A new acylated flavonol glycoside and antioxidant effects of Hedyotis diffusa

Planta Medica

Volumn 66, Issue 4, 2000, Pages 374-377

  Lu, Chai Ming ^a   Yang, Jenq Jer ^b   Wang, Phen Yuh ^c   Lin, Chun Ching ^c  

^a TAJEN INSTITUTE OF TECHNOLOGY   (Taiwan)

^b CHIA NAN UNIVERSITY OF PHARMACY AND SCIENCE   (Taiwan)

^c KAOHSIUNG MEDICAL UNIVERSITY   (Taiwan)

Author keywords

[No Author keywords available]

Indexed keywords

ALLOPURINOL; ANTIOXIDANT; ARACHIDONIC ACID; FERRIC CHLORIDE; GLYCOSIDE; KAEMPFEROL DERIVATIVE; PLANT EXTRACT; TROLOX C;

ANIMAL TISSUE; ANTIOXIDANT ACTIVITY; ARTICLE; CONTROLLED STUDY; DRUG ISOLATION; DRUG STRUCTURE; LIPID PEROXIDATION; LIVER; NONHUMAN; PLANT; RAT; TRADITIONAL MEDICINE;

ACYLATION; ANTIOXIDANTS; FLAVONOIDS; GLYCOSIDES; RUBIACEAE; SPECTRUM ANALYSIS;

ANIMALIA; HEDYOTIS DIFFUSA;

EID: 0034120607     PISSN: 00320943     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2000-8544     Document Type: Article

References (17)

1. 1 Kan WS. 10.15 Rubiaceae, 10. Angiospermae. The Chinese Medicine Publishing Inc. Pharmaceutical Botany, Taipei, Taiwan, R.O.C. 1986:522
2. 2 Yang JJ, Hsu HY, Lin CC. The possible use of Peh-Hue-Juwa-Chi-Cao as an antitumor agent and radioprotector after therapeutic irradiation. Phytotherapy Research 1997; 11:6-10
3. 3 Bojthe-Horvath K, Hetenyi F, Kocsis A, Szabo L, Varga-Balaz M, Mathe Jr I et al. Iridoid glycosides from Galium verum. Phytochemistry 1982; 21:2917-9
4. 4 Takagi S, Yamaki M, Nishihama Y, Ishiguro K. On the iridoid glycosides of the Chinese drug "bai hua she she cao" (Hedyotis diffusa Willd.). Shyoyakugaku Zasshi 1982; 36: 366-9
5. 5 Nishihama Y, Masuda K, Yamaki M, Takagi S, Sakina K. Three new iridoid glycosides from Hedyotis diffusa. Planta Medica 1981; 43: 28-33
6. 6 Huang JT. New iridoids from Oldenlandia diffusa Roxb. Arch. Pharm. 1981; 314: 831-6
7. 7 Halliwell B. Reactive oxygen species in living systems: source, biochemistry and role in human disease. Am. J. Med. 1991; 91: 14S-22S
8. 8 Harborne JB, Mabry TJ, Mabry H. 2.1 Ultraviolet and visible absorption spectroscopy, 2. Ultraviolet-visible and proton magnetic resonance spectroscopy of flavonoids.part In: The Flavonoids, Markham KR, Mabry TJ, editors. Chapman and Hall 1975: 48-60
9. 9 Murakami T, Wada H, Stanley R, Tanaka N, Kido T, Iida H et al. Chemical and chemotaxonomical studies of filices. LXV. A few new flavonol glycosides. Yakugaku Zasshi 1986; 106: 982-8
10. 13C NMR spectroscopy of flavonoids. Heterocycles1981; 16: 2181-236
11. 11 Agrawal PK. NMR spectroscopy in the structural elucidation of oligosaccarides and glycosides. Phytochemistry 1992; 10: 3307-30
12. 12 Lin CC, Chen JY, Namba T. Development of natural crude drug resources from Taiwan (V). Pharmaceutical studies on Chinese crude drug "Peh-hue-juwa-chi-chhau". Shyoyakugaku Zasshi 1987; 41: 180-8
13. 13 Markham KR, Ternai B, Stanley R, Geiger H, Mabry TJ. Carbon-13 NMR studies of flavonoids - III Naturally occurring flavonoid glycosides and their acylated derivatives. Tetrahedron 1978; 34: 1389-97
14. 14 Chang WS, Chang YH, Lu FJ, Chiang HC. Inhibitory effects of phenolics on xanthine oxidase. 1994; 14: 501-6
15. 15 Mc Cord JM, Fridovich I. An enzymatic function for erythro-cuprein (Hemocuprein). J. Biol. Chem. 1969; 244: 6049-58
16. 16 Yoden K, Iio T, Tabata T. Measurement of thiobarbituric acid value in tissue homogenate solubilized with sodium dodecyl sulphate. Yakugaku Zasshi 1980; 100: 553-9
17. 17 Kimuya K, Kubo M, Tani T, Arich S, Okuda H. Studies on Scutellariae Radix. IV. Effects on lipid peroxidation in rat liver homogenate. Chem. Pharm. Bull. 1981; 29: 2610-7