QNZ (EVP4593) EVP4593
QNZ (EVP4593)有效抑制NF-κB激活和TNF-α产生,在Jurkat T细胞中IC50分别为11 nM和7 nM。
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货号:
TK0344 -
规格:
- 1mg
- 2mg
- 5mg
- 10mg
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价格:
¥0.00
QNZ (EVP4593)有效抑制NF-κB激活和TNF-α产生,在Jurkat T细胞中IC50分别为11 nM和7 nM。
| CAS No. | 545380-34-5 |
| 生物活性 | QNZ (EVP4593) shows strong inhibitory effects on NF-κB transcriptional activation and TNF-α production with IC50s of 11 and 7 nM, respectively. QNZ (EVP4593) is a neuroprotective inhibitor of SOC channel. |
| 分子式 | C22H20N4O |
| 分子量 | 356.42 |
| 运输条件 | Room temperature in continental US; may vary elsewhere. |
| 储存条件 | Powder -20°C 3 years |
| 溶解性数据 | DMSO : ≥ 37 mg/mL (103.81 mM) |
| 体外研究 | QNZ (Compound 11q) has a suppressing effect of the NF-κB mediated-inflammatory response. QNZ inhibits edema formation dose-dependently. QNZ (EVP4593) reduces the number of lysosomes/autophagosomes and store-operated channel (SOC) currents in Huntington's disease (HD). Normalization of calcium transport within neurons in response to QNZ is expect to reduce pathology manifestation. A number of lysosomes/autophagosomes are evaluated in HD and WT neurons treated with QNZ using transmission electron microscopy (TEM). Incubation with QNZ reduces the number of lysosomes/autophagosomes in HD GABAergic medium spiny (GABA MS)-like neurons (GMSLNs) by almost two-fold (from 0.41±0.04 to 0.23±0.04; p<0.05), while WT neurons are not affected. This observation is confirmed by examining lysosome content by flow cytometry (FC) analysis. The median fluorescence intensity is reduced by 34±6 % in HD GMSLNs upon QNZ treatment (p<0.05). |
| 纯度及产品资料 | ≥98% |