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S butyrylthiocholine iodide btci

Manufactured by Merck Group
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Sourced in United States, Germany

S-butyrylthiocholine iodide (BTCI) is a chemical compound used as a substrate in enzymatic assays. It is commonly utilized in the measurement of cholinesterase activity, which is relevant in various research and clinical applications.

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Lab products found in correlation

Acetylthiocholine iodide, by Merck Group (2 mentions) Benzylamine, by Merck Group (1 mentions) Toloxatone, by Merck Group (1 mentions) Lazabemide, by Merck Group (1 mentions) Clorgyline, by BioAssay Systems (1 mentions) Pargyline, by BioAssay Systems (1 mentions) Kynuramine, by Merck Group (1 mentions) Mao b, by Merck Group (1 mentions) 5 5 dithiobis 2 nitrobenzoic acid dtnb tacrine, by Merck Group (1 mentions) Recombinant human mao a, by Merck Group (1 mentions) Donepezil, by Merck Group (1 mentions) Ammonium molybdate, by Merck Group (1 mentions) Aluminum chloride, by Merck Group (1 mentions) 2 deoxy d ribose, by Merck Group (1 mentions) 2 2 diphenyl 1 picrylhydrazyl (dpph), by Merck Group (1 mentions) Potassium ferricyanide, by Merck Group (1 mentions) Quercetin, by Merck Group (1 mentions) Folin ciocalteu reagent, by Merck Group (1 mentions) 5 5 dithiobis 2 nitrobenzoic acid dtnb, by Merck Group (1 mentions) Catechin, by Merck Group (1 mentions)

Close spelling variants of this product

Butyrylthiocholine iodide (BTCI) S-butyrylthiocholine iodide Butyrylthiocholine iodide S-butyrylthiocholine Butyrylthiocholine

2 protocols using s butyrylthiocholine iodide btci

1

Enzyme Assays for Neurodegenerative Disorders

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AChE (Type VI-S; from Electrophorus electricus), recombinant human MAO-A, MAO-B, and BChE (from equine serum), acetylthiocholine iodide (ATCI), kynuramine, benzylamine, S-butyrylthiocholine iodide (BTCI), 5,5′-dithiobis (2-nitrobenzoic acid) (DTNB), tacrine, donepezil, toloxatone, and lazabemide were purchased from Sigma-Aldrich (St. Louis, MO, USA). Clorgyline and pargyline (irreversible reference inhibitors of MAO-A and MAO-B, respectively) were from BioAssay Systems (Hayward, CA, USA)40 (link).
Heo J.H., Eom B.H., Ryu H.W., Kang M.G., Park J.E., Kim D.Y., Kim J.H., Park D., Oh S.R, & Kim H. (2020). Acetylcholinesterase and butyrylcholinesterase inhibitory activities of khellactone coumarin derivatives isolated from Peucedanum japonicum Thurnberg. Scientific Reports, 10, 21695.
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2

Comprehensive Antioxidant Evaluation Protocol

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Folin–Ciocalteu reagent, DPPH (1, 1′-diphenyl-2-picrylhydrazyl), aluminum chloride, potassium ferricyanide, and ammonium molybdate were procured from Sigma-Aldrich, India. 2-Deoxy-D-ribose, 2-thiobarbituric acid (TBA), bromocresol green (BCG), catechin, quercetin, 5,5′-dithio-bis-(2-nitro) benzoic acid (DTNB), acetylthiocholine iodide (ATCI), and S-butyrylthiocholine iodide (BTCI) were obtained from Sigma-Aldrich, Germany. All the employed chemicals were of analytical grade.
Al-Amin M.Y., Lahiry A., Ferdous R., Hasan M.K., Kader M.A., Alam A.K., Saud Z.A, & Sadik M.G. (2022). Stephania japonica Ameliorates Scopolamine-Induced Memory Impairment in Mice through Inhibition of Acetylcholinesterase and Oxidative Stress. Advances in Pharmacological and Pharmaceutical Sciences, 2022, 8305271.
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