Synthesis and anticancer activity of novel quinazolinone-based rhodanines
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The compounds synthesized were tested for their antiproliferative activity in vitro against human liver carcinoma cell line (HepG2) and human cervix carcinoma cell
The synthesized compounds were evaluated for in vitro cyto- toxic activity against various cell lines such as HeLa (cervical cancer), MCF-7 (breast cancer), HL-60 (Human promyelo-
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All the compounds synthesized were screened for in-vitro anticancer activity against MCF-7 (Human Breast cancer cell line), Hepg2 (Human Liver cancer cell line), B16
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