Oxyfunctionalization products of terpenoids with dimethyldioxirane and their biological activity

Chemical and Pharmaceutical Bulletin

Volumn 55, Issue 2, 2007, Pages 247-250

  Ogawa, Shoujiro ^a   Hosoi, Keiji ^a   Ikeda, Noriaki ^a   Makino, Mitsuko ^a   Fujimoto, Yasuo ^a   Iida, Takashi ^a  

^a NIHON UNIVERSITY   (Japan)

Author keywords

glucosidase; Dimethyldioxirane; Diterpenoid; Oxyfunctionalization; Triterpenoid

Indexed keywords

11 OXOOLEANOLIC ACID ACETATE; 11 OXOURSOLIC ACID ACETATE; 11,12 DEHYDROURSOLIC LACTONE; 15,16 DEHYDRO 17 HYDROXYKAURENIC ACID; 15,16ALPHA EPOXY 17 HYDROXYKAURENIC ACID; 16,17 DIHYDROXYKAURENIC ACID; 3 O ACETYL 12 OXOOLEANOLIC LACTONE; 3 O ACETYL 12ALPHA CHLOROOLEANAN 28,13 OLIDE; 3 O ACETYL 12ALPHA HYDROXYOLEAN 9 EN 28,13 OLIDE; 3 O ACETYL 12ALPHA HYDROXYOLEANOLIC LACTONE; 3 O ACETYL 20BETA HYDROXYURS 11 EN 28,13 OLIDE; 3 O ACETYL 28 CHLORO 29 OXOLUPEOL; 30 NOR 20 OXOLUPEOL ACETATE; 30 OXOLUPEOL ACETATE; ALPHA GLUCOSIDASE; DIMETHYLDIOXIRANE; ENT 17 CHLORO 16 HYDROXYKAURAN 19 OIC ACID; KAURENIC ACID; LUPEOL ACETATE; OLEANOLIC ACID ACETATE; TERPENOID DERIVATIVE; UNCLASSIFIED DRUG; URSOLIC ACID ACETATE;

ARTICLE; BIOLOGICAL ACTIVITY; CARBON NUCLEAR MAGNETIC RESONANCE; CHROMATOGRAPHY; DEGRADATION KINETICS; DRUG POTENCY; DRUG STRUCTURE; ENZYME INHIBITION; INHIBITION KINETICS; OXIDATION; PROTON NUCLEAR MAGNETIC RESONANCE; SEPARATION TECHNIQUE; SPECTROSCOPY; STRUCTURE ANALYSIS;

ACETATES; ALPHA-GLUCOSIDASES; DITERPENES; EPOXY COMPOUNDS; MAGNETIC RESONANCE SPECTROSCOPY; OLEANOLIC ACID; OXIDATION-REDUCTION; PLANTS, MEDICINAL; TERPENES; TRITERPENES;

EID: 33846947591     PISSN: 00092363     EISSN: 13475223     Source Type: Journal    
DOI: 10.1248/cpb.55.247     Document Type: Article

References (13)

1. Omura T., Ishimura Y., Fujii Y. (eds.), "Cytochrome P-450," Kodansha, Tokyo, 1993.
2. Reese R. B., Steroids, 66, 481-497 (2001).
3. Meunier B., Chem. Rev., 92, 1411-1456 (1992).
4. Ogawa S., Iida T., Goto T., Mano N., Goto J., Nambara T., Org. Biomol. Chem., 2, 1013-1018 (2004).
5. Murry R. W., Chem. Rev., 89, 1187-1201 (1989).
6. Curci R., Dinoi A., Rubino M., Pure Appl. Chem., 67, 811-822 (1995).
7. Parish E. J., Qiu Z., Lipids, 39, 805-809 (2004).
8. Bovicelli T., Lupattelli P., Mincione E., J. Org. Chem., 57, 5052-5054 (1992).
9. Bovicelli P., Lupattelli P., Fiorini V., Tetrahedron Lett., 34, 6103-6104 (1993).
10. Iida T.,Yamaguchi T., Nakamori R., Hikosaka M., Mano N., Goto J., Nambara T., J. Chem. Soc. Perkin Trans. 1, 2001, 2229-2236.
11. Adam W., Bialas J., Hadjiarapoglou L., Chem. Ber., 124, 2377 (1991).
12. Cèrre C., Hofmann A. F., Schteingart C. D., Jia W., Maltby D., Tetrahedron, 53, 435-446 (1997).
13. Asano N., Oseki E., Kaneko K. M., Carbohydr. Res., 258, 255-256 (1994).