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- 文献和实验
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- 保存条件:
Powder: -20°C, 3 years; 4°C, 2 years. In solvent: -80°C, 6 months; -20°C, 1 month.
- 库存:
货期:1-2天
- 供应商:
MedChemExpress LLC
- CAS号:
193620-69-8
- 规格:
10 mM * 1 mL/1 mg/5 mg/10 mg/25 mg/50 mg/100 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥550.0 |
|---|---|---|---|
| 规格: | 1 mg | 产品价格: | ¥190.0 |
| 规格: | 5 mg | 产品价格: | ¥500.0 |
| 规格: | 10 mg | 产品价格: | ¥800.0 |
| 规格: | 25 mg | 产品价格: | ¥1400.0 |
| 规格: | 50 mg | 产品价格: | ¥2400.0 |
| 规格: | 100 mg | 产品价格: | ¥3400.0 |
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TAS-301
CAS No. : 193620-69-8
MCE 国际站:TAS-301
产品活性:TAS-301 是一种平滑肌迁移和增殖抑制剂,能够抑制 PDGF 诱导的 PKC 的活化。
研究领域:Epigenetics | TGF-beta/Smad
作用靶点:PKC
In Vitro: TAS-301 (1-10 μM) concentration-dependently inhibits PKC activation and Ca2+ influx, induced by PDGF, with 62.7% inhibition on PKC activation at 10 μM, and reduces PMA-induced AP-1, with 38% and 67.6% inhibition at 3 and 10 μM, respectively. TAS-301 (0.3-3 μM) dose-dependently reduces the migration of cells induced by growth factors (PDGF-BB, IGF-1,HB-EGF). TAS-301 (1-10 μM) also decreases bFGF-induced BrdU incorporation, especially at 3 and 10 μM.
In Vivo: TAS-301 (3-100 mg/kg, p.o.) dose-dependently reduces the neointimal thickening and I/M ratio and decreases the level of intimal cells in rats 14 days after balloon injury.
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="GeneID:16183" /db_xref="LocusID:16183" /db_xref="MGI:96548" CDS 48..557 /gene="Il2" /note="go_component: extracellular [goid 0005576] [evidence IEA]; go_component: extracellular space [goid 0005615] [evidence TAS] [pmid 12466851]; go_function
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