Conformationally constrained amino acid and dipeptide units can serve in mimics of specific secondary structures for studying relationships between peptide conformation and biological activity. A variety of mimics are required to study systematically the structure-activity relationships in biologica
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ChemInform Abstract: Design, Synthesis, and Conformational Analysis of Azacycloalkane Amino Acids as Conformationally Constrained Probes for Mimicry of Peptide Secondary Structures
β Scribed by Liliane Halab; Francis Gosselin; William D. Lubell
- Publisher
- John Wiley and Sons
- Year
- 2001
- Weight
- 25 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0931-7597
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2000
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English
β 435 KB
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