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193620-69-8

中文名称 3-(双(4-甲氧基苯基)亚甲基)吲哚啉-2-酮
英文名称 TAS-301
CAS 193620-69-8
分子式 C23H19NO3
分子量 357.4
MOL 文件 193620-69-8.mol
更新日期 2024/07/21 13:45:54
193620-69-8 结构式 193620-69-8 结构式

基本信息

中文别名
TAS-301游离态
3-[二(4-甲氧基苯基)亚甲基]-1,3-二氢-2H-吲哚-2-酮
英文别名
CS-1543
TAS 301.TAS301
TAS-301
TAS 301.TAS301
3-[bis(4-methoxyphenyl)methylidene]-1H-indol-2-one
3-[Bis(4-methoxyphenyl)methylene]-1,3-dihydro-2H-indol-2-one
2H-Indol-2-one,3-[bis(4-methoxyphenyl)methylene]-1,3-dihydro-

物理化学性质

储存条件Sealed in dry,Room Temperature
溶解度DMSO: 40 mg/mL
形态solid
颜色Light yellow to yellow

安全数据

安全说明22-24/25
WGK Germany3
3-(双(4-甲氧基苯基)亚甲基)吲哚啉-2-酮价格(试剂级)
报价日期产品编号产品名称CAS号包装价格
2024/01/16S64243-(双(4-甲氧基苯基)亚甲基)吲哚啉-2-酮
TAS-301
193620-69-85mg877.31元
2023/03/20S64243-(双(4-甲氧基苯基)亚甲基)吲哚啉-2-酮
TAS-301
193620-69-825mg2596.51元

常见问题列表

生物活性
TAS-301是平滑肌细胞迁移和增殖的抑制剂,在大鼠颈动脉球囊损伤后抑制内膜增厚。TAS-301 可抑制PDGF诱导的 PKC 激活。
靶点
TargetValue
PKC
()
体外研究

TAS-301 (1-10 μM) concentration-dependently inhibits PKC activation and Ca 2+ 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.

体内研究

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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