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Search Results for " acetyl-coa carboxylase "

20

Compounds

Cat No. Product Name Synonyms Targets
T3510 Olumacostat Glasaretil Acetyl-CoA Carboxylase
Olumacostat glasaretil is a small molecule inhibitor of acetyl coenzyme A carboxylase (ACC). It has been used in trials studying the treatment of Acne Vulgaris.
TQ0243 ND-646 Acetyl-CoA Carboxylase
ND-646 is an orally bioavailable and allosteric inhibitor of the ACC enzymes ACC1 and ACC2(IC50s of 3.5 nM and 4.1 nM for recombinant hACC1 and hACC2, respectively)
T7163 PF-05175157 Acetyl-CoA Carboxylase
PF 05175157 is an inhibitor of acetyl-CoA carboxylase 1 (ACC1) and ACC2 (IC50s = 27, 33, 23.5, and 50.4 nM for human ACC1, human ACC2, rat ACC1, and rat ACC2, respectively
T5046 Haloxyfop Haloxyfop Acid,(±)-Haloxyfop Others , Acetyl-CoA Carboxylase
(±)-Haloxyfop (Haloxyfop Acid) is a herbicide.
T3988 TOFA MDL14514,RMI14514 Acetyl-CoA Carboxylase
TOFA (MDL14514) is an allosteric inhibitor of acetyl-CoA carboxylase-α (ACCA).
T14991 CMS-121 CMS121 Acetyl-CoA Carboxylase
CMS-121, a quinolone derivative, is an orally active acetyl-CoA carboxylase 1 (ACC1) inhibitor. CMS-121 protects HT22 cells against ischemia and oxidative damage (EC50: 7 nM and 200 nM). CMS-121 shows strong neuroprotect...
T1889 CP-640186 CP 640186 Acetyl-CoA Carboxylase
CP-640186 is an isozyme-nonselective Acetyl-CoA carboxylase (ACCase) inhibitor. The IC50s of CP-640186(CP 640186) is 53 nM and 61 nM for rat liver ACC1 and rat skeletal muscle ACC2 respectively.
T3622 CP-640186 hydrochloride CP 640186 HCl Acetyl-CoA Carboxylase
CP-640186 hydrochloride (CP 640186 HCl) is an isozyme-nonselective acetyl-CoA carboxylase (ACC) inhibitor, including rat liver ACC1 (IC50: 53 nM) and rat skeletal muscle ACC2 (IC50: 61 nM); with higher metabolic stabilit...
T7184 Firsocostat ND-630,NDI-010976,GS-0976 Acetyl-CoA Carboxylase
Firsocostat (GS-0976) is an inhibitor of acetyl-CoA carboxylase (ACC) dimerization that inhibits human ACC1 and ACC2 activity (IC50s of 2.1 and 6.1 nM, respectively)
T72180 Acetyl-CoA Carboxylase-IN-1
Acetyl-CoA Carboxylase-IN-1 is a potent inhibitor of acetyl-CoA carboxylase (ACC), exhibiting an inhibition concentration (IC50) of less than 5 nM. This compound also displays antibacterial activity.
T9209 PF-05221304 STAT5 Inhibitor III,NSC 170984,R 6238,,Clesacostat Acetyl-CoA Carboxylase
PF-05221304 (NSC-170984) is an orally active, liver-targeted inhibitor of acetyl-CoA carboxylase (ACC), a rate-limiting enzymes for fatty acid synthesis.
T73350 BAY-3827 Acyltransferase , AMPK
BAY-3827 is a potent and selective AMPK inhibitor with potential antitumor activity, showing antiproliferative activity in an androgen-dependent prostate cancer model. BAY-3827 inhibits the phosphorylation of acetyl CoA ...
T4309 CIL56 CA3 Ferroptosis , ROS
CIL56 (CA3) is a small molecule that induces cellular ferroptosis through the production of iron-dependent reactive oxygen species (ROS). It also induces accumulation of long-chain saturated, monounsaturated, and polyuns...
T70663 ND-654
ND-654 is an acetyl CoA carboxylase inhibitor.
T69277 (±)-Diclofop
(±)-Diclofop is an Acetyl-CoA carboxylase (ACCase) inhibiting herbicide.
T12062 MK-4074 Others
MK-4074 is a liver-specific acetyl-CoA carboxylase ACC1 and ACC2 inhibitor(IC50 of 3 nM).
T36785 Fluazifop-P-butyl
Fluazifop-P-butyl is an arylophenoxypropionate group graminicide that functions as an inhibitor of acetyl-CoA carboxylase (ACCase)[1].
T20135 Diphenamid Trefmid,Enide 50,Enide 50W,Rideon,Fenam,Caswell No. 395
Diphenamid is a chemical compound from the group of acetamides and a herbicide. The effect is based on the inhibition of acetyl-CoA carboxylase.
T61430 S-2E
S-2E is a compound that functions as an orally active, noncompetitive inhibitor of both HMG-CoA reductase and acetyl-CoA carboxylase. It exhibits an anti-hyperlipidemic action, making it suitable for studying conditions ...
T61341 A-908292
A-908292 is a highly potent and selective inhibitor of acetyl-CoA carboxylase 2 (ACC2), displaying an impressive IC50 of 38 nM. This compound serves as a valuable tool in the investigation of fatty acid metabolism [1].
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TargetMol