Cytotoxic and antifungal isoprenylated xanthones and flavonoids from Cudrania fruticosa

Planta Medica

Volumn 71, Issue 3, 2005, Pages 273-274

  Wang, Yong Hong ^a   Hou, Ai Jun ^a   Zhu, Guo Fu ^b   Chen, Dao Feng ^a   Sun, Han Dong ^c  

^a FUDAN UNIVERSITY   (China)

^b SHANGHAI UNIVERSITY OF TRADITIONAL CHINESE MEDICINE   (China)

^c KUNMING INSTITUTE OF BOTANY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

CUDRAFRUTIXANTHONE A; CUDRANIA FRUTICOSA EXTRACT; FLAVONOID; PLANT EXTRACT; UNCLASSIFIED DRUG; XANTHONE DERIVATIVE;

ANALYTIC METHOD; ANTIFUNGAL ACTIVITY; ARTICLE; CYTOTOXICITY; DRUG ISOLATION; ISOPRENYLATION; MINIMUM INHIBITORY CONCENTRATION; PLANT ROOT; PROTON NUCLEAR MAGNETIC RESONANCE; SPECTROSCOPY; STRUCTURE ANALYSIS; TRADITIONAL MEDICINE;

ANTIFUNGAL AGENTS; ANTINEOPLASTIC AGENTS, PHYTOGENIC; CANDIDA ALBICANS; CELL LINE, TUMOR; FLAVONOIDS; HUMANS; INHIBITORY CONCENTRATION 50; MICROBIAL SENSITIVITY TESTS; MORACEAE; PHYTOTHERAPY; PLANT EXTRACTS; PLANT ROOTS; PROTEIN ISOPRENYLATION; XANTHONES;

EID: 16444378358     PISSN: 00320943     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2005-837829     Document Type: Article

References (15)

1. Fukai T, Yonekawa M, Hou AJ, Nomura T, Sun HD, Uno J. Antifungal agents from the roots of Cudrania cochinchinensis against Candida, Cryptococcus, and Aspergillus species. J Nat Prod 2003; 66: 1118-20
2. Zou YS, Hou AJ, Zhu GF, Chen YF, Sun HD, Zhao QS. Cytotoxic isoprenylated xanthones from Cudrania tricuspidata. Bioorg Med Chem 2004; 12: 1947-53
3. Yunnan Medicinal Material Company. Catalogue of Traditional Chinese Medicine in Yunnan. Academic Press, Beijing: 1993: 77
4. Chang CH, Lin CC, Hattori M, Namba T. Four prenylated xanthones from Cudrania cochinchinensis. Phytochemistry 1989; 28: 595-8
5. Chang CH, Lin CC, Kawata Y, Hattori M, Namba T. Prenylated xanthones from Cudrania cochinchinensis. Phytochemistry 1989; 28: 2823-6
6. Hano Y, Matsumoto Y, Sun JY, Nomura T. Structures of three new isoprenylated xanthones, cudraxanthones E, F, and G. Planta Medica 1990; 56: 399-402
7. Hano Y, Matsumoto Y, Sun JY, Nomura T. Structures of four new isoprenylated xanthones, cudraxanthones H, I, J, and K. Planta Medica 1990; 56: 478-81
8. Deshpande VH, Rama Rao AV, Mala Varadan, Venkataraman K. Wood and bark phenolics of Maclura pomifera: four new xanthones. Indian Journal of Chemistry 1973; 11: 518-24
9. Wolfrom ML, Komitsky FJr, Mundell PM. Osage orange pigments. XVI. The structure of alvaxanthone. J Org Chem 1965; 30: 1088-91
10. + exchanger from the bark of Erythrina variegata and the roots of Maclura cochinchinensis. Chem Pharm Bull 1997; 45: 1615-9
11. Ishiguro K, Fukumoto H, Suitani A, Nakajima M, Isoi K. Prenylated xanthones from cell suspension cultures of Hypericum patulum. Phytochemistry 1996; 42: 435-7
12. Monache FD, Ferrari F, Pomponi M. Flavanones and xanthones from Maclura pomifera. Phytochemistry 1984; 23: 1489-91
13. Ingham JL, Keen NT, Hymowitz T. A new isoflavone phytoalexin from fungus-inoculated stems of Glycine wightii. Phytochemistry 1977; 16: 1943-6
14. Wu LJ, Miyase T, Ueno A, Kuroyanagi M, Noro T, Fukushima S. Studies on the constituents of Sophora flavescens Ait. III. Yakugaku Zasshi 1985; 105: 736-41
15. Yang SP, Dong L, Wang Y, Wu Y, Yue JM. Antifungal diterpenoids of Pseudolarix kaempferi, and their structure-activity relationship study. Bioorg Med Chem 2003; 63: 4577-84