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。
Belzutifan (Synonyms: PT2977; MK-6482) 纯度: 99.05%
Belzutifan (PT2977) 是一种口服有效的,选择性 HIF-2α 抑制剂,IC50 为 9 nM。Belzutifan 作为第二代 HIF-2α 抑制剂,可提高效力并改善药代动力学特征。Belzutifan 有抑制透明细胞肾细胞癌 (ccRCC) 作用。
Belzutifan Chemical Structure
CAS No. : 1672668-24-4
规格 | 价格 | 是否有货 | 数量 |
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10 mM * 1 mL in DMSO | ¥6820 | In-stock | |
5 mg | ¥6200 | In-stock | |
10 mg | ¥9800 | In-stock | |
50 mg | 询价 | ||
100 mg | 询价 |
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Belzutifan 相关产品
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生物活性 |
Belzutifan (PT2977) is an orally active and selective HIF-2α inhibitor with an IC50 of 9 nM. Belzutifan, as a second-generation HIF-2α inhibitor, increases potency and improves pharmacokinetic profile. Belzutifan is a potential treatment for clear cell renal cell carcinoma (ccRCC)[1]. |
IC50 & Target |
IC50: 9 nM (HIF-2α)[1] |
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体外研究 (In Vitro) |
Belzutifan (PT2977) potently and dose-dependently reduces mRNA levels of human cyclin D1, a target gene regulated by HIF-2α, and leads to rapid and dose-dependent reduction in EPO expression[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 |
383.34 |
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Formula |
C17H12F3NO4S |
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CAS 号 |
1672668-24-4 |
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运输条件 |
Room temperature in continental US; may vary elsewhere. |
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储存方式 |
-20°C, stored under nitrogen *In solvent : -80°C, 6 months; -20°C, 1 month (stored under nitrogen) |
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溶解性数据 |
In Vitro:
DMSO : 50 mg/mL (130.43 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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