Home Microbiology Parasite inhibitor Oxfendazole For research use only.

Oxfendazole

Synonyms: RS-8858,Fenbendazole sulfoxide

Oxfendazole (RS-8858,Fenbendazole sulfoxide) is a broad spectrum benzimidazole anthelmintic.

Oxfendazole Chemical Structure

Oxfendazole Chemical Structure

CAS No. 53716-50-0

Purity & Quality Control

Batch: S183001 DMSO]10 mg/mL]false]Water]Insoluble]false]Ethanol]Insoluble]false Purity: 100%
100

Oxfendazole Related Products

Biological Activity

Description Oxfendazole (RS-8858,Fenbendazole sulfoxide) is a broad spectrum benzimidazole anthelmintic.
In Vivo
In vivo

Oxfendazole (OX) induces not only mRNA expression of phase I enzymes Cyp1a1, Cyp1a2, but also Nrf2-regulated phase II enzymes such as Gpx2, Nqo1, Yc2, Akr7a3 and Gstm1 in rats, presumably due to an adaptive response against OX-induced oxidative stress. Oxfendazole enhances oxidative DNA damage (as assessed by 8-hydroxydeoxyguanosine; 8-OHdG) and lipid peroxidation (as assessed by thiobarbituric acid-reactive substances; TBARS) in rats. [1] Oxfendazole administered at the therapeutic dose (4.5 mg/kg) and at the highest dose (22.5 mg/kg) increase 1.54- and 2.36-fold the total liver microsomal cytochrome P450 and more particularly the isoenzyme P450IA2 (95% and 184% increases) in rabbit liver. [2] Oxfendazole MRL induces a mutagenic effect in all tested cell types. Oxfendazole exhibits embryotoxicity including teratogenicity. Oxfendazole induces a disturbance in the different biochemical contents of all tested tissues in mice. [3] Oxfendazole increases the incidence and multiplicity of altered foci (4.0- and 3.6-fold, respectively) and hepatocellular adenomas (HCAs) (3.0- and 5.5-fold, respectively). Oxfendazole treatment induces 5.2- and 5.6-fold increases in the number of proliferating cell nuclear antigen (PCNA)-positive cells and single-stranded DNA (ssDNA)-positive cells in HCAs compared with the surrounding tissue, respectively. [4] Oxfendazole and its sulphone metabolite attain a significantly higher plasma concentration and remain much longer in plasma compared with fenbendazole (FBZ) and albendazole (ABZ) and their respective metabolites in dogs. [5]
NCT Number Recruitment Conditions Sponsor/Collaborators Start Date Phases
NCT06367361 Not yet recruiting
Fascioliasis
Universidad Peruana Cayetano Heredia|National Institute of Allergy and Infectious Diseases (NIAID)
 July 2024 Phase 2
NCT04920292 Completed
Filariasis
Swiss Tropical & Public Health Institute|Ifakara Health Institute|Drugs for Neglected Diseases
 April 21 2022 Phase 1
NCT02636803 Withdrawn
Helminthiasis
Johns Hopkins Bloomberg School of Public Health|Universidad Peruana Cayetano Heredia
 November 2019 Phase 2
NCT03035760 Completed
Helminthic Infection
National Institute of Allergy and Infectious Diseases (NIAID)
 May 12 2017 Phase 1
NCT02234570 Completed
Neurocysticercosis
National Institute of Allergy and Infectious Diseases (NIAID)
 November 17 2014 Phase 1

Chemical Information & Solubility

Molecular Weight 315.35 Formula

C15H13N3O3S
CAS No. 53716-50-0 SDF Download Oxfendazole SDF
Smiles COC(=O)NC1=NC2=C(N1)C=C(C=C2)S(=O)C3=CC=CC=C3
Storage (From the date of receipt)

In vitro
Batch:

DMSO : 10 mg/mL ( (31.71 mM) Moisture-absorbing DMSO reduces solubility. Please use fresh DMSO.)

Water : Insoluble

Ethanol : Insoluble


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In vivo
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