Aldometanib

CAS No. 2904601-67-6

Aldometanib( —— )

Catalog No. M35330 CAS No. 2904601-67-6

Aldometanib (LXY-05-029) is an orally active aldolase inhibitor that prevents FBP from binding to v-ATPase-associated aldolase and activates lysosomal AMPK, useful in metabolic homeostasis research .

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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2MG 58 Get Quote
5MG 79 Get Quote
10MG 125 Get Quote
25MG 265 Get Quote
50MG 393 Get Quote
100MG 569 Get Quote
200MG 794 Get Quote
500MG 1215 Get Quote
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Biological Information

  • Product Name
    Aldometanib
  • Note
    Research use only, not for human use.
  • Brief Description
    Aldometanib (LXY-05-029) is an orally active aldolase inhibitor that prevents FBP from binding to v-ATPase-associated aldolase and activates lysosomal AMPK, useful in metabolic homeostasis research .
  • Description
    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.
  • In Vitro
    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.
  • In Vivo
    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.
  • Synonyms
    ——
  • Pathway
    Membrane Transporter/Ion Channel
  • Target
    AMPK
  • Recptor
    AMPK
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    2904601-67-6
  • Formula Weight
    593.46
  • Molecular Formula
    C27H43Cl2IN2
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 100 mg/mL (168.51 mM; Ultrasonic (<60°C)
  • SMILES
    CC1=[N+](C=CN1CCCCCCCCCCCCCCCC)CC2=C(Cl)C=CC=C2Cl.[I-]
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1. Chen-Song Zhang, et al. The aldolase inhibitor aldometanib mimics glucose starvation to activate lysosomal AMPK. Nat Metab. 2022 Oct 10.?
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