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This page is a summary of: The synthesis of non-steroidal anti-inflammatory drug (NSAID)–lantadene prodrugs as novel lung adenocarcinoma inhibitors via the inhibition of cyclooxygenase-2 (COX-2), cyclin D1 and TNF-α-induced NF-κB activation, RSC Advances, January 2014, Royal Society of Chemistry,
DOI: 10.1039/c4ra00280f.
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