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  • Tauroursodeoxycholate dihydrate
Tauroursodeoxycholate dihydrate的可视化放大

Tauroursodeoxycholate dihydrate

Tauroursodeoxycholatedihydrate(TUDCAdihydrate;UR906dihydrate;Taurolitedihydrate)是一种内质网应激抑制剂。Tauroursodeoxycholate显著降低凋亡分子如caspase-3和caspase-12表达。Tauroursodeoxycholate也抑制ERK。

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Tauroursodeoxycholate dihydrate的二维码
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  • 货号: ajce53904
  • CAS: 117609-50-4
  • 别名: 牛磺熊去氧胆酸二水合物; Tauroursodeoxycholic acid dihydrate; TUDCA dihydrate; UR 906 dihydrate
  • 分子式: C26H49NO8S
  • 分子量: 535.73
  • 纯度: >98%
  • 溶解度: DMSO : 83.33 mg/mL (155.54 mM) ,Water:12.5mg/mL(25.02 mM)
  • 储存: Store at -20°C
  • 库存: 现货

Background

Tauroursodeoxycholate dihydrate (TUDCA dihydrate; UR 906 dihydrate; Taurolite dihydrate) is an endoplasmic reticulum (ER) stress inhibitor. Tauroursodeoxycholate significantly reduces expression of apoptosis molecules, such as caspase-3 and caspase-12. Tauroursodeoxycholate also inhibits ERK[1][2]. ERK[1]Caspase-3, Caspase-12[2]



[1]. Kim SY, et al. Tauroursodeoxycholate (TUDCA) inhibits neointimal hyperplasia by suppression of ERK viaPKCα-mediated MKP-1 induction. Cardiovasc Res. 2011 Nov 1;92(2):307-16. [2]. Qin Y, et al. Tauroursodeoxycholic Acid Attenuates Angiotensin II Induced Abdominal Aortic Aneurysm Formation in Apolipoprotein E-deficient Mice by Inhibiting Endoplasmic Reticulum Stress. Eur J Vasc Endovasc Surg. 2017 Mar;53(3):337-345.

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