The selectivity of newly synthesized ergot derivatives to α1- and α2-adrenoceptors, D1- and D2-dopaminergic receptors, muscarinic acetylcholinoceptors and β-adrenoceptors

Author:

Okumura Keiichi,Koike Katsuo,Asai Hajime,Takayanagi Issei

Publisher

Elsevier BV

Subject

Pharmacology

Reference12 articles.

1. Characterization of the binding of [3H]SCH23390, a selective D-1 receptor antagonist ligand, in rat striatum;Billard;Life Sci.,1984

2. The binding of agonists to brain muscarinic receptors;Birdsall;Molec. Pharmac.,1978

3. Relationship between the inhibition constant (Ki) and the concentration of inhibitor which causes 50% inhibition (IC50) of an enzymatic reaction;Cheng;Biochem. Pharmac.,1973

4. Dopamine receptor of the porcine anterior pituitary gland;DeLean;Molec. Pharmac.,1982

5. Pirenzepine distinguishes between different subclass of muscarinic receptors;Hammer;Nature,1980

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