Design, Synthesis and In Vitro Cytotoxic Activity of New 6,9-Disubstituted Purine Analogues

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2020-01-01

Author

Kucukdumlu, Asligul
TUNÇBİLEK, MERAL
GÜVEN, EBRU BİLGET
Atalay, Rengül

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A series of new 6,9-disubstituted purine analogs with 4-substituted piperazine at C-6 and 4-substituted benzyl at N-9 were designed and synthesized in four steps. All synthesized compounds (7-26) were screened initially for their in vitro anticancer activity on Huh7 liver, HCT116 colon and MCF7 breast carcinoma cell lines. Cytotoxic bioactivity studies revealed that all compounds screened, with compound 19 being the exception, were found to have promising cytotoxic activities at IC50 range of 0.05-21.8 mu M against cancer cells Huh7, HCT116 and MCF7. Among the prepared purine analogs, two of them (12 and 22) exhibited excellent cytotoxic activities, with IC50 0.08-0.13 mu M, on Huh7 cells comparable to camptothecin (CPT) and better than cladribine, fludarabine and 5-FU. Afterwards, the evaluation of cytotoxicity of the most potent purine analogs was screened against further hepatocellular cancer (HCC) cell lines. The 6-(4-(4-trifluoromethylphenyl)piperazine (12) and 6-(4-(3,4-dichlorophenyl)piperazine analogs (25) displayed a significant IC50 values (IC50 < 0.1-0.13 mu M) comparable to CPT and better cytotoxic bioactivity when compared with 5-FU, cladribine and fludarabine on HCC cells (Huh7 and HepG2).

Subject Keywords

Purine, Piperazine, Benzyl, Cytotoxic activity

URI

https://hdl.handle.net/11511/30258

Journal

ACTA CHIMICA SLOVENICA

DOI

https://doi.org/10.17344/acsi.2019.5196

Collections

Graduate School of Informatics, Article

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Citation Formats

A. Kucukdumlu, M. TUNÇBİLEK, E. B. GÜVEN, and R. Atalay, “Design, Synthesis and In Vitro Cytotoxic Activity of New 6,9-Disubstituted Purine Analogues,” ACTA CHIMICA SLOVENICA, pp. 70–82, 2020, Accessed: 00, 2020. [Online]. Available: https://hdl.handle.net/11511/30258.