Biosynthesis, asymmetric synthesis, and pharmacology, including cellular targets, of the pyrrole-2-aminoimidazole marine alkaloids

被引:172
作者
Al-Mourabit, Ali [1 ]
Zancanella, Manuel A. [2 ]
Tilvi, Supriya [3 ]
Romo, Daniel [2 ]
机构
[1] CNRS, Inst Chim Subst Nat, Ctr Rech Gif Sur Yvette, UPR 2301, F-91198 Gif Sur Yvette, France
[2] Texas A&M Univ, Dept Chem, College Stn, TX 77842 USA
[3] Natl Inst Oceanog, CSIR, Bioorgan Chem Lab, Panaji 403004, Goa, India
关键词
DIMERIC BROMOPYRROLE ALKALOIDS; PYRROLE-IMIDAZOLE ALKALOIDS; PUMMERER REACTION CHEMISTRY; NATURAL-PRODUCT DIBROMOPHAKELLSTATIN; SPONGE AGELAS-DENDROMORPHA; RAY CRYSTAL-STRUCTURE; ENANTIOSELECTIVE SYNTHESIS; A-D; STEREOSELECTIVE-SYNTHESIS; RELATIVE CONFIGURATION;
D O I
10.1039/c0np00013b
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 (similar to 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.
引用
收藏
页码:1229 / 1260
页数:32
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