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Natural peptide analgesics: the role of solution conformation

โœ Scribed by R. Spadaccini; P.A. Temussi


Book ID
105740560
Publisher
Springer
Year
2001
Tongue
English
Weight
557 KB
Volume
58
Category
Article
ISSN
1420-682X

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๐Ÿ“œ SIMILAR VOLUMES


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โœ Luca D. D'Andrea; Marco Mazzeo; Carla Isernia; Filomena Rossi; Michele Saviano; ๐Ÿ“‚ Article ๐Ÿ“… 1997 ๐Ÿ› Wiley (John Wiley & Sons) ๐ŸŒ English โš– 158 KB ๐Ÿ‘ 1 views

The conformational behavior in solution of a cyclic peptide with sequence cyclo-(Pro 1 -Pro 2 -Dab 3 (cHexA)c[N g HCO]-Leu 4 c[NHCO]-Suc 5 -Gly 6 -) has been throughly investigated with the combined use of nmr and molecular dynamic techniques. The compound, which has been modeled to mimic the FK506

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Nocistatin, a new heptadecapeptide encoded in the bPNP-3 gene, has a powerful biological activity connected with the mechanisms of pain transmission. It does not bind to the opioid receptors but to another brain receptor with high affinity. In order to substantiate these novel biological data with a

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## Synopsis The strategy and tactics of conformational analysis of cyclic peptides in solution is demonstrated by the example of cyclo(-D-Pro-Phe-TPhe-TYp-Phe-). Spin-locked experiments like rotating frame nuclear Overhauser enhancement spectroscopy (ROESY), ROTO, and TOCSY are successfully applie