Journal of Medicinal Chemistry p. 3635 - 3649 (2016)
Update date:2022-08-15
Topics: Anticancer Chemotherapeutic Itraconazole Repurposing Clinically Efficacious
Pace, Jennifer R.
Deberardinis, Albert M.
Sail, Vibhavari
Tacheva-Grigorova, Silvia K.
Chan, Kelly A.
Tran, Raymond
Raccuia, Daniel S.
Wechsler-Reya, Robert J.
Hadden, M. Kyle
Itraconazole (ITZ) is an FDA-approved member of the triazole class of antifungal agents. Two recent drug repurposing screens identified ITZ as a promising anticancer chemotherapeutic that inhibits both the angiogenesis and hedgehog (Hh) signaling pathways. We have synthesized and evaluated first- and second-generation ITZ analogues for their anti-Hh and antiangiogenic activities to probe more fully the structural requirements for these anticancer properties. Our overall results suggest that the triazole functionality is required for ITZ-mediated inhibition of angiogenesis but that it is not essential for inhibition of Hh signaling. The synthesis and evaluation of stereochemically defined des-triazole ITZ analogues also provides key information as to the optimal configuration around the dioxolane ring of the ITZ scaffold. Finally, the results from our studies suggest that two distinct cellular mechanisms of action govern the anticancer properties of the ITZ scaffold.
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