CAS NO: | 15574-96-6 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
100mg | 电议 |
200mg | 电议 |
500mg | 电议 |
1 g | 电议 |
5 g | 电议 |
生物活性 | Pizotifen (Pizotyline) is a potent5-HT2receptor antagonist, with a high affinity for5-HT1Cbinding site. | ||||||||||||||||
IC50& Target |
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体外研究 (In Vitro) | Pizotifen (BC-105) is a potent 5-HT2receptor antagonist, with a high affinity for 5-HT1Cbinding site[1]. Pizotifen is an antidepresent 5-HT2Areceptor antagonist and has the capacity to inhibit serotonin-enhanced ADP-induced platelet aggregation[2]. | ||||||||||||||||
体内研究 (In Vivo) | The weights of the fetuses are significantly reduced by all administered doses of Pipethiadene and Pizotifen (BC-105); the weights of the placentas are significantly reduced after 0.6 and 1.2 mg/kg Pipethiadene and only after the middle dose of Pizotifen. The means of the implantations, live, dead fetuses, resorptions and the occurrence of external, skeletal and visceral anomalies do not differ from the control group. The number of chromosome aberrations in the bone marrow cells of treated mice does not differ significantly from the negative control group. The micronucleus test reveals no elevation in the frequency of micronuclei as compared to the control group. After the two higher doses of both Pipethiadene and Pizotifen (BC-105) maleate, the mitotic indices are lower than in the control group[3]. | ||||||||||||||||
分子量 | 295.44 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C19H21NS | ||||||||||||||||
CAS 号 | 15574-96-6 | ||||||||||||||||
中文名称 | 苯噻啶 | ||||||||||||||||
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 : 20 mg/mL(67.70 mM;Need ultrasonic) H2O :< 0.1 mg/mL(insoluble) 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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