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IM156

A mitochondrial complex I inhibitor and an AMPKα activator

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IM156的二维码
  • 库存: 现货
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  • 包装
    价格
    促销价
    数量
  • 5mg
    ¥1850.00
    1480.00
    - +
  • 10mg
    ¥2825.00
    2260.00
    - +
  • 50mg
    ¥8412.00
    6730.00
    - +
  • 100mg
    ¥13350.00
    10680.00
    - +
已选 0 0
金额: ¥0.00
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  • 货号: ajcx29414
  • CAS: 1422365-94-3
  • 别名: HL156A; HL271 acetate
  • 分子式: C15H20F3N5O3
  • 分子量: 375.35
  • 纯度: >98%
  • 溶解度: DMSO: 100 mg/mL (266.42 mM)
  • 储存: 4°C, protect from light
  • 库存: 现货

Background

IM-156 is an inhibitor of mitochondrial complex I, also known as NADH dehydrogenase (IC50 = 2.2 ?M) and an activator of AMP-activated protein kinase α (AMPKα).1,2 It reduces the oxygen consumption rate (OCR; IC50 = 3.3 ?M) and decreases mitochondrial ATP production in E?-Myc mouse lymphoma cells.1 IM-156 (10, 30, and 50 ?M) increases AMPKα activity in primary rat peritoneal mesothelial cells and protects against chlorhexidine-induced peritoneal fibrosis in rats when administered at a dose of 1 mg/kg.2 It reduces tumor growth in an AT-84 murine oral cancer model and decreases age-related decline in novel object recognition, spatial working, and contextual memory in mice.3,4


1.Izreig, S., Gariepy, A., Kaymak, I., et al.Repression of LKB1 by miR-17~92 sensitizes MYC-dependent lymphoma to biguanide treatmentCell Rep. Med.1(2)100014(2020) 2.Ju, K.D., Kim, H.J., Tsogbadrakh, B., et al.HL156A, a novel AMP-activated protein kinase activator, is protective against peritoneal fibrosis in an in vivo and in vitro model of peritoneal fibrosisAm. J. Physiol. Renal. Physiol.310(5)F342-F350(2016) 3.Lam, T.G., Jeong, Y.S., Kim, S.-A., et al.New metformin derivative HL156A prevents oral cancer progression by inhibiting the insulin-like growth factor/AKT/mammalian target of rapamycin pathwaysCancer Sci.109(3)699-709(2018) 4.Bang, E., Lee, B., Park, J.-O., et al.The improving effect of HL271, a chemical derivative of metformin, a popular drug for type II diabetes mellitus, on aging-induced cognitive declineExp. Neurobiol.27(1)45-56(2018)

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