上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白,专注于信号通路和疾病研究领域。
JNJ-64619178 纯度: 99.79%
JNJ-64619178 是一种伪不可逆的、口服活性的、选择性蛋白精氨酸甲基转移酶 5 (PRMT5) 抑制剂,IC50 为 0.14 nM。JNJ-64619178 有潜力用于肺癌的研究。
JNJ-64619178 Chemical Structure
CAS No. : 2086772-26-9
规格 | 价格 | 是否有货 | 数量 |
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10 mM * 1 mL in DMSO | ¥3084 | In-stock | |
1 mg | ¥1000 | In-stock | |
5 mg | ¥2900 | In-stock | |
10 mg | ¥4900 | In-stock | |
50 mg | ¥12000 | In-stock | |
100 mg | 询价 | ||
200 mg | 询价 |
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JNJ-64619178 相关产品
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生物活性 |
JNJ-64619178 is a selective, orally active and pseudo-irreversible protein arginine methyltransferase 5 (PRMT5) inhibitor with an IC50 of 0.14 nM. JNJ-64619178 has potent activity In lung cancer[1][2]. |
IC50 & Target |
IC50: 0.14 nM (PRMT5)[2] |
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体外研究 (In Vitro) |
JNJ-64619178 binds simultaneously to the S-adenosylmethionine (SAM)- and protein substrate- binding pockets of the PRMT5/MEP50 complex with a pseudo-irreversible mode-of-action. JNJ-64619178 shows potent and broad inhibition of cellular growth[1]. 上海金畔生物科技有限公司 has not independently confirmed the accuracy of these methods. They are for reference only. |
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体内研究 (In Vivo) |
Oral administration of JNJ-64619178 results in efficient inhibition of dimethylation of SMD1/3 proteins, components of the splicing machinery and direct substrates of the methylosome, in several non-small cell lung cancer and small cell lung cancer cancer mouse xenograft models[1]. 上海金畔生物科技有限公司 has not independently confirmed the accuracy of these methods. They are for reference only. |
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Clinical Trial |
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分子量 |
483.36 |
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Formula |
C22H23BrN6O2 |
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CAS 号 |
2086772-26-9 |
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运输条件 |
Room temperature in continental US; may vary elsewhere. |
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储存方式 |
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溶解性数据 |
In Vitro:
DMSO : 125 mg/mL (258.61 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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参考文献 |
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