α-Glucosidase inhibitory constituents from duranta repens

Chemical and Pharmaceutical Bulletin

Volumn 52, Issue 7, 2004, Pages 785-789

  Iqbal, Kiran ^a   Malik, Abdul ^a   Mukhtar, Naveen ^a   Anis, Itrat ^a   Khan, Shamsun Nahar ^a   Choudhary, Muhammad Iqbal ^a  

^a UNIVERSITY OF KARACHI   (Pakistan)

Author keywords

glucosidase inhibition; C alkylated flavonoid; trans clerodane; Verbenaceae

Indexed keywords

3,13 CLERODADIEN 16,15 OLID 18 OIC ACID; 3,7,4' TRIHYDROXY 3' (8'' ACETOXY 7'' METHYLOCTYL) 5,6 DIMETHOXYFLAVONE; 6BETA HYDROXY 5BETA,8BETA,9BETA,10ALPHA CLERODA 3,13 DIEN 16,15 OLID 18 OIC ACID; 7 O ALPHA DEXTRO GLUCOPYRANOSYL 3,4 DIHYDROXY 3' (4'' ACETOXYL 3'' METHYLBUTYL) 5,6 DIMETHOXYFLAVONE; 7 O ALPHA DEXTRO GLUCOPYRANOSYL 3,5 DIHYDROXY 3' (4'' ACETOXYL 3'' METHYLBUTYL) 6,4' DIMETHOXYFLAVONE; ALPHA GLUCOSIDASE INHIBITOR; DURANTA REPENS EXTRACT; FLAVONOID; HARDWICKIIC ACID; PLANT EXTRACT; UNCLASSIFIED DRUG; ALPHA GLUCOSIDASE; ENZYME INHIBITOR;

ALKYLATION; ARTICLE; DRUG ISOLATION; DRUG STRUCTURE; DURANTA REPENS; ENZYME INHIBITION; MEDICINAL PLANT; NONHUMAN; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; SPECTROSCOPY; CHEMISTRY; DRUG ANTAGONISM; ISOLATION AND PURIFICATION; METABOLISM; PLANT; VERBENACEAE;

ALPHA-GLUCOSIDASES; ENZYME INHIBITORS; PLANT COMPONENTS; PLANT EXTRACTS; VERBENACEAE;

EID: 16544387131     PISSN: 00092363     EISSN: 13475223     Source Type: Journal    
DOI: 10.1248/cpb.52.785     Document Type: Article

References (19)

1. Riaz N., Anis I., Malik A., Ahmed Z., Rehman A.-U., Muhammad P., Nawaz S. A., Choudhary M. I., Chem. Pharm. Bull., 51, 252-254 (2003).
2. Khattak I., Anis I., Malik A., Nawaz S. A., Choudhary M. I., Chem. Pharm. Bull., 51, 412-414 (2003).
3. Riaz N., Anis I., Malik A., Ahmed Z., Rehman A.-U., Muhammad P., Shujaat S., Rahman A.-U., Nat. Prod. Res., 17, 247-251 (2003).
4. Perry L. M., Metzger J., "Medicinal Plants of East and South East Asia," The MIT Press, Cambridge, 1980, p. 432.
5. Grainge M., Ahmed S., "Hand Book of Plants with Pest-Control Properties," John Wiley and Sons, New York, 1998, p. 118.
6. Anis I., Ahmed S., Mustafa G., Malik A., Amtul Z., Rahman A.-U., Helv. Chim. Acta, 84, 649-655 (2001).
7. Iqbal K., Anis I., Mukhtar N., Malik A., Fatima N., Chaudhary M. I., Heterocycles, 60, 151-157 (2003), and the references cited therein.
8. Meyer B. N., Ferrigni N. R., Putnam J. E., Jacobsen L. B., Nicholas P. E., McLaughlin J. L., Planta Medica, 45, 31-34 (1982).
9. Sachdev K., Kulshrestha D. K., Indian J. Chem. B, 21, 798-799 (1982).
10. Quastel J. H., Analyst (London), 56, 311 (1951).
11. Voirin B., Phytochemistry, 22, 2107-2145 (1983).
12. Heymann H., Tezuka Y., Kikuchi T., Supriyatna S., Chem. Pharm. Bull., 42, 1202-1207 (1994).
13. Manabe S., Nishino C., Tetrahedron, 42, 3461-3467 (1986).
14. Matsui T., Yoshimoto C., Osajima K., Oki T., Osajima Y., Biosci. Biotech. Biochem., 60, 2019-2022 (1996).
15. Matsuura H., Asakawa C., Kurimoto M., Mizutani J., Biosci. Biotechnol. Biochem., 66, 1576-1578 (2002).
16. Mehta A., Zitzman N., Rudd P. M., Block T. M., Dwek R. A., FEBS Lett., 430, 17-22 (1998).
17. Fischer P. B., Collin M., Karlsson G. B., James W., Butters T. D., Davis S. J., Gordon S., Dwek R. A., Platt F. M., J. Virology, 69, 5791-5797 (1995).
18. Kurihara H., Ando J., Hatano M., Bioorg. Med. Chem. Lett., 5, 1241-1244 (1995).
19. Ali M. S., Jahangir M., Hassan S. S., Choudhary M. I., Phytochemistry, 60, 295-299 (2002).