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9
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T37958 |
Acetyl Coenzyme A trisodium
Acetyl-CoA trisodium |
OXPHOS; Endogenous Metabolite; Autophagy | Apoptosis; Autophagy; Metabolism |
Acetyl Coenzyme A trisodium (Acetyl-CoA trisodium) 是糖代谢和脂代谢的重要化合物,参与三羧酸循环。 | |||
T3510 |
Olumacostat Glasaretil
|
Acetyl-CoA Carboxylase | Metabolism |
Olumacostat glasaretil 是乙酰辅酶A 羧化酶的有效抑制剂。 | |||
T7163 |
PF-05175157
|
Acetyl-CoA Carboxylase | Metabolism |
PF 05175157 是一种广谱的乙酰辅酶 A 羧化酶 (ACC) 抑制剂,对 ACC1 (human),ACC2 (human), ACC1 (rat) 和 ACC2 (rat) 具有抑制作用,IC50分别为 27.0, 33.0, 23.5 和 50.4 nM。 | |||
TQ0243 |
ND-646
|
Acetyl-CoA Carboxylase | Metabolism |
ND-646 是乙酰辅酶 A 羧化酶(ACC)抑制剂,对重组 hACC1 和 hACC2的IC50分别为 3.5 nM 和 4.1 nM。 | |||
T4380 |
Ac-CoA Synthase Inhibitor1
ACSS2 inhibitor |
RSV; Fatty Acid Synthase | Metabolism; Microbiology/Virology |
Ac-CoA Synthase Inhibitor1 (ACSS2 inhibitor) 是一种可逆的醋酸盐依赖性乙酰辅酶 A 合成酶 2 抑制剂,IC50为 0.6 µM,可抑制呼吸道合胞病毒。 | |||
T5046 |
Haloxyfop
Haloxyfop Acid,(±)-Haloxyfop,吡氟氯禾灵 |
Others; Acetyl-CoA Carboxylase | Metabolism; Others |
Haloxyfop (Haloxyfop Acid) 是有效的芳氯氧苯氧丙酸除草剂,广泛应用于阔叶作物的野草。对玉米幼苗叶绿体中乙酰辅酶 A 羧化酶 (EC 6.4.1.2) 具有抑制作用,IC50为 0.5 μM,而对豌豆中该酶无影响。 | |||
T1889 |
CP-640186
CP 640186 |
Acetyl-CoA Carboxylase | Metabolism |
CP-640186 是一种有效的乙酰辅酶 A 羧化酶 (ACC)抑制剂,抑制大鼠肝脏 ACC1 和大鼠骨骼肌 ACC2 的 IC50分别为 53 nM 和 61 nM。 | |||
T14991 |
CMS-121
CMS121 |
Acetyl-CoA Carboxylase | Metabolism |
CMS-121 是喹诺酮衍生物,对乙酰辅酶 A 羧化酶 1 具有抑制作用,具有口服活性。CMS-121具有保护 HT22 细胞免受缺血和氧化损伤的活性,EC50分别为7 nM 和200 nM。CMS-121具有强大的抗炎,抗氧化,神经保护和肾保护作用。 | |||
T3988 |
TOFA
MDL14514,RMI14514 |
Acetyl-CoA Carboxylase | Metabolism |
TOFA (MDL14514) 是有效的乙酰辅酶 A 羧化酶-α (ACCA)的变构抑制剂。 | |||
T3622 |
CP-640186 hydrochloride
CP 640186 HCl,盐酸CP-640186 |
Acetyl-CoA Carboxylase | Metabolism |
CP-640186 hydrochloride (CP 640186 HCl) 是膜渗透性的乙酰辅酶A 羧化酶(ACC)抑制剂,抑制大鼠肝脏ACC1和大鼠骨骼肌ACC2的IC50为53 nM 和61 nM。 | |||
T7184 |
Firsocostat
ND-630,NDI-010976,GS-0976 |
Acetyl-CoA Carboxylase | Metabolism |
Firsocostat (GS-0976) 是有效的乙酰辅酶A 羧化酶 (ACC) 抑制剂,抑制人类 ACC1 和 ACC2 的IC50分别为2.1和6.1 nM。 | |||
T9102 |
WM-3835
|
Apoptosis; Histone Methyltransferase; Histone Acetyltransferase | Apoptosis; Chromatin/Epigenetic |
WM-3835 是一种高特异性 HBO1(KAT7orMYST2) 抑制剂,可直接与 HBO1 33 的乙酰辅酶 A 结合位点结合 WM-3835 激活细胞凋亡,抑制骨肉瘤细胞的增殖,迁移和侵袭。它抑制小鼠中骨肉瘤异种移植物的生长,有抗肿瘤活性。 | |||
T72180 | Acetyl-CoA Carboxylase-IN-1 | ||
Acetyl-CoA Carboxylase-IN-1,一种有效的乙酰辅酶 A 羧化酶 (ACC) 抑制剂,具备抗菌活性,其 IC50 值小于 5 nM。 | |||
T9209 |
PF-05221304
STAT5 Inhibitor III,NSC 170984,R 6238,,Clesacostat |
Acetyl-CoA Carboxylase | Metabolism |
PF-05221304 (NSC-170984) 是一种具有口服活性的肝脏靶向乙酰辅酶A 羧化酶 (ACC) 抑制剂,ACC 是脂肪酸合成的限速酶。 | |||
T9732 |
VY-3-135
|
Fatty Acid Synthase | Metabolism |
VY-3-135 是口服有效的乙酰辅酶 A 合成酶 2 (ACSS2)选择性 抑制剂,IC50为 44 nM,对重组人 ACSS1 或 ACSS3 没有抑制活性。它有效抑制 ACSS2 依赖性脂肪酸代谢,但对肿瘤中的基因表达没有影响。 | |||
T73350 |
BAY-3827
|
Acyltransferase; AMPK | Chromatin/Epigenetic; Metabolism; PI3K/Akt/mTOR signaling |
BAY-3827 是一种具有强效性和选择性的 AMPK 抑制剂,具有潜在的抗肿瘤活性,在雄激素依赖性前列腺癌模型中显示出抗增殖活性。 BAY-3827 抑制乙酰 CoA 羧化酶 1 的磷酸化。 | |||
T4309 |
CIL56
CA3 |
Ferroptosis; ROS | Apoptosis; Immunology/Inflammation |
CIL56 (CA3) 是一种选择性铁死亡诱导剂,可通过产生铁依赖性活性氧来诱导细胞铁死亡。 | |||
T11807 |
L002
|
Others; Histone Acetyltransferase; STAT | Chromatin/Epigenetic; JAK/STAT signaling; Others; Stem Cells |
L002 是一种细胞可渗透的,可逆特定性乙酰转移酶 p300(KAT3B)抑制剂,IC50为 1.98 μM。 它结合乙酰辅酶 A 口袋并竞争性抑制 FATp300 催化结构域,阻断组蛋白乙酰化和 p53 乙酰化,且抑制 STAT3 激活,有用于高血压引起的心脏肥大和纤维化的研究潜力。 | |||
T69277 |
(±)-Diclofop
|
||
(±)-Diclofop is an Acetyl-CoA carboxylase (ACCase) inhibiting herbicide. | |||
T70663 |
ND-654
|
||
ND-654 is an acetyl CoA carboxylase inhibitor. | |||
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. | |||
T76158 | Phosphate acetyltransferase | ||
Phosphate acetyltransferase (磷酸乙酰转移酶) 为一转移酶类,主要应用于生化领域。该酶通过将乙酰基从 acetyl-P 可逆地转移至 CoA,生成 acetyl-CoA 及无机磷酸盐,从而参与乙酸的同化及异化过程。 | |||
T36785 |
Fluazifop-P-butyl
|
||
Fluazifop-P-butyl is an arylophenoxypropionate group graminicide that functions as an inhibitor of acetyl-CoA carboxylase (ACCase)[1]. | |||
T73805 | Acetyl coenzyme A | ||
Acetyl-coenzyme A (Acetyl-CoA) 是一种具有膜非渗透性的中枢代谢中间体,参与 TCA 循环和氧化磷酸化代谢过程。Acetyl-coenzyme A 通过向目标氨基酸残基提供乙酰基团,来完成蛋白质的翻译后乙酰化反应,从而调节各种细胞机制。Acetyl Coenzyme A 也是脂质合成的关键前体。 | |||
T12062 |
MK-4074
|
Others | Others |
MK-4074 is a liver-specific acetyl-CoA carboxylase ACC1 and ACC2 inhibitor(IC50 of 3 nM). | |||
T38473 |
Malonyl Coenzyme A lithium
|
||
Malonyl Coenzyme A (lithium) is a coenzyme A derivative that is utilized in fatty acid and polyketide synthesis and in the transport of α-ketoglutarate across the mitochondrial membrane. Malonyl Coenzyme A (lithium) is formed by the Acetyl CoA Carboxylase-mediated carboxylation of acetyl CoA. Malonyl Coenzyme A (lithium) is exclusively used as the extender unit in the synthesis of bacterial aromatic polyketides. | |||
T33477 |
Monosodium N-acetylglutamate
Sodium N-acetylglutamate (1:1) |
||
Monosodium N-acetylglutamate is the sodium salt of N-acetylglutamate, biosynthesized from glutamate and acetylornithine by ornithine acetyltransferase, and from glutamic acid and acetyl-CoA by the enzyme N-acetylglutamate synthase. | |||
T32598 |
Lauroyl-coenzyme A
Dodecanoyl-coa,Coenzyme A, lauroyl-,Lauroyl-coa |
||
Lauroyl-coenzyme A can function as an acyl group carrier, acetyl-CoA. It can be used as an intermediate in lipid metabolism and is involved in lipid biosynthesis and fatty acid transport. | |||
T36827 |
Acetoacetyl Coenzyme A (sodium salt hydrate)
Acetoacetyl-CoA |
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Acetoacetyl-coenzyme A (acetoacetyl-CoA) is a precursor to HMG-CoA in the isoprenoid pathway.[1],[2] It is reversibly converted to acetyl-CoA by acetoacetyl-CoA thiolase in the mitochondria. Acetoacetyl-CoA thiolase (T2) deficiency results in a build-up of ketone bodies leading to intermittent ketoacidosis.[3],[4] Acetoacetyl-CoA is also an intermediate in the microbial biosynthesis of polyhydroxybutyrate.[5] | |||
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 such as familial hypercholesterolemia and mixed hyperlipidemia [1] [2]. | |||
T40675 |
CP-610431
|
||
CP-610431 is a reversible, ATP-uncompetitive inhibitor of acetyl-CoA carboxylase (ACC), exhibiting isozyme nonselectivity. It inhibits both ACC1 and ACC2 with IC50 values of approximately 50 nM. CP-610431 offers potential application in metabolic syndrome research. | |||
T73796 |
Acetyl coenzyme A lithium
|
||
Acetyl-coenzyme A (Acetyl-CoA) lithium 是一种膜非渗透性的中枢代谢中间体,参与 TCA 循环和氧化磷酸化代谢过程。Acetyl-coenzyme A lithium 通过向目标氨基酸残基提供乙酰基团,来完成蛋白质的翻译后乙酰化反应,从而调节各种细胞机制。Acetyl Coenzyme A lithium 也是脂质合成的关键前体。 | |||
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]. | |||
T75251 | Firsocostat (S enantiomer) | ||
Firsocostat S enantiomer (ND-630 S enantiomer) 是 Firsocostat 的低活性的 S 型异构体。Firsocostat 是乙酰辅酶 A 羧化酶抑制剂。 | |||
T73918 |
Lauroyl coenzyme A lithium
|
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Lauroyl coenzyme A lithium salt 是一种辅酶 A。辅酶 A 作为酰基载体,即乙酰辅酶 A。十二烷酰辅酶 A (C12-CoA) 是一种长链 (C-12) 饱和脂肪酰辅酶 A,用作脂质代谢的中间体,参与脂质生物合成和脂肪酸转运。月桂酰辅酶 A 是底物用于 FAM34A 蛋白和萤火虫荧光素酶的产物。 | |||
T76140 | Acetate kinase (ACK) | ||
Acetate kinase (ACK)是细菌和古菌中普遍存在的酶,能在ATP和二价阳离子的作用下,催化乙酸的磷酸化,从而促进乙酰辅酶A的生成,常应用于生化研究领域。 | |||
T35874 |
CC260
|
||
CC260 is a selective PI5P4Kα and PI5P4Kβ inhibitor with Kis of 40 nM and 30 nM, respectively. CC260 does not inhibit or weakly inhibits other protein kinases, such as Plk1 and RSK2. CC260 can be used for cell energy metabolism, diabetes and cancer research[1]. In cultured C2C12 myotubes, CC260 (20 μM) enhances Insulin-induced Akt phosphorylation at both Thr-308 and Ser-473 but suppresses S6K phosphorylation (Thr-389) by mTORC1[1]. CC260 (2.5 μM, 5 μM, 10 μM, 20 μM) significantly increases phosph... |
Cat. No. | Product Name | Target | Signaling Pathways |
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T5213 |
Acetyl phosphate(lithium potassium)
乙酰磷酸锂钾盐,Lithium potassium acetyl phosphate,Acetylphosphoric acid |
Others; Endogenous Metabolite | Metabolism; Others |
Acetyl phosphate lithium potassium (Lithium potassium acetyl phosphate) 是内源性代谢产物的一种。 | |||
T5267 |
N-Acetyl-L-glutamic acid
Ac-L-Glu-OH,N-乙酰-L-谷氨酰胺,N-Acetylglutamic acid |
Others; Endogenous Metabolite | Metabolism; Others |
N-Acetyl-L-glutamic acid (Ac-L-Glu-OH) 是一种 N-Acyl-L-氨基酸,是动物细胞培养基的组成成分,是一种酿酒酵母和人类的代谢物。 | |||
T13979 |
(S)-3-Hydroxybutanoic acid
L-β-Hydroxybutyric acid,(S)-β-Hydroxybutanoic acid,L-(+)-3-Hydroxybutyric acid,(S)-3-羟基丁酸 |
Endogenous Metabolite | Metabolism |
(S)-3-Hydroxybutanoic acid (L-(+)-3-Hydroxybutyric acid) 是一种正常的人体代谢产物,在患有抑郁症的老年患者中升高。它在人类的肝脏中由乙酰-CoA 合成,当血糖低时能够被脑用作能量来源。 | |||
T12045 |
(-)-Hydroxycitric acid lactone
藤黄内酯,Garcinia lactone |
ATP Citrate Lyase | Metabolism |
(-)-Hydroxycitric acid lactone (Garcinia lactone) 是一种有效的 ATP-柠檬酸裂解酶抑制剂,能够催化柠檬酸盐线粒体外裂解为草酰乙酸和乙酰辅酶 A,限制了脂肪酸合成所需乙酰辅酶 A 单位的可用性。它是一种减肥药,是一种广受欢迎的减肥食品补充剂。 | |||
T5287 |
N-Acetyl-L-aspartic acid
AC-ASP-OH,N-Acetylaspartic acid,N-乙酰-L-天门冬氨酸 |
Others; Endogenous Metabolite | Metabolism; Others |
N-Acetyl-L-aspartic acid (AC-ASP-OH) 是天冬氨酸的衍生物, 是由氨基酸天冬氨酸和乙酰辅酶 A 在神经元中合成的。 | |||
T4947 |
3-Hydroxybutyric acid
Butanoic acid,3-羟基丁酸 |
Endogenous Metabolite | Metabolism |
3-Hydroxybutyric acid (Butanoic acid) 是一种人内源性代谢物,在 I 型糖尿病中升高。它能够调节膜脂的性质。 | |||
T4862 |
Oxaloacetic acid
|
Endogenous Metabolite | Metabolism |
Oxaloacetic acid 是一种代谢中间体,涉及多种途径,如葡萄糖异生、柠檬酸循环、乙醛酸循环、尿素循环、氨基酸合成和脂肪酸合成。 | |||
TN1751 | Hydroxycitric acid | ERK; p38 MAPK; Fatty Acid Synthase | MAPK; Metabolism |
(-)-Hydroxycitric acid (HCA) can inhibit fat synthesis and reduces food intake, the primary mechanism of action of HCA appears to be related to its ability to act as a competitive inhibitor of the enzyme ATP-citrate lyase, which catalyzes the conversion of citrate and coenzyme A to oxaloacetate and acetyl coenzyme A (acetyl-CoA), primary building blocks of fatty acid and cholesterol synthesis. | |||
T1456 |
Doxorubicin
Hydroxydaunorubicin,阿霉素,Adriamycin |
Topoisomerase; AMPK | Chromatin/Epigenetic; DNA Damage/DNA Repair; PI3K/Akt/mTOR signaling |
Doxorubicin (Adriamycin) 是一种有细胞毒性的蒽环类抗生素,具有肿瘤化疗作用。它抑制DNA 拓扑异构酶 I 和拓扑异构酶 II,IC50分别为0.8 μM 和2.67 μM,从而抑制 DNA 复制。它下调AMPK 的基础磷酸化以及下游 acetyl-CoA 羧化酶。它诱导凋亡和自噬 。 |