ALK2-IN-2
Based on 1 publication(s) in Google Scholar
ALK2-IN-2 is an orally active and selective inhibitor of ALK2 (ACVR1), with an IC50 value of 9 nM, and over 700-fold selectivity against ALK3. ALK2-IN-2 can inhibit oxidative stress and protect endothelial cells.
商品は「研究用試薬」です。人や動物の医療用・臨床診断用・食品用の製品ではありません。
研究用途以外に使用した場合、当社は一切の責任を負いかねます。
- 純度: 99.93%
- CAS 番号: 2254409-25-9
- 分子式: C28H27N5O2S
- 分子量:497.61
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保管条件:Powder -20°C, 3 years , 4°C, 2 years ; In solvent -80°C, 2 years , -20°C, 1 year
MedChemExpress(MCE)の使用を引用している文献 ALK2-IN-2
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生物活性
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ACVR1 9 nM (IC50) |
ALK2-IN-2 (Compound 23) can inhibit BMP6-induced transcriptional activity in C2C12 cells, with an EC50 of 8 nM[1].
ALK2-IN-2 (3-100 nM; 6-24 h) has a protective effect on human umbilical vein endothelial cells (HUVECs) and can reduce the damage of oxidative stress to the migration and vascular formation functions of endothelial cells[2].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Cell Line:H2O2 treated HUVECs
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Concentration:3, 9, 27, 50 and 100 nM
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Incubation Time:24 h
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Result:Increased cell viability in a dose-dependent manner.
| Route | Dose (mg/kg) | AUC0→∞ (hr·ng/mL) | t1/2 (h) | Cmax (ng/mL) | CL (mL/min/kg) | Vdss (L/kg) | %F |
| i.v. | 3 | 3220 | 3.5 | / | 16 | 4.6 | / |
| p.o. | 3 | 782 | 4.3 | 67 | / | / | 24 |