Publication | Open Access
Design, synthesis and biological evaluation of fused naphthofuro[3,2-c] quinoline-6,7,12-triones and pyrano[3,2-c]quinoline-6,7,8,13-tetraones derivatives as ERK inhibitors with efficacy in BRAF-mutant melanoma
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Citations
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References
2018
Year
Medicinal ChemistryNatural Product SynthesisMedicineMelanomaBiological EvaluationAnti-cancer AgentErk InhibitorsPharmacologyRadiation OncologyTumor BiologyDrug DiscoveryBraf-mutant Melanoma
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