Side Chain Modifications Change the Binding and Agonist Properties of Endomorphin 2-Reference-Cited by-同舟云学术

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Side Chain Modifications Change the Binding and Agonist Properties of Endomorphin 2

Published:2002-01 Issue:1 Volume:290 Page:153-161
ISSN:0006-291X
Container-title:Biochemical and Biophysical Research Communications
language:en
Short-container-title:Biochemical and Biophysical Research Communications

Author:

Lengyel I.,Orosz G.,Biyashev D.,Kocsis L.,Al-Khrasani M.,Rónai A.,Tömböly Cs.,Fürst Zs.,Tóth G.,Borsodi A.

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Reference49 articles.

1. A potent and selective endogenous agonist for the mu-opiate receptor;Zadina;Nature,1997

2. Pain inhibition by endomorphins;Przewlocki;Ann. N.Y. Acad. Sci.,1999

3. Endogenous opiates: 1998;Vaccarino;Peptides,1999

4. mu Opioid receptor: Role for the amino terminus as a determinant of ligand binding affinity;Chaturvedi;Mol. Brain Res.,2000

5. Proline motifs in peptides and their biological processing;Vanhoof;FASEB J.,1995

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1. The spinal anti-allodynic effects of endomorphin analogs with C-terminal hydrazide modification in neuropathic pain model;Peptides;2020-12

2. Discovery of two novel branched peptidomimetics containing endomorphin-2 and RF9 pharmacophores: Synthesis and neuropharmacological evaluation;Bioorganic & Medicinal Chemistry;2019-02

3. C-terminal hydrazide modification changes the spinal antinociceptive profiles of endomorphins in mice;Peptides;2018-01

4. Pharmacological characterization of EN-9, a novel chimeric peptide of endomorphin-2 and neuropeptide FF that produces potent antinociceptive activity and limited tolerance;Neuropharmacology;2016-09

5. Rational Approach to the Design of Bioactive Peptidomimetics: Recent Developments in Opioid Agonist Peptides;Studies in Natural Products Chemistry;2015

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