<?xml version="1.0" encoding="UTF-8"?>
<xml>
 <records>
  <record>
   <ref-type name="Journal Article">17</ref-type>
   <contributors>
    <authors>
     <author></author>
     <author></author>
     <author></author>
     <author></author>
     <author></author>
    </authors>
   </contributors>
   <titles>
    <title></title>
   </titles>
   <dates>
    <year>2018</year>
    <pub-dates>
     <date>2020-09-16</date>
    </pub-dates>
   </dates>
   <doi>10.1016/j.jmgm.2018.09.002</doi>
   <abstract>A quantitative structureeactivity relationship analysis of the 2-methylquinazolin-4-one and quinazolin-4-imine derivatives, well-known antifolate thymidylate synthase (TYMS) inhibitors, has been performedin the range IC50¼0.4÷380000.0 nmoL/L using the GUSAR 2013 program. Based on the MNA and QNAdescriptors using the self-consistent regression, 6 statistically significant consensus models for predictingthe IC50numerical values have been constructed. These models demonstrate high and moderate prog-nostic accuracies for the training and external validation test sets, respectively. The molecular fragmentsof TYMS inhibitors regulating their antitumor activity are identified. The obtained data open opportu-nities for developing novel promising inhibitors of TYMS.</abstract>
   <urls>
    <web-urls>
     <url>https://repo.bashgmu.ru/publication/4</url>
    </web-urls>
    <pdf-urls>
     <url>https://repo.bashgmu.ru/files/4</url>
    </pdf-urls>
   </urls>
  </record>
 </records>
</xml>
