Synthesis, characterization and in vitro antibacterial activity of thiourea and urea derivatives of steroids

Some heterocyclic systems namely stigmest-6-en-7, 5α thiourea and stigmest-6-en-7, 5α urea derivatives of steroids were synthesized by the reaction of stigmest-5-en-7 one with thiourea/urea in the presence of a few drops of conc. HCl at 80 °C in high yield. All the compounds have been characterized by means of elemental analyses, IR, 1H NMR, 13C NMR and mass spectroscopic data. The antibacterial activity was first tested in vitro by the disk diffusion assay against two Gram-positive and two Gram-negative bacteria, and then the minimum inhibitory concentration (MIC) of compounds were determined. The results showed that steroidal thiourea derivatives inhibit growth as compared to steroidal urea derivatives of both type of the bacteria (Gram-positive and Gram-negative). Compounds 3 and 4 are better antibacterial agents as compared to standard drug chloramphenicol.

Some heterocyclic systems namely stigmest-6-en-7, 5α thiourea and stigmest-6-en-7, 5α urea derivatives of steroids were synthesized by the reaction of stigmest-5-en-7 one with thiourea/urea in the presence of a few drops of conc. HCl at 80 °C in high yield. All the compounds have been characterized by means of elemental analyses, IR, 1H NMR, 13C NMR and mass spectroscopic data. The antibacterial activity of these compounds against two Gram-positive and two Gram-negative bacteria. The results showed that compounds 3 and 4 are better antibacterial agents as compared to standard drug chloramphenicol.Figure optionsDownload as PowerPoint slide