NCT-504
CAS No. 1222765-97-0
NCT-504 ( —— )
产品货号. M35051 CAS No. 1222765-97-0
NCT-504 是选择性的脂质激酶 PIP4Kγ 变构抑制剂,其 IC50 值为 15.8 μM。NCT-504 具有用于亨廷顿氏症疾病研究的潜力。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 2MG | ¥762 | 有现货 |
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| 5MG | ¥1276 | 有现货 |
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| 10MG | ¥2043 | 有现货 |
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| 25MG | ¥3230 | 有现货 |
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| 50MG | ¥4606 | 有现货 |
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| 100MG | ¥6197 | 有现货 |
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| 200MG | ¥8262 | 有现货 |
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| 500MG | 获取报价 | 有现货 |
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| 1G | 获取报价 | 有现货 |
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生物学信息
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产品名称NCT-504
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述NCT-504 是选择性的脂质激酶 PIP4Kγ 变构抑制剂,其 IC50 值为 15.8 μM。NCT-504 具有用于亨廷顿氏症疾病研究的潜力。
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产品描述NCT-504 is a selective allosteric inhibitor of PIP4Kγ, with an IC50 of 15.8 μM. NCT-504 is potential for the research of Huntington's disease.
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体外实验NCT-504 dose not impair the intrinsic ATP-hydrolytic activity of PIP4Kγ in the absence of PI5P substrate.NCT-504 does not inhibit PIP4Kbeta and weakly inhibits PIP4Kalpha phosphorylation of PI5P .NCT-504 dose not inhibit PIP4Kbeta or PIP4Kalpha (IC50 between 50 μM and 100 μM) at 50 μM concentration.NCT-504 elevates the levels of PI(3,5)P2, PI3P and PI5P in MEFs.NCT-504 (10 μM; 12 hours) does not affect cell viability in MEFs.NCT-504 (5 μM, 10 μM; 2 hours, 6 hours) elevates both the induction of autophagy as well as the rate of turnover of autophagic cargo.NCT-504 treatment causes a robust increase in the formation of autolysosomes with only a modest elevation in autophagosomes.NCT-504 increases autophagy flux and decreases huntingtin protein in 293A cells.NCT-504 reduces mHtt protein levels in immortalized striatal cells from knock-in HD mice.Western Blot Analysis Cell Line:HEK293T cells Concentration:5 μM, 10 μM Incubation Time:2 hours, 6 hours Result:Induced autophagosome formation.
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体内实验——
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同义词——
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通路Others
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靶点Other Targets
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受体Others
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研究领域——
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适应症——
化学信息
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CAS Number1222765-97-0
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分子量404.49
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分子式C15H12N6O2S3
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO 中的溶解度 : 125 mg/mL (309.03 mM; 超声助溶 )
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SMILESCn1nnnc1Sc1ncnc2scc(-c3cccc(c3)S(C)(=O)=O)c12
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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
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Eclazolast
Eclazolast (RHC 2871) is a lipophilic anti-allergic compound that inhibits mediator release in a mast cell model.Eclazolast inhibits extracellular secretion by affecting only the direct processes associated with Fc(epsilon)RI in the cell.The effect of Eclazolast is highly dependent on the concentration of antigen that triggers the cell.
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7β-Hydroxyganodereni...
12β-Acetoxy-7β-hydroxy-3,11,15,23-tetraoxo-5a-lanosta-8,20-dien-26-oic acid, a lanostanoid triterpene that can be isolated from Ganoderma lingzhi, exhibits an IC50 of 80.8 μM in MCF-7 cells.
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PNU-142731A
PNU-142731A is an asthma-inhibiting compound with anti-inflammatory activity that induces a decrease in mucus glycoproteins in mice.
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