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Synthesis, Biological Activity, and Conformational Studies of Insect Allatostatin Neuropeptide Analogues Incorporating Turn-Promoting Moieties1Dedicated to Professor Stuart Schreiber on the occasion of his award of the Tetrahedron Prize.1

Authors :
A. I. Scott
Guillermo Moyna
Ronald J. Nachman
Howard J. Williams
Stephen S. Tobe
Source :
Bioorganic & Medicinal Chemistry. 6:1379-1388
Publication Year :
1998
Publisher :
Elsevier BV, 1998.

Abstract

Allatostatins are 6-18 amino acid peptides synthezed by insects to control production of juvenile hormones, which in turn regulate functions including metamorphosis and egg production. Four insect allatostatin neuropeptide analogues incorporating turn-promoting pseudopeptide moieties in the region responsible for biological activity were prepared by solid phase peptide synthetic methods. Bioassay indicated that activities approached those of the natural neuropeptides, and molecular models based on NMR data showed similar conformations and the presence of a beta-turn in the active core region for the four analogues. Differences in activity are believed to be due to differences in bulk and relative position of atoms in the unnatural portion of the analogues, and their differing degrees of conformational freedom. The studies support the feasibility of development of neuropeptide-based insect control agents resistant to peptidase deactivation.

Details

ISSN :
09680896
Volume :
6
Database :
OpenAIRE
Journal :
Bioorganic & Medicinal Chemistry
Accession number :
edsair.doi...........f7db9106842b5674c3a3173796331c43
Full Text :
https://doi.org/10.1016/s0968-0896(98)00129-1