Synthesis and Biological Evaluation of Some Novel 3‐Thioether‐Linked 1,2,4‐Triazole‐Furoate Hybrids

ABSTRACT Herein, we report the successful synthesis of some novel 3‐thioether‐linked 1,2,4‐triazole‐furoate hybrids ( 2a–f and 3a–c ) in excellent yields. Structural characterization of all the compounds was accomplished via NMR spectroscopy and X‐ray crystallography for 2f (CCDC No. 2457105), confirming the formation of the target hybrids. Biological evaluation revealed notably diverse bioactivities: antiproliferative activities of all the compounds against PANC‐1 and three compounds against Huh7 cells were evaluated via CCK‐8 assay, with 3c showing obvious efficacy (IC 50 = 20.37 μg/mL against Huh7). Significantly, 2a displayed potent growth‐promoting effects on the Gram‐negative bacterium Pseudomonas aeruginosa and the fungus Candida albicans , with remarkable promotion rates of 5525.00% and 500%, respectively. In contrast, it exhibited moderate inhibitory effects against Staphylococcus aureus (31.25%), Escherichia coli (55.56%), and Klebsiella pneumoniae (18.75%). 2b , 2d , 2f , and 3b showed remarkable growth‐promoting effects on both wheat stalks and radicles at a concentration of 100 ppm, with their promotion rates reaching 96.3% and 123.9%, 113.5% and 137.9%, 126.1% and 177.7%, 99.4% and 107.6%, respectively, indicating their potential as wheat growth promoters.

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Journal
Journal of Heterocyclic Chemistry
Published
2025-09-04
DOI
https://doi.org/10.1002/jhet.70091
Primary Topic
Synthesis of Organic Compounds
Type
article
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article

Synthesis and Biological Evaluation of Some Novel 3‐Thioether‐Linked 1,2,4‐Triazole‐Furoate Hybrids

Silei Wang, Tongjun Chen, Jiaxin Wu, S. CAI et al.
Journal of Heterocyclic Chemistry
Synthesis of Organic Compounds
article

Synthesis and Biological Evaluation of Some Novel 3‐Thioether‐Linked 1,2,4‐Triazole‐Furoate Hybrids

Silei Wang, Tongjun Chen, Jiaxin Wu, S. CAI, Qi-Chun Ding, Huili Liu, Qiuling Li, Yimin Cai, Yuanjun Zeng, Xuexin Xu
article en

Abstract

ABSTRACT Herein, we report the successful synthesis of some novel 3‐thioether‐linked 1,2,4‐triazole‐furoate hybrids ( 2a–f and 3a–c ) in excellent yields. Structural characterization of all the compounds was accomplished via NMR spectroscopy and X‐ray crystallography for 2f (CCDC No. 2457105), confirming the formation of the target hybrids. Biological evaluation revealed notably diverse bioactivities: antiproliferative activities of all the compounds against PANC‐1 and three compounds against Huh7 cells were evaluated via CCK‐8 assay, with 3c showing obvious efficacy (IC 50 = 20.37 μg/mL against Huh7). Significantly, 2a displayed potent growth‐promoting effects on the Gram‐negative bacterium Pseudomonas aeruginosa and the fungus Candida albicans , with remarkable promotion rates of 5525.00% and 500%, respectively. In contrast, it exhibited moderate inhibitory effects against Staphylococcus aureus (31.25%), Escherichia coli (55.56%), and Klebsiella pneumoniae (18.75%). 2b , 2d , 2f , and 3b showed remarkable growth‐promoting effects on both wheat stalks and radicles at a concentration of 100 ppm, with their promotion rates reaching 96.3% and 123.9%, 113.5% and 137.9%, 126.1% and 177.7%, 99.4% and 107.6%, respectively, indicating their potential as wheat growth promoters.

Journal of Heterocyclic ChemistryVol. 62(11)
Zhangzhou Vocational and Technical College (CN)
Openalex Percentile: Top 74%
Synthesis of Organic Compounds
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Synthesis and Biological Evaluation of Some Novel 3‐Thioether‐Linked 1,2,4‐Triazole‐Furoate Hybrids — Silei Wang, Tongjun Chen, et al. · Journal of Heterocyclic Chemistry (2025) | TGRS Research Map | TGRS