Indoloquinolines: Possible Biogenesis from Common Indole Precursors and their Synthesis using Domino Strategies

Author(s): Prakash T. Parvatkar, Perunninakulath S. Parameswaran

Journal Name: Current Organic Synthesis

Volume 13 , Issue 1 , 2016

Become EABM
Become Reviewer
Call for Editor

Graphical Abstract:


The tetracyclic indoloquinoline alkaloids, cryptolepine, neocryptolepine, isocryptolepine and their analogues, isolated from the West African shrub Cryptolepis sanguinolenta are known to display promising antimalarial, antibacterial, antiviral, antihyperglycemic and cytotoxic properties. Biogenesis of these different linear and angular indoloquinolines are most probably through the reaction of anthranilic acid with selected indole derivatives – indoxyl, oxindole, 3-formyl indole, etc., all by-products during tryptophan biosynthesis from chorismate. As part of our ongoing screening program of bioactive compounds, several of these natural products and their derivatives, including few halogenated metabolites were synthesized in our laboratory using simplified domino approaches. Apart from codifying their probable biosynthetic pathways, this article also summarizes our synthetic studies, most of which were planned mimicking the natural biosynthetic pathways.

Keywords: Alkaloid, biogenesis, Cryptolepis sanguinolenta, domino, indoloquinoline, natural product.

Rights & PermissionsPrintExport Cite as

Article Details

Year: 2016
Page: [58 - 72]
Pages: 15
DOI: 10.2174/1570179412666150511224648
Price: $65

Article Metrics

PDF: 61
PRC: 1