(3)-(4-methoxyfumaroyl)-L-2,3-diaminopropanoic acid oligopeptides
Tri-, tetra-, and pentapeptides containing N super(3)-(4-methoxyfumaroyl)-L-2,3-diaminopropanoic acid (FMDP), an inactivator of glucosamine 6-phosphate synthase of fungal origin (a key enzyme in the biosynthesis of macromolecular components of the fungal cell wall) have been synthesized and investig...
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Published in | Journal of medicinal chemistry Vol. 33; no. 1; pp. 132 - 135 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
01.01.1990
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Subjects | |
Online Access | Get full text |
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Summary: | Tri-, tetra-, and pentapeptides containing N super(3)-(4-methoxyfumaroyl)-L-2,3-diaminopropanoic acid (FMDP), an inactivator of glucosamine 6-phosphate synthase of fungal origin (a key enzyme in the biosynthesis of macromolecular components of the fungal cell wall) have been synthesized and investigated as anticandidal agents. Structure-activity relationships of a series of peptides revealed that tripeptides were generally more active than the other peptides examined. In this study, the lysyl peptide, Lys-Nva-FMDP has been found to be the most active compound in the series. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 content type line 23 ObjectType-Feature-1 |
ISSN: | 0022-2623 |