Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/60821
Full metadata record
DC FieldValueLanguage
dc.contributor.authorSrinivas, Avula-
dc.date.accessioned2022-11-11T09:32:45Z-
dc.date.available2022-11-11T09:32:45Z-
dc.date.issued2022-11-
dc.identifier.issn2583-1321 (Online); 0019-5103 (Print)-
dc.identifier.urihttp://nopr.niscpr.res.in/handle/123456789/60821-
dc.description1199-1204en_US
dc.description.abstractHexa peptide 10 has been prepared by the condensation of tetrapeptide acid and dipeptide amine by using standard coupling reagents EDCI, HOBT and DIPEA. In the same method, terta peptide 8 has also been prepared from the acid of dipeptide 6 and amine salt of dipeptide 7 in dichloromethane. Dipeptide 5 has been prepared from the unnatural amino acid which is prepared from D-Glucose and Xyloses. NMR spectral data of peptides indicates presence of secondary structure in peptides.en_US
dc.language.isoenen_US
dc.publisherNIScPR-CSIR, Indiaen_US
dc.sourceIJC Vol.61(11) [Nov 2022]en_US
dc.subjectUnnatural Aminoacidsen_US
dc.subjectCoupling reactionsen_US
dc.subjectPeptidesen_US
dc.subjectSecondary structureen_US
dc.titleSynthesis of hybrid peptides from unnatural aminoacidsen_US
dc.typeArticleen_US
dc.identifier.doihttps://doi.org/10.56042/ijc.v61i11.68268en_US
Appears in Collections:IJC Vol.61(11) [Nov 2022]

Files in This Item:
File Description SizeFormat 
IJC 61(11) 1199-1204.pdf7.56 MBAdobe PDFView/Open


Items in NOPR are protected by copyright, with all rights reserved, unless otherwise indicated.