Chemical constituents of the bulbs of Habranthus brachyandrus and their cytotoxic activities

Chemical and Pharmaceutical Bulletin

Volumn 57, Issue 10, 2009, Pages 1153-1157

  Jitsuno, Maki ^a   Yokosuka, Akihito ^a   Sakagami, Hiroshi ^b   Mimaki, Yoshihiro ^a  

^a TOKYO UNIVERSITY OF PHARMACY AND LIFE SCIENCES   (Japan)

^b MEIKAI UNIVERSITY SCHOOL OF DENTISTRY   (Japan)

Author keywords

Amaryllidaceae; Flavan derivative; Habranthus brachyandrus; HL 60 cell; HSC 2 cell; Hydroxybutyric acid glucoside

Indexed keywords

AMARYLLIDACEAE ALKALOID; CISPLATIN; ETOPOSIDE; FLAVAN DERIVATIVE; GLUCOSIDE; PHENOL DERIVATIVE;

ANTINEOPLASTIC ACTIVITY; ARTICLE; CANCER CELL CULTURE; CARBON NUCLEAR MAGNETIC RESONANCE; CELL STRAIN HL 60; CONTROLLED STUDY; DRUG CYTOTOXICITY; DRUG ISOLATION; HABRANTHUS BRACHYANDRUS; HUMAN; HUMAN CELL; IC 50; MEDICINAL PLANT; PLANT BULB; PROTON NUCLEAR MAGNETIC RESONANCE; SQUAMOUS CELL CARCINOMA;

CELL LINE, TUMOR; DRUG SCREENING ASSAYS, ANTITUMOR; FLAVANONES; GLUCOSIDES; HL-60 CELLS; HUMANS; LILIACEAE; MAGNETIC RESONANCE SPECTROSCOPY; MOLECULAR CONFORMATION; PHENOLS; PLANT ROOTS;

EID: 70349661827     PISSN: 00092363     EISSN: 13475223     Source Type: Journal    
DOI: 10.1248/cpb.57.1153     Document Type: Article

References (17)

1. Zhong J., Nat. Prod. Rep., 24, 886-905 (2007).
2. Boit H. G., Werner D., Chem. Ber., 92, 2582-2584 (1959).
3. Wildman W. C., Brown C. L., Tetrahedron Lett., 1968, 4573-4576 (1968).
4. Masaoud M., Ripperger H., Porzel A., Adam G., Phytochemistry, 38, 745-749 (1995).
5. Achenbach H., Stocker M., Constenla M. A., Phytochemistry, 27, 1835-1841 (1988).
6. Ghosal S., Singh S. K., Srivastava R. S., Phytochemistry, 24, 151-153 (1985).
7. Ahluwalia V. K., Arora K. K., Mukherjee K., Synthesis, 1984, 346-348 (1984).
8. Ghosal S., Mittal P., Kumar Y., Singh S. K., Phytochemistry, 28, 3193-3196 (1989).
9. Hirai N., Okamoto M., Udagawa H., Yamamuro M., Kato M., Koshimizu K., Biosci. Biotechnol. Biochem., 58, 1679-1684 (1994).
10. Gonzalez A. G., Leon F., Sanchez-Pinto L., Padron J. I., Bermejo J., J. Nat. Prod., 63, 1297-1299 (2000).
11. Kobayashi S., Ishikawa H., Kihara M., Shingu T., Hashimoto T., Chem. Pharm. Bull., 25, 2244-2248 (1977).
12. Hohmann J., Forgo P., Molnar J., Wolfard K., Molnar A., Thalhammer T., Mathe I., Sharples D., Planta Med., 68, 454-457 (2002).
13. Ali A. A., Ramadan M. A., Frahm A. W., Planta Med., 50, 424-427 (1984).
14. Li M., Wu A., Zhou P., Tetrahedron Lett., 47, 3707-3710 (2006).
15. Slade D., Ferreira D., Marais J. P. J., Phytochemistry, 66, 2177-2215 (2005).
16. Haugwitz R. D., Jeffs P. W., Wenkert E., J. Chem. Soc., 1965, 2001-2009 (1965).
17. Boit H. G., Chem. Ber., 87, 1339-1342 (1954).