A New Group of Antibiotics, Hydroxamic Acid Antimycotic Antibiotics. IV. Structures of Enactins Ia, Ib1, Ib2 and Va
Structures of enactins Ia, Ib1, Ib2 and Va were determined by spectroscopic studies using their bis-2, 4-dinitrophenyl derivatives. Both enactins and neoenactins contain L-serine to form the hydroxamic acid structure. Their physico-chemical and biological properties are closely related. The structur...
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Published in: | Chemical & pharmaceutical bulletin Vol. 39; no. 6; pp. 1436 - 1439 |
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Main Authors: | , , , |
Format: | Journal Article |
Language: | English |
Published: |
Tokyo
The Pharmaceutical Society of Japan
1991
Japan Science and Technology Agency |
Subjects: | |
Online Access: | Get full text |
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Summary: | Structures of enactins Ia, Ib1, Ib2 and Va were determined by spectroscopic studies using their bis-2, 4-dinitrophenyl derivatives. Both enactins and neoenactins contain L-serine to form the hydroxamic acid structure. Their physico-chemical and biological properties are closely related. The structures of neoenactin congeners have been previosuly reported and enactins Ia and Va are proved to be 19-hydroxyneoenactin B2 and 14-dihydroneoenactin M1, respectively. Both enactins Ib1 and Ib2 are determined to be 19-hydroxyneoenactin B1 and considered to be diastereoisomers at the 19-position, though their steric structures at this positioin remain to be determined. |
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ISSN: | 0009-2363 1347-5223 |
DOI: | 10.1248/cpb.39.1436 |