Target intelligence / Profile preview

Carnitine O-octanoyltransferase (CROT)

Target
CROT
Molecular classification
Enzyme, Transferase, Acyltransferase
01

Overview

Carnitine O-octanoyltransferase (CROT) is a peroxisomal enzyme involved in fatty acid metabolism, catalyzing the reversible transfer of medium-chain acyl groups from acyl-CoA to carnitine to form acyl-carnitine, which enables export of partially oxidized fatty acids from peroxisomes for further mitochondrial β-oxidation[1][2][3]. CROT thereby acts as a metabolic bridge between peroxisomal and mitochondrial fatty acid oxidation pathways and contributes to cellular lipid and energy homeostasis[1][3]. Regulation of CROT affects not only energy production but also the abundance of lipid-derived signaling molecules, and CROT has been implicated in pathological processes such as vascular calcification and metabolic disorders[2][3]. Genetic or pharmacological modulation of CROT leads to changes in the levels of omega-3 fatty acids and dicarboxylic acids, suggesting potential for biomarker development and therapeutic intervention in cardiovascular and metabolic diseases[2].

Other names
Peroxisomal carnitine O-octanoyltransferaseCOTCarnitine medium-chain acyltransferaseMedium-chain/long-chain carnitine acyltransferaseEasily solubilized mitochondrial carnitine palmitoyltransferaseOvert mitochondrial carnitine palmitoyltransferasePeroxisomal carnitine acyltransferase
02

Mechanism of action

Inhibition of CROT (genetic knockout or siRNA silencing) modulates fatty acid and dicarboxylic acid levels, alters lipid metabolism, and reduces vascular calcification; No direct small-molecule inhibitors in clinical use known

03

Biological functions

Fatty acid β-oxidationLipid metabolismEnergy homeostasisPeroxisome-to-mitochondria fatty acid shuttlingCellular lipid remodeling
04

Disease associations

Cardiovascular disease (e.g., vascular calcification)Metabolic disease (related to fatty acid oxidation)Other (CROT deficiency impacts omega-3 fatty acid metabolism and inflammation)
05

Safety considerations

Potential disruption of energy metabolism due to impaired fatty acid oxidationUnknown long-term effects of CROT inhibition; care in targeting due to broad impact on lipid homeostasis
06

Interacting drugs

Azelaic acid (observed increased levels in CROT deficiency; used in therapy context rather than direct inhibitor)

1 more in the full profile.

07

Biomarkers

Increased plasma/liver omega-3 fatty acids (e.g., EPA, DPA, DHA) in CROT deficiencyElevated dicarboxylic acids, such as tetradecanedioic acid and azelaic acid, in plasma with CROT deficiency

Beyond the preview

Go deeper on Carnitine O-octanoyltransferase (CROT).

Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.

Drug pipeline

Full profile access

Explore the programs pursuing this target and their development progress.

  • Drug candidates
  • Developers
  • Development stage

Clinical trials

Full profile access

Follow the clinical studies evaluating therapies directed at this target.

  • Trial design
  • Status
  • Readouts

Competitive landscape

Full profile access

Compare approaches across drug candidates, modalities, and indications.

  • Programs
  • Modalities
  • Indications

Literature & evidence

Full profile access

Investigate the research and source evidence behind target biology and development.

  • Publications
  • Sources
  • Analysis

Patents

Full profile access

Explore patent activity around therapies and technologies addressing this target.

  • Patents
  • Assignees
  • Technologies

Research & analysis

Full profile access

Connect target biology, drug development, and emerging evidence in your research.

  • Biology
  • Development news
  • Analysis

Bring the full picture into focus.

See how Gosset can support your research on Carnitine O-octanoyltransferase (CROT).

Explore the full profile

Gosset Free

Get started with Gosset.

Enter your work email and we’ll be in touch with next steps.

Work email preferred.

Book a call