CAS 10080-05-4

Formule : 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)

Code InChI : NIMGDPRCIUIRNT-UHFFFAOYSA-N

SMILES : C1CCC(CC1)NC(=O)NCCC2=CC=C(C=C2)S(=O)(=O)N

Glipizide EP Impurity H

CAS : 10080-05-4

Formule : C₁₅H₂₃N₃O₃S

Couleur et forme : White To Off-White Solid

Masse moléculaire : 325.43

Ref: 4Z-G-115

4-[2-[(Cyclohexylcarbamoyl)amino]ethyl]benzenesulphonamide

Produit contrôlé

CAS : 10080-05-4

Formule : C₁₅H₂₃N₃O₃S

Couleur et forme : Neat

Masse moléculaire : 325.43

Ref: 86-MM0942.08

4-(2-(3-Cyclohexylureido)ethyl)benzenesulfonamide

CAS : 10080-05-4

Degré de pureté : 97%

Masse moléculaire : 325.4299927

Ref: 10-F728487

1-Cyclohexyl-3-(p-sulfamoylphenethyl)urea

Produit contrôlé

CAS : 10080-05-4

Impurity 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);

Formule : C₁₅H₂₃N₃O₃S

Couleur et forme : Neat

Masse moléculaire : 325.43

Ref: TR-C988210

Glipizide EP Impurity H

CAS : 10080-05-4

Formule : C₁₅H₂₃N₃O₃S

Masse moléculaire : 325.43

Ref: ST-EA-CP-G11008

4-(2-((Cyclohexylcarbamoyl)amino)ethyl)benzenesulfonamide

CAS : 10080-05-4

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 Mycobacter

Formule : C₁₅H₂₃N₃O₃S

Degré de pureté : Min. 95%

Masse moléculaire : 325.4 g/mol

Ref: 3D-FC180932