Fig. 1From: Two methoxy derivatives of resveratrol, 3,3′,4,5′-tetramethoxy-trans-stilbene and 3,4′,5-trimethoxy-trans-stilbene, suppress lipopolysaccharide-induced inflammation through inactivation of MAPK and NF-κB pathways in RAW 264.7 cellsChemical structures of a 3,4′,5-trans-trihydroxystilbene (resveratrol), b 3,3′,4,5′-tetramethoxy-trans-stilbene (3,3′,4,5′-TMS), and c 3,4′,5-trimethoxy-trans-stilbene (3,4′,5-TMS)Back to article page