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Acrizanib (LHA510) 是一种 VEGFR-2 的抑制剂,其对 BaF3-VEGFR-2 的 IC50 值为 17.4 nM。
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Acrizanib (LHA510) 是一种 VEGFR-2 的抑制剂,其对 BaF3-VEGFR-2 的 IC50 值为 17.4 nM。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
1 mg | ¥ 928 | In stock | |
5 mg | ¥ 2,320 | In stock | |
10 mg | ¥ 3,580 | In stock | |
25 mg | ¥ 5,720 | In stock | |
50 mg | ¥ 7,730 | In stock | |
100 mg | ¥ 9,870 | In stock | |
200 mg | ¥ 13,800 | In stock | |
1 mL x 10 mM (in DMSO) | ¥ 2,270 | In stock |
Acrizanib 相关产品
产品描述 | Acrizanib (LHA510) is a VEGFR-2 inhibitor, with an IC50 of 17.4 nM for BaF3-VEGFR-2. |
靶点活性 | VEGFR2:17.4 nM |
体外活性 | Acrizanib is a VEGFR-2 inhibitor, with an IC50 of 17.4 nM for BaF3-KDR. Acrizanib exhibits ≤10% remaining kinase activity against only 13 wild type kinases: CSF1R, Kit, PDGFRα, PDGFRβ, VEGFR1, VEGFR2, VEGFR3, Fms (soluble VEGFR1), DDR1, DDR2, TIE1, and ABL1 (nonphosphorylated)[1]. |
体内活性 | Rat ocular PK studies with Acrizanib (compound 35) shows a distinctly different profile from that observed with compound 25. While prolonged exposure is once again evident in the PEC, the AUC ratio to the level of Acrizanib in plasma is markedly increased (>21000-fold higher exposure in the PEC than plasma on day 11). Furthermore, unlike 25, Acrizanib also afford much improved retina to plasma AUC exposure ratio after 10 days of dosing (598× for Acrizanib vs 0.8× for 25)[1]. |
别名 | LHA510 |
分子量 | 445.4 |
分子式 | C20H18F3N7O2 |
CAS No. | 1229453-99-9 |
Smiles | CNCc1cc(Oc2ccc3n(ccc3c2)C(=O)Nc2cc(n(C)n2)C(F)(F)F)ncn1 |
密度 | 1.47 g/cm3 (Predicted) |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | ||||||||||||||||||||||||||||||
溶解度信息 | DMSO: 37.8 mg/mL (84.9 mM), Sonication is recommended. | ||||||||||||||||||||||||||||||
溶液配制表 | |||||||||||||||||||||||||||||||
DMSO
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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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