N. Grynberg et al., SYNTHESIS AND IN-VIVO ANTITUMOR-ACTIVITY OF NEW HETEROCYCLIC-DERIVATIVES OF THE 1,3,4-THIADIAZOLIUM-2-AMINIDE CLASS, Anti-cancer drugs, 8(1), 1997, pp. 88-91
Four new mesoionic compounds derivates of -(4-X-cinnamoyl)-1,3,4-thiad
iazalium-2-phenylamine chlorides were synthesized and their antitumor
activities against Ehrlich carcinoma and Sarcoma 180 (S180) were evalu
ated. In the schedule assayed, the derivatives where X = OH and X = NO
2 injected i.p. in mice at a total dose level of 10 and 30 mg/kg respe
ctively caused a significant inhibition of ascitic S180 growth, and at
a dose of 25 mg/kg inhibited the growth of Ehrlich carcinoma. The der
ivatives where X = H and X = OCH3 did not show activity. There are no
significant changes of hematopoietic parameters of the derivatives in
this treatment These data suggest that the presence of more polar subs
tituents, NO2 and OH, strongly increases the antitumor activity of thi
s class of compounds.