Non-fatty acyl polyketide starter in the biosynthesis of vicenistatin, an antitumor macrolactam antibiotic
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference12 articles.
1. Vicenistatin, a novel 20-membered macrocyclic lactam antitumor antibiotic.
2. The structure of hitachimycin, a novel macrocyclic lactam involving β-phenylalanine
3. Biosynthesis of the 17-membered carbocyclic ring of lankacidin antibiotics
4. Biosynthetic studies with carbon-13. Lankacidin group of antibiotics
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1. Biosynthesis of macrolactam antibiotics with β-amino acid polyketide starter units;The Journal of Antibiotics;2024-05-30
2. A versatile route to 2,4,6-trideoxy-4-aminohexoses: Stereoselective syntheses of d -vicenisamine and its epimers via iodocyclization of carbamate;Tetrahedron;2017-12
3. The many roles of glutamate in metabolism;Journal of Industrial Microbiology and Biotechnology;2016-03-01
4. Synthesis and Structure-Activity Relationship of Vicenistatin, a Cytotoxic 20-Membered Macrolactam Glycoside;Chemistry - An Asian Journal;2012-09-27
5. A Natural Protecting Group Strategy To Carry an Amino Acid Starter Unit in the Biosynthesis of Macrolactam Polyketide Antibiotics;Journal of the American Chemical Society;2011-10-25
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