Cytotoxic and antimycobacterial prenylated flavonoids from the roots of Eriosema chinense

Journal of Natural Products

Volumn 72, Issue 6, 2009, Pages 1092-1096

  Sutthivaiyakit, Somyote ^a   Thongnak, Oracha ^a   Lhinhatrakool, Thitima ^a   Yodchun, Orapan ^a   Srimark, Ratree ^a   Dowtaisong, Prisana ^a   Chuankamnerdkarn, Mayuree ^a  

^a RAMKHAMHAENG UNIVERSITY   (Thailand)

Author keywords

[No Author keywords available]

Indexed keywords

DEHYDROLUPINIFOLINOL; DOXORUBICIN; ELLIPTICINE; FLAVONOID; FLEMICHIN D; ISONIAZID; KHONKLONGINOL A; KHONKLONGINOL B; KHONKLONGINOL C; KHONKLONGINOL D; KHONKLONGINOL E; KHONKLONGINOL F; KHONKLONGINOL G; KHONKLONGINOL H; LIGNAN DERIVATIVE; LUPINIFOLIN; LUPINIFOLINOL; RIOSEMAONE A; STREPTOMYCIN; UNCLASSIFIED DRUG; YANGAMBIN;

ANTIBACTERIAL ACTIVITY; ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CELL STRAIN KB; CONTROLLED STUDY; DRUG CYTOTOXICITY; DRUG ISOLATION; DRUG STRUCTURE; ERIOSEMA CHINENSE; HUMAN; HUMAN CELL; LUNG SMALL CELL CANCER; MEDICINAL PLANT; MINIMUM INHIBITORY CONCENTRATION; MYCOBACTERIUM TUBERCULOSIS; NONHUMAN; PLANT ROOT; PROTON NUCLEAR MAGNETIC RESONANCE; SQUAMOUS CELL CARCINOMA;

ANTINEOPLASTIC AGENTS, PHYTOGENIC; ANTITUBERCULAR AGENTS; DRUG SCREENING ASSAYS, ANTITUMOR; FLAVONOIDS; HUMANS; MICROBIAL SENSITIVITY TESTS; MYCOBACTERIUM TUBERCULOSIS; PLANT ROOTS;

ERIOSEMA; MYCOBACTERIUM TUBERCULOSIS;

EID: 67650267725     PISSN: 01633864     EISSN: None     Source Type: Journal    
DOI: 10.1021/np900021h     Document Type: Article

References (17)

1. SmitinandT. Thai Plant Names (Botanical Names-Vernacular Names); Funny Publishing: Bangkok, 1980; p 141.
2. Smalberger, T. M.; Vleggaar, R.; Weber, J. C. Tetrahedron 1974, 30, 3927-3931.
3. Singhal, A. K.; Sharma, R. P.; Thyagarajan, G.; Herz, W.; Govindan, S. V. Phytochemistry 1980, 19, 929-934.
4. Singhal, A. K.; Sharma, R. P.; Madhusudanan, K. P.; Thyagarajan, G.; Herz, W.; Govindan, S. V. Phytochemistry 1981, 20, 803-806.
5. Ma, W. G.; Fuzzati, N.; Li, Q. S.; Yang, C. R.; Stoeckli-Evans, H.; Hostettmann, K. Phytochemistry 1995, 39, 1049-1061.
6. Jain, A. C.; Gupta, R. C.; Sarpal, P. D. Tetrehedron 1978, 34, 3563-3567.
7. (a) Jeffereries, P. R.; Knox, J. R.; White, D. E. Aust. J. Chem. 1961, 14, 175-177.
8. (b) Greger, H.; Hofer, O. Tetrahedron 1980, 36, 3551-3558.
9. Mabry, T. J.; Marklam, K. R.; Thomas, M. B. The Systematic Identification of Flavonoids; Springer-Verlag: New York, 1970; p 268.
10. (a) Gaffield, W. Tetrahedron 1970, 26, 4093-4108.
11. (b) Slade, D.; Ferreira, D.; Marais, J. P. J. Phytochemistry 2005, 66, 2177-2215.
12. Alavez-Solano, D.; Reyes-Chilpa, R.; Jiménez-Estrada, M.; Gómez- Garibay, F.; Chavez-Uribe, I.; Sousa-Sánchez, M. Phytochemistry 2000, 55, 953-957.
13. Mahidol, C; Prawat, H.; Kaweetripob, W.; Ruchirawat, S. Heterocycles 2002, 57, 1287-1292.
14. Jang, D. S.; Cuendet, M.; Hawthorne, M. E.; Kardono, L. B. S.; Kawanishi, K.; Fong, H. H. S.; Mehta, R. G.; Pezzuto, J. M.; Kinghorn, A. D. Phytochemistry 2002, 61, 867-872.
15. (a) Desjardins, R. E.; Canfield, C. J.; Haynes, J. D.; Chulay, J. D. Antimicrob. Agents Chemother. 1979, 16, 710-718.
16. (b) Skehan, P.; Storeng, R.; Scudiero, D.; Monks, A.; McMahon, J.; Vistica, D.; Warren, J. T.; Bokesch, H.; Kenney, S.; Boyd, M. R. J. Natl. Cancer Inst. 1990, 82, 1107-1112.
17. Collins, L. A.; Franzblau, S. G. Antimicrob. Agents Chemother. 1997, 41, 1004-1009.