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Journal of Antibiotics
Volumn 62, Issue 8, 2009, Pages 435-437
Xanthoradones, new potentiators of imipenem activity against methicillin-resistant Staphylococcus aureus, produced by Penicillium radicum FKI-3765-2 II. Structure elucidation
Author keywords

Fungal metabolites; Imipenem potentiator; Methicillin resistant Staphylococcus aureus (MRSA); Structure elucidation; Xanthoradone; Xanthoviridicatin
Indexed keywords

ANTIINFECTIVE AGENT; IMIPENEM; UNCLASSIFIED DRUG; XANTHORADONE A; XANTHORADONE B;
EID: 70249105402     PISSN: 00218820     EISSN: None     Source Type: Journal    
DOI: 10.1038/ja.2009.61     Document Type: Article
Times cited : (13)
References (6)
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    • Yamazaki, H., Nonaka, K., Masuma, R., Omura, S.&Tomoda, H. Xanthoradones, new potentiators of imipenem activity against methicillin-resistant Staphylococcus aureus, produced by Penicillium radicum FKI-3765-2 I. Taxonomy, fermentation, isolation and biological properties. J. Antibiot. 62, 431-434 (2009).
    • (2009) J. Antibiot , vol.62 , pp. 431-434
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  • 2
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    • Isolation, structure, and HIV-1 integrase inhibitory activity of xanthoviridicatin E and F, two novel fungal metabolites produced by Penicillium chrysogenum
    • Singh, S. B. et al. Isolation, structure, and HIV-1 integrase inhibitory activity of xanthoviridicatin E and F, two novel fungal metabolites produced by Penicillium chrysogenum. Helv. Chim. Acta. 86, 3380-3385 (2003).
    • (2003) Helv. Chim. Acta. , vol.86 , pp. 3380-3385
    • Singh, S.B.1
  • 3
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    • Structure of xanthoviridicatins D and xanthoviridicatin G, metabolites of penicillium viridicatum: application of proton and carbon-13 NMR spectroscopy
    • Stack, M. E., Mazzola, E. P.&Eppley, R. M. Structure of xanthoviridicatins D and xanthoviridicatin G, metabolites of Penicillium viridicatum: application of proton and carbon-13 NMR spectroscopy. Tetrahedron Lett. 52, 4989-4992 (1979).
    • (1979) Tetrahedron Lett. , vol.52 , pp. 4989-4992
    • Stack, M.E.1    Mazzola, E.P.2    Eppley, R.M.3
  • 4
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    • Synthesis, biosynthesis, and absolute configuration of vioxanthin
    • Bode, S. E., Drochner, D.&Muller, M. Synthesis, biosynthesis, and absolute configuration of vioxanthin. Angew. Chem. Int. Ed. Engl. 46, 5916-5920 (2007).
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  • 5
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    • Fungal products. Part XIII. Xanthomegnin, viomellin, rubrosulphin, and viopurpurin, pigments from Aspergillus sulphureus and Aspergillus melleus
    • Durley, R. C., MacMillan, J., Simpson, T. J., Glen, A. T.&Turner, W. B. Fungal products. Part XIII. Xanthomegnin, viomellin, rubrosulphin, and viopurpurin, pigments from Aspergillus sulphureus and Aspergillus melleus. J. Chem. Soc. Perkin. Trans. 1 2, 163-169 (
    • (1975) J. Chem. Soc. Perkin. Trans , vol.2 , pp. 163-169
    • Durley, R.C.1    MacMillan, J.2    Simpson, T.J.3    Glen, A.T.4    Turner, W.B.5
  • 6
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    • Kitamura, J.&Nozawa, Y. Genotoxicity of quinine pigments from pathogenic fungi
    • Mori, H., Kawai, K., Ohbayashi, F., Kitamura, J.&Nozawa, Y. Genotoxicity of quinine pigments from pathogenic fungi. Mutat. Res. 122, 29-34 (1983).
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    • Mori, H.1    Kawai, K.2    Ohbayashi, F.3

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.