
Aldometanib
CAS No. 2904601-67-6
Aldometanib ( —— )
产品货号. M35330 CAS No. 2904601-67-6
Aldometanib (LXY-05-029) 是一种醛缩酶抑制剂。Aldometanib 可以激活溶酶体腺苷-磷酸活化蛋白激酶 AMPK 并降低血糖。Aldometanib 可用于代谢稳态的研究。
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
2MG | ¥491 | 有现货 |
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5MG | ¥670 | 有现货 |
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10MG | ¥1066 | 有现货 |
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25MG | ¥2252 | 有现货 |
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50MG | ¥3339 | 有现货 |
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100MG | ¥4835 | 有现货 |
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200MG | ¥6747 | 有现货 |
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500MG | ¥10328 | 有现货 |
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1G | 获取报价 | 有现货 |
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生物学信息
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产品名称Aldometanib
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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
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产品简述Aldometanib (LXY-05-029) 是一种醛缩酶抑制剂。Aldometanib 可以激活溶酶体腺苷-磷酸活化蛋白激酶 AMPK 并降低血糖。Aldometanib 可用于代谢稳态的研究。
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产品描述Aldometanib (LXY-05-029) is an orally active aldolase inhibitor. Aldometanib can activate lysosomal adenosine monophosphate-activated protein kinase (AMPK) and decreases blood glucose. Aldometanib can be used for the research of metabolic homeostasis.
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体外实验Western Blot Analysis Cell Line:Mouse primary hepatocytes, MEFs cells Concentration:0-1000 nM Incubation Time:2 h Result:Activated AMPK in mouse embryonic fibroblasts (MEFs) and mouse primary hepatocytes cells.Immunofluorescence Cell Line:MEFs cells Concentration:5 nM Incubation Time:2 h Result:Inhibited TRPVs and induces AXIN lysosomal translocation.
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体内实验Animal Model:Lean mice Dosage:0-10 mpk Administration:Oral Result:Decreased fasting blood glucose and improved glucose tolerance, promoted muscular TBC1D1 phosphorylation and glucose uptake.Animal Model:Obese hyperglycaemic mice Dosage:2-10 mpk Administration:Oral, twice daily, for a week Result:Decreased blood glucose, lowered blood glucose in a muscular AMPK-dependent manner reduced hepatic TAG, improved insulin sensitivity, increased glucose disposal rates, inhibited TAG synthesis in liver and primary hepatocytes, decreased fat mass.Animal Model:NASH mice Dosage:2 mpk Administration:Oral, twice-daily, for a month Result:Decreased histological scores used to describe the features of NASH, reduced apoptosis rate of hepatic cells, inhibited inflammatory responses in the liver of NASH mice and improved glucose tolerance of NASH mice.Animal Model:C. elegans Dosage:0-50 μM Administration:Oral, 0-50 days Result:Promoted oxidative stress resistance and mitochondrial functions in C. elegans.Animal Model:C57BL/6 mice Dosage:100 μg/mL Administration:Oral Result:Extended lifespan, elevated NAD+ levels and mitochondrial oxidative respiration, rejuvenated muscle function in aged mice.
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同义词——
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通路Membrane Transporter/Ion Channel
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靶点AMPK
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受体AMPK
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研究领域——
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适应症——
化学信息
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CAS Number2904601-67-6
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分子量593.46
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分子式C27H43Cl2IN2
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO 中的溶解度 : 100 mg/mL (168.51 mM; 超声助溶 (<60°C)
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SMILESCC1=[N+](C=CN1CCCCCCCCCCCCCCCC)CC2=C(Cl)C=CC=C2Cl.[I-]
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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1. Chen-Song Zhang, et al. The aldolase inhibitor aldometanib mimics glucose starvation to activate lysosomal AMPK. Nat Metab. 2022 Oct 10.?