New cytotoxic biflavonoids from Selaginella delicatula

Planta Medica

Volumn 71, Issue 7, 2005, Pages 659-665

  Chen, Jih Jung ^a   Duh, Chang Yih ^b   Chen, Jinn Fen ^c  

^a TAJEN INSTITUTE OF TECHNOLOGY   (Taiwan)

^b NATIONAL SUN YAT SEN UNIVERSITY   (Taiwan)

^c Taitung District Agricultural Research and Extension Station   (Taiwan)

Author keywords

2,3 dihydroamentoflavone 7,4 ,7 trimethyl ether; Biflavonoids; Robustaflavone 4 ,4 dimethyl ether; Robustaflavone 7,4 4 trimethyl ether; Selaginella delicatula; Selaginellaceae

Indexed keywords

2'',3'' DIHYDROISOCRYPTOMERIN 7 METHYL ETHER; 2,3 DIHYDROAMENTOFLAVONE 7,4' DIMETHYL ETHER; 2,3 DIHYDROAMENTOFLAVONE 7,4',7'' TRIMETHYL ETHER; ALPHA TOCOPHERYLQUINONE; BIFLAVONOID; PLANT EXTRACT; ROBUSTAFLAVONE 4',4''' DIMETHYL ETHER; ROBUSTAFLAVONE 7,4',4''' TRIMETHYL ETHER; UNCLASSIFIED DRUG;

ANIMAL CELL; ARTICLE; CELL STRAIN HT29; CONTROLLED STUDY; CYTOTOXICITY; DRUG ACTIVITY; DRUG ISOLATION; DRUG STRUCTURE; HUMAN; HUMAN CELL; MOUSE; NONHUMAN; SELAGINELLA; SELAGINELLA DELICATULA; SPECTROSCOPY; STRUCTURE ANALYSIS;

ANIMALS; ANTINEOPLASTIC AGENTS, PHYTOGENIC; CELL LINE, TUMOR; FLAVONOIDS; HT29 CELLS; HUMANS; LEUKEMIA P388; MAGNETIC RESONANCE SPECTROSCOPY; MICE; PHYTOTHERAPY; PLANT COMPONENTS, AERIAL; PLANT EXTRACTS; SELAGINELLACEAE;

SELAGINELLA DELICATULA; SELAGINELLACEAE;

EID: 23644455460     PISSN: 00320943     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2005-871273     Document Type: Article

References (16)

1. Tsai JL, Shieh WC. Selaginellaceae in Flora of Taiwan. 2nd edition. Editorial Committee of the Flora of Taiwan, Taipei, Taiwan: 1994; Vol. 1: 45-57
2. Okigawa M, Hwa CW, Kawano N, Rahman W. Biflavones in Selaginella species. Phytochemistry 1971; 10: 3286-7
3. Lee SW, Chen ZT, Chen MT, Chen CM. Biflavones of Selaginella doederlenii Hieron. Chin Pharm J 1992; 44: 537-41
4. Lin RC, Skaltsounis AL, Seguin E, Tillequin F, Koch M. Phenolic constituents of Selaginella doederleinii. Planta Med 1994; 60: 168-70
5. Silva GL, Chai H, Gupta MP, Farnsworth NR, Cordell GA, Pezzuto JM et al. Cytotoxic biflavonoids from Selaginella willdenowii. Phytochemistry 1995; 40: 129-34
6. Sun CM, Syu WJ, Huang YT, Chen CC, Ou JC. Selective cytotoxicity of ginkgetin from Selaginella moellendorffii. J Nat Prod 1997; 60: 382-4
7. Lin LC, Kuo YC, Chou CJ. Cytotoxic biflavonoids from Selaginella delicatula. J Nat Prod 2000; 63: 627-30
8. Voirin B. Distribution des composés polyphénoliques chez es lycopodinées. Phytochemistry 1972; 11: 257-62
9. Teresa J de P, Urones JG, Marcos IS, Ferreras JF, Bertelloni AML, Barcala PB. Diterpenoids from Nepeta tuberosa subsp. reticulata. Phytochemistry 1987; 26: 1481-6
10. Mosmann T. Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. J Immunol Methods 1983; 65: 55-63
11. Chen JJ, Duh CY, Huang HY, Chen IS. Furoquinoline alkaloids and cytotoxic constituents from the leaves of Melicope semecarpifolia. Planta Med 2003; 69: 542-6
12. 13C NMR studies of some naturally occurring amentoflavone and hinokiflavone biflavonoids. Phytochemistry 1987; 26: 3335-7
13. Li SH, Zhang HJ, Niu XM, Yao P, Sun HD, Fong HHS. Chemical constituents from Amentotaxus yunnanensis and Torreya yunnanensis. J Nat Prod 2003; 66: 1002-5
14. Chen JJ, Huang YC, Chen YC, Huang YT, Wang SW, Peng CY et al. Cytotoxic amides from Piper sintenense. Planta Med 2002; 68: 980-5
15. Kojima H, Sato N, Hatano A, Ogura H. Sterol glucosides from Prunella vulgaris. Phytochemistry 1990; 29: 2351-5
16. Geran RI, Greenberg NH, Macdonald MM, Schumacher AM, Abbott BJ. Protocols for screening chemical agents and natural products against animal tumors and other biological systems. Cancer Chemother Rep, 3 1972; 3: 1-103