Endomorphin-1 and endomorphin-2 differentially interact with specific binding sites for substance P (SP) aminoterminal SP1–7 in the rat spinal cord-Reference-Cited by-同舟云学术

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Endomorphin-1 and endomorphin-2 differentially interact with specific binding sites for substance P (SP) aminoterminal SP1–7 in the rat spinal cord

Published:2006-04 Issue:4 Volume:27 Page:753-759
ISSN:0196-9781
Container-title:Peptides
language:en
Short-container-title:Peptides

Author:

Botros Milad,Hallberg Mathias,Johansson Tobias,Zhou Qin,Lindeberg Gunnar,Frändberg Per-Anders,Tömböly Csaba,Tóth Géza,Le Grevès Pierre,Nyberg Fred

Publisher

Elsevier BV

Subject

Cellular and Molecular Neuroscience,Endocrinology,Physiology,Biochemistry

Reference29 articles.

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3. Relationship between the inhibition constant (K1) and the concentration of inhibitor which causes 50 per cent inhibition (I50) of an enzymatic reaction;Cheng;Biochem Pharmacol,1973

4. Lack of evidence of kappa2-selective activation of G-proteins: kappa opioid receptor stimulation of [35S] GTPgammaS binding in guinea pig brain;Childers;Biochem Pharmacol,1998

5. Neuropeptide conversion to bioactive fragments—an important pathway in neuromodulation;Hallberg;Curr Protein Pept Sci,2003

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1. The amino-terminal heptapeptide of the algesic substance P provides analgesic effect in relieving chronic neuropathic pain;European Journal of Pharmacology;2021-02

2. Endomorphins: structure, localization, immunoregulatory activity;Problems of Endocrinology;2020-08-04

3. Targeting Neuropathic Pain: Pathobiology, Current Treatment and Peptidomimetics as a New Therapeutic Opportunity;Current Medicinal Chemistry;2020-03-27

4. Synthesis and Preclinical Evaluation of the First Carbon-11 Labeled PET Tracers Targeting Substance P1–7;Molecular Pharmaceutics;2018-10-18

5. From the Anti-Nociceptive Substance P Metabolite Substance P (1-7) to Small Peptidomimetics;Current Protein & Peptide Science;2018-09-07

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