货号:A515238
同义名:
Furoxone; Trifurox
Furazolidone是一种硝基呋喃衍生物,具有抗菌和抗原虫活性,能够抑制 AML1-ETO 转化细胞,并对 Gram-positive 和 Gram-negative 细菌具有灭菌作用。


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| 描述 | Furazolidone (FZD) is a nitrofuran derivative with antiprotozoal and antibacterial activity, inhibits AML1-ETO (Acute myeloid leukemia ) transformed cells with IC50 value of 12.7 μM[3]. Biological in vitro evaluations demonstrated that free FZD and the FZD:β-CD complexes presented significant leishmanicidal activity against L. amazonensis with IC50 values of 6.16 μg/mL and 1.83 μg/mL for the complexes prepared by kneading and lyophilization, respectively[4]. Moreover, furazolidone was more effective and better tolerated than quinacrine for the treatment of giardiasis[5]. Furazolidone is known to induce a condition of cardiomyopathy in turkeys, which could be used as a model to study alpha 1-antitrypsin deficiency in man[6]. |
| Concentration | Treated Time | Description | References | |
| human hepatocyte L02 cells | 10-60 µg/mL | 24 hours | To evaluate the effect of FZD on L02 cell viability, results showed FZD reduced cell viability in a dose-dependent manner. | Molecules. 2016 Aug 22;21(8):1061 |
| Helicobacter pylori | ≥2 mg/l | 72 hours | To evaluate the resistance of Furazolidone against Helicobacter pylori, the results showed a resistance rate of 0.28% (6/2109). | Front Cell Infect Microbiol. 2022 Sep 8;12:970630 |
| Giardia lamblia WB C6 | 100 μM | Evaluate the inhibitory effect of furazolidone on Giardia lamblia, results showed that furazolidone was reduced by TrxR, increasing toxicity to the parasite. | Int J Parasitol Drugs Drug Resist. 2016 Dec;6(3):148-153 | |
| Pseudomonas bacteria (Pseudomonas sp. OS4, P. plecoglossicida IsA, Pseudomonas sp. MChB) | 5 mg/L | 24 hours | To assess the effect of furazolidone on bacterial metabolic activity, results showed that FZD combined with saponins significantly reduced bacterial metabolic activity, demonstrating a synergistic bactericidal effect. | World J Microbiol Biotechnol. 2023 Jun 5;39(8):221 |
| Human colon epithelial cells CCD 841CoN | 5 mg/L | 48 hours | To evaluate the cytotoxicity of furazolidone combined with saponins, results showed an IC50 of 1.28 µg/mL for FZD, and the addition of saponins did not significantly alter its cytotoxicity. | World J Microbiol Biotechnol. 2023 Jun 5;39(8):221 |
| Escherichia coli K12 | 2.5 μg/mL | 24 hours | Evaluate the synergy between Furazolidone and Sodium Deoxycholate, showing FICI of 0.125, indicating synergistic inhibition | BMC Microbiol. 2020 Jan 6;20(1):5 |
| peripheral blood mononuclear cells (PBMC) | >20 µM | 72 hours | To evaluate the cytotoxicity of Furazolidone on PBMC, results showed no cytotoxic activity on the viability and proliferation of PBMC populations up to 20 µM. | Antimicrob Agents Chemother. 2018 Mar 27;62(4):e01834-17 |
| Neonatal rat cardiomyocytes (NRCMs) | 6.25–100 μM | 48 hours | To evaluate the effects of furazolidone on cardiomyocyte viability and mitochondrial membrane potential, showing dose-dependent decreases in cell viability and MMP | PLoS One. 2013 Jun 20;8(6):e66779 |
| Administration | Dosage | Frequency | Description | References | ||
| Sprague-Dawley rats | Furazolidone-induced dilated cardiomyopathy model | Gavage | 0.3 mg/bodyweight (g)/day | Once daily for 8 weeks | Induced dilated cardiomyopathy model for subsequent stem cell and gene therapy studies | J Cell Mol Med. 2015 Aug;19(8):1868-76 |
| Sprague-Dawley rats | Furazolidone-induced dilated cardiomyopathy model | Oral | 700 ppm | Daily administration for thirty weeks | To establish a rat model of furazolidone-induced dilated cardiomyopathy, showing enlarged LV dimensions, reduced systolic and diastolic functions, myocardial fibrosis, and mitochondrial damage | PLoS One. 2013 Jun 20;8(6):e66779 |
| NCT号 | 适应症或疾病 | 临床期 | 招募状态 | 预计完成时间 | 地点 |
| NCT03320538 | Peptic Ulcer Disease | Not Applicable | Recruiting | July 1, 2019 | China, Jiangxi ... 展开 >> Jiangxi University of Traditional Chinese Medicine Recruiting Nanchang, Jiangxi, China, 330004 Contact: Xu Zhou, Ph.D. +8618780085060 zhouxu_ebm@hotmail.com Contact: Xiaofan Chen, Ph.D. +86079187118012 841347982@qq.com 收起 << |
| NCT02689583 | Gastritis Gas... 展开 >>tric Ulcer 收起 << | Not Applicable | Unknown | - | - |
| NCT02934048 | Therapeutic Duration ... 展开 >> Helicobacter Pylori Antimicrobial Susceptibility Test Eradication 收起 << | Phase 4 | Unknown | June 2017 | - |
| 计算器 | ||||
| 存储液制备 | ![]() |
1mg | 5mg | 10mg |
|
1 mM 5 mM 10 mM |
4.44mL 0.89mL 0.44mL |
22.21mL 4.44mL 2.22mL |
44.41mL 8.88mL 4.44mL |
|
| CAS号 | 67-45-8 |
| 分子式 | C8H7N3O5 |
| 分子量 | 225.16 |
| SMILES Code | O=C1OCCN1/N=C/C2=CC=C([N+]([O-])=O)O2 |
| MDL No. | MFCD00010550 |
| 别名 | Furoxone; Trifurox; Furazolidon; Furazolidine; Tikofuran; Nitrofuroxon; Nitrofurazolidone; Nifulidone; NSC 6469 |
| 运输 | 蓝冰 |
| 存储条件 |
In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Keep in dark place, sealed in dry, room temperature |
| 溶解方案 |
DMSO: 4 mg/mL(17.77 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 |
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