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CEP-11981是一种具有口服活性的TIE2/泛VEGFR抑制剂,具有广泛的酪氨酸激酶抑制活性,能够抗肿瘤和抗血管生成,可用于难治性实体瘤。
CEP-11981是一种具有口服活性的TIE2/泛VEGFR抑制剂,具有广泛的酪氨酸激酶抑制活性,能够抗肿瘤和抗血管生成,可用于难治性实体瘤。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
1 mg | ¥ 6,410 | In stock | |
5 mg | ¥ 12,800 | In stock | |
10 mg | ¥ 17,200 | In stock | |
25 mg | ¥ 25,600 | In stock |
CEP-11981 相关产品
产品描述 | CEP-11981 is an orally active TIE2/pan-VEGFR inhibitor with broad tyrosine kinase inhibitory activity, exhibiting antitumour and anti-angiogenic effects, and is applicable for the treatment of refractory solid tumours. |
体内活性 | Calcium channel-modulator-1 (20 mg/kg ; p.o.) causes a 35-37% decrease in systolic blood pressure in spontaneously hypertensive rats. However, iv administration of Calcium channel-modulator-1 to anesthetized spontaneously hypertensive rats causes a decrease in blood pressure.[1] |
分子量 | 477.56 |
分子式 | C28H27N7O |
CAS No. | 856691-93-5 |
Smiles | O=C1NCC=2C1=C3C4=CN(N=C4CCC3=C5C2C6=CC(=CC=C6N5CC(C)C)NC7=NC=CC=N7)C |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
以上为“体内实验配液计算器”的使用方法举例,并不是具体某个化合物的推荐配制方式,请根据您的实验动物和给药方式选择适当的溶解方案。
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