Author(s)

Ryan Beni, William Boadi, Kaleh Karim, Jawzah Alnakhli, Samiyah Alhamed

Department of Chemistry, Tennessee State University, Nashville, TN, USA.

Leuprorelin^® (LEP) is an FDA drug for breast cancer and prostate cancer treatment. There are several reported adverse effects such as transient hypertension, excessive salivation, and increased dysuria during treatment with LEP. In this study, the efficacy and toxicity of LEP were modified by using a drug delivery system to adjust the physicochemical properties. In this regard, Leuprorelin^® conjugates of triphenylmethanol derivatives (TPMs) were synthesized as prodrugs. Comparative antiproliferative assays showed that LEP-TPMs conjugates had significantly higher antiproliferative activities than the corresponding non-covalent physical mixtures of the TPMs and LEP against human invasive ductal carcinoma (BT-549), human prostate carcinoma (PC3), human lung cancer (A549) and mouse pre-adipocytes (3T3-L1) cells.

Prodrugs, Leuprorelin, Polyphenols, Prostate Cancer, Triphenylmethanol, Prodrugs

Beni, R. , Boadi, W. , Karim, K. , Alnakhli, J. and Alhamed, S. (2019) Synthesis and Antiproliferative Activities of Triphenylmethanol Conjugates of Leuprorelin. Open Journal of Medicinal Chemistry, 9, 37-47. doi: 10.4236/ojmc.2019.92002.