Title : Palmitoylethanolamide, a naturally occurring lipid, is an orally effective intestinal anti-inflammatory agent.

Pub. Date : 2015 Jan

PMID : 25205418






4 Functional Relationships(s)
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1 BACKGROUND AND PURPOSE: Palmitoylethanolamide (PEA) acts via several targets, including cannabinoid CB1 and CB2 receptors, transient receptor potential vanilloid type-1 (TRPV1) ion channels, peroxisome proliferator-activated receptor alpha (PPAR alpha) and orphan G protein-coupled receptor 55 (GRR55), all involved in the control of intestinal inflammation. palmidrol transient receptor potential cation channel, subfamily V, member 1 Mus musculus
2 BACKGROUND AND PURPOSE: Palmitoylethanolamide (PEA) acts via several targets, including cannabinoid CB1 and CB2 receptors, transient receptor potential vanilloid type-1 (TRPV1) ion channels, peroxisome proliferator-activated receptor alpha (PPAR alpha) and orphan G protein-coupled receptor 55 (GRR55), all involved in the control of intestinal inflammation. palmidrol transient receptor potential cation channel, subfamily V, member 1 Mus musculus
3 BACKGROUND AND PURPOSE: Palmitoylethanolamide (PEA) acts via several targets, including cannabinoid CB1 and CB2 receptors, transient receptor potential vanilloid type-1 (TRPV1) ion channels, peroxisome proliferator-activated receptor alpha (PPAR alpha) and orphan G protein-coupled receptor 55 (GRR55), all involved in the control of intestinal inflammation. palmidrol transient receptor potential cation channel, subfamily V, member 1 Mus musculus
4 BACKGROUND AND PURPOSE: Palmitoylethanolamide (PEA) acts via several targets, including cannabinoid CB1 and CB2 receptors, transient receptor potential vanilloid type-1 (TRPV1) ion channels, peroxisome proliferator-activated receptor alpha (PPAR alpha) and orphan G protein-coupled receptor 55 (GRR55), all involved in the control of intestinal inflammation. palmidrol transient receptor potential cation channel, subfamily V, member 1 Mus musculus