This invention provides substituted pyrimidine compounds that are useful in treating a patient having a disease or cancer. The compounds of this invention are useful as multi-enzyme antifolates selectively targeting the folate receptor (FR). Further, a method of making 5-and 6-substituted cyclopenta[d]pyrimidine for nonclassical and classical antifolates as TS and DHFR inhibitors is provided.
本发明提供了可用于治疗患有疾病或癌症的取代
嘧啶化合物。本发明的化合物可用作多酶抗叶酸类药物,选择性地靶向叶酸受体(FR)。此外,还提供了一种制备5-和6-取代环戊[d]
嘧啶的方法,用于非经典和经典抗叶酸类药物,作为
TS和DHFR
抑制剂。