Three new triterpenoids from Salacia hainanensis Chun et How showed effective anti-α-glucosidase activity

Phytochemistry Letters

Volumn 5, Issue 3, 2012, Pages 432-437

  Huang, Jian ^a   Guo, Zheng Hong ^a   Cheng, Peng ^a   Sun, Bo Hang ^a   Gao, Hui Yuan ^a  

^a SHENYANG PHARMACEUTICAL UNIVERSITY   (China)

Author keywords

Glucosidase; 2 ,3 Dihydroxylup 20(29) ene; 24,25,26 Trihydroxytirucall 7 en 3 one; 30 Hydroxy D:A friedo olean 1 en 3 one; Salacia hainanensis Chun et How

Indexed keywords

(2BETA,3BEBTA DIHYDROXYLUP 20(29) ENE; 21ALPHA HYDROXY D:A FRIEDO OLEAN 3 ONE; 24,25,26 TRIHYDROXYTIRUCALL 7 EN 3 ONE; 30 HYDROXY D:A FRIEDO OLEAN 1 EN 3 ONE; ALPHA GLUCOSIDASE; ENZYME INHIBITOR; HYDROXY D:A FRIEDO OLEAN 3 ONE; OLIBANUMOL J; TRITERPENOID; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CONTROLLED STUDY; DRUG MECHANISM; DRUG STRUCTURE; ENZYME ACTIVITY; ENZYME INHIBITION; MASS SPECTROMETRY; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; SALACIA; SALACIA HAINANENSIS;

EID: 84865042176     PISSN: 18743900     EISSN: 18767486     Source Type: Journal    
DOI: 10.1016/j.phytol.2012.03.016     Document Type: Article

References (11)

1. K. Akinobu, M. Toshio, M. Hisashi, and Y. Masayuki Structures of new friedelane- and norfriedelane-type triterpenes and polyacylated eudesmane-type sesquiterpene from Salacia chinensis Linn. (S. prinoides DC., Hippocrateaceae) and radical scavenging activities of principal constituents Chem. Pharm. Bull. 51 2003 1051 1055
2. C. Betanco, R. Freire, A.G. Gonzaiez, J.A. Salazar, C. Pascard, and T. Prange Three triterpenes and other terpenoids from Catha cassinoides Phytochemistry 19 1980 1989 1993
3. A.M. Dulcie, K. Maria, A.M. Hamdani, and A.H.T. David Triterpenoids from Owenia cepiodora Phytochemistry 49 1998 2457 2460
4. V.A. Facundo, C.H.S. Andrade, E.R. Silveira, R. Braz-Filhoa, and C.D. Hufford Triterpenes and flavonoids from Combretum leprosum Phytochemistry 32 1993 411 415
5. N. Hiroshi, S. Hideyo, H. Teruhisa, K. Ryoji, R.Y. Wu, and K.H. Lee Antitumour triterpenes of Maytenus diversifolia Phytochemistry 25 1986 479 485
6. I. Kanji, S. Hiroshi, S. Motoyoshi, and S. Koichiro Phenyl glucosides from a hairy root culture of Swertia japonica Phytochemistry 29 1990 3823 3825
7. Y. Masayuki, M. Toshio, M. Hisashi, T. Genzoh, and M. Osamu Absolute stereostructure of potent α-glucosidase inhibitor, salacinol, with unique thiosugar sulfonium sulfate inner salt structure from Salacia reticulata Bioorg. Med. Chem. 10 2002 1547 1554
8. Y. Masayuki, N. Norihisa, S. Hiroshi, T. Miki, K. Yuzo, and M. Hisashi Polyphenol constituents from Salacia species: quantitative analysis of mangiferin with α-glucosidase and aldose reductase inhibitory activities Yakugaku Zasshi. 121 2001 371 378
9. Y. Masayuki, M. Toshio, O. Hideo, and M. Hisashi Absolute stereostructures of olibanumols A, B, C, H, I, and J from olibanum, gum-resin of Boswellia carterii, and inhibitors of nitric oxide production in lipopolysaccharide-activated mouse peritoneal macrophages Chem. Pharm. Bull. 57 2009 957 964
10. T. Matsui, T. Ueda, T. Oki, K. Sugita, N. Terahara, and K. Matsumoto α-Glucosidase inhibitory action of natural acylated anthocyanins. 1. Survey of natural pigments with potent inhibitory activity J. Agric. Food Chem. 49 2001 1948 1951 (Pubitemid 32816843)
11. N.S. William, C.S. Mary, P.R. Lynton, B.M. Michael, J.M. Edward, L.Q. Chen, B.B. Robert, N. Pichaya, and R.J. Betsy Triterpenoid constituents in the bark of Balanops australiana Aust. J. Chem. 53 2000 809 812