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奥吩达唑 /Oxfendazole {[allProObj[0].p_purity_real_show]}

货号:A193817 同义名: 奥芬哒唑 / Oxfenbendazole;HOE 8105

Oxfendazole是fenbendazole的亚砜形式,是一种广谱苯并咪唑类驱虫药。

Oxfendazole 化学结构 CAS号:53716-50-0
Oxfendazole 化学结构
CAS号:53716-50-0
Oxfendazole 3D分子结构
CAS号:53716-50-0
Oxfendazole 化学结构 CAS号:53716-50-0
Oxfendazole 3D分子结构 CAS号:53716-50-0
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Oxfendazole 纯度/质量文件 产品仅供科研

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Oxfendazole 生物活性

描述 Oxfendazole, a veterinary medicine belonging to the benzimidazole family of anthelmintic drugs, has demonstrated substantial activity against the tissue stages of Taenia solium and has potential to be developed as an effective therapy for neurocysticercosis. Oxfendazole was rapidly absorbed with a mean plasma half-life ranging from 8.5 to 11 h. The renal excretion of oxfendazole was minimal[3]. Oxfendazole (OFZ) is effective against A. suum when used at a single high oral dose of 30 mg/kg[4]. The efficacy of oxfendazole in the reduction of O. lupi mfs was evaluated by microfilarial count and by assessing the percentage of mfs (microfilariae) reduction and mean microfilaricidal efficacy. The mean microfilaricidal efficacy of oxfendazole in the treatment of canine onchocercosis by O. lupi at D30, D90 and D180 was 41%, 81% and 90%, in G2 and 40%, 65% and 70%, in G3, respectively[5]. Oxfendazole also suppressed the cell growth of non‑small cell lung cancer (NSCLC) cells, and overexpression of c‑Src decreased the cytotoxicity of oxfendazole against NSCLC cells[6].

Oxfendazole 临床研究

NCT号 适应症或疾病 临床期 招募状态 预计完成时间 地点
NCT01584362 Tenia Solium Infection Phase 1 Withdrawn(study conducted unde... 展开 >>r Clinical Trials Agreement as NIAID registration NCT02234570) 收起 << - -
NCT03435718 Trichuris Infection Phase 2 Not yet recruiting October 2021 -
NCT02636803 Helminthiasis Phase 2 Not yet recruiting February 2020 -

Oxfendazole 参考文献

[1]Dewa Y, Nishimura J, et al. Involvement of oxidative stress in hepatocellular tumor-promoting activity of oxfendazole in rats. Arch Toxicol. 2009 May;83(5):503-11.

[2]Gleizes C, Eeckhoutte C, et al. Inducing effect of oxfendazole on cytochrome P450IA2 in rabbit liver. Consequences on cytochrome P450 dependent monooxygenases. Biochem Pharmacol. 1991 Jun 15;41(12):1813-20.

[3]An G, Murry DJ, Gajurel K, et al. Pharmacokinetics, Safety, and Tolerability of Oxfendazole in Healthy Volunteers: a Randomized, Placebo-Controlled First-in-Human Single-Dose Escalation Study. Antimicrob Agents Chemother. 2019;63(4):e02255-18. Published 2019 Mar 27

[4]Ceballos L, Canton C, Cadenazzi G, et al. Oxfendazole kinetics in pigs: In vivo assessment of its pattern of accumulation in Ascaris suum. Exp Parasitol. 2019;199:52‐58

[5]Colella V, Maia C, Pereira A, et al. Evaluation of oxfendazole in the treatment of zoonotic Onchocerca lupi infection in dogs. PLoS Negl Trop Dis. 2018;12(1):e0006218. Published 2018 Jan 29

[6]Xu D, Tian W, Jiang C, Huang Z, Zheng S. The anthelmintic agent oxfendazole inhibits cell growth in non‑small cell lung cancer by suppressing c‑Src activation. Mol Med Rep. 2019;19(4):2921‐2926

Oxfendazole 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

3.17mL

0.63mL

0.32mL

15.86mL

3.17mL

1.59mL

31.71mL

6.34mL

3.17mL

Oxfendazole 技术信息

CAS号53716-50-0
分子式C15H13N3O3S
分子量 315.347
别名 奥芬哒唑 ;Oxfenbendazole;HOE 8105;Fenbendazole sulfoxide
运输蓝冰
存储条件

In solvent -20°C:3-6个月-80°C:12个月

Pure form Sealed in dry,Room Temperature

溶解度

DMSO: 30 mg/mL(95.13 mM),配合低频超声,并水浴加热至45℃助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

动物实验配方
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