Dapaconazole,98.95%
产品编号:Bellancom-16719| CAS NO:1269726-67-1| 分子式:C19H15Cl2F3N2O| 分子量:415.24
达巴康唑作为一种抗真菌药物,抑制甾醇14α-脱甲基酶细胞色素P450活性,IC50为1.4μM。
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Dapaconazole
产品介绍 | Dapaconazole 作为一种抗真菌化合物,抑制 sterol 14α-demethylase cytochrome P450 活性的 IC50 值为 1.4 μM。 | ||||||||||||||||
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生物活性 | Dapaconazole, as an antifungal agent, inhibits sterol 14α-demethylase cytochrome P450 activity with an IC50 of 1.4 μM. | ||||||||||||||||
体外研究 |
Dapaconazole inhibits sterol 14α-demethylase cytochrome P450 activity with an IC50 of 1.4 ± 0.3 μM. 西域 has not independently confirmed the accuracy of these methods. They are for reference only. | ||||||||||||||||
体内研究 |
Dapaconazole (20 mg/kg; p.o.) shows that the bioavailability is 97.3 %. 西域 has not independently confirmed the accuracy of these methods. They are for reference only.
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体内研究 |
Dapaconazole (20 mg/kg; p.o.) shows that the bioavailability is 97.3 %. 西域 has not independently confirmed the accuracy of these methods. They are for reference only.
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性状 | Solid | ||||||||||||||||
溶解性数据 |
In Vitro:
DMSO : 100 mg/mL (240.82 mM; Need ultrasonic) 配制储备液
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请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 In Vivo:
请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照 In Vitro 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,建议您现用现配,当天使用;
以下溶剂前显示的百
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运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
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参考文献 |

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