Powder: -20°C for 3 years | In solvent: -80°C for 1 year
SAR407899 is Rho kinase inhibitor potently inhibits endothelin-1-induced constriction of renal resistance arteries.
パッケージサイズ | 在庫状況 | 単価(税別) | |||
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2 mg | 在庫あり | ¥ 7,500 | |||
5 mg | 在庫あり | ¥ 12,000 | |||
10 mg | 在庫あり | ¥ 19,500 | |||
25 mg | 在庫あり | ¥ 35,500 | |||
50 mg | 在庫あり | ¥ 57,000 | |||
100 mg | 在庫あり | ¥ 90,500 | |||
1 mL * 10 mM (in DMSO) | 在庫あり | ¥ 13,000 |
説明 | SAR407899 is Rho kinase inhibitor potently inhibits endothelin-1-induced constriction of renal resistance arteries. |
ターゲット&IC50 | ROCK2:102 nM (IC50), ROCK1:276 nM (IC50) |
In vivo | In vivo, SAR407899 dose-dependently induced rabbit penile erection, with greater potency and longer duration of action than sildenafil[1]. |
動物実験 | Compared the effects of SAR407899, the Rho-kinase inhibitor Y-27632 and the PDE5 inhibitor sildenafil for their ability to relax corpus cavernosum strips contracted with phenylephrine in healthy and diabetic animals. Strips were obtained from WKY, spontaneous hypertensive (SHR), control CD, and diabetic CD rats, humans, control and diabetic rabbits. Diabetes was induced by streptozotocin or alloxan injection. In vivo penile erection (length) induced by drugs was measured in conscious rabbits[1]. |
分子量 | 244.29 |
分子式 | C14H16N2O2 |
CAS No. | 923359-38-0 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
DMSO: 6 mg/mL (24.56 mM)
You can also refer to dose conversion for different animals. 詳細
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SAR407899 923359-38-0 Cell Cycle/Checkpoint Cytoskeletal Signaling Stem Cells ROCK Rho Rho-associated kinase ROK SAR-407899 Rho-kinase Rho-associated protein kinase SAR 407899 inhibit Inhibitor inhibitor