Research Article

Synthesis and characterization of 1,2,4-triazole containing hydrazide-hydrazones derived from (S)-Naproxen as anticancer agents

Volume: 22 Number: 4 June 27, 2025
EN

Synthesis and characterization of 1,2,4-triazole containing hydrazide-hydrazones derived from (S)-Naproxen as anticancer agents

Abstract

A novel series of new naproxen derivatives (S)-ethyl{[4-(4-fluorophenyl)-5-[(1-(6-methoxynaphtalen-2- yl)ethyl)]-4H-1,2,4-triazole-3-yl]sulphanyl}acetate (5), (S)-2-({5-[1-(6-methoxynaphtalen-1-yl)ethyl]-4-fluorophenyl-4H1,2,4-triazole-3-yl}sulphanyl)acetohydrazide (6), 2-{[5-[1-(6-methoxynaphtalen-2-yl)ethyl]-4-(4-fluorophenyl)-4H-1,2,4- triazole-3-yl]sulphanyl}-N'-[(substituted)methylidene]acetohydrazides (7a-m) were synthesized, in this study. The structures of compounds 5, 6 and 7a-m were defined by spectral (1H-NMR, 13C-NMR, HR-MS and FT-IR) methods and their purity was proven by elemental analysis, thin layer chromatography and high pressure liquid chromatography. These compounds were evaluated for in vitro anticancer activity by using MTS method against PC-3 and DU-143 (androgen-independent human prostate cancer cell lines) and LNCaP (androgen-sensitive human prostate adenocarcinoma) prostate cancer cell lines. Cisplatin was used as the positive sensitivity reference standard. Compounds (7a-m) exhibited anticancer activity with IC50 values of 87.2-400 µM against prostate cancer cell lines.

Keywords

References

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Details

Primary Language

English

Subjects

Pharmaceutical Chemistry

Journal Section

Research Article

Publication Date

June 27, 2025

Submission Date

April 4, 2018

Acceptance Date

May 22, 2018

Published in Issue

Year 2018 Volume: 22 Number: 4

APA
Han, M. İ., Bekçi, H., Cumaoğlu, A., & Küçükgüzel, Ş. G. (2025). Synthesis and characterization of 1,2,4-triazole containing hydrazide-hydrazones derived from (S)-Naproxen as anticancer agents. Journal of Research in Pharmacy, 22(4), 559-569. https://doi.org/10.12991/jrp.2018.98
AMA
1.Han Mİ, Bekçi H, Cumaoğlu A, Küçükgüzel ŞG. Synthesis and characterization of 1,2,4-triazole containing hydrazide-hydrazones derived from (S)-Naproxen as anticancer agents. J. Res. Pharm. 2025;22(4):559-569. doi:10.12991/jrp.2018.98
Chicago
Han, Muhammed İhsan, Hatice Bekçi, Ahmet Cumaoğlu, and Ş. Güniz Küçükgüzel. 2025. “Synthesis and Characterization of 1,2,4-Triazole Containing Hydrazide-Hydrazones Derived from (S)-Naproxen As Anticancer Agents”. Journal of Research in Pharmacy 22 (4): 559-69. https://doi.org/10.12991/jrp.2018.98.
EndNote
Han Mİ, Bekçi H, Cumaoğlu A, Küçükgüzel ŞG (June 1, 2025) Synthesis and characterization of 1,2,4-triazole containing hydrazide-hydrazones derived from (S)-Naproxen as anticancer agents. Journal of Research in Pharmacy 22 4 559–569.
IEEE
[1]M. İ. Han, H. Bekçi, A. Cumaoğlu, and Ş. G. Küçükgüzel, “Synthesis and characterization of 1,2,4-triazole containing hydrazide-hydrazones derived from (S)-Naproxen as anticancer agents”, J. Res. Pharm., vol. 22, no. 4, pp. 559–569, June 2025, doi: 10.12991/jrp.2018.98.
ISNAD
Han, Muhammed İhsan - Bekçi, Hatice - Cumaoğlu, Ahmet - Küçükgüzel, Ş. Güniz. “Synthesis and Characterization of 1,2,4-Triazole Containing Hydrazide-Hydrazones Derived from (S)-Naproxen As Anticancer Agents”. Journal of Research in Pharmacy 22/4 (June 1, 2025): 559-569. https://doi.org/10.12991/jrp.2018.98.
JAMA
1.Han Mİ, Bekçi H, Cumaoğlu A, Küçükgüzel ŞG. Synthesis and characterization of 1,2,4-triazole containing hydrazide-hydrazones derived from (S)-Naproxen as anticancer agents. J. Res. Pharm. 2025;22:559–569.
MLA
Han, Muhammed İhsan, et al. “Synthesis and Characterization of 1,2,4-Triazole Containing Hydrazide-Hydrazones Derived from (S)-Naproxen As Anticancer Agents”. Journal of Research in Pharmacy, vol. 22, no. 4, June 2025, pp. 559-6, doi:10.12991/jrp.2018.98.
Vancouver
1.Muhammed İhsan Han, Hatice Bekçi, Ahmet Cumaoğlu, Ş. Güniz Küçükgüzel. Synthesis and characterization of 1,2,4-triazole containing hydrazide-hydrazones derived from (S)-Naproxen as anticancer agents. J. Res. Pharm. 2025 Jun. 1;22(4):559-6. doi:10.12991/jrp.2018.98

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