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Chinese Journal of Natural Medicines (English Ed.) ; (6): 545-550, 2021.
Article Dans Anglais | WPRIM | ID: wpr-888784

Résumé

For local treatment of ulcerative colitis, a new azoreductase driven prodrug CDDO-AZO from bardoxolone methyl (CDDO-Me) and 5-aminosalicylate (5-ASA) was designed, synthesized and biologically evaluated. It is proposed that orally administrated CDDO-AZO is stable before reaching the colon, while it can also be triggered by the presence of azoreductase in the colon to fragment into CDDO-Me and 5-ASA, generating potent anti-colitis effects. Superior to olsalazine (OLS, a clinically used drug for ulcerative colitis) and CDDO-Me plus 5-ASA, CDDO-AZO significantly attenuated inflammatory colitis symptoms in DSS-induced chronic colitis mice, which suggested that CDDO-AZO may be a promising anti-ulcerative colitis agent.


Sujets)
Animaux , Souris , Colite/traitement médicamenteux , Mésalazine/pharmacologie , Nitroréductases , Acide oléanolique/pharmacologie , Promédicaments
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