Electrogenerated chemiluminescence (ECL) of six new ethyne-based acridine derivatives (1-6) has been studied. The new acridine derivatives were synthesized by cross-coupling of 9-chloroacridine and corresponding donor-substituted phenylethynes under modified Sonogashira conditions. The donor groups were varied in the order of increasing steric hindrance and donor strength at the donor site. The...

Lewis et al. (14, 15) reported the results of a survey of various derivatives of acridine as pos sible inhibitors of the growth of tumors in mice. Among the series of 70 acridine derivatives which they tested, sixteen 9-aminoacridine compounds were found to inhibit the growth of tumors to the extent that, after 14 days of treatment, they were th@— @ theaveragesizeoftumorsinuntreatedcon trol m...

Stabilization of G-quadruplex structures formed from telomeric DNA, by means of G-quadruplex selective ligands, is a means of inhibiting the telomerase enzyme. This makes G-quadruplex an emerging target for cancer therapy. The objective of the current 3D QSAR study is to uncover structural requirements for acridine derivatives, which would eventually assist and complement the rational drug-desi...

multi drug resistance (mdr) is a serious obstacle in the management of breast cancer. therefore, overcoming mdr using novel anticancer agents is a top priority for medicinal chemists. it was found that dihydropyridines lacking calcium antagonistic activity (e.g acridinediones) possess mdr modifier potency. in this study, the capability of four novel acridine-1,8-diones derivatives 3a-d were eva...