derivatives of thiazolidinone ring systems are known to act as anti-hiv infections , analgesic, anti-bacterial, anti-convulsant, anti parasitic, potential anti-inflammatory and herbicidal agents. due biological activities of thiazolidinones ring, several methods for their synthesis have been illustrated in literature. imidazolidine-2-thiones were synthesized by the oxidative cyclization of 1-be...

Detection of substances tasting bitter to humans occurs in diverse organisms including the social amoeba Dictyostelium discoideum. To establish a molecular mechanism for bitter tastant detection in Dictyostelium, we screened a mutant library for resistance to a commonly used bitter standard, phenylthiourea. This approach identified a G-protein-coupled receptor mutant, grlJ(-), which showed a si...

Derivatives of thiazolidinone ring systems are known to act as anti-HIV infections , analgesic, anti-bacterial, anti-convulsant, anti parasitic, potential anti-inflammatory and herbicidal agents. Due biological activities of thiazolidinones ring, several methods for their synthesis have been illustrated in literature. Imidazolidine-2-thiones were synthesized by the oxidative cyclization of 1-be...

the phenylthiourea-substituted triethoxysilane as a silane agent was synthesized and grafted on highly ordered nanoporous silica (lus-1) with a textured morphology and hexagonal array. this material (tu-lus-1) contained 0.8 mmol/g of soft base phenylthiourea group and surface area 760 m2g-1 and was able to adsorb 0.75 mmolhg/g of tu-lus-1 in endothermic reaction.

The phenylthiourea-substituted triethoxysilane as a silane agent was synthesized and grafted on highly ordered nanoporous silica (LUS- 1) with a textured morphology and hexagonal array. This material (Tu-LUS-1) contained 0.8 mmol/g of soft base phenylthiourea group and surface area 760 m2 g-1  and was able to adsorb 0.75 mmolHg/g of TU-LUS-1 in endothermic reaction.

New 1-benzhydryl-3-phenylurea derivatives and their 1-benzhydryl-3-phenylthiourea isosteres were synthesized and evaluated for their human CB1 and CB2 cannabinoid receptor affinity. These compounds proved to be selective CB1 cannabinoid receptor ligands, acting as inverse agonists in a [35S]-GTPgammaS assay. The affinity of 3,5,5'-triphenylimidazolidine-2,4-dione and 3,5,5'-triphenyl-2-thioxoim...

[structure: see text] A neutral receptor with a rigid hydrazine spacer, N-p-(dimethylamino)benzamido-N'-phenylthiourea, was prepared, and its dual fluorescence in acetonitrile was found to show response toward the presence of anions such as AcO(-), H(2)PO(4)(-), HSO(4)(-), Br(-), Cl(-), F(-), and ClO(4)(-) with high sensitivity and selectivity toward AcO(-).