Cytotoxicity of salicylaldehyde benzoylhydrazone analogs and their transition metal complexes: quantitative structure-activity relationships. (Q33887277)

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English	Cytotoxicity of salicylaldehyde benzoylhydrazone analogs and their transition metal complexes: quantitative structure-activity relationships.	scientific article

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3 November 2019

Cytotoxicity of salicylaldehyde benzoylhydrazone analogs and their transition metal complexes: quantitative structure-activity relationships (English)

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10643654%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

transition metal

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5

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3 November 2019

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E W Ainscough

1

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3 November 2019

A M Brodie

2

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3 November 2019

W A Denny

3

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3 November 2019

G J Finlay

4

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3 November 2019

J D Ranford

6

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3 November 2019

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1 November 1999

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3 November 2019

Journal of Inorganic Biochemistry

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3 November 2019

77

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3 November 2019

3-4

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3 November 2019

125-133

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3 November 2019

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

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Complexes of salicylaldehyde acylhydrazones: cytotoxicity, QSAR and crystal structure of the sterically hindered t-butyl dimer

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Dicopper(II) Complexes of the Antitumor Analogues Acylbis(salicylaldehyde hydrazones) and Crystal Structures of Monomeric [Cu(2)(1,3-propanedioyl bis(salicylaldehyde hydrazone))(H(2)O)(2)].(ClO(4))(2).3H(2)O and Polymeric [{Cu(2)(1,6-hexanedioyl bis

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10.1016/S0162-0134(99)00131-2

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