Target intelligence / Profile preview

Carboxylesterase 1d (Ces1d (mouse); sometimes CES1D is used in literature)

Target
Ces1d (mouse); sometimes CES1D is used in literature
Molecular classification
Enzyme, Serine hydrolase, Lipase, Alpha/beta fold hydrolase family
01

Overview

Carboxylesterase 1d (Ces1d) is a member of the carboxylesterase family of enzymes found predominantly in mouse liver, lung, and adipose tissue[4][5]. It belongs to the serine hydrolase superfamily and regulates hydrolysis of neutral lipids such as triacylglycerols and cholesterol esters, as well as xenobiotic esters and amides[6]. Ces1d is essential for intracellular lipid and cholesterol homeostasis and is a major metabolic enzyme in lung and liver tissues, especially alveolar macrophages[5]. It is involved in the breakdown of lipid mediators and participates in immune regulation, being a target of organophosphate toxins. While the exact role of Ces1d in cholesterol ester hydrolysis remains debated, its knockout impairs regulation of inflammation and may disrupt cholesterol efflux in experimental models[6]. Ces1d is considered a key metabolic enzyme relevant for pharmacology, toxicology, and metabolic disease research in mice[5][6].

Other names
Ces1dCes1d proteinhepatic carboxylesteraseserine esterase 1d
02

Mechanism of action

Drug metabolism via hydrolysis of ester and amide bonds in drugs and prodrugs. Lipid hydrolysis (triacylglycerol, thioester, cholesterol ester metabolism). Regulation of lipid-derived signaling molecules, effect on immune cells.

03

Biological functions

Drug metabolism (hydrolysis of esters, amides, and xenobiotics)Lipid metabolism (hydrolyzes triacylglycerols and participates in cholesterol ester metabolism)Regulation of intracellular cholesterol availability and effluxImmunomodulation via effects on lipid mediatorsDetoxification (target of organophosphate poisoning)
04

Disease associations

Inflammation (modulates immune cell response and inflammatory mediators)Metabolic disease (involvement in lipid/cholesterol metabolism)Potential role in atherosclerosis (controversial)No direct link to cancer or neurodegenerative disease established in mouse, but human CES1 is involved in cancer and metabolic syndrome
05

Safety considerations

Inhibition by organophosphates may lead to impaired immune response and increased susceptibility to poisoningGenetic manipulation (knockout) can alter cholesterol and lipid metabolism, affecting inflammation and metabolic balancePotential off-target effects in drug development due to broad substrate specificity
06

Interacting drugs

Organophosphate pesticides (inhibit activity)

2 more in the full profile.

07

Biomarkers

Ces1d expression levels in mouse lung and alveolar macrophages as indicator of inflammation and lipid metabolic statusCES1 genetic variants in humans are used for pharmacogenomic profiling for drug response (no established clinical biomarker in mouse)

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