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Lonidamine is a derivative of indazole-3-carboxylic acid, which for a long time, has been known to inhibit aerobic glycolysis in cancer cells. It seems to enhance aerobic glycolysis in normal cells, but suppress glycolysis in cancer cells. This is most likely through the inhibition of the mitochondrially bound hexokinase. Later studies in Ehrlich ascites…
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cells glycolysis inhibit cancer combination derivative aerobic enhance showed anticancer agents brain tumours temozolomide acid normal hexokinase gamendazole indazole-3-carboxylic long
| Subject | Predicate | Object | Confidence | Src |
|---|---|---|---|---|
| Lonidamine | 3D model (JSmol) | Interactive image | 1.00 | infobox |
| Lonidamine | ATC code | L01XX07 (WHO) | 1.00 | infobox |
| Lonidamine | CAS Number | 50264-69-2 Y | 1.00 | infobox |
| Lonidamine | ChEBI | CHEBI:50138 | 1.00 | infobox |
| Lonidamine | ChemSpider | 36170 N | 1.00 | infobox |
| Lonidamine | CompTox Dashboard (EPA) | DTXSID5020782 | 1.00 | infobox |
| Lonidamine | ECHA InfoCard | 100.051.356 | 1.00 | infobox |
| Lonidamine | Formula | C15H10Cl2N2O2 | 1.00 | infobox |
| Lonidamine | KEGG | D07257 Y | 1.00 | infobox |
| Lonidamine | Molar mass | 321.16 g·mol−1 | 1.00 | infobox |
| Lonidamine | PubChem CID | 39562 | 1.00 | infobox |
| Lonidamine | UNII | U78804BIDR | 1.00 | infobox |
| Lonidamine | is a | derivative of indazole-3-carboxylic acid | 0.90 | text |
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