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)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 102 In Stock
5MG 93 In Stock
10MG 135 In Stock
25MG 224 In Stock
50MG 324 In Stock
100MG 484 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

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.
molnova catalog
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