Biosynthesis, asymmetric synthesis, and pharmacology, including cellular targets, of the pyrrole-2-aminoimidazole marine alkaloids
DRS at CSIR-National Institute of Oceanography
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Title |
Biosynthesis, asymmetric synthesis, and pharmacology, including cellular targets, of the pyrrole-2-aminoimidazole marine alkaloids
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Creator |
Al-Mourabit, A.
Zancanella, M.A. Tilvi, S. Romo, D. |
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Subject |
marine alkaloids
asymmetric syntheses structural complexity |
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Description |
The pyrrole-2-aminoimidazole (P-2-AI) alkaloids are a growing family of marine alkaloids, now numbering well over 150 members, with high topographical and biological information content. Their intriguing structural complexity, rich and compact stereochemical content, high N to C ratio (~1 : 2), and increasingly studied biological activities are attracting a growing number of researchers from numerous disciplines world-wide. This review surveys advances in this area with a focus on the structural diversity, biosynthetic hypotheses with increasing, but still rare, verifying experimental studies, asymmetric syntheses, and biological studies, including cellular target receptor isolation studies, of this stimulating and exciting alkaloid family
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Date |
2011-07-29T07:26:48Z
2011-07-29T07:26:48Z 2011 |
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Type |
Journal Article
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Identifier |
Natural Product Reports, vol.28(7); 2011; 1229-1260
http://drs.nio.org/drs/handle/2264/3889 |
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Language |
en
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Rights |
An edited version of this paper was published by and © The Royal Society of Chemistry 2011. http://dx.doi.org/10.1039/C0NP00013B
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Publisher |
The Royal Society of Chemistry
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