Article detail · 2022
Exploration of 1,2,3-triazole linked benzenesulfonamide derivatives as isoform selective inhibitors of human carbonic anhydrase
Journal
BIOORGANIC & MEDICINAL CHEMISTRYISSN 0968-0896
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YÖKSİS
OpenAlex
Open access · green
SJR Q2
JCR Q1
Citations 101
Top 10%
Percentile 98.4%
FWCI 7.43
- Year
- 2022
- Type
- article
Data source split
- YÖKSİS YÖKSİS article record
- YÖKSİS venue BIOORGANIC & MEDICINAL CHEMISTRY
- Catalog match (ISSN) Bioorganic and Medicinal Chemistry
- OpenAlex OpenAlex enrichment (abstract, citations, topics)
Abstract
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Topics
Citations
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101 citations
OpenAlex cited_by_count (cache / database)
160 publications in the local catalog that cite this work (OpenAlex reference match; not the full global list).
- Discovery of novel benzenesulfonamides incorporating 1,2,3-triazole scaffold as carbonic anhydrase I, II, IX, and XII inhibitors 2023
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- Enzyme inhibition, molecular docking, and density functional theory studies of new thiosemicarbazones incorporating the 4‐hydroxy‐3,5‐dimethoxy benzaldehyde motif 2023
- Synthesis and characterization of novel acyl hydrazones derived from vanillin as potential aldose reductase inhibitors 2023
- Enzyme inhibition, molecular docking, and density functional theory studies of new thiosemicarbazones incorporating the 4‐hydroxy‐3,5‐dimethoxy benzaldehyde motif 2022
- Novel spiroindoline derivatives targeting aldose reductase against diabetic complications: Bioactivity, cytotoxicity, and molecular modeling studies 2024
- Novel spiroindoline derivatives targeting aldose reductase against diabetic complications: Bioactivity, cytotoxicity, and molecular modeling studies 2024