1995
DOI: 10.1016/0223-5234(96)88318-8
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Neurotropic activity of aldehyde and ketone thiosemicarbazones with a heterocyclic component

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Cited by 21 publications
(13 citation statements)
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“…Thiosemicarbazones of -N-heterocyclic carbaldehydes act as tridentate ligands. The biological activity of the thiosemicarbazone depends on the parent aldehyde or ketone (Padhye & Kauffman, 1985;Liberta & West, 1992;Lukevics et al, 1995). Among thousands of screened compounds (Klayman et al, 1979), 2-acetylpyridine thiosemicarbazones were the ®rst compounds reported as potent antimalarial agents.…”
Section: Commentmentioning
confidence: 99%
“…Thiosemicarbazones of -N-heterocyclic carbaldehydes act as tridentate ligands. The biological activity of the thiosemicarbazone depends on the parent aldehyde or ketone (Padhye & Kauffman, 1985;Liberta & West, 1992;Lukevics et al, 1995). Among thousands of screened compounds (Klayman et al, 1979), 2-acetylpyridine thiosemicarbazones were the ®rst compounds reported as potent antimalarial agents.…”
Section: Commentmentioning
confidence: 99%
“…Recently, there has been considerable interest in the coordination chemistry of thiosemicarbazones because of their biological and carcinostatic activities (Liu et al, 1995;Lukevics et al, 1996) and their non-linear optical properties (Tian et al, 1997;Liu et al, 1999). It has been postulated that extensive electron delocalization in the thiosemicarbazone moiety helps the free thiosemicarbazone ligands and their metal complexes to exhibit SHG (second harmonic generation) ef®ciency (Tian et al, 1997;Liu et al, 1999).…”
Section: Commentmentioning
confidence: 99%
“…Such systems found to have potential applications in biological and material science. Thiosemicarbazone and thiocarbazone belong to a large group of thiourea derivatives, which have shown wide biological activities .…”
Section: Thiocarbohydrazidesmentioning
confidence: 99%