A 740003
目录号: A11316
P2X7 receptor 拮抗剂
A 740003 是一种新型的 P2X7 受体竞争性拮抗剂(IC50 值分别为人类 40 nM 和大鼠 18 nM)。
Discription | A 740003 is a novel competitive antagonist of P2X7 receptors (IC50 values = 40 nM for human and 18 nM for rat). | |||||
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Cell Research |
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目录号 | A11316 |
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分子式 | C26H30N6O3 |
分子量 | 474.6 |
CAS号 | 861393-28-4 |
SMILES | CC(C)(C)C(NC(=O)CC1=CC(=C(C=C1)OC)OC)/N=C(/NC#N)\NC2=CC=CC3=C2C=CC=N3 |
其他名称 | A740003, A-740003 |
储存条件 | Store lyophilized at -20ºC, keep desiccated. |
In vitro | DMSO | 85 mg/mL (179.11 mM) | |
Water | Insoluble | ||
Ethanol | 1 mg/mL | ||
* <1 mg/ml means slightly soluble or insoluble. * Please note that Adooq tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations. |
Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
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0.1 mM | 21.07 mL | 105.35 mL | 210.7 mL |
0.5 mM | 4.21 mL | 21.07 mL | 42.14 mL |
1 mM | 2.11 mL | 10.54 mL | 21.07 mL |
5 mM | 0.42 mL | 2.11 mL | 4.21 mL |
Calculate the dilution required to prepare a stock solution. This equation is commonly abbreviated as: C1V1 = C2V2