Date published: 2026-4-26

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ACAA1 Inhibitors

ACAA1 Inhibitors are a group of chemical compounds that target and reduce the activity of the enzyme acetyl-CoA acyltransferase 1 (ACAA1). ACAA1 is an enzyme that plays a crucial role in the breakdown and oxidation of fatty acids within the peroxisomes, a type of organelle responsible for various metabolic functions including the beta-oxidation of very long-chain fatty acids. Inhibitors of ACAA1 would interfere with the enzyme's catalytic function, which is the final step of the peroxisomal fatty acid beta-oxidation pathway, where acetyl-CoA is produced from the breakdown of fatty acids. The inhibition could occur through various mechanisms, such as direct binding to the active site of the enzyme, thus preventing substrate access, or by binding to allosteric sites to induce a conformational change in the enzyme that results in a decrease in its catalytic efficiency.

Techniques such as competitive inhibition assays can help determine whether the inhibitors compete with substrates for binding to the enzyme's active site, while non-competitive inhibition assays could reveal if the inhibitors act on other parts of the enzyme. Structural studies involving techniques like X-ray crystallography or nuclear magnetic resonance (NMR) could yield detailed insights into how these inhibitors interact with ACAA1 at the molecular level. The systematic study of ACAA1 Inhibitors serves to deepen scientific understanding of fatty acid metabolism within peroxisomes and the role of ACAA1 in these biochemical pathways. By selectively inhibiting ACAA1, researchers can examine the broader implications of disrupting this particular step in the metabolic process, potentially revealing compensatory pathways or the interdependence of metabolic networks within the cell.Moreover, the exploration of ACAA1 Inhibitors could contribute to the fundamental knowledge of enzyme inhibition and its effects on metabolic processes, thereby enriching the field of enzymology and metabolic biochemistry.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Triacsin C Solution in DMSO

76896-80-5sc-200574
sc-200574A
100 µg
1 mg
$187.00
$843.00
14
(1)

Triacsin C is an inhibitor of long-chain acyl-CoA synthetase, which reduces the availability of acyl-CoA. ACAA1 requires acyl-CoA substrates for its thiolase activity, thus Triacsin C indirectly diminishes ACAA1 function by substrate limitation.

rac Perhexiline Maleate

6724-53-4sc-460183
10 mg
$188.00
(0)

Perhexiline inhibits carnitine palmitoyltransferase (CPT1), leading to reduced mitochondrial uptake of long-chain fatty acids. This reduction in substrate availability for beta-oxidation indirectly diminishes ACAA1 activity, as fewer products of beta-oxidation are available for ACAA1 to process.

(+)-Etomoxir sodium salt

828934-41-4sc-215009
sc-215009A
5 mg
25 mg
$151.00
$506.00
3
(2)

Etomoxir binds irreversibly to CPT1, blocking fatty acid transport into mitochondria for beta-oxidation. This blockade reduces the production of acetyl-CoA, a direct substrate for ACAA1, thereby indirectly diminishing its activity.

Vanillin

121-33-5sc-251423
sc-251423A
100 g
500 g
$44.00
$124.00
1
(1)

Vanillin is a natural inhibitor of CPT1, which indirectly leads to reduced beta-oxidation and a concomitant decrease in acetyl-CoA levels. This reduction in acetyl-CoA availability indirectly diminishes ACAA1 functional activity.

1,1-Dimethylbiguanide, Hydrochloride

1115-70-4sc-202000F
sc-202000A
sc-202000B
sc-202000C
sc-202000D
sc-202000E
sc-202000
10 mg
5 g
10 g
50 g
100 g
250 g
1 g
$20.00
$43.00
$63.00
$156.00
$260.00
$510.00
$31.00
37
(1)

1,1-Dimethylbiguanide is a CPT1 inhibitor that prevents the transport of fatty acids into mitochondria, thereby reducing beta-oxidation and indirectly diminishing the availability of acetyl-CoA for ACAA1.

Ranolazine

95635-55-5sc-212769
1 g
$109.00
3
(1)

Ranolazine inhibits partial fatty acid oxidation, leading to a decrease in acetyl-CoA production. With less acetyl-CoA available for ACAA1 to process, its functional activity is indirectly diminished.

Bongkrekic acid

11076-19-0sc-205606
100 µg
$400.00
10
(1)

Bongkrekic acid is a CPT1 inhibitor in rodents and is presumed to function similarly in humans. By inhibiting CPT1, it reduces substrate entry for beta-oxidation, leading to less acetyl-CoA for ACAA1 and thus indirectly diminishing its activity.