目录号 | 产品详情 | 靶点 | |
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T2846 | Antibacterial AChE | ||
Isoimperatorin 是 Angelica dahurica 根的甲醇提取物,是一种抗炎剂,有效抑制乙酰胆碱酯酶,IC50为 74.6 μM。 | |||
T23131 | AChE | ||
PE 154是一种强效的 acetylcholinesterase (AChE) 和 butyrylcholinesterase (BChE) 荧光抑制剂 ,IC50 分别为 280 pM 和 16 nM。PE 154 在组织化学分析中常用来标记 β 淀粉样蛋白斑块。 | |||
T80671 | Antifungal | ||
ACHE-IN-38 是一种有效的Acetylcholinesterase 抑制剂,可用于合成具有抗炎、抗肿瘤和抗菌活性的化合物。 | |||
T77352 | |||
ACHE Inhibitor 12 对乙酰胆碱酯酶具有抑制作用,IC50值为0.38 µM。 | |||
TN6919 | Beta Amyloid AChE | ||
Methyl tridecanoate 能够适度抑制 β-淀粉样蛋白聚集,弱抑制乙酰胆碱酯酶。 | |||
T7500 | AChR | ||
Isoxazole (1,2-oxazole) 是乙酰胆碱酯酶 (AChE) 的抑制剂。异恶唑的配体结合并抑制 Sxc-反转运蛋白。 | |||
TN1091 | AChE | ||
Dehydronuciferine 是一种乙酰胆碱酯酶抑制剂,其 IC50=25 μg/mL,是从 Nelumbo nucifera Gaertn 的叶子中分离得到。 | |||
T8907 | MAO Monoamine Oxidase | ||
Minaprine dihydrochloride 是一种可逆的单胺氧化酶 MAO-A 抑制剂,对乙酰胆碱酯酶有微弱抑制,是一种抗抑郁类化合物。 | |||
TN1589 | AChE | ||
Dihydrowithaferin A 是一种从 Withania somnifera 中分离出来的 withanolide,具有抗乙酰胆碱酯酶 (AChE) 的活性。饮食中的Dihydrowithaferin A 可以预防或减少肿瘤的生长。 | |||
T1612 | AChR AChE | ||
Neostigmine methyl sulfate (Syntostigmin) 是一种乙酰胆碱酯酶的可逆抑制剂, 不能透过血脑屏障。 |
目录号 | 产品名/同用名 | 种属 | 表达系统 | ||
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TMPY-01742 | Acetylcholinesterase Protein, Mouse, Recombinant (His) | Mouse | HEK293 | ||
Acetylcholinesterase, also known as ACHE, is an enzyme that degrades (through its hydrolytic activity) the neurotransmitter acetylcholine, producing choline and an acetate group. Acetylcholinesterase plays a crucial role in nerve impulse transmission at cholinergic synapses by rapid hydrolysis of the neurotransmitter acetylcholine (ACh). ACHE appears to be a potential therapeutic target at muscle injuries including organophosphate myopathy. It is an externally oriented membrane-bound enzyme and its main physiological role is termination of chemical transmission at cholinergic synapses and secretory organs by rapid hydrolysis of the neurotransmitter acetylcholine (ACh). ACHE plays important roles in the cholinergic system, and its dysregulation is involved in a variety of human diseases. ACHE was significantly down-regulated in the cancerous tissues of 69.2% of hepatocellular carcinoma (HCC) patients, and the low ACHE expression in HCC was correlated with tumor aggressiveness, an elevated risk of postoperative recurrence, and a low survival rate. Both the recombinant ACHE protein and the enhanced expression of ACHE significantly inhibited HCC cell growth in vitro and tumorigenicity in vivo. ACHE as a tumor growth suppressor in regulating cell proliferation, the relevant signaling pathways, and the drug sensitivity of HCC cells. Thus, ACHE is a promising independent prognostic predictor for HCC recurrence and the survival of HCC patients. ACHE is responsible for the hydrolysis of acetylcholine in the nervous system. It is inhibited by organophosphate and carbamate pesticides. However, this enzyme is only slightly inhibited by organophosphorothionates.
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TMPJ-00695 | CuTA Protein, Human, Recombinant (His) | Human | E. coli | ||
Protein CutA (CUTA) posseses a signal peptide and is widely expressed in brain. CUTA mayforms part of a complex of membrane proteins attached to acetylcholinesterase (AChE). CUTA takes part in cellular tolerance to a broad range of divalent cations other than copper. Alternate transcriptional splice variants, both protein-coding and non-protein-coding, have been found.
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TMPH-03234 | Acetylcholinesterase Protein, Rat, Recombinant (His) | Rat | E. coli | ||
Terminates signal transduction at the neuromuscular junction by rapid hydrolysis of the acetylcholine released into the synaptic cleft.
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TMPY-01693 | Butyrylcholinesterase Protein, Human, Recombinant (His) | Human | HEK293 | ||
Butyrylcholinesterase (BCHE), also known as cholinesterase or BuChE, is an enzyme defined as "pseudo" or "non-neuronal" cholinesterase. Butyrylcholinesterase (BCHE) is widely distributed in the nervous system as well as blood plasma. It is constitutively similar to the neuronal acetylcholinesterase, and is a non-specific cholinesterase which hydrolyses many different choline esters. Butyrylcholinesterase (BCHE) is a glycoprotein of 4 identical subunits, that were arranged as a dimer of dimers with each dimer composed of two identical subunits joined by interchain disulfide bonds. Butyrylcholinesterase (BCHE) behaves principally similar to the true enzyme and thus can play a similar role in nerve conduction, although it participates probably only in relatively slow conductive processes and could be involved in other nervous system functions and in neurodegenerative diseases. It can hydrolyze toxic esters such as cocaine or scavenge organophosphorus pesticides and nerve agents. Purified human serum cholinesterase combines in its active surface an anionic and an esteratic site, similar to true cholinesterase. It has been demonstrated that butyrylcholinesterase (BCHE) may have a greater role in cholinergic transmission than previously surmised, making BChE inhibition an important therapeutic goal in Alzheimer's disease.
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TMPY-01596 | Butyrylcholinesterase Protein, Mouse, Recombinant (His) | Mouse | HEK293 | ||
Butyrylcholinesterase (BCHE), also known as cholinesterase or BuChE, is an enzyme defined as "pseudo" or "non-neuronal" cholinesterase. Butyrylcholinesterase (BCHE) is widely distributed in the nervous system as well as blood plasma. It is constitutively similar to the neuronal acetylcholinesterase, and is a non-specific cholinesterase which hydrolyses many different choline esters. Butyrylcholinesterase (BCHE) is a glycoprotein of 4 identical subunits, that were arranged as a dimer of dimers with each dimer composed of two identical subunits joined by interchain disulfide bonds. Butyrylcholinesterase (BCHE) behaves principally similar to the true enzyme and thus can play a similar role in nerve conduction, although it participates probably only in relatively slow conductive processes and could be involved in other nervous system functions and in neurodegenerative diseases. It can hydrolyze toxic esters such as cocaine or scavenge organophosphorus pesticides and nerve agents. Purified human serum cholinesterase combines in its active surface an anionic and an esteratic site, similar to true cholinesterase. It has been demonstrated that butyrylcholinesterase (BCHE) may have a greater role in cholinergic transmission than previously surmised, making BChE inhibition an important therapeutic goal in Alzheimer's disease.
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