Partial and full agonism in endomorphin derivatives: Comparison by null and operational model

Author:

Rónai András Z.,Al-Khrasani Mahmoud,Benyhe Sándor,Lengyel Imre,Kocsis László,Orosz György,Tóth Géza,Kató Erzsébet,Tóthfalusi László

Publisher

Elsevier BV

Subject

Cellular and Molecular Neuroscience,Endocrinology,Physiology,Biochemistry

Reference53 articles.

1. The effect of endomorphins on the release of 3H-norepinephrine from rat nucleus tractus solitarii slices;Al-Khrasani;Regul Peptides,2003

2. Receptor constants for endomorphin-1 and endomorphin-1-ol indicate differences in efficacy and receptor occupancy;Al-Khrasani;Eur J Pharmacol,2001

3. Stimulation of guanosine-5′-O-(3-[35S]thio)triphosphate binding by endogenous opioids acting at a cloned μ receptor;Alt;J Pharmacol Exp Ther,1998

4. Tyr-d-Ala-(Me)Phe-chloromethyl ketone: a μ-specific affinity label for the opioid receptor;Benyhe;Neuropeptides,1987

5. Novel opioid peptides derived from mitochondrial cytochrome b: cytochrophins;Brantl;Eur J Pharmacol,1985

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