| S8893 |
Firsocostat (GS-0976, ND-630)
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Firsocostat (GS-0976, ND-630) is a reversible inhibitor of acetyl CoA carboxylase (ACC) with IC50s of 2.1 nM, 6.1 nM for hACC1 and hACC2, respectively.
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Adv Sci (Weinh), 2024, 11(46):e2401311
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Nat Commun, 2023, 14(1):1362
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Genome Med, 2022, 14(1):67
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| S6690 |
TOFA
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TOFA is an allosteric inhibitor of acetyl-CoA carboxylase-α (ACCA). Inside the cell, this compound is converted to TOFyl-CoA (5-tetradecyloxy-2-furoyl-CoA), exerting an allosteric inhibition on ACCA. It blocks fatty acid synthesis and induces cell death in a dose-dependent manner.
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J Clin Invest, 2025, e190215
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J Transl Med, 2025, 23(1):1055
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Oncotarget, 2025, 16:532-544
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| S6672 |
PF-05175157
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PF-05175157 is a broad-spectrum effective ACC inhibitor with IC50 of 27.0 nM, 33.0 nM, 23.5 nM and 50.4 nM for human ACC1, human ACC2, rat ACC1, and rat ACC2, respectively.
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Nat Commun, 2025, 16(1):509
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Cancer Cell Int, 2023, 23(1):83
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Liver Res-Prc, 2023, Volume 7, Issue 2 Pages 124-135
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| S8377 |
ND646
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ND-646 is an allosteric inhibitor of the ACC (Acetyl-CoA carboxylase) enzymes that prevents ACC subunit dimerisation to suppress fatty acid synthesis with IC50 of 3.5 nM and 4.1 nM for hACC1 and hACC2, respectively.
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Cancer Discov, 2023, 13(2):496-515
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Cancer Sci, 2023, 114(4):1651-1662
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| S6753 |
CP 640186
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CP 640186 is an isozyme-nonselective ACC (Acetyl-CoA carboxylase) inhibitor with IC50 values of 53 and 61 nM for rat liver ACC1 and rat skeletal muscle ACC2, respectively.
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Exp Ther Med, 2020, 20(1):521-529
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Molecules, 2015, 20(9):16221-34
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| S5519 |
4-Methylsalicylic acid
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4-Methylsalicylic acid (m-Cresotic acid, 2-Hydroxy-4-methylbenzoic acid, m-Cresotinic acid, 2-Hydroxy-p-toluic acid) is used to inhibit the medium chain acyl-CoA synthetase.
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| S6145 |
PF-05221304
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PF-05221304 is an orally bioavailable, liver-targeted inhibitor of acetyl-CoA carboxylase (ACC), an enzyme that catalyses the first committed step in de novo lipogenesis (DNL).
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| S6112 |
Oxalacetic acid
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Oxalacetic acid (Oxaloacetic acid, 2-Oxosuccinic acid, Ketosuccinic acid) is an intermediate of the citric acid cycle, where it reacts with acetyl-CoA to form citrate, catalysed by citrate synthase. It is also involved in gluconeogenesis, urea cycle, glyoxylate cycle, amino acid synthesis, and fatty acid synthesis. Oxaloacetate is also a potent inhibitor of Complex II.
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