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Peptide Scanning for Studying Structure-Activity Relationships in Drug Discovery

期刊

CHEMICAL BIOLOGY & DRUG DESIGN
卷 81, 期 1, 页码 148-165

出版社

WILEY-BLACKWELL
DOI: 10.1111/cbdd.12042

关键词

aza-amino acid; conformational constraint; Freidinger lactam; peptidomimetic; scan; stapled peptide

资金

  1. Natural Sciences and Engineering Research Council of Canada (NSERC)
  2. Canadian Institutes of Health Research (CIHR) [TGC-114046]
  3. University of Leicester

向作者/读者索取更多资源

Peptide-based therapeutics have grown in importance over the last few decades. Furthermore, peptides have been extensively used as lead compounds in the drug discovery process to investigate the nature of chemical space required for molecular recognition and activity at a variety of targets. This critical commentary reviews scanning techniques, which employ natural and non-proteinogenic amino acids to facilitate understanding of structural requirements for peptide biological activity. The value of sequence analysis by such methods is highlighted by examples, in which the elements for peptide affinity and activity have been elucidated and employed to prepare peptidomimetic leads for drug development.

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