产品说明书

TAS-301

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Chemical Structure| 193620-69-8 同义名 : -
CAS号 : 193620-69-8
货号 : A200976
分子式 : C23H19NO3
纯度 : 99%+
分子量 : 357.4
MDL号 : MFCD05865245
存储条件:

粉末 Sealed in dry,Room Temperature

液体 -20°C:3-6个月-80°C:12个月

溶解度 :

DMSO: 40 mg/mL(111.92 mM),注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

动物实验配方:
生物活性
描述 TAS-301 inhibits PKC activation and Ca2+ influx in a concentration-dependent manner, induced by PDGF, achieving 62.7% inhibition at 10 μM. It also reduces PMA-induced AP-1 activity, with 38% and 67.6% inhibition at concentrations of 3 and 10 μM, respectively[1]. Dose-dependently, TAS-301 (0.3-3 μM) curtails cell migration induced by various growth factors (PDGF-BB, IGF-1, HB-EGF) and diminishes bFGF-induced BrdU incorporation, particularly at 3 and 10 μM[2].
实验方案
1mg 5mg 10mg

1 mM

5 mM

10 mM

2.80mL

0.56mL

0.28mL

13.99mL

2.80mL

1.40mL

27.98mL

5.60mL

2.80mL

参考文献

[1]Muranaka Y, et al. TAS-301, an inhibitor of smooth muscle cell migration and proliferation, inhibits intimal thickening after balloon injury to rat carotid arteries. J Pharmacol Exp Ther. 1998 Jun;285(3):1280-6.

[2]Sasaki E, et al. TAS-301 blocks receptor-operated calcium influx and inhibits rat vascular smooth muscle cell proliferation induced by basic fibroblast growth factor and platelet-derived growth factor. Jpn J Pharmacol. 2000 Nov;84(3):252-8.