(±)-Felodipine-d5

Modify Date: 2024-01-02 18:51:23

(±)-Felodipine-d5 structure	Common Name	(±)-Felodipine-d5
	CAS Number	1242281-38-4	Molecular Weight	389.28
	Density	1.3±0.1 g/cm3	Boiling Point	471.5±45.0 °C at 760 mmHg
	Molecular Formula	C₁₈H₁₄D₅Cl₂NO₄	Melting Point	N/A
	MSDS	N/A	Flash Point	239.0±28.7 °C

Use of (±)-Felodipine-d5

Felodipine-d5 is deuterium labeled Felodipine. Felodipine, a dihydropyridine, is a potent, vasoselective calcium channel antagonist. Felodipine lowers blood pressure (BP) by selective action on vascular smooth muscle, especially in the resistance vessels. Felodipine, an anti-hypertensive agent, induces autophagy. Felodipine can cross the blood-brain barrier[1][2][3].

Name	(±)-Felodipine-d5
Synonym	More Synonyms

Description	Felodipine-d5 is deuterium labeled Felodipine. Felodipine, a dihydropyridine, is a potent, vasoselective calcium channel antagonist. Felodipine lowers blood pressure (BP) by selective action on vascular smooth muscle, especially in the resistance vessels. Felodipine, an anti-hypertensive agent, induces autophagy. Felodipine can cross the blood-brain barrier[1][2][3].
Related Catalog	Signaling Pathways >> Membrane Transporter/Ion Channel >> Calcium Channel Research Areas >> Cardiovascular Disease Signaling Pathways >> Autophagy >> Autophagy
In Vitro	Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs[1].
References	[1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53(2):211-216. [2]. Johnson JD, et al. Calcium and calmodulin antagonists binding to calmodulin and relaxation of coronary segments. J Pharmacol Exp Ther. 1983;226(2):330-334. [3]. Siddiqi FH, et al. Felodipine induces autophagy in mouse brains with pharmacokinetics amenable to repurposing [published correction appears in Nat Commun. 2019 Jun 4;10(1):2530]. Nat Commun. 2019;10(1):1817. Published 2019 Apr 18. [4]. Yiu, S. and E.E. Knaus, Synthesis, biological evaluation, calcium channel antagonist activity, and anticonvulsant activity of felodipine coupled to a dihydropyridine-pyridinium salt redox chemical delivery system. J Med Chem, 1996. 39(23): p. 4576-82.

Density	1.3±0.1 g/cm3
Boiling Point	471.5±45.0 °C at 760 mmHg
Molecular Formula	C₁₈H₁₄D₅Cl₂NO₄
Molecular Weight	389.28
Flash Point	239.0±28.7 °C
Exact Mass	388.100494
LogP	4.83
Vapour Pressure	0.0±1.2 mmHg at 25°C
Index of Refraction	1.550

(Â±)-Felodipine-d5

(2H5)Ethyl methyl 4-(2,3-dichlorophenyl)-2,6-dimethyl-1,4-dihydro-3,5-pyridinedicarboxylate

3,5-Pyridinedicarboxylic acid, 4-(2,3-dichlorophenyl)-1,4-dihydro-2,6-dimethyl-, ethyl-d5 methyl ester

(±)-Felodipine-d5

Use of (±)-Felodipine-d5

Names

(±)-Felodipine-d5 Biological Activity

Chemical & Physical Properties

Synonyms