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Paromomycin Sulfate
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
Paromomycin Sulfate图片
CAS NO:1263-89-4
包装与价格:
包装价格(元)
10 mM * 1 mL in Water电议
500mg电议
1 g电议
5 g电议
10 g电议

产品名称
硫酸巴龙霉素
Aminosidine sulfate
产品介绍
Paromomycin (Aminosidine) sulfate 是一种的广谱氨基糖苷类抗生素 (antibiotic),具有杀螨杀菌作用,是新霉素 (HY-B0470) 衍生物。Paromomycin sulfate 通过与细菌 30S 核糖体 A 位点的 RNA 寡核苷酸特异性结合,使 mRNA 的翻译提前终止,并抑制蛋白质合成。Paromomycin sulfate 可用于细菌和寄生虫感染的研究。
生物活性

Paromomycin (Aminosidine) sulfate, a neomycin (HY-B0470) derivative, is a broad spectrumaminoglycosideantibioticwith amebicidal and bactericidal effects. Paromomycin sulfate prematures termination of translation of mRNA and inhibits protein synthesis by specifically binds to the RNA oligonucleotide at the A site ofbacterial30S ribosomes. Paromomycin sulfate can be used for the research ofbacterialand parasitic infections[1][2][3].

IC50& Target

Aminoglycoside

 

Amebae

 

体外研究
(In Vitro)

Paromomycin sulfate (500 μg/ml) reduces intracellular parasitic forms by 97.2% compared to control in Caco-2 cells and reduces the percentage of intracellularC. parvumforms by 99.5% in HCT-8 cells[2].

体内研究
(In Vivo)

Paromomycin sulfate (oral gavage; 50 mg/kg-200 mg/kg; once daily; for five consecutive days two weeks post infection) reduces the number of oocyst per gram of feces and intestine. It shows minimal focal inflammation in only 20% of the sections at 50 mg/kg from the intestines of mice infected withC. parvumand only 10% of focal inflammation at 200 mg/kg[1].

Animal Model:Male Swiss albino mice[1]
Dosage:50 mg/kg-200 mg/kg
Administration:Oral gavage; 50 mg/kg-200 mg/kg; once daily; for five consecutive days two weeks post infection
Result:Was against cryptosporidiosis in vivo.
Clinical Trial
分子量

713.71

性状

Solid

Formula

C23H47N5O18S

CAS 号

1263-89-4

中文名称

硫酸新霉素杂质E

结构分类
  • Antibiotics
  • Other Antibiotics
来源

Streptomyces rimosus NRRL 2455

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

4°C, sealed storage, away from moisture

*In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)

溶解性数据
In Vitro: 

H2O : 100 mg/mL(140.11 mM;ultrasonic and warming and heat to 80℃)

Ethanol : 1 mg/mL(1.40 mM;Need ultrasonic)

DMSO : 1 mg/mL(1.40 mM;ultrasonic and warming and heat to 80℃)

配制储备液
浓度溶剂体积质量1 mg5 mg10 mg
1 mM1.4011 mL7.0056 mL14.0113 mL
5 mM0.2802 mL1.4011 mL2.8023 mL
10 mM0.1401 mL0.7006 mL1.4011 mL
*

请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效
储备液的保存方式和期限:-80℃, 6 months; -20℃, 1 month (sealed storage, away from moisture)。-80℃ 储存时,请在 6 个月内使用,-20℃ 储存时,请在 1 个月内使用。

In Vivo:

请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照In Vitro方式配制澄清的储备液,再依次添加助溶剂:

——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用; 以下溶剂前显示的百
分比是指该溶剂在您配制终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶

  • 1.

    请依序添加每种溶剂: PBS

    Solubility: 100 mg/mL (140.11 mM); Clear solution; Need ultrasonic

*以上所有助溶剂都可在本网站选购。