Epub ahead of printNew substituted 1,4-naphthoquinones have been prepared in good overall yields through the naphthol route. The cytotoxicity of these compounds was tested in vitro on MCF-7 breast tumor cells. The most active compound 14 displayed an IC50 of 15microM.OBJECTIVE: To investigate the cytotoxicity of new naphthoquinones derivatives on MCF-7 cells.METHOD: Synthesis of new naphtoquinones derivatives and in vitro evaluation of their cytotoxicity on MCF-7 cells (rezasurin cell-based assay). RESULTS: Starting from Ethyl 4-hydroxy-6,7-dimethoxy-2-naphthoate, four naphthoquinones were prepared and exhibited substantial cytotoxicity against MCF-7 cells.CONCLUSION: Preliminary studies of the structure-activity relationship have shown the...
Chrysophanol and 1,8-di-O-hexylchrysophanol derivatives having nucleic acid bases at position 5 were...
Chrysophanol and 1,8-di-O-hexylchrysophanol derivatives having nucleic acid bases at position 5 were...
Chrysophanol and 1,8-di-O-hexylchrysophanol derivatives having nucleic acid bases at position 5 were...
Epub ahead of printNew substituted 1,4-naphthoquinones have been prepared in good overall yields thr...
Epub ahead of printNew substituted 1,4-naphthoquinones have been prepared in good overall yields thr...
In this study, eight naphthoquinone derivatives were synthesized in yields ranging from 52 to 96% us...
In this study, eight naphthoquinone derivatives were synthesized in yields ranging from 52 to 96% us...
To examine the effect of hydrophobicity on the anticancer activity of 1,4-naphthoquinone derivative...
To examine the effect of hydrophobicity on the anticancer activity of 1,4-naphthoquinone derivative...
The cytotoxicity of a series of aminonaphthoquinones resulting from the reaction of suitable aminoac...
Colorectal cancer (CRC) is a disease with high incidence and mortality, constituting the fourth most...
Synthesizing bioactive small molecules by structural modification of 1,4-naphthoquinone was the prim...
Chrysophanol and 1,8-di-O-hexylchrysophanol derivatives having nucleic acid bases at position 5 were...
Eleven 2,3-(substituted)-1,4-naphthoquinone derivatives were synthesized in yields ranging from 52-8...
Chrysophanol and 1,8-di-O-hexylchrysophanol derivatives having nucleic acid bases at position 5 were...
Chrysophanol and 1,8-di-O-hexylchrysophanol derivatives having nucleic acid bases at position 5 were...
Chrysophanol and 1,8-di-O-hexylchrysophanol derivatives having nucleic acid bases at position 5 were...
Chrysophanol and 1,8-di-O-hexylchrysophanol derivatives having nucleic acid bases at position 5 were...
Epub ahead of printNew substituted 1,4-naphthoquinones have been prepared in good overall yields thr...
Epub ahead of printNew substituted 1,4-naphthoquinones have been prepared in good overall yields thr...
In this study, eight naphthoquinone derivatives were synthesized in yields ranging from 52 to 96% us...
In this study, eight naphthoquinone derivatives were synthesized in yields ranging from 52 to 96% us...
To examine the effect of hydrophobicity on the anticancer activity of 1,4-naphthoquinone derivative...
To examine the effect of hydrophobicity on the anticancer activity of 1,4-naphthoquinone derivative...
The cytotoxicity of a series of aminonaphthoquinones resulting from the reaction of suitable aminoac...
Colorectal cancer (CRC) is a disease with high incidence and mortality, constituting the fourth most...
Synthesizing bioactive small molecules by structural modification of 1,4-naphthoquinone was the prim...
Chrysophanol and 1,8-di-O-hexylchrysophanol derivatives having nucleic acid bases at position 5 were...
Eleven 2,3-(substituted)-1,4-naphthoquinone derivatives were synthesized in yields ranging from 52-8...
Chrysophanol and 1,8-di-O-hexylchrysophanol derivatives having nucleic acid bases at position 5 were...
Chrysophanol and 1,8-di-O-hexylchrysophanol derivatives having nucleic acid bases at position 5 were...
Chrysophanol and 1,8-di-O-hexylchrysophanol derivatives having nucleic acid bases at position 5 were...
Chrysophanol and 1,8-di-O-hexylchrysophanol derivatives having nucleic acid bases at position 5 were...