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描述 | MRT-81 is a strong antagonist of human and rodent smoothened (Smo) receptors, exhibiting an IC50 value of 41 nM in Shh-light2 cells and demonstrating potent hedgehog pathway inhibition. MRT-81 is utilized in cancer research[1]. |
体外研究 | MRT-81 inhibits the differentiation of mesenchymal pluripotent C3H10T1/2 cells into alkaline phosphatase-positive osteoblasts induced by the Smo agonist SAG (0.1 µM), with an IC50 value of 64 nM[1]. MRT-81, ranging from 1-1000 nM, potently antagonizes SAG (0.01 µM)-induced proliferation of rat granule cell precursors (GCPs) with an IC50 value of less than 10 nM[1]. MRT-81 blocks BODIPY-cyclopamine (5 nM) binding to human Smo in a dose-dependent manner within a concentration range of 0 to 1000 nM for 2 hours at 37 °C, achieving an IC50 of 63 nM in HEK-hSmo cells[1]. |
计算器 | ||||
存储液制备 | ![]() |
1mg | 5mg | 10mg |
1 mM 5 mM 10 mM |
1.80mL 0.36mL 0.18mL |
9.00mL 1.80mL 0.90mL |
18.00mL 3.60mL 1.80mL |
CAS号 | 1263132-08-6 |
分子式 | C31H29N3O5S |
分子量 | 555.64 |
SMILES Code | O=C(C1=CC=C(C2=CC=CC=C2)C=C1)NC3=CC(NC(NC(C4=CC(OC)=C(OC)C(OC)=C4)=O)=S)=CC=C3C |
MDL No. | N/A |
别名 | |
运输 | 蓝冰 |
InChI Key | CTXQODCQOSYYDE-UHFFFAOYSA-N |
Pubchem ID | 56964692 |
存储条件 |
In solvent -20°C:3-6个月-80°C:12个月 Pure form Sealed in dry, 2-8°C |
溶解方案 |
DMSO: 105 mg/mL(188.97 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 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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