7-Ethoxyresorufin-d5

Modify Date: 2024-01-10 14:27:18

7-Ethoxyresorufin-d5 structure	Common Name	7-Ethoxyresorufin-d5
	CAS Number	2749329-28-8	Molecular Weight	246.27
	Density	N/A	Boiling Point	N/A
	Molecular Formula	C₁₄H₆D₅NO₃	Melting Point	N/A
	MSDS	N/A	Flash Point	N/A

Use of 7-Ethoxyresorufin-d5

7-Ethoxyresorufin-d5 is deuterium labeled 7-Ethoxyresorufin. 7-Ethoxyresorufin (Resorufin ethyl ether) is a fluorometric substrate and competitive inhibitor of cytochrome P450, especially CYP1A1. 7-Ethoxyresorufin also inhibits NO synthase[1][2].

Name	7-Ethoxyresorufin-d5

Description	7-Ethoxyresorufin-d5 is deuterium labeled 7-Ethoxyresorufin. 7-Ethoxyresorufin (Resorufin ethyl ether) is a fluorometric substrate and competitive inhibitor of cytochrome P450, especially CYP1A1. 7-Ethoxyresorufin also inhibits NO synthase[1][2].
Related Catalog	Signaling Pathways >> Metabolic Enzyme/Protease >> Cytochrome P450 Research Areas >> Others Signaling Pathways >> Immunology/Inflammation >> NO Synthase
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]. C G Li, et al. Inhibition of NO-medicate responses by 7-ethoxyresorufin, a substrate and competitive inhibitor of cytochrome P450. Br J Pharmacol. 1996 May;118(1):57-62. [3]. Thomas K H Chang, et al. Enzymatic analysis of cDNA-expressed human CYP1A1, CYP1A2, and CYP1B1 with 7-ethoxyresorufin as substrate. Methods Mol Biol. 2006;320:85-90.

Molecular Formula	C₁₄H₆D₅NO₃
Molecular Weight	246.27

7-Ethoxyresorufin-d5

Use of 7-Ethoxyresorufin-d5

Names

7-Ethoxyresorufin-d5 Biological Activity

Chemical & Physical Properties