Log In Sign up
The largest database of trusted experimental protocols

5 5 dithiobis 2 nitrobenzoic acid dtnb tacrine

Manufactured by Merck Group
Visit Supplier
Sourced in United States

5,5′-dithiobis (2-nitrobenzoic acid) (DTNB) is a chemical compound used as a reagent in various biochemical and analytical applications. Tacrine is a drug that was previously used for the treatment of Alzheimer's disease.

Automatically generated - may contain errors

Lab products found in correlation

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) Acetylthiocholine iodide, by Merck Group (1 mentions) Mao b, by Merck Group (1 mentions) S butyrylthiocholine iodide btci, by Merck Group (1 mentions) Recombinant human mao a, by Merck Group (1 mentions) Donepezil, by Merck Group (1 mentions) Dimethyl sulfoxide (dmso), by Merck Group (1 mentions)

Close spelling variants of this product

5,5′-dithiobis(2-nitrobenzoic acid) (DTNB), 5,5′-dithiobis(2-nitrobenzoic acid) Dithiobis-2-nitrobenzoic acid Tacrine

2 protocols using 5 5 dithiobis 2 nitrobenzoic acid dtnb tacrine

1

Enzyme Assays for Neurodegenerative Disorders

Check if the same lab product or an alternative is used in the 5 most similar protocols
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.
+ Open protocol
+ Expand
2

Cholinesterase Inhibition Assay Protocol

Check if the same lab product or an alternative is used in the 5 most similar protocols
All HPLC solvents were purchased from Guangdong Guanghua Sci-Tech Co. Ltd. (Guangzhou, China). Acetylcholinesterase (C3389), acetylthiocholine iodide (A5751), butyrylcholinesterase (C1057), butyrylthiocholine iodide (B3253), and 5,5-dithiobis (2-nitrobenzoic acid) (DTNB), tacrine and dimethylsulfoxide (DMSO) were purchased from Sigma-Aldrich Co. (St. Louis, Missouri, United States). All chemicals and solvents used in column chromatography and assays were acquired from commercial sources.
Wu Y., Su X., Lu J., Wu M., Yang S.Y., Mai Y., Deng W, & Xue Y. (2022). In Vitro and in Silico Analysis of Phytochemicals From Fallopia dentatoalata as Dual Functional Cholinesterase Inhibitors for the Treatment of Alzheimer’s Disease. Frontiers in Pharmacology, 13, 905708.
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!