Iprodione

CAS : 36734-19-7

Ref. 3D-FI24646

Informations sur le produit

• Nom: Iprodione
• Synonymes: 3-(3,5-Dichlorophenyl)-N-(1-methylethyl)-2,4-dioxo-1-imidazolidinecarboxamideChipco 26019Glycophen, 3-(3,5-Dichlorophenyl)-N-(1-methylethyl)-2,4-dioxo-1-imidazolidinecarboxamide, 3-(3,5-Dichlorophenyl)-N-isopropyl-2,4-dioxoimidazolidine-1-carboxamide, 3-(3,5-Dichlorphenyl)-2,4-dioxo-N-isopropylimidazolidin-1-carboxamid, 3-(3,5-dichlorophenyl)-2,4-dioxo-N-isopropylimidazolidine-1-carboxamide, 3-(3,5-diclorofenil)-2,4-dioxo-N-isopropilimidazolidina-1-carboxamida, Botrix, Chipco 26019, Civet, Glycophen, Glycophene, Iprodial, Iprodin, Iprodion, Junheling, Kidan, Lfa 2043, Promidione, Quintalic, Rovral, Rovral 500 Aqua, Rovral 50WP, Rovral Aquaflo, Rovral Flo, Rovral Flo 255SC, Rovral Green GT, Rovral PM, Rp 26019, Verisan, Xiuan, Yijunniao
• CAS: 36734-19-7

Description

Iprodione is an ester hydrochloride that belongs to the class of fungicides. It has been shown to have high resistance and is used in vitro assays to detect mutants with a high degree of resistance. Iprodione inhibits the growth of wild-type strains, but not resistant mutants, by inhibiting protein synthesis at the ribosome level, blocking the polymerase chain reaction and DNA replication. This prevents transcription and replication of genetic material. Iprodione also inhibits nitrite ion production in wild-type strains and has genotoxic effects on cultured human cells. The drug is metabolized through a number of metabolic transformations, including hydrolysis by esterases or glucuronidases, oxidation by cytochrome P450 enzymes, reduction by glutathione reductase, or conjugation with glucuronic acid.

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 330.17 g/mol
• Formule: C₁₃H₁₃Cl₂N₃O₃
• Degré de pureté: Min. 95%
• Couleur/Forme: Powder
• InChI: InChI=1S/C13H13Cl2N3O3/c1-7(2)16-12(20)17-6-11(19)18(13(17)21)10-4-8(14)3-9(15)5-10/h3-5,7H,6H2,1-2H3,(H,16,20)
• Code InChI: InChIKey=ONUFESLQCSAYKA-UHFFFAOYSA-N
• SMILES: CC(C)NC(=O)N1CC(=O)N(c2cc(Cl)cc(Cl)c2)C1=O