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Chemical Compound Review

vicenistatin     (3E,5E,7S,8S,10E,13E,15E,19S)- 8-[(2R,4S,5S...

Synonyms: CHEMBL1797115, AC1O5QK7, C15688, 150999-05-6
 
 
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Disease relevance of vicenistatin

  • Vicenistatin, an antitumor antibiotic isolated from Streptomyces halstedii, is a unique 20-membered macrocyclic lactam with a novel aminosugar vicenisamine [1].
 

High impact information on vicenistatin

  • The vicenistatin biosynthetic gene cluster (vin) spanning approximately 64 kbp was cloned and sequenced [1].
  • In the January issue of Chemistry & Biology, Kakinuma and coworkers reported on the vicenistatin biosynthetic gene cluster and demonstrated in vitro glycosylation of its aglycone core, raising the possibility of producing analogs with altered sugar residues [2].
  • A unique feature of the vicenistatin PKS is that the loading module contains only an acyl carrier protein domain, in contrast to other known PKS-loading modules containing certain activation domains [1].
 

Associations of vicenistatin with other chemical compounds

 

Analytical, diagnostic and therapeutic context of vicenistatin

References

  1. Cloning, sequencing, and functional analysis of the biosynthetic gene cluster of macrolactam antibiotic vicenistatin in Streptomyces halstedii. Ogasawara, Y., Katayama, K., Minami, A., Otsuka, M., Eguchi, T., Kakinuma, K. Chem. Biol. (2004) [Pubmed]
  2. New start and finish for complex polyketide biosynthesis. Caffrey, P. Chem. Biol. (2004) [Pubmed]
  3. Involvement of glutamate mutase in the biosynthesis of the unique starter unit of the macrolactam polyketide antibiotic vicenistatin. Ogasawara, Y., Kakinuma, K., Eguchi, T. J. Antibiot. (2005) [Pubmed]
  4. Vicenistatin, a novel 20-membered macrocyclic lactam antitumor antibiotic. Shindo, K., Kamishohara, M., Odagawa, A., Matsuoka, M., Kawai, H. J. Antibiot. (1993) [Pubmed]
 
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