4.6 Article

N-Glycoconjugates: Selective colorimetric chemosensors for aspartic acid and cysteine

期刊

JOURNAL OF MOLECULAR STRUCTURE
卷 1241, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.molstruc.2021.130644

关键词

Glycoconjugates; Amino acids; Chemosensor; Hydrogen bonding; Molecular recognition

资金

  1. Science and Engineering Research Board (SERB) [EMR/2016/007105]
  2. DST FIST
  3. UGC SAP

向作者/读者索取更多资源

This study explores the selective recognition of naturally occurring amino acids using five glycopeptide-based receptors. The receptors containing specific amino acid moieties interact selectively with certain amino acids, as confirmed by UV-visible and H-1 NMR spectroscopy, and single crystal X-ray diffraction studies.
Selective recognition of naturally occurring amino acids have been explored using five glycopeptide-based receptors with the help of UV-visible and H-1 NMR spectroscopy, while structures of two glycopeptides have been established via single crystal X-ray diffraction studies. The receptors containing alanine, valine, isoleucine and methionine moieties interact selectively with aspartic acid, while phenylalanine derivative with cysteine. (C) 2021 Elsevier B.V. All rights reserved.

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