Santosh N Mokale*, Nikhil S Sakle, Swati A Bhavale, Deepak K Lokwani and Vishakha Shelke Pages 1009 - 1015 ( 7 )
Methods: A novel series of isoxazole (S21-S30) derivatives were designed, synthesized and screened for their anticancer activity against estrogen receptor-positive MCF-7 and negative MDA-MB-435 breast cancer cell lines. The synthesized derivative has the ability to inhibit the growth of the human breast cancer cell line at low concentrations. In vivo anticancer activity was performed on virgin female sprague dawley rats.
Results: The result shows that compound S23 has more selectivity and marked estrogen modulator activity than the standard tamoxifen.
Chalcone, isoxazole, breast cancer, estrogen receptor, S21-S30, tamoxifen.
Y.B.Chavan college of pharmacy, Aurangabad, Y.B. Chavan College of Pharmacy - Pharmacology Aurangabad, Maharashtra, Y.B. Chavan College of Pharmacy - Pharm Chemistry Aurangabad, maharashtra, Y.B. Chavan College of Pharmacy - Pharm Chemistry Aurangabad, maharashtra, Y.B. Chavan College of Pharmacy - Pharm Chemistry Aurangabad, maharashtra