Design, Synthesis, in Silico and in Vitro Dipeptidyl Peptidase‐4 Activity of Triazole‐Based Heterocyclic Compounds

1,2,3-triazole-based ring connected with pyridazine, triazine, methyl pyrazole, diphenyl pyrazole, and phthalimide moieties through propylene linker has been synthesized for antidiabetic evaluation via click chemistry. The antidiabetic evaluations have been done by molecular docking studies and in-vitro tests against the dipeptidyl peptidase-4 (DPP-4) enzyme. The molecular docking studies have revealed that compounds 22, 23, 29, and 30 showed hydrogen bonds with the DPP-4 enzyme while in-vitro tests have revealed that compound 30 has (IC<sub>50</sub> values 12.82 nM), exhibited potent activity compared to the standard drug, sitagliptin (14.8 nM). Among the heterocyclic compounds, phthalimide and pyrazole derivatives were found more potent for DPP-4 inhibitors.

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Journal
Chemistry & Biodiversity
Published
2024-12-24
DOI
https://doi.org/10.1002/cbdv.202402381
Primary Topic
Click Chemistry and Applications
Type
article
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article

Design, Synthesis, in Silico and in Vitro Dipeptidyl Peptidase‐4 Activity of Triazole‐Based Heterocyclic Compounds

Manisha Nidhar, Ranjeet Ranjan Kumar, Ashish Kumar Tewari
Chemistry & Biodiversity
Click Chemistry and Applications
article

Design, Synthesis, in Silico and in Vitro Dipeptidyl Peptidase‐4 Activity of Triazole‐Based Heterocyclic Compounds

Manisha Nidhar, Ranjeet Ranjan Kumar, Ashish Kumar Tewari
article en

Abstract

1,2,3-triazole-based ring connected with pyridazine, triazine, methyl pyrazole, diphenyl pyrazole, and phthalimide moieties through propylene linker has been synthesized for antidiabetic evaluation via click chemistry. The antidiabetic evaluations have been done by molecular docking studies and in-vitro tests against the dipeptidyl peptidase-4 (DPP-4) enzyme. The molecular docking studies have revealed that compounds 22, 23, 29, and 30 showed hydrogen bonds with the DPP-4 enzyme while in-vitro tests have revealed that compound 30 has (IC<sub>50</sub> values 12.82 nM), exhibited potent activity compared to the standard drug, sitagliptin (14.8 nM). Among the heterocyclic compounds, phthalimide and pyrazole derivatives were found more potent for DPP-4 inhibitors.

Chemistry & BiodiversityVol. 22(5)
University of Allahabad (IN), Banaras Hindu University (IN)
Openalex Percentile: Top 82%
Click Chemistry and Applications
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Design, Synthesis, in Silico and in Vitro Dipeptidyl Peptidase‐4 Activity of Triazole‐Based Heterocyclic Compounds — Manisha Nidhar, Ranjeet Ranjan Kumar, et al. · Chemistry & Biodiversity (2024) | TGRS Research Map | TGRS