Literature DB >> 8621357

Structure of the spiroketal-macrolide ossamycin.

H A Kirst1, J S Mynderse, J W Martin, P J Baker, J W Paschal, J L Rios Steiner, E Lobkovsky, J Clardy.   

Abstract

Ossamycin is a cytotoxic agent of undetermined structure that was originally isolated in 1965 from culture broths of Streptomyces hygroscopicus var. ossamyceticus. Its overall structure and relative stereochemistry have now been determined by single crystal X-ray diffraction studies. Absolute stereochemistry was established according to the previously determined configuration of its aminosaccharide constituent, ossamine. The aglycone of ossamycin possesses a 24-membered macrolide ring system onto which is incorporated both a 6,6-spiroketal and 5-membered hemiketal ring system. The overall three-dimensional structure possesses features in common with the related macrocyclic antibiotics dunaimycin, cytovaricin, and A82548A.

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Year:  1996        PMID: 8621357     DOI: 10.7164/antibiotics.49.162

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


  7 in total

Review 1.  ATP synthase and the actions of inhibitors utilized to study its roles in human health, disease, and other scientific areas.

Authors:  Sangjin Hong; Peter L Pedersen
Journal:  Microbiol Mol Biol Rev       Date:  2008-12       Impact factor: 11.056

2.  Association of Streptomyces community composition determined by PCR-denaturing gradient gel electrophoresis with indoor mold status.

Authors:  Elisabet Johansson; Tiina Reponen; Jarek Meller; Stephen Vesper; Jagjit Yadav
Journal:  Environ Monit Assess       Date:  2014-10-22       Impact factor: 2.513

3.  Total synthesis and stereochemical assignment of (-)-ushikulide A.

Authors:  Barry M Trost; Brendan M O'Boyle; Daniel Hund
Journal:  J Am Chem Soc       Date:  2009-10-21       Impact factor: 15.419

4.  Exploiting orthogonally reactive functionality: synthesis and stereochemical assignment of (-)-ushikulide A.

Authors:  Barry M Trost; Brendan M O'Boyle
Journal:  J Am Chem Soc       Date:  2008-12-03       Impact factor: 15.419

5.  Integration of Genomic Data with NMR Analysis Enables Assignment of the Full Stereostructure of Neaumycin B, a Potent Inhibitor of Glioblastoma from a Marine-Derived Micromonospora.

Authors:  Min Cheol Kim; Henrique Machado; Kyoung Hwa Jang; Lynnie Trzoss; Paul R Jensen; William Fenical
Journal:  J Am Chem Soc       Date:  2018-08-20       Impact factor: 15.419

6.  The biosynthetic pathway to ossamycin, a macrocyclic polyketide bearing a spiroacetal moiety.

Authors:  Oksana Bilyk; Markiyan Samborskyy; Peter F Leadlay
Journal:  PLoS One       Date:  2019-04-30       Impact factor: 3.240

7.  Biosynthetic origin of butyrolactol A, an antifungal polyketide produced by a marine-derived Streptomyces.

Authors:  Enjuro Harunari; Hisayuki Komaki; Yasuhiro Igarashi
Journal:  Beilstein J Org Chem       Date:  2017-03-08       Impact factor: 2.883

  7 in total

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