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Literature summary for 3.1.1.8 extracted from

  • Correa-Basurto, J.; Bello, M.; Rosales-Hernandez, M.C.; Hernandez-Rodriguez, M.; Nicolas-Vazquez, I.; Rojo-Dominguez, A.; Trujillo-Ferrara, J.G.; Miranda, R.; Flores-Sandoval, C.A.
    QSAR, docking, dynamic simulation and quantum mechanics studies to explore the recognition properties of cholinesterase binding sites (2014), Chem. Biol. Interact., 209, 1-13.
    View publication on PubMed

Inhibitors

Inhibitors Comment Organism Structure
(2Z)-4-[(2-aminophenyl)amino]-4-oxobut-2-enoic acid one of the best inhibitors Homo sapiens
(2Z)-4-[(4-nitrophenyl)amino]-4-oxobut-2-enoic acid weak inhibition Homo sapiens
1-(2-nitrophenyl)-1H-pyrrole-2,5-dione weak inhibition Homo sapiens
1-(2-nitrophenyl)pyrrolidine-2,5-dione weak inhibition Homo sapiens
1-(3-aminophenyl)pyrrolidine-2,5-dione one of the best inhibitors Homo sapiens
3-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)benzoic acid one of the best inhibitors Homo sapiens
4-[(2-aminophenyl)amino]-4-oxobutanoic acid one of the best inhibitors Homo sapiens
4-[(3-aminophenyl)amino]-4-oxobutanoic acid weak inhibition Homo sapiens

Organism

Organism UniProt Comment Textmining
Homo sapiens
-
-
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
butyrylthiocholine + H2O
-
Homo sapiens butyrate + thiocholine
-
?

Synonyms

Synonyms Comment Organism
BChE
-
Homo sapiens
butyrylcholinesterase
-
Homo sapiens