Kupchik E J, Pisano M A, Raghunath A V, Cardona R A, Formaini N, Alleguez C
J Pharm Sci. 1975 Jul;64(7):1259-62. doi: 10.1002/jps.2600640736.
Six N-substituted N'-cyano-S-(trimethylstannyl)isothioureas were synthesized by the reaction of (trimethylstannyl)cyanamide with various organic isothiocyanates. The IR spectrum of each compound was obtained over the 4000-30-cm(-1) range, and some bands were assigned. The six new compounds and five previously synthesized N-substituted N'-cyano-S-(triphenylstannyl)isothioureas were tested for and were found to exhibit antifungal activity. N-Phenyl-N'-cyano-S-(triphenylstannyl)isothiourea was also investigated for antibacterial activity and was observed to be especially inhibitory toward Gram-positive species. The antimicrobial activity of two compounds was compared to that of the oxygen analogs of these compounds.
通过(三甲基锡基)氰胺与各种有机异硫氰酸酯反应合成了六种N-取代的N'-氰基-S-(三甲基锡基)异硫脲。在4000 - 30 cm⁻¹范围内获得了每种化合物的红外光谱,并对一些谱带进行了归属。对这六种新化合物和五种先前合成的N-取代的N'-氰基-S-(三苯基锡基)异硫脲进行了测试,发现它们具有抗真菌活性。还研究了N-苯基-N'-氰基-S-(三苯基锡基)异硫脲的抗菌活性,发现其对革兰氏阳性菌具有特别的抑制作用。将两种化合物的抗菌活性与其氧类似物的抗菌活性进行了比较。