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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Rasale, Dnyaneshwar B. | en_US |
dc.contributor.author | Maity, Indrajit | en_US |
dc.contributor.author | Das, Apurba Kumar | en_US |
dc.date.accessioned | 2022-05-05T15:51:40Z | - |
dc.date.available | 2022-05-05T15:51:40Z | - |
dc.date.issued | 2014 | - |
dc.identifier.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 | en_US |
dc.identifier.issn | 1359-7345 | - |
dc.identifier.other | EID(2-s2.0-84907075325) | - |
dc.identifier.uri | https://doi.org/10.1039/c4cc03835e | - |
dc.identifier.uri | https://dspace.iiti.ac.in/handle/123456789/9904 | - |
dc.description.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. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Royal Society of Chemistry | en_US |
dc.source | Chemical Communications | en_US |
dc.subject | 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 | en_US |
dc.title | In situ generation of redox active peptides driven by selenoester mediated native chemical ligation | en_US |
dc.type | Journal Article | en_US |
Appears in Collections: | Department of Chemistry |
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