Literature DB >> 7622429

Balmoralmycin, a new angucyclinone, and two related biosynthetic shunt products containing a novel ring system.

K U Bindseil1, P Hug, H H Peter, F Petersen, B E Roggo.   

Abstract

A new angucyclinone, named balmoralmycin (1), was isolated as an inhibitor of protein kinase C-alpha (PKC-alpha) from the Streptomyces strain P6417. Chemical screening of extracts of the same strain resulted in the detection of two decaketides with unusual structural features (2 and 3). Both compounds belong to a recently described structural class of secondary metabolites which arises from engineered biosynthesis of a recombinant Streptomyces strain. The isolation of compounds of this class from a wild-type strain has never been reported before.

Entities:  

Mesh:

Substances:

Year:  1995        PMID: 7622429     DOI: 10.7164/antibiotics.48.457

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


  2 in total

Review 1.  A comprehensive review of glycosylated bacterial natural products.

Authors:  Sherif I Elshahawi; Khaled A Shaaban; Madan K Kharel; Jon S Thorson
Journal:  Chem Soc Rev       Date:  2015-11-07       Impact factor: 54.564

2.  Tandem Intramolecular Benzyne-Furan Cycloadditions. Total Synthesis of Vineomycinone B(2) Methyl Ester.

Authors:  Steven M Sparks; Chi-Li Chen; Stephen F Martin
Journal:  Tetrahedron       Date:  2007-08-27       Impact factor: 2.457

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.