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 |
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| 5MG | 93 | In Stock |
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| 10MG | 135 | In Stock |
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| 25MG | 224 | In Stock |
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| 50MG | 324 | In Stock |
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| 100MG | 484 | In Stock |
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| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameFX-11
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NoteResearch use only, not for human use.
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Brief DescriptionFX-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).
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DescriptionFX-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.
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In VitroWestern 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.
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In VivoAnimal 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.
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Synonyms——
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PathwayMetabolic Enzyme/Protease
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TargetDehydrogenase
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RecptorDehydrogenase
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Research Area——
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Indication——
Chemical Information
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CAS Number213971-34-7
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Formula Weight350.41
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Molecular FormulaC22H22O4
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 250 mg/mL (713.45 mM; Ultrasonic )
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SMILESCCCc1c(O)c(O)c(C(O)=O)c2cc(Cc3ccccc3)c(C)cc12
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1. EC Calvaresi. Small molecule inhibitors of lactate dehydrogenase a as an anticancer strategy. 2014.
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