X-ray diffraction study of copper (II) complexes of pyridoxal isonicotinoyl hydrazone
Author:
Publisher
Wiley
Subject
Condensed Matter Physics,General Materials Science,General Chemistry
Reference6 articles.
1. : The Power Methods in X-ray Crystallography, New York 1958, p. 119
2. Synthesis, absorption, and toxicity of N1,N8-bis(2,3-dihydroxybenzoyl)spermidine, a potent iron chelator
3. Cytotoxic chelators and chelates 1. Inhibition of DNA synthesis in cultured rodent and human cells by aroylhydrazones and by a copper(II) complex of salicylaldehyde benzoyl hydrazone
4. A study of intracellular iron metabolism using pyridoxal isonicotinoyl hydrazone and other synthetic chelating agents
5. , unpublished work
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1. Prediction of protonation constants of hydrazones and Schiff bases derived from pyridoxal 5′-phosphate, pyridoxal, 3-hydroxyisonicotinaldehyde and salicylic aldehyde;Journal of Molecular Liquids;2023-11
2. Stability of Cu(II) and Zn(II) Complexes with Pyridinecarbohydrazones of Pyridoxal-5-phosphate in Aqueous Solution;Russian Journal of General Chemistry;2018-07
3. Influence of regioisomerism on stability, formation kinetics and ascorbate oxidation preventive properties of Schiff bases derived from pyridinecarboxylic acids hydrazides and pyridoxal 5′-phosphate;Journal of Molecular Liquids;2017-09
4. Pyridoxal hydrazonato molybdenum(vi) complexes: assembly, structure and epoxidation (pre)catalyst testing under solvent-free conditions;RSC Advances;2014-08-14
5. The iron chelator pyridoxal isonicotinoyl hydrazone (PIH) and its analogues prevent damage to 2-deoxyribose mediated by ferric iron plus ascorbate;Biochimica et Biophysica Acta (BBA) - General Subjects;2000-10
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