Marine Drugs · 2020 · 13 citations · 17 references
PharmacyBiochemistryPharmacologyDrug DiscoveryOrganic ChemistryStructure-activity RelationshipsMarine Bioactive CompoundsMarine Natural ProductsTerpenoid BiosynthesisAntiproliferative AgentsAntiproliferative Drug ActionBioactive Compounds From Marine FungiBioactive Marine MetabolitesCircular DichroismCircular Dichroism AnalysisElectronic Circular DichroismSecondary Metabolite Gene Clusters
Five new compounds 15R-17,18-dehydroxantholipin (1), (3E,5E,7E)-3-methyldeca-3,5,7-triene-2,9-dione (2) and qinlactone A–C (3–5) were identified from mangrove Streptomyces qinglanensis 172205 with “genetic dereplication,” which deleted the highly expressed secondary metabolite-enterocin biosynthetic gene cluster. The chemical structures were established by spectroscopic methods, and the absolute configurations were determined by electronic circular dichroism (ECD). Compound 1 exhibited strong anti-microbial and antiproliferative bioactivities, while compounds 2–4 showed weak antiproliferative activities.
17
Roberto Cammi, J. Tomasi · Journal of Computational Chemistry · 1995 · 1.4K citations
Actinomycetes for Marine Drug Discovery Isolated from Mangrove Soils and Plants in China
Kui Hong, An-Hui Gao, Qing-Yi Xie et al. · Marine Drugs · 2009 · 372 citations · Full text