Design, synthesis, characterization and non-steroidal anti-inflammatory activity of novel oxazolone derivatives
By: Muthubhupathi, G
.
Contributor(s): Selvakumar, M.
Publisher: Raipur Asian Pharma Press 2023Edition: Vol.13(3), Jul-Sep.Description: 145-152p.Subject(s): PHARMACEUTICSOnline resources: Click here
In:
Asian journal of pharmaceutical researchSummary: An innovative sequence of Oxazolone derivatives were synthesized via chemical reaction including Preparation of benzoyl glycine crystals and Synthesis of oxazolone derivatives. The synthesized compounds such as P- Chlorobenaldehyde, 4-Fluro benaldehyde, Cinnamaldehyde, 2-Chloro benaldehyde, and O- Anisaldehyde were elucidated by Fourier Transform-Infra Red (FT-IR) spectrometer and showed its corresponding peaks. The in- vitro anti-inflammatory activity of synthesized compounds by protein denaturation assay exhibited very good significant anti-inflammatory activity. Additionally, the test compounds 2-Chloro benzaldehyde had nearest IC50 value to the standard diclofenac sodium when compared to all other test compounds, and demonstrated highest zone of inhibition at the low concentration used to exhibit the high potency.
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Articles Abstract Database
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School of Pharmacy Archieval Section | Not for loan | 2023-1648 |
An innovative sequence of Oxazolone derivatives were synthesized via chemical reaction including Preparation of benzoyl glycine crystals and Synthesis of oxazolone derivatives. The synthesized compounds such as P- Chlorobenaldehyde, 4-Fluro benaldehyde, Cinnamaldehyde, 2-Chloro benaldehyde, and O- Anisaldehyde were elucidated by Fourier Transform-Infra Red (FT-IR) spectrometer and showed its corresponding peaks. The in- vitro anti-inflammatory activity of synthesized compounds by protein denaturation assay exhibited very good significant anti-inflammatory activity. Additionally, the test compounds 2-Chloro benzaldehyde had nearest IC50 value to the standard diclofenac sodium when compared to all other test compounds, and demonstrated highest zone of inhibition at the low concentration used to exhibit the high potency.
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