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| | pyridoxal isonicotinoyl hydrazone Basic information |
| Product Name: | pyridoxal isonicotinoyl hydrazone | | Synonyms: | Pyridoxal isonicotinoyl hydrazone (PIH);NSC 77674;PIH(Pyridoxal isonicotinoyl hydrazine);PIH - CAS 737-86-0 - Calbiochem;Pyridoxal isonicotinoyl hydrazine;4-Pyridinecarboxylic acid, 2-[[3-hydroxy-5-(hydroxymethyl)-2-methyl-4-pyridinyl]methylene]hydrazide;N'-((3-Hydroxy-5-(hydroxymethyl)-2-methylpyridin-4-yl)methylene)isonicotinohydrazide;inhibit,pyridoxal isonicotinoyl hydrazone,Inhibitor | | CAS: | 737-86-0 | | MF: | C14H14N4O3 | | MW: | 286.29 | | EINECS: | | | Product Categories: | | | Mol File: | 737-86-0.mol |  |
| | pyridoxal isonicotinoyl hydrazone Chemical Properties |
| Melting point | 261-262 °C (decomp) | | density | 1.35±0.1 g/cm3(Predicted) | | storage temp. | +2C to +8C | | solubility | DMF: 1 mg/ml; DMSO: 5 mg/ml; Ethanol: 0.5 mg/ml | | form | Yellow solid | | pka | 8.04±0.10(Predicted) |
| | pyridoxal isonicotinoyl hydrazone Usage And Synthesis |
| Uses | Pyridoxal Isonicotinoyl Hydrazone is a cell-permeable non-toxic iron chelator of the aroyl hydrazone class. | | General Description | A cell-permeable, non-toxic tridendate iron (Fe3+) chelator of the aroyl hydrazone class. Even at low concentrations, highly effective in mobilizing Fe3+ from cells and preventing its uptake from transferrin, even at low concentrations. Exhibits similar specificity and binding affinity as Deferoxamine Mesylate (Cat. No. 252750) but has greater access to mitochondrial iron. Also useful for the management of iron overload disease in experimental models. Inhibits the induction of heme containing indoleamine 2,3-dioxygenase activity. |
| | pyridoxal isonicotinoyl hydrazone Preparation Products And Raw materials |
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