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Lonidamine

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Catalog No. T0239Cas No. 50264-69-2
Alias Diclondazolic Acid, DICA, AF1890

Lonidamine (Diclondazolic Acid) is an indazole carboxylic acid derivative, principally inhibiting aerobic glycolytic activity, by its effect on mitochondrially-bound hexokinase (HK).

Lonidamine

Lonidamine

🥰Excellent
Purity: 97.36%
Catalog No. T0239Alias Diclondazolic Acid, DICA, AF1890Cas No. 50264-69-2
Lonidamine (Diclondazolic Acid) is an indazole carboxylic acid derivative, principally inhibiting aerobic glycolytic activity, by its effect on mitochondrially-bound hexokinase (HK).
Pack SizePriceAvailabilityQuantity
2 mg$33In Stock
5 mg$45In Stock
10 mg$58In Stock
25 mg$75In Stock
50 mg$117In Stock
100 mg$152In Stock
500 mg$373In Stock
1 g$555In Stock
1 mL x 10 mM (in DMSO)$50In Stock
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Purity:97.36%
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Product Introduction

Bioactivity
Description
Lonidamine (Diclondazolic Acid) is an indazole carboxylic acid derivative, principally inhibiting aerobic glycolytic activity, by its effect on mitochondrially-bound hexokinase (HK).
Targets&IC50
Mitochondrial pyruvate carrier:2.5 μM (Ki)
In vitro
In mice carrying glioma tumors, Lonidamine (160 mg/kg) effectively reduced tumor growth.
In vivo
In both normal and tumor cells, Lonidamine reduces oxygen consumption while augmenting aerobic glycolysis in normal cells, thereby inhibiting aerobic glycolysis in tumor cells. The compound induces apoptosis at a concentration of 50 mg/ml in resistant cell lines, including the human breast cancer cell line MCF-7 ADR(r) and the LB9 multiform glioblastoma cell line, which exhibit resistance to doxorubicin and nitrosourea.
AliasDiclondazolic Acid, DICA, AF1890
Chemical Properties
Molecular Weight321.16
FormulaC15H10Cl2N2O2
Cas No.50264-69-2
SmilesOC(=O)c1nn(Cc2ccc(Cl)cc2Cl)c2ccccc12
Relative Density.1.47 g/cm3
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 60 mg/mL (186.82 mM), Sonication is recommended.
Ethanol: 1.6 mg/mL (5 mM)
Solution Preparation Table
Ethanol/DMSO
1mg5mg10mg50mg
1 mM3.1137 mL15.5686 mL31.1371 mL155.6856 mL
5 mM0.6227 mL3.1137 mL6.2274 mL31.1371 mL
DMSO
1mg5mg10mg50mg
10 mM0.3114 mL1.5569 mL3.1137 mL15.5686 mL
20 mM0.1557 mL0.7784 mL1.5569 mL7.7843 mL
50 mM0.0623 mL0.3114 mL0.6227 mL3.1137 mL
100 mM0.0311 mL0.1557 mL0.3114 mL1.5569 mL

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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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