| Literature DB >> 26084575 |
Sang-Jip Nam1, Christopher A Kauffman1, Paul R Jensen1, Curtis E Moore1, Arnold L Rheingold1, William Fenical1.
Abstract
Chemical investigation of a marine actinomycete within the family Streptomycetaceae (our strain CNQ-149) has led to the isolation of the unprecedented alkaloids, actinobenzoquinoline (1) and actinophenanthrolines A-C (2-4). The chemical structures of 1-4 were assigned by interpretation of NMR spectroscopic data, and their absolute configurations were assigned by X-ray analysis. Actinobenzoquinoline possesses a 5-methyloxazolidin-4-one moiety and a dihydrobenzo[h]quinoline core structure, while actinophenanthrolines A-C are composed of hydroxypropanamide-substituted 1,7-phenanthroline core skeletons.Entities:
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Year: 2015 PMID: 26084575 DOI: 10.1021/acs.orglett.5b01387
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005