124 Results for "

Cholinesterase Inhibitors

" in MedChemExpress (MCE) Product Catalog:
Products (124)

124 Results for "Cholinesterase Inhibitors" in MCE Product Catalog:

13
13 Publications Verification
Cat. No.: HY-138097
CAS No.: 115066-04-1
Purity:  ≥98.0%
α-NETA is a potent and noncompetitive choline acetyltransferase (ChA) inhibitor with an IC50 of 9 μM. α-NETA is a potent ALDH1A1 (IC50=0.04 µM) and chemokine-like receptor-1 (CMKLR1) antagonist. α-NETA weakly inhibits cholinesterase (ChE; IC50=84 µM) and acetylcholinesterase (AChE; IC50=300 µM). α-NETA has anti-cancer activity .
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5
5 Cited Publications
Cat. No.: HY-107569
CAS No.: 78824-30-3
Purity:  ≥99.0%
Garcinol, a polyisoprenylated benzophenone harvested from Garcinia indica, exerts anti-cholinesterase properties towards acetyl cholinesterase (AChE) and butyrylcholinesterase (BChE) with IC50s of 0.66 μM and 7.39 μM, respectively . Garcinol also inhibits histone acetyltransferases (HATs, IC50= 7 μM) and p300/CPB-associated factor (PCAF, IC50 = 5 μM). Garcinol has anti-inflammatory and anti-cancer activity .
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2
2 Cited Publications
Cat. No.: HY-B0423
CAS No.: 114-80-7
Synonyms: Eustigmin bromide; Neoserine bromide
Target:  

Cholinesterase (ChE)

Research Areas:  

Neurological Disease

Neostigmine (Eustigmin) Bromide is an orally active and reversible cholinesterase inhibitor that acts on myasthenia gravis to prolong and intensify the muscarinic and nicotinic effects of acetylcholine. Neostigmine Bromide can be used in anesthesia to reverse the neuromuscular blockade produced by competitive neuromuscular blockers .
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2
2 Cited Publications
Cat. No.: HY-B0207A
CAS No.: 101-26-8
Target:  

Cholinesterase (ChE)

Research Areas:  

Cardiovascular Disease

Pyridostigmine bromide is an orally active cholinesterase (ChE) inhibitor that can be used in cardiovascular disease research .
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2
2 Cited Publications
Cat. No.: HY-107825
CAS No.: 577-85-5
Purity:  99.92%
Flavonol is a cholinesterase (ChE) inhibitor, with an IC50 value of 120 μM and a Ki value of 74 μM. Flavonol has antioxidant, free radical-scavenging, antibacterial properties, and immune modulation functions. Flavonol inhibits the PriA helicase of Staphylococcus aureus. Flavonol can suppress the production of NO in LPS-activated RAW 264.7 cells by inhibiting the expression of the iNOS enzyme. Flavonol shows protective and analgesic effects in mice through various neuronal pathways. Flavonol can be used in research related to tumors and atherosclerosis diseases .
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2
2 Cited Publications
Cat. No.: HY-N4225
CAS No.: 85547-22-4
Aaptamine is an alkaloid that can be isolated from the sponge Aaptos suberitoides. Aaptamine is a competitive antagonist of the α-adrenergic receptor, as well as an inhibitor of the proteasome and cholinesterase. Aaptamine is cytotoxic to tumor cells and can induce apoptosis, cell cycle arrest of tumor cells, and the expression of p21 through a p53-independent pathway. Aaptamine has multiple activities such as anti-tumor, antioxidant, antibacterial, and analgesic effects .
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2
2 Cited Publications
Cat. No.: HY-N6865
CAS No.: 38691-95-1
Groenlandicine, a protoberberine alkaloid, is a cholinesterase inhibitor (AChE (IC50 = 0.54 μM), BChE (IC50 = 3.32 μM)). Groenlandicine non-competitively inhibits BACE1 (IC50 = 19.68 μM, Ki = 21.2) and inhibits RLAR (IC50 = 140.1 μM), HRAR (IC50 = 154.2 μM), and total ROS generation (IC50 = 51.78 μM) in vitro. Groenlandicine suppresses osteosarcoma cell proliferation while promoting apoptosis. Groenlandicine inhibits the tumor growth when combined with Cisplatin (HY-17394). Groenlandicine can be used for the study on osteosarcoma, Alzheimer's disease and diabetes mellitus .
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2
2 Cited Publications
Cat. No.: HY-B1885
CAS No.: 122-14-5
Fenitrothion is a broad-spectrum and orally active insecticide/acaricide. Fenitrothion inhibits cholinesterase, AMPKα and IRS1/PI3K/AKT. Fenitrothion causes Apoptosis, reduces SOD activity. Fenitrothion shows insecticidal effect against Rhyzopertha dominica and Tribolium castaneum adults. Fenitrothion is widely used in cotton crops, vegetable crops, fruit crops and field crops, especially rice. Fenitrothion can be used for brain and spleen toxicology studies .
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1
1 Cited Publications
Cat. No.: HY-17368
CAS No.: 123441-03-2
Synonyms: ENA 713 free base; SDZ-ENA 713 free base
Target:  

Cholinesterase (ChE)

Research Areas:  

Neurological Disease

Rivastigmine (ENA 713 free base) is an orally active and potent cholinesterase (ChE) inhibitor and inhibits butyrylcholinesterase (BChE) and acetylcholinesteras (AChE) with IC50s of 0.037 μM , 4.15 μM, respectively. Rivastigmine can pass the blood brain barrier (BBB). Rivastigmine is a parasympathomimetic or cholinergic agent used for the research of mild to moderate dementia of the Alzheimer's type and dementia due to Parkinson's disease .
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1
1 Cited Publications
Cat. No.: HY-11017
CAS No.: 129101-54-8
Purity:  99.03%
Synonyms: ENA 713; SDZ-ENA 713
Target:  

Cholinesterase (ChE)

Research Areas:  

Neurological Disease

Rivastigmine tartrate (ENA 713; SDZ-ENA 713) is an orally active and potent cholinesterase (ChE) inhibitor and inhibits butyrylcholinesterase (BChE) and acetylcholinesteras (AChE) with IC50s of 0.037 μM, 4.15 μM, respectively. Rivastigmine tartrate can pass the blood brain barrier (BBB). Rivastigmine tartrate is a parasympathomimetic or cholinergic agent used for the research of mild to moderate dementia of the Alzheimer's type and dementia due to Parkinson's disease .
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Cat. No.: HY-17530
CAS No.: 1646-88-4
Aldicarb sulfone is one of the metabolites of the carbamate pesticide Aldicarb and has insecticidal activity. Aldicarb sulfone is also an inhibitor of cholinesterase .
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Cat. No.: HY-107416
CAS No.: 83654-05-1
Purity:  99.41%
Synonyms: U-57908
RHC 80267 (U-57908) is a potent and selective inhibitor of diacylglycerol lipase (DAGL) (with IC50 of 4 μM in canine platelets). RHC-80267 inhibits cholinesterase activity with an IC50 of 4 μM, thereby enhancing the relaxation evoked by acetylcholine. RHC 80267 also inhibits COX and the hydrolysis of phosphatidylcholine (PC) .
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Cat. No.: HY-119577
CAS No.: 15876-67-2
Purity:  ≥99.0%
Synonyms: Distigmine dibromide
Target:  

Cholinesterase (ChE)

Research Areas:  

Neurological Disease

Ubretid is a potent inhibitor of plasma cholinesterase. Ubretid therefore delays the hydrolysis of suxamethonium and prolongs its action, similar to the effects shown by other anticholinesterase agents, such as pyridostigmine and donepezil. Ubretid has the potential for the research of urinary retention prolongs the effect of suxamethonium. Ubretid is commonly prescribed for the research of myasthenia gravis and for difficulty in emptying the bladder .
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Cat. No.: HY-B1626A
CAS No.: 56-94-0
Synonyms: BC-48
Target:  

Cholinesterase (ChE)

Research Areas:  

Neurological Disease

Demecarium Bromide (BC-48) is a potent cholinesterase inhibitor, with an apparent affinity (Kiapp) of 0.15 μM . Demecarium Bromide (BC-48) is used as a glaucoma agent .
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Cat. No.: HY-B0207AS
CAS No.: 2375858-08-3
Pyridostigmine-d6 (bromide) is the deuterium labeled Pyridostigmine, which is a parasympathomimetic and a reversible cholinesterase inhibitor.
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Cat. No.: HY-W022759
CAS No.: 5336-90-3
Target:  

Cholinesterase (ChE)

Research Areas:  

Others

9-Acridinecarboxylic acid is a precursor of a cholinesterase inhibitor, and its derivatives have nanomolar inhibitory potency against AChE and BChE .
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Cat. No.: HY-W203728
CAS No.: 14403-45-3
L-β-Imidazolelactic acid is an inhibitor of Cholinesterase and Monoamine oxidase, and also the final metabolite of L-Histidine (HY-N0832). L-β-Imidazolelactic acid increases the activity of Superoxide dismutase. L-β-Imidazolelactic acid is applicable to research related to liver cirrhosis and histidinemia .
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Cat. No.: HY-I0020
CAS No.: 510-77-0
Synonyms: (-)-Narwedine; Narwedin
Target:  

Cholinesterase (ChE)

Research Areas:  

Neurological Disease

Galanthaminone (Narwedin) is a competitive and reversible cholinesterase (AChE) inhibitor; is used for the treatment of mild to moderate Alzheimer's disease and various other memory impairments.
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Cat. No.: HY-136838
CAS No.: 142698-19-9
Purity:  99.91%
Synonyms: (R)-E2020 free base
Target:  

Cholinesterase (ChE)

Research Areas:  

Neurological Disease Cancer

(R)-Donepezil is a R-enantiomer of Donepezil (HY-14566). Donepezil is a specific and potent AChE inhibitor .
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Cat. No.: HY-107275
CAS No.: 25650-68-4
Purity:  99.51%
Ebeiedinone, a steroidal alkaloid from Fritillaria species, inhibits the bioactivity of human whole blood cholinesterase (ChE) at the concentration of 0.1 mM, with the inhibitory effects of 69.0% .
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