Results 111 to 120 of about 24,444 (255)

A Bioorthogonally Synthesized and Disulfide-Containing Fluorescence Turn-On Chemical Probe for Measurements of Butyrylcholinesterase Activity and Inhibition in the Presence of Physiological Glutathione [PDF]

open access: gold, 2020
Ming-Mao Gong   +10 more
openalex   +1 more source

Comparison of the Binding of Reversible Inhibitors to Human Butyrylcholinesterase and Acetylcholinesterase: A Crystallographic, Kinetic and Calorimetric Study

open access: yesMolecules, 2017
Acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) hydrolyze the neurotransmitter acetylcholine and, thereby, function as coregulators of cholinergic neurotransmission.
Terrone L. Rosenberry   +6 more
doaj   +1 more source

GWAS of butyrylcholinesterase activity identifies four novel loci, independent effects within BCHE and secondary associations with metabolic risk factors [PDF]

open access: bronze, 2011
Beben Benyamin   +14 more
openalex   +1 more source

Synthesis, Analysis, Cholinesterase-Inhibiting Activity and Molecular Modelling Studies of 3-(Dialkylamino)-2-hydroxypropyl 4-[(Alkoxy-carbonyl)amino]benzoates and Their Quaternary Ammonium Salts

open access: yesMolecules, 2017
Tertiary amines 3-(dialkylamino)-2-hydroxypropyl 4-[(alkoxycarbonyl)amino]benzoates and their quaternary ammonium salts were synthesized. The final step of synthesis of quaternary ammonium salts was carried out by microwave-assisted synthesis.
Tereza Padrtova   +9 more
doaj   +1 more source

Novel Drug-Like Fluorenyl Derivatives as Selective Butyrylcholinesterase and Β-Amyloid Inhibitors for the Treatment of Alzheimer's Disease

open access: green, 2023
Anna Pasieka   +11 more
openalex   +1 more source

Structure-activity correlations for organophosphorus ester anticholinesterases. Part 2: CNDO/2 calculations applied to ester hydrolysis rates [PDF]

open access: yes
Quantitative structure-activity relationships are presented for the hydrolysis of organophosphorus esters, RR'P(O)X, where R and R' are alkyl and/or alkoxy groups and X is fluorine, chlorine or a phenoxy group.
Golub, M. A.   +3 more
core   +1 more source

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