Lupane triterpenoid derivatives

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Carbohydrate doai

Patent

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

514 25, 514 53, 514 61, 514169, 514172, 514176, 514178, 536 41, 536 5, 536 187, 5361231, 53612313, A61K 31705, C07J 1700

Patent

active

056438842

ABSTRACT:
This invention relates generally to the field of medicinal chemistry, and more specifically to derivatives of a subclass of triterpenoid acids that have multi-medicament properties, that is derivatives of the lupane, betulinic acid, formulations containing such, and their use to prevent or treat certain diseases, and preferably to derivatives or analogues of betulinic acid, that have the following structural formula (1): ##STR1## wherein: Y is OR.sup.1, NR.sup.1.sub.2, O.sup.- M.sup.1 ;

REFERENCES:
patent: 3934027 (1976-01-01), Hess et al.
patent: 4173648 (1979-11-01), Pifferi et al.
patent: 5356880 (1994-10-01), Kurono et al.
patent: 5519008 (1996-05-01), Rao et al.
patent: 5527890 (1996-06-01), Rao et al.
Juodvirsis et al., CA 72:111711, 1969, "Synthesis of triterpene glycosides", Izr. Sib. Otd. Akad. Nauk. SSSR. (Russian).
Otsuka, H. et al., "Studies on Anti-Inflammatory Agents. V. A New Anti-Inflammatory Constituent of Pyracantha Crenulata ROEM," Chem. and Pharm. Bulletin, vol. 29, No. 11, pp. 3099-3104 (1981).
Inada, A. et al., "Phytochemical Studies on Meliaceous Plants. VIII. Structures and Inhibitory Effects on Epstein-Barr Virus Activation of Triterpenoids from Leaves of Chisocheton Macrophyllus KING," Chem. and Pharm. Bulletin, vol. 41, No. 3, pp. 617-619 (1993).
Sheth, K. et al., "Tumor Inhibitory Agent from Hyptis Emoryi (Labiatae)," Journal of Pharm. Sci., vol. 61, No. 11, p. 1819 (1972).
Chemical Abstracts, vol. 89, No. 25, Abstract No. 211956 (Kingston, D. et al.) (1978).
Chemical Abstracts, vol. 109, No. 17, Abstract No. 146343 (Tomas-Barberan, F. et al.) (1988).
Chemical Abstracts, vol. 111, No. 25, Abstract No. 228964 (Chen, R. et al.) (1989).
Chemical Abstracts, vol. 110, No. 19, Abstract No. 170211 (Choi, Y.H. et al.) (1989).
Chemical Abstracts, vol. 103, No. 25, Abstract No. 211168 (Fang, X. et al.) (1985).
Miles, D.H. et al., "Tumor Inhibitors I: Preliminary Investigation of Antitumor Activity of Sarracenia Flava," Journal of Pharm. Sci., vol. 63, No. 4, pp. 613-615 (1974).
Supplementary European Search Report issued May 31, 1996.
B.N. Rao et al., Siayl Lewis X Mimics Derived from a Pharmacophore Search Are Selectin Inhibitors with Anti-Inflammatory Activity, J. of Biol. Chem., vol. 269, No. 31, pp. 19663-19666 (1994).
Otsuka, et al., "Studies on Anti-inflammatory Agents. V..sup.1) A New Anti-inflammatory Constituent of Pyracantha crenulata Roem .sup.2) ", Chem.Pharm.Bull. 29:11:3099-3104 (1981).
Yasukawa, et al., "Sterol and Triterpene Derivatives from Plants Inhibit the Effects of a Tumor Promoter, and Sitosterol and Betulinic Acid Inhibit Tumor Formation in Mouse Skin Two-Stage Carcinogenesis," Oncology 48:72-76 (1991).
Heby, "Ornithine Decarboxylase as Target of Chemotherapy," Adv.Enzyme Regul., 24:103-124 (1985).
Choi, et al., "Ellagic Acid Derivatives of Agrostistachys hookeri.sup.1," Planta Medica, pp. 511-513 (1988).
CA 86:68400, 1976, Hiller et al., "Isolation of betulic acid 3-0.beta.-d-glcoside", a saponin from Eryngium bromelififolium Delar., (German) 1976.

LandOfFree

Say what you really think

Search LandOfFree.com for the USA inventors and patents. Rate them and share your experience with other people.

Rating

Lupane triterpenoid derivatives does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Lupane triterpenoid derivatives, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Lupane triterpenoid derivatives will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFUS-PAI-O-597180

  Search
All data on this website is collected from public sources. Our data reflects the most accurate information available at the time of publication.