Novel 1,4‐Disubstituted 1,2,3‐Triazoles Accessed via Click Chemistry: Their Molecular Docking, Anti‐inflammatory and Antioxidant Evaluation

Abstract The present research highlights a simple method for the preparation of novel triazoles using click chemistry, which were fully characterized using 1 H and 13 C NMR, as well as HRMS analytical techniques. All triazole derivatives were further evaluated for their antioxidant and anti‐inflammatory properties, along with ADME and molecular docking studies. The in vitro anti‐inflammatory activity of the synthesized triazoles 4c and 4d showed significant IC 50 values of 34.12 ± 0.55 µg/mL and 35.57 ± 0.35 µg/mL, respectively, and was further supported by DPPH assay results with IC 50 values of 37.29 ± 0.86 µg/mL and 41.50 ± 0.68 µg/mL for 4c and 4d, respectively. The biological data were promising, while molecular docking provided insights into their binding interactions. Additionally, ADME analysis further supported their potential as drug candidates.

Authors

Institutions

Publication Details

Journal
ChemistrySelect
Published
2025-08-01
DOI
https://doi.org/10.1002/slct.202501657
Citations
1
Primary Topic
Click Chemistry and Applications
Type
article
Field-Weighted Citation Impact
0.94

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Novel 1,4‐Disubstituted 1,2,3‐Triazoles Accessed via Click Chemistry: Their Molecular Docking, Anti‐inflammatory and Antioxidant Evaluation

Prakash N. Chavan, Padma B. Dandge, Shankar Hangirgekar, Sneha Rochlani et al.
1 citations
ChemistrySelect
Click Chemistry and Applications
0.94
article

Novel 1,4‐Disubstituted 1,2,3‐Triazoles Accessed via Click Chemistry: Their Molecular Docking, Anti‐inflammatory and Antioxidant Evaluation

Prakash N. Chavan, Padma B. Dandge, Shankar Hangirgekar, Sneha Rochlani, Pramod S. Patil, Nisha Nerlekar, Sandeep Sankpal, Akshay Gurav, Prasad Swami, Lalit Bhosale, Prashant D. Ladkat
article en
1 citations

Abstract

Abstract The present research highlights a simple method for the preparation of novel triazoles using click chemistry, which were fully characterized using 1 H and 13 C NMR, as well as HRMS analytical techniques. All triazole derivatives were further evaluated for their antioxidant and anti‐inflammatory properties, along with ADME and molecular docking studies. The in vitro anti‐inflammatory activity of the synthesized triazoles 4c and 4d showed significant IC 50 values of 34.12 ± 0.55 µg/mL and 35.57 ± 0.35 µg/mL, respectively, and was further supported by DPPH assay results with IC 50 values of 37.29 ± 0.86 µg/mL and 41.50 ± 0.68 µg/mL for 4c and 4d, respectively. The biological data were promising, while molecular docking provided insights into their binding interactions. Additionally, ADME analysis further supported their potential as drug candidates.

ChemistrySelectVol. 10(30)
Shivaji University (IN), Rayat Shikshan Sanstha (IN), Atmiya University (IN), Dr. Vitthalrao Vikhe Patil Foundation’s Medical College (IN), Bharati Vidyapeeth (Deemed to be University) (IN)
Shivaji University, Kolhapur, Science and Engineering Research Board
Openalex Percentile: Top 23%
Click Chemistry and Applications
0.94
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.