@article{ajps20251312,
author={{Kumar, Utsav and Sharma, Nitin and Tyagi, Harsh and Ajeet, Ajeet and Kumar, Babita and Ain, Shabnam and Ain, Qurratul},
title={Designing and Evaluation of Novel Thiazole Derivatives As COX Inhibitor by <i>Iv</i>lcb: <i>In-vitro</i> Like Computational Bioassay &amp; Docking Analysis},
journal={American Journal of Pharmacological Sciences},
volume={13},
number={1},
pages={6--18},
year={2025},
url={https://pubs.sciepub.com/ajps/13/1/2},
issn={2327-672X},
abstract={COX (Cyclooxygenase) is also known as prostaglandin-endoperoxide synthase (PTGS) which is responsible for inflammation and related issues. In the present study eleven thiazole derivatives were designed and computationlly evaluated for their inhibitory activity against COX enzyme. All eleven novel designed molecules were evaluated by <i>Iv</i>LCB: <i>In-vitro</i> like computational bioassay and SwissDock. These molecules were also evaluated for their ADME descriptors and bioactivity prediction using Molinspiration for bioacitivity scores for the drug targets like GPCR ligands, kinase inhibitors, ion channel modulators, nuclear receptors etc. As per the analysis done it was found that designed molecule 2A8 shows High activity pattern, good % inhibition and strong binding ability to PDB ID: 4M11 with 14 hydrogen bonds and binding affinity of -10 kcal/mol.},
doi={10.12691/ajps-13-1-2}
publisher={Science and Education Publishing}
}