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Moniliformin (sodium salt)
诱导有丝分裂停滞在中期,是提取自镰孢镰刀菌中的有效,水溶性的霉菌毒素。
目录号: PC10016 纯度: ≥98%
CAS No. :71376-34-6
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中文名称
Moniliformin (sodium salt)
中文别名
1-羟基-1-环丁烯-3,4-二酮钠;串珠镰刀菌素;串珠镰刀菌素钾盐;苊醌;3-羟基-3-环丁烯二酮钠盐
英文名称
Moniliformin (sodium salt)
英文别名
3-Cyclobutene-1,2-dione,3-hydroxy-, sodium salt (1:1);Moniliformin, sodium salt;Moniliformin;Moniliformin Sodium;Moniliformin sodium salt solution;sodium,3,4-dioxocyclobuten-1-olate;1-Hydroxycyclobut-1-ene-3,4-dione;1-Hydroxycyclobut-1-ene-3,4-dione sodium salt;3-CYCLOBUTENE-1,2-DIONE,3-HYDROXY-,SODIUM SALT;3-Hydroxy-3-cyclobutenedione sodium salt;Moniliformin sodium salt from Fusarium moniliforme;Moniliformin sodium salt from Fusarium proliferatum;Moniliformin sodium salt
Cas No.
71376-34-6
分子式
C4Ho3-.Na+
分子量
120.04
包装储存

4°C, sealed storage, away from moisture

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

生物活性

Moniliformin sodium salt is a potent mycotoxin isolate from Fusarium moniliforme.

性状

Solid

体外研究(In Vitro)

Fusarium moniliforme NRRL 6322 produces about 600 mg of recoverable moniliformin, a mycotoxic metabolite, per kg of corn grit medium. Several strains of Fusarium moniliforme produce in laboratory culture more than 800 mg of moniliformin per kg of growth substrate. Monocytes-derived macrophages exposed to moniliformin during the differentiation process present a decrease of endocytosis ability, and a decrease of CD71 and HLA-DR expression.

Medlife has not independently confirmed the accuracy of these methods. They are for reference only.

体内研究(In Vivo)

Moniliformin is less toxic to mice, with an LD50 of 20.9 mg per kg for the females and 29.1 mg per kg of body weight for the males. As in the case of the chicks, mice surviving the toxin demonstrated no ill effects; the mice or chicks that died became recumbent in 4 to 6 h after treatment and died within 24 h. In 4-day-old chicken embryos, a sharp LD50 of 2.8 μg per embryo is obtained with no overt gross teratogenic effects in the survivors. Rats treated with the highest dose of moniliformin show decreased activity followed by acute heart failure and death. The rats of the lower doses (<9mg/kg b.w.) show no signs of toxicity. The daily intake of moniliformin strongly reduces the phagocytic activity of neutrophils in all dose groups. The decrease continued in the satellite group during the follow-up period, indicating a severe impact on the immune system and a LOAEL value of 3mg/kg b.w. for moniliformin. Moniliformin is rapidly excreted into urine, ranging between 20.2 and 31.5% daily and shows no signs of accumulation. The concentration of moniliformin in faeces is less than 2%, which suggests efficient absorption from the gastrointestinal tract.

Medlife has not independently confirmed the accuracy of these methods. They are for reference only.

运输条件

Room temperature or refrigerated transportation.

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)

结构分类
来源

Fusarium moniliforme

参考文献
溶解度数据
体外研究: 

H2O : 100 mg/mL (833.06 mM; Need ultrasonic)

DMSO : ≥ 45 mg/mL (374.88 mM)

* "≥" means soluble, but saturation unknown.

配制储备溶液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 8.3306 mL 41.6528 mL 83.3056 mL
5 mM 1.6661 mL 8.3306 mL 16.6611 mL
10 mM 0.8331 mL 4.1653 mL 8.3306 mL
*

产品不同,其溶解度不同。建议根据产品选择合适的溶剂配制储备溶液;配成溶液后,建议分装保存,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°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)。-80°C 储存时,建议在 6 个月内使用,-20°C 储存时,建议在 1 个月内使用。

体内研究:

建议根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都建议先按照 体外研究 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.

    建议依照次序添加每种溶剂: PBS

    Solubility: 33.33 mg/mL (277.66 mM); Clear solution; Need ultrasonic

*
搜索质检报告(COA)

1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

The molarity calculator equation
Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)
The dilution calculator equation
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
This equation is commonly abbreviated as: C1V1 = C2V2