CAS NO: | 483367-10-8 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
5mg | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
生物活性 | Purmorphamine is asmoothened/Smo receptoragonist with anEC50of 1 μM. | ||||||||||||||||
IC50& Target | IC50: 1.5 μM (Smoothened) | ||||||||||||||||
体外研究 (In Vitro) | Purmorphamine (10, 20 μM) in combination with sirolimus significantly decreases cell numbers according to the MTT assay. Purmorphamine induces up-regulation of alkaline phosphatase activity and expression of RUNX-2 at day 14. Up-regulation of osteocalcin is detected at the 3 and 5 μM doses of purmorphamine on day 14 post-induction. Matrix mineralization remains unchanged in the presence or absence of purmorphamine[1]. Purmorphamine induces STAT3 phosphorylation in mouse ES cell line ES14 and mesenchymal stem cell line C3H10T1/2[2]. Purmorphamine up-regulates the expressionof markers of the osteoblast phenotype-ALP activity and bone-like nodule formationd-in human bonemarrow mesenchymal cells[3]. | ||||||||||||||||
分子量 | 520.62 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C31H32N6O2 | ||||||||||||||||
CAS 号 | 483367-10-8 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
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溶解性数据 | In Vitro: DMSO : 33.33 mg/mL(64.02 mM;Need ultrasonic) 配制储备液
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