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Results: 3
Inhibition of in vitro lymphoproliferation by three novel iron chelators of the pyridoxal and salicyl aldehyde hydrazone classes
Authors: van Reyk, D Sarel, S Hunt, N
Citation: D. Van Reyk et al., Inhibition of in vitro lymphoproliferation by three novel iron chelators of the pyridoxal and salicyl aldehyde hydrazone classes, BIOCH PHARM, 60(4), 2000, pp. 581-587
Domain-structured N-1,N-2-derivatized hydrazines as inhibitors of ribonucleoside diphosphate reductase: Redox-cycling considerations
Authors: Sarel, S Fizames, C Lavelle, F Avramovici-Grisaru, S
Citation: S. Sarel et al., Domain-structured N-1,N-2-derivatized hydrazines as inhibitors of ribonucleoside diphosphate reductase: Redox-cycling considerations, J MED CHEM, 42(2), 1999, pp. 242-248
Iron chelators of the pyridoxal-based class. Part 7. The synthesis and single crystal structure of 1-(N-ethoxycarbonylmethylpyridoxyledenium)-2-(pyrimidyl)hydrazine salts
Authors: Sarel, S Avramovici-Grisaru, S Cohen, S
Citation: S. Sarel et al., Iron chelators of the pyridoxal-based class. Part 7. The synthesis and single crystal structure of 1-(N-ethoxycarbonylmethylpyridoxyledenium)-2-(pyrimidyl)hydrazine salts, HETEROCYCLE, 49, 1998, pp. 393-404
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