SYNTHESIS AND PHARMACOLOGICAL EVALUATION OF NOVEL ACETAMIDE DERIVATIVES FOR ANTIPSYCHOTIC ACTIVITY

Abstract: - The present study reports the synthesis and pharmacological evaluation of a series of novel acetamide derivatives designed to explore their potential antipsychotic activity. The compounds were synthesized through standard acylation techniques, and their structures were confirmed using FT-IR, ^1H-NMR, ^13C-NMR, and mass spectrometry. The synthesized derivatives were screened using established behavioral models in rodents, including amphetamine-induced hyperlocomotion and apomorphine-induced stereotypy. Several compounds showed significant reductions in hyperactivity and stereotypic movements, indicating possible dopamine receptor antagonism. Catalepsy assessments were performed to evaluate extrapyramidal side-effect liability, and select derivatives exhibited favorable activity with minimal motor impairment compared to reference antipsychotic drugs. Preliminary structure–activity relationship analysis suggested that specific substituent modifications enhanced pharmacological responses. Overall, the findings indicate that these novel acetamide derivatives may serve as promising lead molecules for further development of safer and more effective antipsychotic agents.

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Publication Details

Journal
Zenodo (CERN European Organization for Nuclear Research)
Published
2025-11-21
DOI
https://doi.org/10.5281/zenodo.17838223
Primary Topic
Pharmacological Receptor Mechanisms and Effects
Type
article
Field-Weighted Citation Impact
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article

SYNTHESIS AND PHARMACOLOGICAL EVALUATION OF NOVEL ACETAMIDE DERIVATIVES FOR ANTIPSYCHOTIC ACTIVITY

Zenodo (CERN European Organization for Nuclear Research)
Pharmacological Receptor Mechanisms and Effects
article

SYNTHESIS AND PHARMACOLOGICAL EVALUATION OF NOVEL ACETAMIDE DERIVATIVES FOR ANTIPSYCHOTIC ACTIVITY

article en

Abstract

Abstract: - The present study reports the synthesis and pharmacological evaluation of a series of novel acetamide derivatives designed to explore their potential antipsychotic activity. The compounds were synthesized through standard acylation techniques, and their structures were confirmed using FT-IR, ^1H-NMR, ^13C-NMR, and mass spectrometry. The synthesized derivatives were screened using established behavioral models in rodents, including amphetamine-induced hyperlocomotion and apomorphine-induced stereotypy. Several compounds showed significant reductions in hyperactivity and stereotypic movements, indicating possible dopamine receptor antagonism. Catalepsy assessments were performed to evaluate extrapyramidal side-effect liability, and select derivatives exhibited favorable activity with minimal motor impairment compared to reference antipsychotic drugs. Preliminary structure–activity relationship analysis suggested that specific substituent modifications enhanced pharmacological responses. Overall, the findings indicate that these novel acetamide derivatives may serve as promising lead molecules for further development of safer and more effective antipsychotic agents.

Zenodo (CERN European Organization for Nuclear Research)
IFTM University (IN)
Openalex Percentile: Top 42%
Pharmacological Receptor Mechanisms and Effects
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