, new less toxic ThS
inhibitors must be sought and created. The GUSAR 2013 program was used to study
and quinazolin-4-imine derivatives, well-known antifolate thymidylate synthase (TYMS)
inhibitors, has been
Zhao, X.,
Sun, J.,
Su, W.,
Shan, H.,
Zhang, B.,
Wang, Y.,
Shabanova, A.,
Shan, H.,
Liang, H. (2018) fibroblasts. Additionally, we determined that luzindole, a melatonin receptor
inhibitor, reduced the anti