Antioxidative flavonoids from Cleistocalyx operculatus buds

Chemical and Pharmaceutical Bulletin

Volumn 56, Issue 12, 2008, Pages 1725-1728

  Min, Byung Sun ^a   Van Thu, Cao ^b   Dat, Nguyen Tien ^c   Dang, Nguyen Hai ^c   Jang, Han Su ^d   Hung, Tran Manh ^a  

^a Catholic University of Daegu   (South Korea)

^b HANOI UNIVERSITY OF PHARMACY   (Viet Nam)

^c GRADUATE UNIVERSITY OF SCIENCE AND TECHNOLOGY   (Viet Nam)

^d Gyeongbuk Institute for Bio industry   (South Korea)

Author keywords

Anti oxidant; Cleistocalyx operculatus; Flavonoid; Myrtaceae

Indexed keywords

1,1 DIPHENYL 2 PICRYLHYDRAZYL; 3' FORMYL 4',6',4 TRIHYDROXY 2' METHOXY 5' METHYLCHALCONE; 3' FORMYL 6',4 DIHYDROXY 2' METHOXY 5' METHYLCHALCONE 4' O BETA DEXTRO GLUCOPYRANOSIDE; 8 FORMYL 6 METHYLNARINGENIN; 8 FORMYL 6 METHYLNARINGENIN 7 O BETA DEXTRO GLUCOPYRANOSIDE; FLAVONOID; PLANT EXTRACT; SCAVENGER; UNCLASSIFIED DRUG;

ANTIOXIDANT ACTIVITY; ARTICLE; BUD; CLEISTOCALYX OPERCULATUS; DRUG ISOLATION; DRUG SCREENING; DRUG STRUCTURE; IC 50; IN VITRO STUDY; MYRTACEAE; NONHUMAN; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; STRUCTURE ANALYSIS;

ANTIOXIDANTS; BETA-GLUCOSIDASE; CIRCULAR DICHROISM; FLAVONOIDS; FLOWERS; HYDROLYSIS; MAGNETIC RESONANCE SPECTROSCOPY; MULTIENZYME COMPLEXES; MYRTACEAE; PICRATES; PLANT EXTRACTS; SPECTROMETRY, MASS, ELECTROSPRAY IONIZATION; SPECTROPHOTOMETRY, INFRARED; SPECTROPHOTOMETRY, ULTRAVIOLET;

EID: 57349116180     PISSN: 00092363     EISSN: 13475223     Source Type: Journal    
DOI: 10.1248/cpb.56.1725     Document Type: Article

References (16)

1. Loi D. T., "Vietnamese Medicinal Plants and Ingredients," Medical Publishing House, Hanoi, 2001, pp. 423-424.
2. Ye C. L., Lu Y. H., Wei D. Z., Phytochemistry, 65, 445-447 (2004).
3. Woo A. Y., Waye M. M., Kwan H. S., Chan M. C., Chau C. F., Cheng C. H., Vasc. Pharmacol., 38, 163-168 (2002).
4. Lu Y. H., Du C. B., Wu Z. B., Ye C. L., Liu J. W., Wei D. Z., Zhongguo Zhong Yao Za Zhi, 28, 964-966 (2003).
5. Mai T. T., Chuyen N. V., Biosci. Biotechnol. Biochem., 71, 69-76 (2007).
6. Nomura M., Yamakawa K., Hirata Y., Niwa M., Shoyakugaku Zasshi, 47, 408-410 (1993).
7. Zhang F. X., Liu M. F., Lu R. R., Zhiwu Xuebao, 32, 469-472 (1990).
8. Dung N. X., Luu H. V., Khoi T. T., Leclercq P. A., J. Essent. Oil Res., 6, 661-662 (1994).
9. Ye C. L., Liu J. W., Wei D. Z., Lu Y. H., Qian F., Cancer Chemother. Pharmacol., 56, 70-74 (2005).
10. Ye C. L., Liu Y., Wei D. Z., J. Pharm. Pharmacol., 59, 553-559 (2007).
11. Ye C. L., Qian F., Wei D. Z., Lu Y. H., Liu J. W., Leuk. Res., 29, 887-892 (2005).
12. Norbedo C., Ferraro G., Coussio J. D., J. Nat. Prod., 45, 635-636 (1982).
13. Gaffield W., Tetrahedron, 26, 4093-4108 (1970).
14. Karikome H., Mimaki Y., Sashida Y., Phytochemistry, 30, 315-319 (1991).
15. Zhao J., Nakamura N., Hattori M., Kuboyama T., Tohda C., Komatsu K., Chem. Pharm. Bull., 50, 760-765 (2002).
16. Min B. S., Na M. K., Oh S. R., Ahn K. S., Jeong G. S., Li G., Lee S. K., Joung H., Lee H. K., J. Nat. Prod., 67, 1980-1984 (2004).