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
CD spectral study of Dnp derivatives of amino acids and peptides for their configurational and conformational analysis
✍ Scribed by Masao Kawai; Ukon Nagai; Yoshihito Inai; Hatsuo Yamamura; Ryougo Akasaka; Shigeru Takagi; Yoshihisa Miwa; Tooru Taga
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 2005
- Tongue
- English
- Weight
- 247 KB
- Volume
- 80
- Category
- Article
- ISSN
- 0006-3525
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✦ Synopsis
Abstract
Rules relating the stereochemistry of N‐Dnp (Dnp: 2,4‐dinitrophenyl) derivatives of α‐amino acids and peptides and the sign of the Cotton effects at the longest wavelength band (ca. 400 nm) are surveyed. Some new data and insights concerning the CD spectra of Dnp–α‐amino acids are included: i.e., the spectra of Dnp derivatives as the composite of the corresponding o‐nitrophenyl and p‐nitrophenyl derivatives; the crystal structure of Dnp–I‐phenylalanine and its solid‐state CD spectra; the CD spectra of Dnp–α‐amino acids containing sulfur atom on their side chains; and the theoretical approach to the CD spectra using molecular orbital method‐based calculation. Conformational analyses of cyclic and linear peptides by the CD spectra of their Dnp derivatives are also discussed. © 2005 Wiley Periodicals, Inc. Biopolymers (Pept Sci), 2005
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