Posaconazole

目录号: A10744

CYP3A4 抑制剂

Posaconazole

Posaconazole Chemical Structure

CAS NO. 171228-49-2

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。

库存: 现货

规格 价格 数量
5 mg
¥ 600.00
10 mg
¥ 1,000.00
25 mg
¥ 1,800.00
50 mg
¥ 3,000.00
10mM * 1mL in DMSO
¥ 1,430.00
Warning 产品仅用于科学研究,不针对患者销售,望谅解.

产品详情

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.
In lyophilized form, the chemical is stable for 36 months.
In solution, store at -20ºC and use within 3 months to prevent loss of potency. Aliquot to avoid multiple freeze/thaw cycles.

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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