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AGI-1067

CAS No. 216167-82-7

AGI-1067 ( Succinobucol;AGI 1067;AGI1067 )

产品货号. M13448 CAS No. 216167-82-7

AGI-1067 (Succinobucol) is a potent inhibitor of TNF-α-inducible expression of VCAM-1, MCP-1 and E-selectin (IC50=6,10 and 25 uM).

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
5MG ¥381 有现货
10MG ¥648 有现货
25MG ¥1320 有现货
50MG ¥2252 有现货
100MG ¥3856 有现货
500MG ¥8505 有现货
1G 获取报价 有现货

生物学信息

  • 产品名称
    AGI-1067
  • 注意事项
    本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
  • 产品简述
    AGI-1067 (Succinobucol) is a potent inhibitor of TNF-α-inducible expression of VCAM-1, MCP-1 and E-selectin (IC50=6,10 and 25 uM).
  • 产品描述
    AGI-1067 (Succinobucol) is a potent inhibitor of TNF-α-inducible expression of VCAM-1, MCP-1 and E-selectin (IC50=6,10 and 25 uM) with concurrent antioxidant and lipid-modulating properties; inhibits atherosclerosis in LDL receptor-deficient and apolipoprotein E-deficient mice, also reduces VCAM-1 and MCP-1 mRNA levels in lungs of LPS-stimulated mice; inhibits atherosclerosis not only via its lipid-lowering effects but also by having direct anti-inflammatory effects on the vessel wall.Diabetes Phase 3 Clinical
  • 同义词
    Succinobucol;AGI 1067;AGI1067
  • 通路
    Others
  • 靶点
    Other Targets
  • 受体
    Others
  • 研究领域
    Metabolic Disease
  • 适应症
    Diabetes

化学信息

  • CAS Number
    216167-82-7
  • 分子量
    616.92
  • 分子式
    C35H52O5S2
  • 纯度
    >98% (HPLC)
  • 溶解度
    DMSO: Soluble ( < 1 mg/ml refers to the product slightly soluble or insoluble )
  • SMILES
    O=C(O)CCC(OC1=C(C(C)(C)C)C=C(SC(C)(SC2=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C2)C)C=C1C(C)(C)C)=O
  • 化学全称
    4-(4-((1-((3,5-bis(1,1-Dimethylethyl)-4-hydroxyphenyl)sulfanyl)-1-methylethyl)sulfanyl)-2,6-bis(1,1-dimethylethyl)phenoxy)-4-oxobutanoic acid

运输与储存

  • 储存条件
    (-20℃)
  • 运输条件
    With Ice Pack
  • 稳定性
    ≥ 2 years

参考文献

1. Sundell CL, et al. J Pharmacol Exp Ther. 2003 Jun;305(3):1116-23.
2. Meng CQ, et al. Bioorg Med Chem Lett. 2002 Sep 16;12(18):2545-8.
3. Tardif JC, et al. Circulation. 2003 Feb 4;107(4):552-8.
4. Kunsch C, et al. J Pharmacol Exp Ther. 2004 Mar;308(3):820-9.
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