Levamlodipine (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Levamlodipine" in English language version.

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chiralemcure.com

"Asomex by Emcure" (PDF). Medical Update Newsletter. 20 (1): 1–2. January 2010. Archived from the original (PDF) on 4 March 2016.

Burges RA, Gardiner DG, Gwilt M, Higgins AJ, Blackburn KJ, Campbell SF, et al. (January 1987). "Calcium channel blocking properties of amlodipine in vascular smooth muscle and cardiac muscle in vitro: evidence for voltage modulation of vascular dihydropyridine receptors". Journal of Cardiovascular Pharmacology. 9 (1): 110–119. doi:10.1097/00005344-198701000-00018. PMID 2434785. S2CID 40257612.
Goldmann S, Stoltefuss J (December 1991). "1,4-Dihydropyridines: Effects of Chirality and Conformation on the Calcium Antagonist and Calcium Agonist Activities". Angewandte Chemie International Edition in English. 30 (12): 1559–1578. doi:10.1002/anie.199115591.
Goldmann S, Stoltefuss J, Born L (September 1992). "Determination of the absolute configuration of the active amlodipine enantiomer as (-)-S: a correction". Journal of Medicinal Chemistry. 35 (18): 3341–3344. doi:10.1021/jm00096a005. PMID 1388206.
Park JY, Kim KA, Park PW, Lee OJ, Ryu JH, Lee GH, et al. (November 2006). "Pharmacokinetic and pharmacodynamic characteristics of a new S-amlodipine formulation in healthy Korean male subjects: a randomized, open-label, two-period, comparative, crossover study". Clinical Therapeutics. 28 (11): 1837–1847. doi:10.1016/j.clinthera.2006.11.008. PMID 17213004.

"Levamlodipine maleate". FDA-Approved Drugs. U.S. Food and Drug Administration.

Thacker HP (April 2007). "S-amlodipine--the 2007 clinical review". Journal of the Indian Medical Association. 105 (4): 180–2, 184, 186 passim. PMID 17822186.
Burges RA, Gardiner DG, Gwilt M, Higgins AJ, Blackburn KJ, Campbell SF, et al. (January 1987). "Calcium channel blocking properties of amlodipine in vascular smooth muscle and cardiac muscle in vitro: evidence for voltage modulation of vascular dihydropyridine receptors". Journal of Cardiovascular Pharmacology. 9 (1): 110–119. doi:10.1097/00005344-198701000-00018. PMID 2434785. S2CID 40257612.
Goldmann S, Stoltefuss J, Born L (September 1992). "Determination of the absolute configuration of the active amlodipine enantiomer as (-)-S: a correction". Journal of Medicinal Chemistry. 35 (18): 3341–3344. doi:10.1021/jm00096a005. PMID 1388206.
Park JY, Kim KA, Park PW, Lee OJ, Ryu JH, Lee GH, et al. (November 2006). "Pharmacokinetic and pharmacodynamic characteristics of a new S-amlodipine formulation in healthy Korean male subjects: a randomized, open-label, two-period, comparative, crossover study". Clinical Therapeutics. 28 (11): 1837–1847. doi:10.1016/j.clinthera.2006.11.008. PMID 17213004.
Pathak L, Kerkar PG, Manade VG (March 2004). "Multicentric, clinical trial of S-Amlodipine 2.5 mg versus Amlodipine 5 mg in the treatment of mild to moderate hypertension--a randomized, double-blind clinical trial". The Journal of the Association of Physicians of India. 52: 197–202. PMID 15636308.

Bhandari P, Shah C, Surwade S (2008-01-01), Chirality-Today and Tomorrow's Way of Treatment, retrieved 2021-10-22

"Asomex by Emcure" (PDF). Medical Update Newsletter. 20 (1): 1–2. January 2010. Archived from the original (PDF) on 4 March 2016.