2012
DOI: 10.1016/j.phytol.2012.06.015
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Antimalarial and antitubercular C-glycosylated benz[α]anthraquinones from the marine-derived Streptomyces sp. BCC45596

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Cited by 45 publications
(25 citation statements)
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“…Supong and colleagues reported a novel C -glycosylated benz[ a ]anthraquinone derivative, urdamycinone E ( 78 ) isolated from a marine Streptomyces sp. BCC45596 that potently inhibited P. falciparum K1 strain [84]. …”
Section: Marine Compounds With Antibacterial Antifungal Antiprotmentioning
confidence: 99%
See 1 more Smart Citation
“…Supong and colleagues reported a novel C -glycosylated benz[ a ]anthraquinone derivative, urdamycinone E ( 78 ) isolated from a marine Streptomyces sp. BCC45596 that potently inhibited P. falciparum K1 strain [84]. …”
Section: Marine Compounds With Antibacterial Antifungal Antiprotmentioning
confidence: 99%
“…Avilés and colleagues isolated two new tricyclic diterpenes ( 91 , 92 ) from the Bahamian marine sponge Svenzea flava that displayed moderate antimycobacterial activity against M. tuberculosis H37Rv, the data suggesting that “the isoneoamphilectane backbone” may be “responsible for the observed activity” [95]. In addition to the antimalarial activity described earlier, Supong and colleagues reported that the novel C -glycosylated benz[ a ]anthraquinone derivative, urdamycinone E ( 78 ), inhibited M. tuberculosis strain H37Rv [84]. …”
Section: Marine Compounds With Antibacterial Antifungal Antiprotmentioning
confidence: 99%
“…Yang and coworkers [100] reported the isolation of anthraquinone derivative, 3-acetoxy-4-deoxybostrycin ( Figure 23.10), from a marine-derived fungus Nigrospora, which exhibited promising activity against B. cereus with an MIC value of 48.8 nM, which was stronger than that of the positive control ciprofloxacin (MIC ¼ 1250 nM). C-glycosylated benz[a]anthraquinone derivatives [101], urdamycinone E, urdamycinone G, dehydroxyaquayamycin ( Figure 23.10), isolated from the marine Streptomycetes sp. exhibited potent activity against M. tuberculosis MICs of 3.13e12.50 mg/mL.…”
Section: Antimicrobial Agents From Marine Sourcesmentioning
confidence: 99%
“…Appendices N-Q) allowed to support the presence of dehydroxyaquayamycin by comparison against reported data(Supong et al, 2012). HR-ESI-MS of this sample resulted in…”
mentioning
confidence: 89%
“…Data1:SA-A3-X11-5- 31 dehydroxyaquayamycin. This metabolite was previously described as natural product from marine actinobacteria (Supong et al, 2012), originally obtained as dehydrated product of aquayamycin during its structure elucidation (Sezaki et al, 1970). Data12:SA-A3-X11-5-2.lcd PDA Ch12 420nm,4nm…”
Section: Measurement Of Colony Areasmentioning
confidence: 99%