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Posaconazole主要是CYP3A4的抑制剂,但不抑制其他CYP酶的活性。也是甾醇C14+脱甲基酶抑制剂的抑制剂,IC50为0.25μM。泊沙康唑的终末消除半衰期中位数为15-35小时。
靶点信息
lanosterol 14α-demethylase | ||||
In vitro (25°C) | DMSO | 90 mg/mL (128.42 mM) | |
Water | Insoluble | ||
Ethanol | Insoluble | ||
In vivo | 1% DMSO+30% polyethylene glycol+1% Tween 80 | 28 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 |
---|---|---|---|
0.1 mM | 14.27 mL | 71.35 mL | 142.69 mL |
0.5 mM | 2.85 mL | 14.27 mL | 28.54 mL |
1 mM | 1.43 mL | 7.13 mL | 14.27 mL |
5 mM | 0.29 mL | 1.43 mL | 2.85 mL |
*The above data is based on the productmolecular weight 700.8 . Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.
目录号 | A10744 |
---|---|
作用机制 | Inhibitor (抑制剂) |
M. Wt | 700.8 |
Formula | C37H42F2N8O4 |
Purity | >99% |
Storage | Store lyophilized at -20ºC, keep desiccated. |
CAS No. | 171228-49-2 |
Synonyms | Noxafil |
SMILES | CC[C@@H]([C@H](C)O)N1C(=O)N(C=N1)C2=CC=C(C=C2)N3CCN(CC3)C4=CC=C(C=C4)OC[C@H]5C[C@](OC5)(CN6C=NC=N6)C7=C(C=C(C=C7)F)F |
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