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Lipases are esterase enzymes that catalyze the hydrolysis of ester bonds within hydrophobic lipids. The diverse class of lipase enzymes includes diacylglycerol lipase (DAGL) and lipoprotein lipase (LPL) and endothelial lipase (LIPG).
|Cat No||Product Name / Activity|
|Endothelial lipase and lipoprotein lipase inhibitor|
|Pancreatic, gastric and carboxylester lipase inhibitor; antiobesity and antihypercholesterolemic activity|
|Diacylglycerol lipase inhibitor|
|Selective endothelial lipase inhibitor; orally bioavailable|
Lipases are esterase enzymes that catalyze the hydrolysis of ester bonds within hydrophobic lipids. This is a diverse class of enzymes and includes diacylglycerol lipase and lipoprotein lipase (E.C. 18.104.22.168), and endothelial lipase (E.C. 22.214.171.124).
Diacylglycerol lipase (DAGL) catalyzes the conversion of 1,2,diacylglycerol (DAG) into the endocannabinol, 2'arachidonylglycerol (2'AG). 2'AG is a cannabinoid receptor 1 (CB1) agonist and is involved in the inhibition of neurotransmitter release. There are two DAGL isoforms; DAGLα and DAGLβ. Both isoforms are associated with the plasma membrane and are stimulated by Ca2+. They are found throughout the central nervous system, where they appear to be targeted exclusively to post-synaptic neuronal membranes.
Endothelial lipase (LIPG) is a vascular lipase which is synthesized in endothelial cells. LIPG hydrolyzes the phospholipids of VLDL, chylomicrons and HDL; it also displays triglyceride lipase activity.
Lipoprotein lipase (LPL), like LIPG, is a vascular lipase, however it is not synthesized in endothelial cells. It is anchored to the capillary endothelium by proteoglycans and catalyzes the hydrolysis of triglycerides to release free fatty acids into the circulation. LPL therefore initiates the processing of triglyceride-rich lipoproteins such as chylomicrons and VLDL.
Tocris offers the following scientific literature for Lipases to showcase our products. We invite you to request* or download your copy today!
*Please note that Tocris will only send literature to established scientific business / institute addresses.
|Gene||Species||Gene Symbol||Gene Accession No.||Protein Accession No.|