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Cat. No. | Product Name | Target | Signaling Pathways |
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T78350 |
Glutamate dehydrogenase
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Glutamate dehydrogenase为存在于原核生物与真核生物线粒体中的酶类,适用于氨、α-酮戊二酸、L-谷氨酸及脲酶的酶促反应检测。 | |||
T73616 |
Glutamate dehydrogenase (NAD(P))
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Glutamate dehydrogenase NAD(P) (GLDH)(谷氨酸脱氢酶 NAD(P))是一种存在于肝细胞、肾组织、脑、肌肉和肠细胞的线粒体酶,主要应用于生化研究。作为尿素循环的一环,该酶催化谷氨酸的逆向氧化脱氨反应,生成α-酮戊二酸(α-KG)。 | |||
T4173 |
R162
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Dehydrogenase | Metabolism |
R162 是谷氨酸脱氢酶 (GDH1/GLUD1) 抑制剂,具有抗癌的活性。 | |||
T37405 |
Octanoyl Coenzyme A (sodium salt)
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Octanoyl coenzyme A (octanoyl-CoA) is a medium-chain acyl CoA and a metabolic intermediate in mitochondrial fatty acid β-oxidation. Levels of octanoyl-CoA are increased in the liver of patients with Reye's syndrome and β-oxidation of octanoyl-CoA by medium-chain acyl CoA dehydrogenase (MCADH) is decreased in patients with MCADH deficiency (MCD). Octanoyl-CoA inhibits citrate synthase and glutamate dehydrogenase. | |||
T64276 |
Octanoyl coenzyme A lithium
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Octanoyl coenzyme A lithium 是一种脂肪酸酰基辅酶 A 的衍生物。Octanoyl coenzyme A lithium 能够抑制柠檬酸合成酶和谷氨酸脱氢酶 (IC50: 0.4-1.6 mM)。 | |||
T71305 |
Clofibric Acid-d4
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Clofibric acid-d4 is intended for use as an internal standard for the quantification of clofibric acid by GC- or LC-MS. Clofibric acid is a peroxisome proliferator-activated receptor α (PPARα) agonist (EC50 = 50 µM in a transactivation assay) and the active metabolite of clofibrate. It is formed from clofibrate by tissue and serum esterases. Dietary administration of clofibric acid (0.067-0.22%) reduces serum cholesterol, phospholipid, and triglyceride levels in rats. It decreases glutamate oxal... | |||
T77217 | Saccharopine hydrochloride | ||
Saccharopine hydrochloride(L-Saccharopine hydrochloride)是赖氨酸降解的中间体,兼具线粒体毒性。该化合物由赖氨酸-酮戊二酸还原酶催化赖氨酸与α-酮戊二酸生成。继而,糖精脱氢酶作用于Saccharopine hydrochloride,生成α-氨基己酸酯半醛和谷氨酸。其通过干扰线粒体的稳态平衡,对生物体的发育造成损害。 | |||
T37671 |
CAY10608
CAY10608 |
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N-Methyl-D-aspartate (NMDA) receptors are Ca2+ permeable ligand-gated channels of the central nervous system that are activated after binding of the co-agonists glutamate and glycine. CAY10608 is a propanolamine that potently, selectively, and non-competitively antagonizes the NR2B subunit of NMDA receptors (IC50 = 50 nM). It does not inhibit NR1, NR2A, NR2C, and NR2D subunits and has no significant effects on α-amino-3-hydroxy-5-methyl-4-isoxazolepropioinic acid (AMPA) or kainate receptors. CAY... | |||
T83813 |
8-Azidoadenosine-5'-O-diphosphate sodium
8-azido-ADP,Click Tag™ 8-Azidoadenosine-5'-O-diphosphate |
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8-Azidoadenosine-5'-O-diphosphate(8-azido-ADP)是ATP前体和嘌呤受体配体ADP的可点击形式。8-azido-ADP的放射性标记形式已被用作各种蛋白质的光亲和标签,包括从牛脑中分离的谷氨酸脱氢酶(GDH)同工酶,以及从兔网织红细胞中分离的真核翻译起始因子2(eIF2)和鸟苷核苷酸交换因子(GEF)。 | |||
T74893 | EGCG-4″-sulfate | ||
EGCG-4″-sulfate,作为绿茶中的主要多酚成分,具有抑制细胞增殖和诱导细胞凋亡的功能。它通过抑制谷氨酸脱氢酶1/2(GDH1/2, GLUD1/2)活性,发挥作用。此外,EGCG-4″-sulfate在对抗结直肠癌、髓性白血病、甲状腺癌等多种癌症中显示出显著的抗癌、抗氧化和抗炎效果[2]。 | |||
T83820 |
TNP-GTP sodium
TNP-Guanosine 5'-triphosphate |
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TNP-GTP是一种荧光衍生物,源自蛋白质合成与糖异生的能量底物鸟苷三磷酸(GTP)。其在水中激发波长为410 nm时,发射最大波长为552 nm,而在40%和80%的N,N-二甲基甲酰胺中,其荧光强度增加,发射波长分别向544 nm和532 nm移动,这是因为N,N-二甲基甲酰胺的极性比水小。TNP-GTP是谷氨酸脱氢酶的抑制剂(Ki = 2.7 μM)。当与谷氨酸脱氢酶结合时,TNP-GTP的荧光强度增加,且发射波长从552 nm变为545 nm,此效果可以通过加入GTP来阻断。TNP-GTP还是嘌呤P2X2和P2X2/3受体的拮抗剂(IC50s分别为0.4和1.2 nM)。它还选择性抑制大鼠可溶性鸟苷酸环化酶(sGC; Ki = 11 nM)高于牛肝谷氨酸脱氢酶(GDH; Ki = 2.7 µM)以及钙调素依赖的B. pertussis腺苷酸环化酶(AC)毒素(Kis在存在锰或镁时分别为20和320 µM)。 |
Cat. No. | Product Name | Target | Signaling Pathways |
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T4920 |
2-Ketoglutaric acid Sodium
Oxoglutaric acid,AKG,2-oxoglutarate monobasic,LPHA-酮戊二酸钠,α-Ketoglutaric acid sodium salt |
Tyrosinase; Endogenous Metabolite | Metabolism; Proteases/Proteasome |
2-Ketoglutaric acid Sodium (AKG) 是一种三羧酸循环的中间产物,它可以由谷氨酸通过谷氨酸脱氢酶氧化脱氨产生,也可以作为磷酸吡哆醛依赖的转氨化反应的产物(由支链氨基酸转氨酶介导),其中谷氨酸是常见的氨基供体。 |