FX-11

CAS No. 213971-34-7

FX-11( —— )

Catalog No. M33364 CAS No. 213971-34-7

FX-11 (LDHA Inhibitor FX11) is A potent, selective and competitive specific inhibitor of lactate dehydrogenase A (LDHA) with a Ki of 8 μM. FX-11 can activate PKM2 (pyruvate kinase M2).

Purity : >98% (HPLC)

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Biological Information

  • Product Name
    FX-11
  • Note
    Research use only, not for human use.
  • Brief Description
    FX-11 (LDHA Inhibitor FX11) is A potent, selective and competitive specific inhibitor of lactate dehydrogenase A (LDHA) with a Ki of 8 μM. FX-11 can activate PKM2 (pyruvate kinase M2).
  • Description
    FX-11 is a potent, selective, reversible and competitive lactate dehydrogenase A (LDHA) inhibitor, with a Ki of 8 μM. FX-11 reduces ATP levels and induces oxidative stress, ROS production and cell death. FX-11 shows antitumor activity in lymphoma and pancreatic cancer xenografts.
  • In Vitro
    Western Blot Analysis Cell Line:P493 cellsConcentration:9 μM Incubation Time:24 h, 48 h Result:Showed a decrease in ATP levels, accompanied by activation of AMP kinase and phosphorylation of its substrate acetyl-CoA carboxylase.Cell Proliferation Assay Cell Line:BxPc-3 and MIA PaCa-2 cells Concentration:0-100 μM Incubation Time:72 h Result:Reduced cell metabolic activity in a concentration-dependent manner, showed a significant reduction in cell proliferation, with IC50 values of 49.27 μM and 60.54 μM for BxPc-3 and MIA PaCa-2 cells, respectively.
  • In Vivo
    Animal Model:Male SCID mice and RH-Foxn1nu mice (human P493 B-cell xenografts)Dosage:42 μg/mouse (2.1 mg/kg) Administration:IP; daily for 10-14 daysResult:Resulted in a remarkable inhibition of tumor growth, inhibited tumor xenograft progression.Animal Model:Immunocompromised CD-1 mice (6-8 weeks; 20-25 g, n=5 per group )Dosage:2 mg/kg, 1 mg/kg+15 mg/kg TEPP-46, 2 mg/kg+30 mg/kg TEPP-46 Administration:IP (100 μL), daily, for 3 weeks Result:Significantly lowered LDHA activity in plasma and tumor lysates; significantly lowered the expression of the proliferation marker Ki-67; significantly decreased proliferation indices were observed in tumor sections; significantly delayed tumor growth.
  • Synonyms
    ——
  • Pathway
    Metabolic Enzyme/Protease
  • Target
    Dehydrogenase
  • Recptor
    Dehydrogenase
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    213971-34-7
  • Formula Weight
    350.41
  • Molecular Formula
    C22H22O4
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 250 mg/mL (713.45 mM; Ultrasonic )
  • SMILES
    CCCc1c(O)c(O)c(C(O)=O)c2cc(Cc3ccccc3)c(C)cc12
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1. EC Calvaresi. Small molecule inhibitors of lactate dehydrogenase a as an anticancer strategy. 2014.
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