《Characterization of the promiscuous N-acyl CoA transferase, LgoC, in legonoxamine biosynthesis》 was written by Maglangit, Fleurdeliz; Alrashdi, Saad; Renault, Justine; Trembleau, Laurent; Victoria, Catherine; Tong, Ming Him; Wang, Shan; Kyeremeh, Kwaku; Deng, Hai. Product Details of 51644-96-3 And the article was included in Organic & Biomolecular Chemistry in 2020. The article conveys some information:
More than 500 siderophores are known to date, but only three were identified to be aryl-containing hydroxamate siderophores, legonoxamines A and B from Streptomyces sp. MA37, and aryl ferrioxamine 2 from Micrococcus luteus KLE1011. Siderophores are produced by microorganisms to scavenge iron from the environment, thereby making this essential metal nutrient available to the microbe. We demonstrate here that LgoC from MA37 is responsible for the key aryl-hydroxamate forming step in legonoxamine biosynthesis. Biochem. characterization established that LgoC displays considerable promiscuity for the acylation between N-hydroxy-cadaverine and SNAC (N-acetylcysteamines) thioester derivatives The experimental part of the paper was very detailed, including the reaction process of tert-Butyl (5-aminopentyl)carbamate(cas: 51644-96-3Product Details of 51644-96-3)
Some of the reported applications of tert-Butyl (5-aminopentyl)carbamate(cas: 51644-96-3) include: synthesis of of a supermacrocycle that self-assemble to form organic nanotubes., preparation of water-soluble unsymmetrical sulforhodamine fluorophores from monobrominated sulfoxanthene dye, synthesis of functionalized porphyrins as biocompatible carrier system for photodynamic therapy (PDT).Product Details of 51644-96-3
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics