
CAS 10080-05-4
:Fórmula:C15H23N3O3S
InChI:InChI=1S/C15H23N3O3S/c16-22(20,21)14-8-6-12(7-9-14)10-11-17-15(19)18-13-4-2-1-3-5-13/h6-9,13H,1-5,10-11H2,(H2,16,20,21)(H2,17,18,19)
Clave InChI:NIMGDPRCIUIRNT-UHFFFAOYSA-N
SMILES:C1CCC(CC1)NC(=O)NCCC2=CC=C(C=C2)S(=O)(=O)N
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Glipizide impurity 11
CAS:Glipizide impurity 11 is an impurity of Glipizide.Fórmula:C15H23N3O3SPeso molecular:325.426Glipizide EP Impurity H
CAS:Fórmula:C15H23N3O3SForma y color:White To Off-White SolidPeso molecular:325.434-[2-[(Cyclohexylcarbamoyl)amino]ethyl]benzenesulphonamide
CAS:Producto controladoFórmula:C15H23N3O3SForma y color:NeatPeso molecular:325.431-Cyclohexyl-3-(p-sulfamoylphenethyl)urea
CAS:Producto controladoImpurity Glipizide EP Impurity H
Applications 1-Cyclohexyl-3-(p-sulfamoylphenethyl)urea (Glipizide EP Impurity H) is an impurity of Glipizide (G410225).
References Jurca, B. et al.: J. Therm. Anal. Calor., 62, 859 (2000);Fórmula:C15H23N3O3SForma y color:NeatPeso molecular:325.434-(2-((Cyclohexylcarbamoyl)amino)ethyl)benzenesulfonamide
CAS:4-(2-((Cyclohexylcarbamoyl)amino)ethyl)benzenesulfonamide is a research and development impurity standard that is used for the synthesis of drug products. CAS No. 10080-05-4, 4-(2-((Cyclohexylcarbamoyl)amino)ethyl)benzenesulfonamide is a synthetic compound that has been shown to be metabolized in humans and in rats. It has been extensively evaluated as a potential antituberculosis drug candidate and shown to inhibit bacterial growth by binding to DNA-dependent RNA polymerase, thereby preventing transcription and replication. This active form 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. In vitro studies have demonstrated its efficacy against MycobacterFórmula:C15H23N3O3SPureza:Min. 95%Peso molecular:325.4 g/mol






