Fungi are ubiquitous in nature, and typically cause little or no environmental or pathogenic
damage to their plant, animal, and human hosts. However, a small but growing number of …

There has been substantial attention in the expansion of new thiosemicarbazide derivatives
with diverse biological activities in recent years. Therefore, many scientists have prepared …

Previously, we demonstrated that the potent antiproliferative activity of the di-2-pyridylketone
thiosemicarbazone (DpT) series of Fe chelators was due to their ability to induce Fe …

Thiosemicarbazone analogs of papaveraldine and related compounds 1–6 were
synthesized and evaluated for cytotoxic and antimalarial activities. The cytotoxic activity was …

Compounds 1–30 showed varying degree of α-glucosidase inhibition with IC 50 values
ranging between 187 and 420 μ M. Compounds 1, 2, 3, 6, 8, 12, and 4 (IC 50= 187.7±3.05 …

New imidazole derived thiosemicarbazones and hydrazones were prepared by
condensation of 4 (5)-imidazole carboxaldehyde, 4-(1 H-imidazole-1-yl) benzaldehyde and …

Malaria is a potentially life-threatening disease, affecting approx. 214 million people
worldwide. Malaria is caused by a protozoan, Plasmodium falciparum, which is transmitted …

Original results are presented in the field of research that addresses the extension of the
reaction of residue of acyl-thiosemicarbazide fixation on the structure of 5 …

Phenoxyacetohydrazide Schiff base analogs 1–28 have been synthesized and their in vitro
β-glucouoronidase inhibition potential studied. Compounds 1 (IC50= 9.20±0.32 µM), 5 …

A series of metal complexes of Cu (II) and Ni (II) having the general composition [M (L) X2]
with benzil bis (thiosemicarbazone) has been prepared and characterized by element …