Das, Ananta Kumar Islam, A. F. M. Mahmudul Rouf, Md. Abdur Paul, Prosenjit Hassan, Md. Jahid Roy, Saurabh Esha, Esrat Jahan Hossain, Md. Selim Hossain, Md. Monir Hossain, Md. Emdad Saha, Koushik 2025-01-07T05:30:44Z 2025-01-07T05:30:44Z 2024-12-30 2024-12 https://pubs.kist.re.kr/handle/201004/151491 The study aims to synthesize benzamide derivatives of p-aminophenol (PAP) by reacting with 4-benzoyl chloride. The reaction of PAP yields four derivatives: P-1 [N-(4-hydroxyphenyl)benzamide], P-2 [4 &apos;-bromo-N-(4-hydroxyphenyl)benzamide], P-3 [4 &apos;-nitro-N-(4-hydroxyphenyl)benzamide] and P-4 [3 &apos;,5 &apos;-dintro-N-(4-hydroxyphenyl)benzamide] and evaluation of biological activity. PAP derivatives hot plate analgesic test produced a significant analgesic effect. The higher analgesic activities were observed at 60 min for all derivatives P-1, P-2, P-3, and P-4 at 47.65, 48.13, 47.08, and 45.47%, respectively. Derivatives of PAP were also shown to have statistically significant (p < 0.001) analgesic efficacy in the writhing test. The maximum percent inhibition of the writhing by P-2 (82.11%). In vivo anti-inflammatory examination confirmed that P-1, P-2, and P-4 prevented carrageenan-induced rat paw edema for 60-240 min. The toxicity of PAP derivatives P-1 and P-4 was lower than paracetamol. Experiments demonstrate that derivatives exhibit less cytotoxicity. The compounds P-3 and P-4 inhibited egg and bovine albumin denaturation better at lower dosages in anti-inflammatory experiments. Molecular docking and ADMET showed that derivatives might inhibit COX-1 and COX-2. Also, P-4 demonstrated the highest binding affinity (-8.2 kcal/mol) for COX-1 and P-1 (-8.4 kcal/mol) for COX-2. According to computational and experimental studies, PAP derivatives may inhibit cyclooxygenase to relieve pain, inflammation, and fever. English WILEY-V C H VERLAG GMBH Synthesis and Biological Evaluation of p-Aminophenol Derivatives Applying In Vivo, Ex Vivo, and In Silico Approach Article 10.1002/slct.202404333 1 ChemistrySelect, v.9, no.46 ChemistrySelect 9 46 N scie scopus 001373515000001 2-s2.0-85211480909 Chemistry, Multidisciplinary Chemistry Article PARACETAMOL MECHANISM ACETAMINOPHEN Analgesic Anti-inflammatory Antipyretic Molecular docking PAP