The present invention has identified thiaprophyrin, selenaporphyrin, and carotenoid porphyrin compounds that bind the G-quadruplex formed by the folding of single-stranded human telomeric DNA. These compounds have been shown to be effective telomerase and c-myc inhibitors and are contemplated to be useful in developing cancer treatments.
本发明已经确定了
硫代
卟啉、
硒代
卟啉和类
胡萝卜素卟啉化合物,这些化合物与由单链人类端粒DNA折叠形成的G-四链体结合。这些化合物已被证明是有效的端粒酶和c-myc
抑制剂,并被考虑用于开发癌症治疗。