Author/Authors :
Raed A. Al-Qawasmeh، نويسنده , , Yoon Lee، نويسنده , , Ming-Yu Cao، نويسنده , , Xiaoping Gu، نويسنده , , Aikaterini Vassilakos، نويسنده , , Jim A. Wright، نويسنده , , Aiping Young، نويسنده ,
Abstract :
Clotrimazole (CLT) 1, a synthetic anti-fungal imidazole derivative, inhibits tumor cell proliferation and angiogenesis. In the current study, flow cytometric analysis demonstrated that the decrease in tumor cell growth by CLT 1 was associated with inhibition of cell cycle progression at the G1–S phase transition, resulting in G0–G1 arrest. A series of CLT 1 analogues has been generated in order to develop CLT 1 derivatives that are devoid of the imidazole moiety which is responsible for the hepatoxicity associated with CLT 1 while retaining CLT 1 efficacy. The majority of these analogues demonstrate in vitro antiproliferative activity ranging from submicromolar to micromolar concentrations.