Journal of Natural Products · 2003 · 50 citations · 12 references
PharmacyMedicinal ChemistryMicrobiologyDrug DiscoveryStructure-activity RelationshipsSynthetic Medicinal ChemistryAntibacterial AgentsAntibacterial PharmacologyNatural Product Drug DiscoveryStructure-activity Relationship AnalysisAntimicrobial MetabolitesMinimum Inhibitory Concentration DeterminationMinimum Inhibitory Concentration TestingSpectroscopic Identification
Bioactivity-directed fractionation of the methanolic extract of the stem and fruits of Senna obliqua led to the isolation of two known antimycobacterial natural products, quinquangulin (1) and rubrofusarin (2). Both compounds had minimum inhibitory concentrations (MICs) of 12.0 microg/mL against Mycobacteriatuberculosis in radiometric culture. This is the first report of antimycobacterial activity associated with naphthopyrone compounds. Their structures were determined by spectroscopic means including 1D and 2D NMR techniques and further confirmed by X-ray crystallographic analysis.
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Tsutomu Hatano, Hiroshi UEBAYASHI, Hideyuki Ito et al. · Chemical and Pharmaceutical Bulletin · 1999 · 197 citations · Full text
Studies in the biochemistry of micro-organisms
J. N. Ashley, Betty C. Hobbs, Harold Raistrick · Biochemical Journal · 1937 · 92 citations · Full text