Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractDiscovery of a linear lead antagonist to the insect pheromone biosynthesis activating neuropeptide (PBAN)    Next AbstractEmissions of biogenic VOC from forest ecosystems in central Europe: estimation and comparison with anthropogenic emission inventory »

J Pept Res


Title:Insect neuropeptide antagonist. Part II. Synthesis and biological activity of backbone cyclic and precyclic PBAN antagonists
Author(s):Zeltser I; Ben-Aziz O; Schefler I; Bhargava K; Altstein M; Gilon C;
Address:"Department of Organic Chemistry, The Hebrew University of Jerusalem, Givat Ram-91904, Jerusalem, Israel"
Journal Title:J Pept Res
Year:2001
Volume:58
Issue:4
Page Number:275 - 284
DOI: 10.1034/j.1399-3011.2001.00914.x
ISSN/ISBN:1397-002X (Print) 1397-002X (Linking)
Abstract:"A new approach for the design and synthesis of pheromone biosynthesis activating neuropeptide (PBAN) agonists and antagonists using the backbone cyclization and cycloscan concepts is described. Two backbone cyclic (BBC) libraries were synthesized: library I (Ser library) was based on the active C-terminal hexapeptide sequence Tyr-Phe-Ser-Pro-Arg-Leu-NH2 of PBAN1-33NH2; whereas library II (D-Phe library) was based on the sequence of the PBAN lead linear antagonist Arg-Tyr-Phe-d-Phe-Pro-Arg-Leu-NH2. In both libraries the Pro residue was replaced by the BBC building unit Nalpha-(omega-aminoalkyl) Gly having various lengths of alkyl chain. The peptides of the two libraries were tested for agonistic and antagonistic activity. Four precyclic peptides based on two of the BBC antagonists were also synthesized; their activity revealed that a negative charge at the N-terminus of the peptide abolished antagonistic activity. We also describe the use of the reagent SiCl3I for selective deprotection of the Boc group from the building unit prior to on-resin amino-end to backbone-nitrogen (AE-BN) cyclization, during solid-phase synthesis with Fmoc chemistry"
Keywords:"Animals Drug Design Female Hormone Antagonists/*chemical synthesis/*pharmacology Insecta/chemistry/drug effects Moths/chemistry/drug effects Neuropeptides/agonists/*antagonists & inhibitors Peptide Library Peptides, Cyclic/*chemical synthesis/*pharmacolog;"
Notes:"MedlineZeltser, I Ben-Aziz, O Schefler, I Bhargava, K Altstein, M Gilon, C eng Research Support, Non-U.S. Gov't Denmark 2001/10/19 J Pept Res. 2001 Oct; 58(4):275-84. doi: 10.1034/j.1399-3011.2001.00914.x"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 22-09-2024