PU02 | MedChemExpress (MCE)
品牌 | 厂商性质 | 产地 | 货期 | 价格 |
---|---|---|---|---|
MedChemExpress (MCE) | 生产商 | 美国 | 现货 | 770 |
性能特点
PU02 是 6-MP (HY-13677) 的一个衍生物,是 5-HT3 受体的负变构调节剂,其在 HEK293 细胞测得的转染 5-HT3A 和 5-HT3AB 受体后的 IC50 值分别
规格 | CAS号 | 价格 | 操作 |
---|---|---|---|
10 mM * 1 mL | 313984-77-9 | ¥770.00 | 询底价 |
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PU02
CAS No. : 313984-77-9
MCE 国际站:PU02
产品活性:PU02 是 6-MP (HY-13677) 的一个衍生物,是 5-HT3 受体的负变构调节剂,其在 HEK293 细胞测得的转染 5-HT3A 和 5-HT3AB 受体后的 IC50 值分别为 0.36 和 0.73 μM。
研究领域:GPCR/G Protein | Neuronal Signaling | Apoptosis
作用靶点:5-HT Receptor | Apoptosis
In Vitro: PU02 (NMMP) (0-200 μM) leads to a steady decrease in cell viability of HepG2 cells (IC50=48.585 μM). PU02 (NMMP) shows less toxicity on L02 cells than did 6-MP after 48 h of treatment.
PU02 (NMMP) at 6.25 or 25 μM exhibits inhibitory effects on the viability of the tested cell lines, including SMMC-7721, MDA-MB-231, RKO and HCT-8 cells.
PU02 (NMMP) induces cell cycle arrest at the G2/M phase. PU02 (NMMP) downregulats the expression of cyclin B1/D1 and CDK4 in a time-dependent manner in HepG2 cells,but the expression of cyclin E is not affected.
PU02 (NMMP)-treated cells exhibits a significant increase in caspase-3 cleavage, suggesting enhanced apoptotic activity.
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