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BAY-7598 is a potent, selective, and orally bioavailable MMP12 inhibitor (IC50s: 0.085, 0.67, and 1.1 nM for human/murine/rat MMP12).

BAY-7598 is a potent, selective, and orally bioavailable MMP12 inhibitor (IC50s: 0.085, 0.67, and 1.1 nM for human/murine/rat MMP12).
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 25 mg | ¥ 26,600 | 3-6月 | |
| 50 mg | ¥ 33,800 | 3-6月 | |
| 100 mg | ¥ 42,500 | 3-6月 |
| 产品描述 | BAY-7598 is a potent, selective, and orally bioavailable MMP12 inhibitor (IC50s: 0.085, 0.67, and 1.1 nM for human/murine/rat MMP12). |
| 靶点活性 | MMP12 (murine):0.67 nM , MMP12 (human):0.085 nM , MMP12 (rat):1.1 nM |
| 体外活性 | BAY-7598 inhibits human MMP2, MMP3, MMP7, MMP8, MMP9, MMP10, MMP13, MMP14, and MMP16 (IC50s: 44, 360, 600, 15, 460, 12, 67, 250, and 940 nM). BAY-7598 inhibits murine MMP2, MMP3, MMP7, MMP8, and MMP9 (IC50s: 45, 270, 130, 54, and 210 nM). BAY-7598 inhibits rat MMP2, MMP8, and MMP9 (IC50s: 45, 67, and 1000 nM). |
| 体内活性 | BAY-7598 has moderate terminal elimination half-life (t1/2=4.1 h and 4.6 h for mouse (5.0 mg/kg, p.o.), mouse (0.3 mg/kg, iv), respectively). |
| 分子量 | 505.56 |
| 分子式 | C28H31N3O6 |
| CAS No. | 1816257-74-5 |
| Smiles | C([C@H]1[C@H](C(O)=O)[C@@H](C(=O)C2=CC=C(OCCC3CCOCC3)C=C2)CC1)N4C(=O)C=5C(N=N4)=CC=CC5 |
| 密度 | 1.39 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. |
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。
对于不同动物的给药剂量换算,您也可以参考 更多