Discovery of novel thiazole derivatives containing pyrazole scaffold as PPAR-γ Agonists, α-Glucosidase, α-Amylase and COX-2 inhibitors; Design, synthesis and in silico study.
- DOI
- 10.1016/j.bioorg.2024.107760
- Published
- 2024 Nov
- Container
- Bioorganic chemistry
- Publisher
- Not recorded
- Open access
- no
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Cite this work
BibTeX
@article{allodium:10.1016/j.bioorg.2024.107760,
title = {Discovery of novel thiazole derivatives containing pyrazole scaffold as PPAR-γ Agonists, α-Glucosidase, α-Amylase and COX-2 inhibitors; Design, synthesis and in silico study.},
author = {Fadaly WAA and Elshewy A and Nemr MTM and Abdou K and Sayed AM and Kahk NM},
year = {2024},
journal = {Bioorganic chemistry},
doi = {10.1016/j.bioorg.2024.107760},
url = {https://doi.org/10.1016/j.bioorg.2024.107760}
}RIS
TY - JOUR TI - Discovery of novel thiazole derivatives containing pyrazole scaffold as PPAR-γ Agonists, α-Glucosidase, α-Amylase and COX-2 inhibitors; Design, synthesis and in silico study. AU - Fadaly WAA AU - Elshewy A AU - Nemr MTM AU - Abdou K AU - Sayed AM AU - Kahk NM PY - 2024 JO - Bioorganic chemistry DO - 10.1016/j.bioorg.2024.107760 UR - https://doi.org/10.1016/j.bioorg.2024.107760 ER -
APA
WAA, F., A, E., MTM, N., K, A., AM, S., & NM, K. (2024). Discovery of novel thiazole derivatives containing pyrazole scaffold as PPAR-γ Agonists, α-Glucosidase, α-Amylase and COX-2 inhibitors; Design, synthesis and in silico study.. Bioorganic chemistry. https://doi.org/10.1016/j.bioorg.2024.107760
Source records
- pubmed · retrieved 2026-11-11T01:00:36.879Z
- europe-pmc · retrieved 2026-11-11T01:00:36.905Z