21578-47-2Relevant academic research and scientific papers
Antimicrobial activity and structural study of disubstituted Thiourea Derivatives
Cunha, Silvio,MacEdo Jr., Fernando C.,Costa, Giselle A. N.,Rodrigues Jr., Manoel T.,Verde, Rosival B. V.,De Souza Neta, Lourdes C.,Vencato, Ivo,Lariucci, Carlito,Sa, Fernando P.
, p. 511 - 516 (2007)
The antimicrobial activity of six N-phenyl- and fourteen N-benzoylthiourea derivatives were evaluated from their Minimal Inhibitory Concentration (MIC) values using the microdilution procedure against ten microorganisms. Most of the compounds exhibited selective activity against fungi and Gram-positive bacteria, which were very effectively inhibited by some of the tested thioureas. Additionally, SAR considerations and four novel X-ray diffraction structures of N-benzoylthioureas are included. Springer-Verlag 2007.
Synthesis 1-acyl-3-(2'-aminophenyl) thioureas as anti-intestinal nematode prodrugs
Duan, Li-Ping,Xue, Jia,Xu, Li-Li,Zhang, Hao-Bing
experimental part, p. 6941 - 6947 (2011/02/22)
A series of 1-acyl-3-(2'-aminophenyl) thiourea derivatives were designed and synthesized. The structures of all the newly synthesized compounds were identified by IR, elemental analysis, 1H-NMR and 13C-NMR. Their anti-intestinal nema
REACTIONS OF CARBONYL ISOTHIOCYANATES WITH NUCLEOPHILIC BIFUNCTIONAL REAGENTS
Uher, Michal,Berkes, Dusan,Lesko, Jan,Floch, Lubomir
, p. 1651 - 1658 (2007/10/02)
Reactions of benzoyl-, 2-furoyl-, acetyl-, and trichloroacetyl isothiocyanates with 1,2-diaminobenzene, 2-aminophenol, 5,6-diamino-1,3-uracil and 2,3-diaminopyridine were investigated.Formation of the individual products and their IR, UV and electron impa
