Target intelligence / Profile preview

Cytochrome P450 family 4 subfamily X member 1 (CYP4X1)

Target
CYP4X1
Molecular classification
Enzyme, Monooxygenase, Cytochrome P450 superfamily
01

Overview

Cytochrome P450 family 4 subfamily X member 1 (CYP4X1) is a member of the cytochrome P450 superfamily of enzymes, functioning as a monooxygenase that catalyzes diverse reactions including the metabolism of arachidonic acid and the endocannabinoid anandamide[1][2][4]. CYP4X1 is highly expressed in the brain, with lower expression in tissues such as prostate, lung, and neurovascular systems[1][4]. It is implicated in the regulation of fatty acid and endocannabinoid metabolism, neurovascular function, and possibly energy homeostasis, as knockout mouse models display increased body weight and adiposity[4]. Its role in human disease is under investigation, with some studies connecting its expression to tumor biology (notably in brain and breast cancers) and to rare neurological disorders[2][4]. Despite these links, CYP4X1 remains an orphan enzyme, with limited knowledge about its physiological substrates, drug interactions, or therapeutic applications[1][4].

Other names
CYP4X1Cytochrome P450 4X1CYPIVX1Cytochrome P450 family 4 subfamily X polypeptide 1UNQ1929/PRO4404MGC40051
02

Mechanism of action

Inhibition of monooxygenase activity affecting fatty acid and endocannabinoid metabolism (inferred from the enzyme’s biochemical role) Potential modulation of neurovascular signaling via alteration of arachidonic acid and anandamide metabolism[4]

03

Biological functions

Fatty acid metabolismEndocannabinoid metabolismDrug metabolismCholesterol and steroid synthesisRegulation of energy balanceNeurovascular function
04

Disease associations

Cancer (potential role in brain and breast cancer)Obesity/metabolic dysfunctionNeurovascular disordersBietti crystalline corneoretinal dystrophyAkinetic mutismOther (experimental evidence for energy homeostasis impairment in knockout mice)
05

Safety considerations

Limited safety data; challenges include orphan status and unclear physiological roles[1][4]Potential for metabolic disruption affecting lipid and endocannabinoid pathways
06

Interacting drugs

Only a few inhibitors reported; no widely validated small-molecule inhibitors or approved drugs specifically targeting CYP4X1
07

Biomarkers

Currently none established for clinical use; research suggests potential as a marker for certain brain- and breast-cancer types[4]

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