Oxfendazole

For research use only.

Catalog No.S1830 Synonyms: RS-8858

1 publication

Oxfendazole Chemical Structure

CAS No. 53716-50-0

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

Selleck's Oxfendazole has been cited by 1 publication

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Biological Activity

Description Oxfendazole (RS-8858) is a broad spectrum benzimidazole anthelmintic.
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]

Protocol

Solubility (25°C)

In vitro DMSO 10 mg/mL (31.71 mM)
Water Insoluble
Ethanol Insoluble

* Please note that Selleck tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations.

Chemical Information

Molecular Weight 315.35
Formula

C15H13N3O3S

CAS No. 53716-50-0
Storage powder
in solvent
Synonyms RS-8858
Smiles COC(=O)NC1=NC2=C(N1)C=C(C=C2)S(=O)C3=CC=CC=C3

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Clinical Trial Information

NCT Number Recruitment interventions Conditions Sponsor/Collaborators Start Date Phases
NCT04920292 Not yet recruiting Drug: Oxfendazole|Drug: Placebo Filariasis Swiss Tropical & Public Health Institute|Ifakara Health Institute|Drugs for Neglected Diseases September 1 2021 Phase 1
NCT02636803 Withdrawn Drug: oxfendazole|Drug: albendazole Helminthiasis Johns Hopkins Bloomberg School of Public Health|Universidad Peruana Cayetano Heredia November 2019 Phase 2
NCT03035760 Completed Drug: Oxfendazole Helminthic Infection National Institute of Allergy and Infectious Diseases (NIAID) May 12 2017 Phase 1
NCT02234570 Completed Drug: Oxfendazole|Other: Placebo Neurocysticercosis National Institute of Allergy and Infectious Diseases (NIAID) November 17 2014 Phase 1

Tech Support

Answers to questions you may have can be found in the inhibitor handling instructions. Topics include how to prepare stock solutions, how to store inhibitors, and issues that need special attention for cell-based assays and animal experiments.

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Cell Lines Assay Type Concentration Incubation Time Formulation Activity Description PMID