Total Synthesis and Anti-inflammatory Evaluation of Penchinone A and Its Structural Analogues.
J Org Chem
; 82(21): 11566-11572, 2017 11 03.
Article
em En
| MEDLINE
| ID: mdl-29019238
ABSTRACT
The first total synthesis and biological evaluation of penchinone A and its structural analogues are described. The key steps for the preparation of penchinone A derivatives involve the oxime-directed palladium(II)-catalyzed oxidative acylation, Claisen rearrangement, and base-mediated olefin migration. This transformation efficiently provides a range of allyl-substituted biaryl ketones with site-selectivity and functional group compatibility. In addition, all synthetic compounds were screened for anti-inflammatory activity against nitric oxide (NO), tumor necrosis factor alpha (TNF-α), and interleukin-6 (IL-6) with lipopolysaccharide (LPS)-induced RAW264.7 cells. Generally, a range of penchinone A derivatives potently inhibited NO, TNF-α, and IL-6 productions, compared to dexamethasone as a positive control. Notably, penchinone A (8g) and its derivatives (8e and 8f) were found to exhibit anti-inflammatory activity stronger than that of dexamethasone.
Texto completo:
1
Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Anti-Inflamatórios não Esteroides
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Interleucina-6
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Fator de Necrose Tumoral alfa
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Lignanas
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Óxido Nítrico
Limite:
Animals
Idioma:
En
Ano de publicação:
2017
Tipo de documento:
Article