Conformational studies of stereoisomeric 14-membered cyclic enkephalin analogues containing 1-naphthyialanine at the fourth position: Chirality effect of leucine at the fifth position on biological activity and receptor selectivity-Reference-Cited by-同舟云学术

Conformational studies of stereoisomeric 14-membered cyclic enkephalin analogues containing 1-naphthyialanine at the fourth position: Chirality effect of leucine at the fifth position on biological activity and receptor selectivity

Published:1991-06 Issue:7 Volume:31 Page:877-898
ISSN:0006-3525
Container-title:Biopolymers
language:en
Short-container-title:Biopolymers

Author:

Yamazaki Toshimasa,Said-Nejad Odile E.,Schiller Peter W.,Goodman Murray

Publisher

Wiley

Subject

Organic Chemistry,Biomaterials,Biochemistry,General Medicine,Biophysics

Reference38 articles.

1. & Eds. (1984) The Peptides, Vol. 6. Academic Press, Orlando, FL.

2. & Eds. (1986) Opioid Peptides: Medicinal Chemistry, NIDA Research Monographs, Vol. 69. Government Printing Office, Washington, DC.

3. (1984) in The Peptides, Vol. 6, & Eds., Academic Press, Orlando, FL, pp. 219-298.

4. Cyclic and acyclic partial retro-inverso enkephalinamides: Mu receptor selective enzyme resistant analogs

5. Synthesis and biological activity of linear and cyclic enkephalins modified at the Gly3-Phe4amide bond

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