生物活性 | ||||||||||
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体外研究 (In Vitro) |
KAAD-Cyclopamine inhibits pathway activation induced by 1 μM purmorphamine with an IC50 of 3 nM, wheras this cyclopamine derivative has an IC50 of 100 nM in Shh-LIGHT2 cells stimulated with 10 μM purmorphamine[1]. MCE has not independently confirmed the accuracy of these methods. They are for reference only. |
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分子量 |
697.99 |
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性状 |
固体 |
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Formula |
C44H63N3O4 |
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CAS 号 | ||||||||||
运输条件 |
Room temperature in continental US; may vary elsewhere. |
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储存方式 |
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纯度 & 产品资料 |
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参考文献 |
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