CAS 54029-12-8: (±)-Albendazole sulfoxide
Formula:C12H15N3O3S
InChI:InChI=1S/C12H15N3O3S/c1-3-6-19(17)8-4-5-9-10(7-8)14-11(13-9)15-12(16)18-2/h4-5,7H,3,6H2,1-2H3,(H2,13,14,15,16)
InChI key:InChIKey=VXTGHWHFYNYFFV-UHFFFAOYSA-N
SMILES:S(CCC)(=O)C=1C=C2C(N=C(NC(OC)=O)N2)=CC1
Synonyms:- Albendazole S-oxide
- Albendazole Sulfoxide
- Carbamic acid, N-[6-(propylsulfinyl)-1H-benzimidazol-2-yl]-, methyl ester
- Carbamic acid, [5-(propylsulfinyl)-1H-benzimidazol-2-yl]-, methyl ester
- Methyl [5-(propylsulfinyl)-1H-benzimidazol-2-yl]carbamate
- N-(4-hydroxyphenyl)methanesulfonamide
- Ricobendazole
- Rs 8852
- Rycobendazole
- methyl (5-propylsulfinyl-3H-benzoimidazol-2-yl)aminoformate
- methyl [6-(propylsulfinyl)-1H-benzimidazol-2-yl]carbamate
- See more synonyms
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Albendazole-sulfoxide 100 µg/mL in Acetonitrile
CAS:Formula:C12H15N3O3SColor and Shape:Single SolutionMolecular weight:281.33Albendazole Sulfoxide
CAS:Formula:C12H15N3O3SPurity:>98.0%(N)Color and Shape:White to Light yellow powder to crystalMolecular weight:281.33Albendazole EP Impurity B (Albendazole Sulfoxide, Ricobendazole)
CAS:Formula:C12H15N3O3SColor and Shape:Off-White SolidMolecular weight:281.33GB 31658.11-2021 Albendazole and metabolites Mixture 47 2-20 µg/mL in Acetonitrile
CAS:Controlled ProductColor and Shape:MixtureMethyl (6-(propylsulfinyl)-1H-benzo[d]imidazol-2-yl)carbamate
CAS:Purity:97%Molecular weight:281.3299865722656Albendazole Sulfoxide
CAS:Impurity Albendazole EP Impurity B Applications Albendazole Sulfoxide (Albendazole EP Impurity B) is a metabolite of Albendazole, an anthelmintic. References Dominguez, L., et al.: Farmaco, 50, 697 (1995), De Laurentis, N., et al.: Pharm. Pharmacol Lett., 6, 2: 51 (1996)Formula:C12H15N3O3SColor and Shape:White To BrownMolecular weight:281.33Albendazole EP Impurity B-d7 (Albendazole Sulfoxide-d7, Ricobendazole-d7)
CAS:Formula:C12H8D7N3O3SColor and Shape:Pale Yellow SolidMolecular weight:288.37Albendazole sulfoxide
CAS:Albendazole sulfoxide is a sulfoxide of albendazole. The molecular docking analysis of the two molecules showed that the sulfoxide group is located in the same position as the hydroxyl group on albendazole. It has been shown that this replacement of hydroxyl with a sulfoxide group increases the solubility and stability of albendazole, which may be due to hydrogen bonding interactions between these groups. Albendazole sulfoxide has been shown to be an effective treatment for infections caused by parasites such as helminths. However, it should not be used in combination with drugs that are metabolized by cytochrome P450 enzymes because it can inhibit their activity.Formula:C12H15N3O3SPurity:Min. 97 Area-%Color and Shape:White PowderMolecular weight:281.33 g/molAlbendazole-sulfoxide 1000 µg/mL in Acetonitrile:Methanol
CAS:Controlled ProductFormula:C12H15N3O3SColor and Shape:Single SolutionMolecular weight:281.33Smart Solutions™ v59 PharmaVetResiMix Kit 1
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Color and Shape:MixtureAlbendazole Sulfoxide-d7
CAS:Controlled ProductApplications Albendazole Sulfoxide-d7 is the isotope labelled metabolite of Albendazole (A511620), an anthelmintic agent. References Dominguez, L., et al.: Farmaco, 50, 697 (1995), De Laurentis, N., et al.: Pharm. Pharmacol Lett., 6, 2: 51 (1996)Formula:C12H8D7N3O3SColor and Shape:NeatMolecular weight:288.37Methyl [5-Propylsulphinyl)-1H-benzimidazol-2-yl]carbamate
CAS:Controlled ProductFormula:C12H15N3O3SColor and Shape:NeatMolecular weight:281.33
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