Literature DB >> 2584147

The structure of vacidin A, an aromatic heptaene macrolide antibiotic. II. Stereochemistry of the antibiotic.

P Sowiński1, P Gariboldi, J K Pawlak, E Borowski.   

Abstract

On the basis of coupling constants and rotating frame nuclear Overhauser effect spectroscopy of vacidin A methoxycarbonylmethylamide, the stereochemistry of the antibiotic was established. The configuration of the aglycone was determined as (3R,7R,9R,11S,13S,15R,17S,18R,19S,21R, 36S,37R,38S). The aminosugar constituent of the antibiotic was identified as beta-(D)-mycosamine. The chiral center at C-41 remains to be assigned.

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Year:  1989        PMID: 2584147     DOI: 10.7164/antibiotics.42.1639

Source DB:  PubMed          Journal:  J Antibiot (Tokyo)        ISSN: 0021-8820            Impact factor:   2.649


  2 in total

1.  The stereostructure of candicidin D.

Authors:  Katarzyna Szwarc; Paweł Szczeblewski; Paweł Sowiński; Edward Borowski; Jan Pawlak
Journal:  J Antibiot (Tokyo)       Date:  2015-02-25       Impact factor: 2.649

2.  Analytical studies on ascosin, candicidin and levorin multicomponent antifungal antibiotic complexes. The stereostructure of ascosin A2.

Authors:  Paweł Szczeblewski; Tomasz Laskowski; Bartosz Kubacki; Marta Dziergowska; Magda Liczmańska; Jakub Grynda; Paweł Kubica; Agata Kot-Wasik; Edward Borowski
Journal:  Sci Rep       Date:  2017-01-09       Impact factor: 4.379

  2 in total

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