| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1376053 | Bioorganic & Medicinal Chemistry Letters | 2007 | 7 Pages |
Amide derivatives of 5,6-dimethoxy-2,3-dihydro-1H-inden(-1-yl)acetic acid were synthesized and evaluated for their anti-inflammatory and analgesic activity. Few selected compounds were also screened for their antipyretic, anti-arthritic, and ulcerogenic potential. Most of the compounds exhibited good activity profile and were free of gastrointestinal toxicity of common NSAIDs. However these compounds failed to decrease secondary lesions of adjuvant induced arthritis and also did not inhibit TNF-α in lipopolysaccharide induced pyresis.
Graphical abstractA series of 5,6-dimethoxy-2,3-dihydro-1H-inden(-1-yl)acetic acid amides were synthesized and screened for their anti-inflammatory and related biological activities. The synthesized compounds showed long duration of anti-inflammatory activity and were free from ulcerogenicity liability of common NSAIDs.Figure optionsDownload full-size imageDownload as PowerPoint slide
