
ML-180
CAS No. 863588-32-3
ML-180 ( SR1848 )
产品货号. M22607 CAS No. 863588-32-3
ML-180 是一种有效的孤儿核受体肝受体同源物 1 (LRH-1; NR5A2) 反向激动剂(IC50 为 3.7 μM)。ML-180(0.5-5 μM;24 小时)显示出对 cyclin-D1 和 cyclin-D1 的显着抑制作用。 cyclin-E1 在肝细胞中的表达,但对 SK-OV-3 细胞中的抑制影响不大[2]。 ML-180(5 μM;24 小时)导致 LRH-1 表达快速降低,并有效抑制内源性 LRH-1 信号传导。
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
2MG | ¥356 | 有现货 |
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5MG | ¥567 | 有现货 |
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10MG | ¥940 | 有现货 |
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25MG | ¥1766 | 有现货 |
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50MG | ¥3094 | 有现货 |
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100MG | ¥4682 | 有现货 |
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200MG | 获取报价 | 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ML-180
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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ML-180 是一种有效的孤儿核受体肝受体同源物 1 (LRH-1; NR5A2) 反向激动剂(IC50 为 3.7 μM)。ML-180(0.5-5 μM;24 小时)显示出对 cyclin-D1 和 cyclin-D1 的显着抑制作用。 cyclin-E1 在肝细胞中的表达,但对 SK-OV-3 细胞中的抑制影响不大[2]。 ML-180(5 μM;24 小时)导致 LRH-1 表达快速降低,并有效抑制内源性 LRH-1 信号传导。
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产品描述ML-180 is a potent orphan nuclear receptor liver receptor homolog 1 (LRH-1; NR5A2) inverse agonist (IC50 of 3.7 μM) .ML-180 (0.5-5 μM; 24 hours) shows a significant inhibition of cyclin-D1 and cyclin-E1 expression in hepatic cells, but has little effect on repression in SK-OV-3 cells. ML-180 (5 μM; 24 hours) leads to a rapid decrease of LRH-1 expression and efficiently represses endogenous LRH-1 signaling. ML-180 has a statistically significant decrease of both LRH-1 and SHP mRNA in adrenal glands and pancreatic tissue.
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体外实验ML-180 (SR1848; 0.01-100 μM; 48 hours) shows diminished capacity to proliferate at concentrations above 1 μM, and the EC50 being roughly 2.8 μM in Huh-7 cells. ML-180 inhibits cell proliferation in an LRH-1-dependent manner. ML-180 (0.5-5 μM; 24 hours) shows a significant inhibition of cyclin-D1 and cyclin-E1 expression in hepatic cells, but has little effect on repression in SK-OV-3 cells. ML-180 (5 μM; 24 hours) leads to a rapid decrease of LRH-1 expression and efficiently represses endogenous LRH-1 signaling. ML-180 (0.5-5 μM; 24 hours) inhibits LRH-1 mRNA expression in a dose-dependent manner. ML-180 (5 μM; 2 hours) rapidly and significantly decreases the mRNA levels of LRH-1 receptor and its downstream targets (CYP19, GATA3, and GATA4) in Huh-7 and HepG2 cells. Cell Proliferation Assay Cell Line:Huh-7 cells Concentration: 0.01, 0.1, 1, 10, 100 μM Incubation Time:48 hours Result:Showed diminished capacity to proliferate at concentrations above 1 μM.Cell Cycle Analysis Cell Line:Huh-7 cells Concentration:0.5, 1, 5 μM Incubation Time:24 hours Result: Showed a significant inhibition of cyclin-D1 and cyclin-E1 expression in hepatic cells.Western Blot Analysis Cell Line:Huh-7 cells Concentration:5 μM Incubation Time:24 hours Result:Significantly reduced the LRH-1 protein levels.RT-PCRCell Line:Huh-7 cells Concentration:0.5, 1, 5 μM Incubation Time:24 hours Result:Inhibited LRH-1 mRNA expression in a dose-dependent manner.
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体内实验ML-180 (SR1848; 30 mg/kg; i.p.; daily; for 10 days) has a statistically significant decrease of both LRH-1 and SHP mRNA in adrenal glands and pancreatic tissue. Animal Model:8-week-old C57Bl/6J mice Dosage:30 mg/kg Administration:IP; daily; for 10 days Result:Had a statistically significant decrease of both LRH-1 and SHP mRNA in adrenal glands and pancreatic tissue.
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同义词SR1848
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通路Others
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靶点Other Targets
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受体orphan nuclear receptor NR5A2
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研究领域——
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适应症——
化学信息
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CAS Number863588-32-3
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分子量388.89
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分子式C20H25ClN4O2
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纯度>98% (HPLC)
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溶解度DMSO:11 mg/mL (28.28 mM; Need ultrasonic)
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SMILESClc1cccc(c1)N1CCN(CC1)c1cc(=O)n(C2CCCCC2)c(=O)[nH]1
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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
1. Busby S, et al. Discovery of Inverse Agonists for the Liver Receptor Homologue-1 (LRH1; NR5A2).