Solvent-modulated second harmonic generation in <i>N</i>-alkylated thiohydantoin derivatives: synthesis, characterization, and first-principle insights. [PDF]
Ali MA +5 more
europepmc +1 more source
Study of the optical properties of 2-thiohydantoin derivatives [PDF]
Smarandachea, Adriana +6 more
openaire +2 more sources
Synthesis and evaluation of novel thiohydantoin derivatives for antidiabetic activity using in silico in vitro and in vivo methods. [PDF]
Bukhari A +5 more
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A new polymorph of 1-acetyl-2-thiohydantoin
The crystal structure of a new polymorph of 1-acetyl-2-thiohydantoin has been determined by X-ray diffraction. The crystal, C5H6N2O2S, belongs to space group P1 with cell dimensions of a = 4.9865(7)Å, b = 5.5716(7)Å, c = 12.544(2)Å, a = 74.793(8)°, b = 80.413(9)°, g = 85.001(10)°. The final R1 value is 0.036 for 1304 reflections (I > 2.0s(I)).
openaire +1 more source
[3 + 2] Cycloaddition of thioformylium methylide with various arylidene-azolones in the synthesis of 7-thia-3-azaspiro[4.4]nonan-4-ones. [PDF]
Rudik DI +7 more
europepmc +1 more source
Synthesis of novel 2-thiohydantoin derivatives as potential anti-diabetic drugs
M.Sc. (Chemistry)Department of ChemistryThiohydantoin is a hydantoin with one carbonyl group replaced with a thiocarbonyl group. In this study five series (glycinates, alaninates, butanoates, vallinates and norvalinates) of thiohydantoin derivatives (21a-
Tshishonga, Unarine
core
In vitro assays identified thiohydantoins with anti-trypanosomatid activity and molecular modelling studies indicated possible selective CYP51 inhibition. [PDF]
Camargo PG +9 more
europepmc +1 more source
Design, eco-friendly synthesis, and molecular docking studies of isatin hybrids as promising therapeutic agents (anticancer, anticholinesterase inhibitor, α-glucosidase inhibitor, and anti-MRSA). [PDF]
Seliem IA.
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Chiral Recognition of Chiral (Hetero)Cyclic Derivatives Probed by Tetraaza Macrocyclic Chiral Solvating Agents via <sup>1</sup>H NMR Spectroscopy. [PDF]
Wang Y +8 more
europepmc +1 more source
A guide to using small-molecule ferroptosis inhibitors. [PDF]
Pratt DA, Dixon SJ.
europepmc +1 more source

