Target intelligence / Profile preview

Arylacetamide deacetylase (AADAC)

Target
AADAC
Molecular classification
Enzyme, Amidase signature enzyme family, Lipase/Esterase (shares homology and functional features)
01

Overview

Arylacetamide deacetylase (AADAC) is a microsomal enzyme encoded by the AADAC gene and primarily located in the liver and gastrointestinal tract, with expression also observed in the brain and other tissues. It belongs to the amidase signature enzyme family, sharing sequence and structural homology with lipases and carboxylesterases. AADAC catalyzes the hydrolysis of arylacetamide, ester, and amide bonds in a variety of drugs and xenobiotics, forming metabolites that are more readily excreted by the body. Its activity is central in drug detoxification, prodrug activation, and influences the pharmacokinetics and safety of several clinically important medications. Genetic variation in AADAC contributes to differential drug responses and adverse reactions in human populations. Furthermore, AADAC’s protein-protein interactions link it to cancer and metabolic diseases, making it relevant in both pharmaceutical metabolism studies and clinical pharmacogenetics.

Other names
AADACMicrosomal arylacetamide deacetylaseDACCES5A1
02

Mechanism of action

Hydrolysis of prodrugs to active drugs or metabolites Deacetylation of arylacetamide and related compounds Detoxification of xenobiotics through amide/ester hydrolysis

03

Biological functions

Drug metabolism and detoxificationXenobiotic metabolism (hydrolysis of esters and amides)Lipid metabolismProdrug activationPhase I drug metabolismFormation of metabolites for excretionRegulation of cancer cell proliferation, migration, and viability (via protein-protein interaction with APP)
04

Disease associations

Cancer (expression upregulation linked to better prognosis in several tumor types; interacts with cancer-related proteins)Drug-induced liver injury/adverse drug reactionsGenetic variants linked to Tourette syndromePotential roles in hypertension, diabetes, and obesity (via interaction partners)
05

Safety considerations

Interindividual variability in drug metabolism due to genetic polymorphismsDrug interactions or altered drug efficacy based on AADAC activity or expressionRisk of drug-induced toxicity, especially liver injury, from altered AADAC-mediated metabolism
06

Interacting drugs

Flutamide

7 more in the full profile.

07

Biomarkers

Genetic polymorphisms in AADAC affecting drug metabolism and toxicity riskExpression/activity levels for predicting therapy response or risk of adverse reactions

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