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Furazolidone/呋喃唑酮 {[allProObj[0].p_purity_real_show]}

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。

Furazolidone/呋喃唑酮 化学结构 CAS号:67-45-8
Furazolidone/呋喃唑酮 化学结构
CAS号:67-45-8
Furazolidone/呋喃唑酮 3D分子结构
CAS号:67-45-8
Furazolidone/呋喃唑酮 化学结构 CAS号:67-45-8
Furazolidone/呋喃唑酮 3D分子结构 CAS号:67-45-8
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Furazolidone/呋喃唑酮 纯度/质量文件 产品仅供科研

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Furazolidone/呋喃唑酮 生物活性

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].

Furazolidone/呋喃唑酮 细胞实验

Cell Line
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

Furazolidone/呋喃唑酮 动物实验

Species
Animal Model
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

Furazolidone/呋喃唑酮 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
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 -

Furazolidone/呋喃唑酮 参考文献

[1]Jiang X, Sun L, et al. A novel application of furazolidone: anti-leukemic activity in acute myeloid leukemia. PLoS One. 2013 Aug 9;8(8):e72335. doi: 10.1371/journal.pone.0072335. eCollection 2013.

[2]Alam MI, Paget T, et al. Formulation and advantages of furazolidone in liposomal drug delivery systems. Eur J Pharm Sci. 2016 Mar 10;84:139-45.

[3]Jiang X, Sun L, Qiu JJ, et al. A novel application of furazolidone: anti-leukemic activity in acute myeloid leukemia. PLoS One. 2013;8(8):e72335. Published 2013 Aug 9.

[4]Carvalho SG, Siqueira LA, Zanini MS, et al. Physicochemical and in vitro biological evaluations of furazolidone-based β-cyclodextrin complexes in Leishmania amazonensis. Res Vet Sci. 2018;119:143–153.

[5]Craft JC, Murphy T, Nelson JD. Furazolidone and quinacrine. Comparative study of therapy for giardiasis in children. Am J Dis Child. 1981;135(2):164–166.

[6]Ali BH. Some pharmacological and toxicological properties of furazolidone. Vet Res Commun. 1983;6(1):1–11.

Furazolidone/呋喃唑酮 实验方案

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

Furazolidone/呋喃唑酮 技术信息

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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