CAS 54029-12-8
:(±)-Albendazole sulfoxide
Description:
(±)-Albendazole sulfoxide is a chemical compound that serves as a metabolite of the anthelmintic drug albendazole, which is widely used to treat parasitic infections. It is characterized by its sulfoxide functional group, which contributes to its biological activity. The compound is typically a white to off-white solid, exhibiting low solubility in water but higher solubility in organic solvents. Its molecular structure includes a benzimidazole ring, which is crucial for its pharmacological properties. (±)-Albendazole sulfoxide is known for its ability to inhibit the polymerization of tubulin, thereby disrupting microtubule formation in parasites. This mechanism of action makes it effective against a variety of helminths and some protozoa. The compound is also notable for its relatively low toxicity in humans, which enhances its therapeutic profile. In terms of stability, it is generally stable under normal conditions but may degrade under extreme pH or temperature. Overall, (±)-Albendazole sulfoxide plays a significant role in the treatment of parasitic diseases, contributing to the efficacy of albendazole-based therapies.
Formula:C12H15N3O3S
InChI:InChI=1/C7H9NO3S/c1-12(10,11)8-6-2-4-7(9)5-3-6/h2-5,8-9H,1H3
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
- Albendazole oxide
- Albendazole sulphoxide
- ALBENDAZOLE SULFOXIDE/RICOBENDAZOLE
- Rycobendzole
- Albendazole Oxide, Ricobendazole, RS-8852
- RICOBENDAZOLEC
- methyl N-(5-propylsulfinyl-3H-benzoimidazol-2-yl)carbamate
- See more synonyms
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Found 19 products.
Albendazole EP Impurity B-d7 (Albendazole Sulfoxide-d7, Ricobendazole-d7)
CAS:Formula:C12H8D7N3O3SColor and Shape:Pale Yellow SolidMolecular weight:288.37Albendazole EP Impurity B (Albendazole Sulfoxide, Ricobendazole)
CAS:Formula:C12H15N3O3SColor and Shape:Off-White SolidMolecular weight:281.33Smart Solutions™ v59 PharmaVetResiMix Kit 1
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Color and Shape:MixtureMethyl [5-Propylsulphinyl)-1H-benzimidazol-2-yl]carbamate
CAS:Controlled ProductFormula:C12H15N3O3SColor and Shape:NeatMolecular weight:281.33Albendazole-sulfoxide 100 µg/mL in Acetonitrile
CAS:Formula:C12H15N3O3SColor and Shape:Single SolutionMolecular weight:281.33Albendazole-sulfoxide 1000 µg/mL in Acetonitrile:Methanol
CAS:Controlled ProductFormula: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 sulfoxide
CAS:Albendazole sulfoxide (Ricobendazole) is a metabolite of Albendazole, an anthelmintic.Formula:C12H15N3O3SPurity:97.29%Color and Shape:White To Off-White PowderMolecular weight:281.33Albendazole Sulfoxide-d7
CAS:Controlled Product<p>Applications Albendazole Sulfoxide-d7 is the isotope labelled metabolite of Albendazole (A511620), an anthelmintic agent.<br>References Dominguez, L., et al.: Farmaco, 50, 697 (1995), De Laurentis, N., et al.: Pharm. Pharmacol Lett., 6, 2: 51 (1996)<br></p>Formula:C12H8D7N3O3SColor and Shape:NeatMolecular weight:288.37Albendazole Sulfoxide
CAS:<p>Impurity Albendazole EP Impurity B<br>Applications Albendazole Sulfoxide (Albendazole EP Impurity B) is a metabolite of Albendazole, an anthelmintic.<br>References Dominguez, L., et al.: Farmaco, 50, 697 (1995), De Laurentis, N., et al.: Pharm. Pharmacol Lett., 6, 2: 51 (1996)<br></p>Formula:C12H15N3O3SColor and Shape:White To BrownMolecular weight:281.33Albendazole sulfoxide
CAS:<p>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.</p>Formula:C12H15N3O3SPurity:Min. 97 Area-%Color and Shape:White PowderMolecular weight:281.33 g/molMethyl (6-(propylsulfinyl)-1H-benzo[d]imidazol-2-yl)carbamate
CAS:Purity:97%Molecular weight:281.3299866GB 31658.11-2021 Albendazole and metabolites Mixture 47 2-20 µg/mL in Acetonitrile
CAS:Controlled ProductColor and Shape:Mixture












