4.5 Review

Perspectives on Chemopreventive and Therapeutic Potential of Curcumin Analogs in Medicinal Chemistry

期刊

MINI-REVIEWS IN MEDICINAL CHEMISTRY
卷 10, 期 5, 页码 372-387

出版社

BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/138955710791330891

关键词

Curcumin; chemoprevention; therapy; synthetic analog

资金

  1. National Cancer Institute, NIH [R01CA083695, R01CA131151, R01CA132794]
  2. University of Texas MD Anderson Cancer Center [5P20-CA101936]
  3. NATIONAL CANCER INSTITUTE [R01CA083695, R01CA132794, R01CA131151, P20CA101936] Funding Source: NIH RePORTER

向作者/读者索取更多资源

Curcumin is a natural polyphenol derived from the plant Curcuma longa, commonly called turmeric. Extensive research over past 50 years has indicated that this polyphenol is highly pleiotropic molecule capable of preventing and treating various cancers. The anticancer potential of Curcumin is severely affected by its limited systemic and target tissue bioavailability and rapid metabolism. In the present review article, we provide a summarized account of different drug delivery systems employed for tackling the problem of curcumin's bioavailability such as liposomes, phospholipid complexes and nanoparticles. Concomitantly we have reviewed the large volume of literature reports describing structural modifications of Curcumin and the anticancer potential of its analogs. Some of the difluorocurcumin analogs allowing longer circulation times and preferential accumulation in the pancreas seem to offer promising leads for conducting first in-depth animal studies and subsequently clinical trials for the use of these analogs for prevention of tumor progression and/or treatments of human malignancies.

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