In situ generation of redox active peptides driven by selenoester mediated native chemical ligation

Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/9904

Title:	In situ generation of redox active peptides driven by selenoester mediated native chemical ligation
Authors:	Rasale, Dnyaneshwar B. Maity, Indrajit Das, Apurba Kumar
Keywords:	cysteinylglycine\|dipeptide\|disulfide\|ester\|nanomaterial\|oxidizing agent\|peptide\|selenium derivative\|ester\|nanotube\|peptide\|redox active peptide\|selenoester\|unclassified drug\|atomic force microscopy\|chemistry\|oxidation reduction reaction\|synthesis\|ultrastructure\|article\|chemical reaction\|gel\|high performance liquid chromatography\|hydrogen bond\|native chemical ligation\|oxidation reduction reaction\|phase transition\|protein conformation\|protein synthesis\|Dipeptides\|Disulfides\|Esters\|Microscopy, Atomic Force\|Nanostructures\|Oxidants\|Oxidation-Reduction\|Peptides\|Selenium Compounds
Issue Date:	2014
Publisher:	Royal Society of Chemistry
Citation:	Rasale, D. B., Maity, I., & Das, A. K. (2014). In situ generation of redox active peptides driven by selenoester mediated native chemical ligation. Chemical Communications, 50(77), 1139711400. https://doi.org/10.1039/C4CC03835E
Abstract:	Redox active peptides are generated through selenoester mediated native chemical ligation (NCL). Distinct nanostructures, such as nanotubes to nanofibrillar architectures, were observed for self-assembling soft materials. © 2014 The Partner Organisations.
URI:	https://doi.org/10.1039/c4cc03835e https://dspace.iiti.ac.in/handle/123456789/9904
ISSN:	1359-7345
Type of Material:	Journal Article
Appears in Collections:	Department of Chemistry

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