Chemistry and Biology of Fascaplysin, a Potent Marine-Derived CDK-4 Inhibitor

Author(s): S. B. Bharate, S. Manda, N. Mupparapu, N. Battini, R. A. Vishwakarma

Journal Name: Mini-Reviews in Medicinal Chemistry

Volume 12 , Issue 7 , 2012

Become EABM
Become Reviewer


Marine natural products offer an abundant source of pharmacologically active agents with great diversity and complexity, and the potential to produce valuable therapeutic entities. Indole alkaloids is one of the important class of marine-derived secondary metabolites, with wide occurrence amongst variety of marine sources such as sponges, tunicates, algae, worms and microorganisms and have been extensively studied for their biological activities. Among this chemical family, a sponge-derived bis-indole alkaloid fascaplysin (1) exhibited broad range of bioactivities including antibacterial, antifungal, antiviral, anti-HIV-1-RTase, p56 tyrosine kinase inhibition, antimalarial, anti-angiogenic, antiproliferative activity against numerous cancer cell lines, specific inhibition of cyclin-dependent kinase-4 (IC50 350 nM) and action as a DNA intercalator. In the present review, the chemical diversity of natural as well as synthetic analogues of fascaplysin has been reviewed with a detailed account on synthetic reports and pharmacological studies. Our analysis of the structure-activity relationships of this family of compounds highlights the existence of various potential leads for the development of novel anticancer agents.

Keywords: Fascaplysin, anticancer, cyclin-dependent kinase, CDK-4, marine natural products, anti-angiogenic, acorn worms, unicates, symbiotic bacteria, stereochemistry

Rights & PermissionsPrintExport Cite as

Article Details

Year: 2012
Page: [650 - 664]
Pages: 15
DOI: 10.2174/138955712800626719
Price: $65

Article Metrics

PDF: 34