Literature DB >> 26465962

Unciaphenol, an Oxygenated Analogue of the Bergman Cyclization Product of Uncialamycin Exhibits Anti-HIV Activity.

David E Williams1, Helen Bottriell1, Julian Davies2, Ian Tietjen3, Mark A Brockman3,4, Raymond J Andersen1.   

Abstract

Unciaphenol (2), an oxygenated analogue of the Bergman cyclization product of the enediyne uncialamycin (1), has been isolated along with 1 from cultures of the actinomycete Streptomyces uncialis. It is proposed that the C-22 OH substituent in 2 might arise from the attack of a nucleophilic oxygen species on the p-benzyne diradical intermediate IA in the Bergman cyclization of 1. 2 shows in vitro anti-HIV activity against viral strains that are resistant to clinically utilized anti-retroviral therapies.

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Year:  2015        PMID: 26465962     DOI: 10.1021/acs.orglett.5b02664

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  2 in total

1.  Genome Mining of Micromonospora yangpuensis DSM 45577 as a Producer of an Anthraquinone-Fused Enediyne.

Authors:  Xiaohui Yan; Jian-Jun Chen; Ajeeth Adhikari; Dong Yang; Ivana Crnovcic; Nan Wang; Chin-Yuan Chang; Christoph Rader; Ben Shen
Journal:  Org Lett       Date:  2017-10-31       Impact factor: 6.005

2.  C-N-Coupled Metabolites Yield Insights into Dynemicin A Biosynthesis.

Authors:  Douglas R Cohen; Craig A Townsend
Journal:  Chembiochem       Date:  2020-04-29       Impact factor: 3.164

  2 in total

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