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|---|---|---|---|---|---|---|---|
| {[ item.pr_size ]} |
{[ getRatePriceInt(item.pr_rmb, 1,1) ]} {[ getRatePriceInt(item.pr_rmb_sale, 1,1) ]} {[ suihuo_tips(item.pr_tag_price, item.pr_am) ]} |
{[ getRatePriceInt(item.pr_rmb, 1,1) ]} {[ getRatePriceInt(item.pr_rmb,item.pr_rate,1) ]} {[ suihuo_tips(item.pr_tag_price, item.pr_am) ]} |
{[ getRatePriceInt(item.pr_rmb, 1,1) ]}{[ suihuo_tips(item.pr_tag_price, item.pr_am) ]} | {[ getRatePrice(item.pr_rmb_sale, 1,1,item.mem_isinteger) ]} {[ getRatePrice(item.pr_rmb,item.pr_rate,item.mem_rate,item.mem_isinteger) ]} {[ getRatePrice(item.pr_rmb,1,item.mem_rate,item.mem_isinteger) ]} | 现货 | 1周 咨询 | - + |
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| 描述 | Dimethylmalonate is a competitive SDH (succinate dehydrogenase) inhibitor. It led to an increase in succinate in the cytosol, presumably by impairing the oxidation of succinate to fumarate, and also boosted LPS-induced succinate accumulation. Limiting succinate oxidation by dimethylmalonate induced an anti-inflammatory response at 10mM in BMDMs. Dimethylmalonate, at dose of 160 mg/kg, i.p., also showed anti-inflammatory effect on LPS-induced sepsis mice model. It decreased serum levels of IL-1β and boosted IL-10, but had no significant effect on TNF-α, as well as reduced IL-1β and PHD3 expression in the spleen[1]. |
| 作用机制 | Dimethylmalonate is a competitive SDH inhibitor. |
| Dose | mice: 160mg/kg, i.p.[1] |
| 计算器 | ||||
| 存储液制备 | ![]() |
1mg | 5mg | 10mg |
|
1 mM 5 mM 10 mM |
7.57mL 1.51mL 0.76mL |
37.85mL 7.57mL 3.78mL |
75.69mL 15.14mL 7.57mL |
|
| CAS号 | 108-59-8 |
| 分子式 | C5H8O4 |
| 分子量 | 132.11 |
| SMILES Code | O=C(OC)CC(OC)=O |
| MDL No. | MFCD00008460 |
| 别名 | |
| 运输 | 蓝冰 |
| InChI Key | BEPAFCGSDWSTEL-UHFFFAOYSA-N |
| Pubchem ID | 7943 |
| 存储条件 |
In solvent -20°C:3-6个月-80°C:12个月 |
| 溶解方案 |
DMSO: 105 mg/mL(794.76 mM),配合低频超声助溶,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 H2O: 100 mg/mL(756.92 mM),配合低频超声助溶 以下溶解方案都请先按照体外实验的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
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