淡江大學機構典藏:Item 987654321/118898
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    Title: Discovery of a more potent anti-cancer agent than C4-benzazole 1,8-naphthalimide derivatives against murine melanoma
    Authors: Tung, Chi-Hua;Lu, Yen-Ta;Kao, Wei-Ting;Liu, Jen-Wei;Lai, Yi-Hsuan;Jiang, Shinn-Jong;Chen, Hao-Ping;Shih, Tzenge-Lien
    Date: 2020-06-24
    Issue Date: 2020-07-13 12:10:27 (UTC+8)
    Abstract: Three novel naphthalimide‐based derivatives were synthesized and tested in vitro as anticancer agents. Our previous report of the C4‐benzazole 1,8‐naphthalimide derivatives showed good inhibition against murine melanoma. We aimed to synthesize more potent agents and found that compound 5 reported in this article behaved 5‐ to 10‐fold potency than our previous best results. The unique structure of compound 5 consisted of a naphthalimide framework in which C4 position was linked with an ethylenediamine group where the amino group was coupled with a 2‐piconic acid moiety. Compound 5 exhibited the most potent inhibitory activity toward human DNA topoisomerase II proteins with IC50 value (2.6 ± 0.1 μM) against murine B16F10 melanoma cells among the three target compounds synthesized in this study. In accordance with this finding, the results of molecular docking also revealed that compound 5 has the highest affinity with human DNA topoisomerase II among the selected compounds. Compound 5 , therefore, has high potential for becoming a lead compound.
    Relation: Journal of the Chinese Chemical Society 67(7), 1254-1262
    DOI: 10.1002/jccs.202000019
    Appears in Collections:[Graduate Institute & Department of Chemistry] Journal Article

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