3-α-Chlorimperialine: an M2-selective muscarinic receptor antagonist that penetrates into brain
Author:
Publisher
Elsevier BV
Subject
Pharmacology
Reference11 articles.
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2. Muscarinic receptor subtype selectivity of novel heterocyclic QNB analogues;Baumgold;Life Sci.,1991
3. Use of ex vivo binding to measure the brain concentrations of putative radioligands;Baumgold;Nucl. Med. Biol.,1992
4. Characterization of the interaction of the cervane alkaloid imperialine, at muscarinic receptors in vitro;Eglen;Naunyn-Schmied. Arch. Pharmacol.,1992
5. Molecular probes for muscarinic receptors based on amine congeners of pirenzepine and telenzepine;Jacobson;Bioorgan. Med. Chem. Lett.,1992
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1. Orally active and selective benzylidene ketal M2 muscarinic receptor antagonists for the treatment of Alzheimer's disease;Drug Development Research;2002-07
2. Muscarinic receptors of the M2 subtype in human and bovine trabecular meshwork;Graefe's Archive for Clinical and Experimental Ophthalmology;2001-04
3. Therapeutic Opportunities for Muscarinic Receptors in the Central Nervous System;Journal of Medicinal Chemistry;2000-11-01
4. Subtypes of muscarinic receptors in rat duodenum A comparison with rabbit vas deferens, rat atria, guinea-pig ileum and gallbladder by using imperialine;General Pharmacology: The Vascular System;1999-04
5. 3-α-Chloro-imperialine, a potent blocker of cholinergic presynaptic modulation of glutamatergic afferents in the rat neostriatum;Neuropharmacology;1998-12
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