CAS NO: | 68047-06-3 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
5mg | 电议 |
10mg | 电议 |
25mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
生物活性 | 4-Hydroxytamoxifen ((Z)-4-Hydroxytamoxifen) is an orally active, selectiveestrogen receptor modulator(SERM). 4-Hydroxytamoxifen ((Z)-4-Hydroxytamoxifen) inducesCRISPR/Cas9systems based on ER mediated nucleus translocation[1][2][3][4]. | ||||||||||||||||
IC50& Target[1][2] |
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体外研究 (In Vitro) | 4-Hydroxytamoxifen (Monohydroxytamoxifen) is a selective ostrogen receptor antagonist, with an IC50of 3.3 nM for the [3H]oestradiol binding to oestrogen receptor. 4-Hydroxytamoxifen (10, 100 nM) enables to inhibit the binding of [3H]oestradiol to the human 8 S oestrogen receptor[1]. 4-Hydroxytamoxifen activates intein-linked inactive Cas9, reduces off-target CRISPR-mediated gene editing. In human cells, conditionally active Cas9s modify target genomic sites with up to 25-fold higher specificity than wild-type Cas9[2]. | ||||||||||||||||
体内研究 (In Vivo) | 4-Hydroxytamoxifen (0.2, 1 and 5 μg/day, p.o.) causes a dose-related decrease in uterine wet weight of immature rats[1]. 4-Hydroxytamoxifen (6 μg/0.1 mL sesame oil/day, s.c.) effectively attenuates methamphetamine-induced nigrostriatal dopamine depletions in bothsexes of intact and gonadectomized C57BL/6 J mice. 4-Hydroxytamoxifen does not alter the dopamine content levels in the striatum[3]. | ||||||||||||||||
Clinical Trial | |||||||||||||||||
分子量 | 387.51 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C26H29NO2 | ||||||||||||||||
CAS 号 | 68047-06-3 | ||||||||||||||||
中文名称 | 4-羟基他莫昔芬 | ||||||||||||||||
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 : 50 mg/mL(129.03 mM;ultrasonic and warming and heat to 60℃) Ethanol : 20 mg/mL(51.61 mM;Need ultrasonic) 配制储备液
* 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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