The origins of cyanobactin chemistry and biology

被引:16
|
作者
Jaspars, Marcel [1 ]
机构
[1] Univ Aberdeen, Marine Biodiscovery Ctr, Dept Chem, Old Aberdeen AB24 3UE, Scotland
基金
英国生物技术与生命科学研究理事会;
关键词
TUNICATE LISSOCLINUM-PATELLA; CYCLIC-PEPTIDES; MARINE TUNICATE; MACROCYCLIZATION; ASCIDIACYCLAMIDE; DIVERSITY; DISCOVERY; SYMBIONT; PATHWAY; ROUTE;
D O I
10.1039/c3cc49252d
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The correct structure of the symmetrical cyanobactin, ascidiacyclamide, was published in Chemical Communications by Hamamoto et al. in 1983. The cyanobactin family of compounds are cyclic peptides with modifications including azole/azoline rings, D-stereocentres and in some cases prenyl groups. Although related compounds were isolated earlier by Ireland et al., two of the three published structures later had to be corrected. Hamamoto's ascidiacyclamide structure assisted the understanding of the chemistry, bioactivity, biological origin and biosynthesis of this group of compounds. Cyanobactins are of interest as new chemotypes for the treatment of a range of diseases, in particular those in which extended binding sites are implicated.
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页码:10174 / 10176
页数:3
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