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- W4382502050 abstract "Aim: The previously reported dual histone deacetylase type II (HDAC II) / topoisomerase type I (Topo I) inhibitors suffer pharmacokinetic limitations because of their huge molecular weights. Materials & methods: We report the design and synthesis of a smarter novel set of uracil-linked Schiff bases (19–30) as dual HDAC II/Topo I inhibitors keeping the essential pharmacophoric features. Cytotoxicity of all compounds was assessed against three cancer cell lines. Studies of their effects on the apoptotic BAX and antiapoptotic BCL2 genes, molecular docking studies, and absorption, distribution, metabolism and excretion studies were conducted. Results: Compounds 22, 25 and 30 exhibited significant activities. The bromophenyl derivative 22 displayed the best selectivity index, with IC 50 values against HDAC II and Topo I of 1.12 and 13.44 μM, respectively. Conclusion: Compound 22 could be considered a lead HDAC II/Topo I inhibitor." @default.
- W4382502050 created "2023-06-30" @default.
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- W4382502050 date "2023-06-01" @default.
- W4382502050 modified "2023-10-16" @default.
- W4382502050 title "Design and synthesis of novel uracil-linked Schiff bases as dual histone deacetylase type II/topoisomerase type I inhibitors with apoptotic potential" @default.
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- W4382502050 doi "https://doi.org/10.4155/fmc-2023-0112" @default.
- W4382502050 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/37381751" @default.
- W4382502050 hasPublicationYear "2023" @default.
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