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About This Item
Empirical Formula (Hill Notation):
C12H15N3O3S
CAS Number:
Molecular Weight:
281.33
NACRES:
NA.77
UNSPSC Code:
12352119
Beilstein/REAXYS Number:
677664
MDL number:
description
Modulation and Signaling
Quality Level
assay
≥97% (HPLC)
form
solid
color
white to beige
suitability
HPTLC
storage temp.
2-8°C
SMILES string
CCCS(=O)c1ccc2[nH]c(NC(=O)OC)nc2c1
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
VXTGHWHFYNYFFV-UHFFFAOYSA-N
General description
Albendazole sulfoxide is a blood-brain barrier main metabolite of anti-parasitic agent albendazole that acts as a antihelminthic. It binds to colchicine binding site of β-tubulin and prevents polymerization. Albendazole sulfoxide exhibits greater affinity to parasitic β-tubulin than to mammalian.
Application
Metabolomics research
Biochem/physiol Actions
Ricobendazole is a key metabolite of albendazole and acts as an anthelmintic. It has been shown to induce apoptosis in human cancer cell line HT-29, possibly by arresting cell cycle at the G2/M phase.
Other Notes
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signalword
Warning
hcodes
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - Repr. 2 - Skin Sens. 1 - STOT RE 2 Oral
target_organs
Adrenal gland,spleen,male reproductive organs,Blood
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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Lidia Radko et al.
Journal of veterinary research, 61(3), 313-319 (2018-07-07)
Albendazole is used to treat endoparasitic diseases in animals and humans. After oral administration, it is quickly oxidised into its pharmacologically active metabolite albendazole sulfoxide and then to sulfone. However, it is not clear which compound is responsible for toxic
Global Trade Item Number
| SKU | GTIN |
|---|---|
| SMB01325-100MG | 04065266715293 |


