Cite
In vitro metabolism of the M1-muscarinic agonist 5-(2-ethyl-2H-tetrazol-5-yl)-1-methyl-1,2,3,6-tetrahydropyridine by human hepatic cytochromes P-450 determined at pH 7.4 and 8.5.
MLA
Jensen, K. G., and L. Dalgaard. “In Vitro Metabolism of the M1-Muscarinic Agonist 5-(2-Ethyl-2H-Tetrazol-5-Yl)-1-Methyl-1,2,3,6-Tetrahydropyridine by Human Hepatic Cytochromes P-450 Determined at PH 7.4 and 8.5.” Drug Metabolism and Disposition: The Biological Fate of Chemicals, vol. 27, no. 1, Jan. 1999, pp. 125–32. EBSCOhost, widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=cmedm&AN=9884321&authtype=sso&custid=ns315887.
APA
Jensen, K. G., & Dalgaard, L. (1999). In vitro metabolism of the M1-muscarinic agonist 5-(2-ethyl-2H-tetrazol-5-yl)-1-methyl-1,2,3,6-tetrahydropyridine by human hepatic cytochromes P-450 determined at pH 7.4 and 8.5. Drug Metabolism and Disposition: The Biological Fate of Chemicals, 27(1), 125–132.
Chicago
Jensen, K G, and L Dalgaard. 1999. “In Vitro Metabolism of the M1-Muscarinic Agonist 5-(2-Ethyl-2H-Tetrazol-5-Yl)-1-Methyl-1,2,3,6-Tetrahydropyridine by Human Hepatic Cytochromes P-450 Determined at PH 7.4 and 8.5.” Drug Metabolism and Disposition: The Biological Fate of Chemicals 27 (1): 125–32. http://widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=cmedm&AN=9884321&authtype=sso&custid=ns315887.