Date published: 2026-5-6

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ATP-citrate synthase Inhibitors

ATP-citrate synthase inhibitors constitute a class of chemical compounds that exert their effects by selectively targeting the enzyme ATP-citrate synthase (ACLY). ATP-citrate synthase is a crucial enzyme involved in cellular energy metabolism and lipid biosynthesis, playing a pivotal role in the conversion of citrate and coenzyme A to acetyl-CoA and oxaloacetate. This enzymatic conversion is a key step in the generation of cytoplasmic acetyl-CoA, which serves as a precursor for various lipid molecules, including fatty acids and cholesterol. Inhibition of ATP-citrate synthase disrupts this metabolic pathway, leading to alterations in lipid production and cellular energy balance. Structurally diverse, ATP-citrate synthase inhibitors feature compounds with distinct chemical scaffolds that interact with specific regions of the enzyme, thereby modulating its activity. The inhibitory action may occur through competitive binding to the enzyme's active site or by disrupting the enzyme's conformational dynamics, impeding its catalytic function. The significance of ATP-citrate synthase inhibitors lies in their potential to regulate cellular metabolism, particularly lipid homeostasis. By targeting this enzymatic node, these inhibitors may have implications in understanding fundamental cellular processes and serve as valuable tools for investigating the intricate interplay between energy metabolism and lipid synthesis. Further research into the specific mechanisms of action and potential downstream effects of ATP-citrate synthase inhibitors may unveil new insights into cellular biochemistry.
Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

MEDICA 16

87272-20-6sc-203131
sc-203131A
5 mg
10 mg
$192.00
$265.00
1
(1)

MEDICA 16 acts as an ATP-citrate synthase, catalyzing the condensation of acetyl-CoA and oxaloacetate to form citrate. Its unique binding affinity for the active site enhances substrate specificity, promoting efficient energy metabolism. The enzyme's kinetic properties reveal a sigmoidal response to substrate concentration, indicative of allosteric regulation. Additionally, MEDICA 16's structural flexibility allows for dynamic interactions with cofactors, optimizing its catalytic efficiency in metabolic pathways.

Fluoroacetic acid

144-49-0sc-507258
5 g
$822.00
(0)

Fluoroacetic acid is a potent inhibitor of ATP-citrate synthase, disrupting the citric acid cycle by mimicking acetyl-CoA. Its fluorinated structure enhances binding affinity through specific interactions with active site residues, altering enzyme kinetics. The presence of the electronegative fluorine atom influences the acid's reactivity, promoting unique pathways in metabolic processes. This compound's distinct behavior as an acid halide allows for selective inhibition, impacting cellular energy metabolism.

Radicicol

12772-57-5sc-200620
sc-200620A
1 mg
5 mg
$92.00
$333.00
13
(1)

Binds to Hsp90, which is indirectly associated with ACL stability, thus can decrease ACL activity.

Oxalomalic acid sodium salt

89304-26-7sc-295985
sc-295985A
1 mg
5 mg
$52.00
$156.00
(0)

Inhibits ACL by mimicking its substrate oxaloacetate, thus competitively inhibiting enzyme activity.

FK-866

658084-64-1sc-205325
sc-205325A
5 mg
10 mg
$143.00
$250.00
12
(1)

Inhibits NAD biosynthesis, which is necessary for ACL function, thereby indirectly reducing ACL activity.

Itaconic acid

97-65-4sc-250207
sc-250207A
100 g
1 kg
$29.00
$52.00
(0)

Modulates the cellular redox state, indirectly affecting ACL activity due to changes in cellular metabolism.