The molal volumes of atropine and hyoscine in relation to their respective potencies
Author:
Publisher
Wiley
Subject
Pharmacology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1476-5381.1984.tb16236.x/fullpdf
Reference16 articles.
1. The size of hydroxyl groups in solution and the changes in size associated with the ionization of phenolic, carboxylic and amino groups in phenolic quaternary ammonium salts, nicotine and some amino acids: possible implications for drug-water and drug-receptor interactions;BARLOW;Br. J. Pharmac.,1980
2. A comparison of phenylalkyl and phenoxyalkyl trimethylammonium and triethylammonium salts; their apparent molal volume at infinite dilution and effects on the frog rectus and guinea-pig ileum preparations;BARLOW;Br. J. Pharmac.,1973
3. The size of the hydroxl group and its contribution to the affinity of atropine for muscarinic-sensitive acetylcholine receptors;BARLOW;Br. J. Pharmac.,1980
4. Affinities of the protonated and nonprotonated forms of hyoscine and hyoscine N-oxide for muscarinic receptors of the guinea-pig ileum and a comparison of their size in solution with that of atropine;BARLOW;Br. J. Pharmac.,1981
5. Solubility parameters;BARTON;Chem. Reviews,1975
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1. Enthalpy-entropy relationship in drug-cholinoceptor interaction: a new approach;British Journal of Pharmacology;1985-08
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