1215631-57-4

1215631-57-4 structure

Name: Iprodione-d5
Chemical Name: 3-[3,5-Dichloro(2H3)phenyl]-N-isopropyl-2,4-dioxo(2H2)imidazolidine-1-carboxamide
CAS Number: 1215631-57-4
Molecular Formula: C₁₃H₈D₅Cl₂N₃O₃
Molecular Weight: 335.197
Catalog: Signaling Pathways Anti-infection Fungal
Create Date: 2018-05-10 14:06:43
Modify Date: 2024-02-06 21:03:30
Iprodione-d5 is the deuterium labeled Iprodione[1]. Iprodione, a dicarboximide fungicide, has a highly specific action, with a capacity to cause oxidative damage through production of free oxygen radicals (ROS). Iprodione does not appear to be species selective[2].

Name	3-[3,5-Dichloro(2H3)phenyl]-N-isopropyl-2,4-dioxo(2H2)imidazolidine-1-carboxamide
Synonyms	3-[3,5-Dichloro(H)phenyl]-N-isopropyl-2,4-dioxo(H)imidazolidine-1-carboxamide 1-Imidazolidine-5,5-d-carboxamide, 3-(3,5-dichlorophenyl-2,4,6-d)-N-(1-methylethyl)-2,4-dioxo- 3-[3,5-Dichloro(H)phenyl]-N-isopropyl-2,4-dioxo-1-(H)imidazolidinecarboxamide

Description	Iprodione-d5 is the deuterium labeled Iprodione[1]. Iprodione, a dicarboximide fungicide, has a highly specific action, with a capacity to cause oxidative damage through production of free oxygen radicals (ROS). Iprodione does not appear to be species selective[2].
Related Catalog	Research Areas >> Infection Signaling Pathways >> Anti-infection >> Fungal
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 Feb;53(2):211-216. [2]. Radice S, et al. Effect of iprodione, a dicarboximide fungicide, on primary cultured rainbow trout (Oncorhynchus mykiss) hepatocytes. Aquat Toxicol. 2001;54(1-2):51-58.