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

Journal of Inorganic Biochemistry

Volumn 72, Issue 3-4, 1998, Pages 155-162

  Koh, L L ^a   Kon, O L ^b   Loh, K W ^a   Long, Y C ^a   Ranford, J D ^a   Tan, A L C ^c   Tjan, Y Y ^a  

^a NATIONAL UNIVERSITY OF SINGAPORE   (Singapore)

^b NATIONAL UNIVERSITY OF SINGAPORE   (Singapore)

^c INSTITUTE OF MOLECULAR AND CELL BIOLOGY   (Singapore)

Author keywords

[No Author keywords available]

Indexed keywords

COPPER COMPLEX; HYDRAZONE DERIVATIVE; SALICYLALDEHYDE ACYLHYDRAZONE; UNCLASSIFIED DRUG;

ARTICLE; COMPLEX FORMATION; CRYSTAL STRUCTURE; DIMERIZATION; DRUG CYTOTOXICITY; DRUG SOLUBILITY; DRUG STRUCTURE; LIGAND BINDING; LIPOPHILICITY; QUANTITATIVE STRUCTURE ACTIVITY RELATION; STEREOSPECIFICITY; STRUCTURE ANALYSIS;

ALDEHYDES; ANTINEOPLASTIC AGENTS; CRYSTALLOGRAPHY, X-RAY; DIMERIZATION; HUMANS; HYDRAZONES; STRUCTURE-ACTIVITY RELATIONSHIP; TUMOR CELLS, CULTURED;

EID: 0032469763     PISSN: 01620134     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0162-0134(98)10075-2     Document Type: Article

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