pyridoxal has been researched along with 2-naphthol in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (50.00) | 18.7374 |
| 1990's | 2 (50.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Baker, E; Gross, S; Ponka, P; Richardson, D | 1 |
| Miles, EW | 1 |
| Fales, HM; Gin, JB; Miles, EW | 1 |
| Milnes, K; Richardson, DR | 1 |
4 other study(ies) available for pyridoxal and 2-naphthol
| Article | Year |
|---|---|
Evaluation of the iron chelation potential of hydrazones of pyridoxal, salicylaldehyde and 2-hydroxy-1-naphthylaldehyde using the hepatocyte in culture.
Topics: Animals; Benzaldehydes; Cells, Cultured; Dialysis; Hydrazones; Intracellular Membranes; Iron; Iron Chelating Agents; Liver; Naphthols; Pyridoxal; Tissue Distribution | 1992 |
Reaction of 5 -pyridoxal methyl chloride, an analog of pyridoxal 5'-phosphate, with the B protein of Escherichia coli tryptophan synthetase.
Topics: Amino Acids; Apoproteins; Bacterial Proteins; Binding Sites; Chlorine; Circular Dichroism; Electrophoresis, Paper; Escherichia coli; Hydro-Lyases; Imines; Macromolecular Substances; Naphthols; Optical Rotation; Picolines; Pyridoxal; Pyridoxal Phosphate; Pyridoxine; Serine; Spectrometry, Fluorescence; Spectrophotometry; Tryptophan Synthase | 1972 |
5-(2-Chloroethyl)-3-hydroxy-2-methyl-4-pyridinecarboxaldehyde ( 5 -pyridoxal methyl chloride) and its reaction with N -acetyl-L-lysine to form a new cyclic imino acid derivative of homopyridoxal.
Topics: Acetates; Alkylation; Amino Acids; Chlorine; Cyclization; Hydrogen-Ion Concentration; Imines; Indicators and Reagents; Isomerism; Lysine; Magnetic Resonance Spectroscopy; Mass Spectrometry; Molecular Conformation; Naphthols; Picolines; Pyridoxal; Pyridoxal Phosphate; Pyridoxine; Spectrometry, Fluorescence; Spectrophotometry; Spectrophotometry, Ultraviolet | 1972 |
The potential of iron chelators of the pyridoxal isonicotinoyl hydrazone class as effective antiproliferative agents II: the mechanism of action of ligands derived from salicylaldehyde benzoyl hydrazone and 2-hydroxy-1-naphthylaldehyde benzoyl hydrazone.
Topics: Antineoplastic Agents; Apoptosis; Benzaldehydes; Cell Cycle; Cell Division; Deferoxamine; DNA Fragmentation; Drug Design; Drug Resistance, Neoplasm; Drug Screening Assays, Antitumor; Ferritins; Growth Inhibitors; HL-60 Cells; Humans; Hydrazones; Iron; Iron Chelating Agents; Isoniazid; Ligands; Molecular Structure; Naphthols; Neoplasm Proteins; Neoplasms; Pyridoxal; Structure-Activity Relationship; Transferrin; Tumor Cells, Cultured | 1997 |