Page last updated: 2024-08-18

2-naphthol and deferoxamine

2-naphthol has been researched along with deferoxamine in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	2 (100.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Cabantchik, ZI; Loyevsky, M; Ponka, P; Tsafack, A	1
Milnes, K; Richardson, DR	1

Other Studies

2 other study(ies) available for 2-naphthol and deferoxamine

Article	Year
Mode of action of iron (III) chelators as antimalarials. IV. Potentiation of desferal action by benzoyl and isonicotinoyl hydrazone derivatives. The Journal of laboratory and clinical medicine, 1996, Volume: 127, Issue:6 Topics: Animals; Antimalarials; Deferoxamine; Drug Synergism; Ferric Compounds; Humans; Hydrazones; Iron Chelating Agents; Isoniazid; Kinetics; Naphthols; Plasmodium falciparum; Spectrometry, Fluorescence	1996
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. Blood, 1997, Apr-15, Volume: 89, Issue:8 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

Article

Year

Mode of action of iron (III) chelators as antimalarials. IV. Potentiation of desferal action by benzoyl and isonicotinoyl hydrazone derivatives.

The Journal of laboratory and clinical medicine, 1996, Volume: 127, Issue:6

Topics: Animals; Antimalarials; Deferoxamine; Drug Synergism; Ferric Compounds; Humans; Hydrazones; Iron Chelating Agents; Isoniazid; Kinetics; Naphthols; Plasmodium falciparum; Spectrometry, Fluorescence

1996

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.

Blood, 1997, Apr-15, Volume: 89, Issue:8

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