Literature summary extracted from

Orhan, I.; Kartal, M.; Tosun, F.; Sener, B.
Screening of various phenolic acids and flavonoid derivatives for their anticholinesterase potential (2008), Z. Naturforsch. C, 62, 829-832.

Inhibitors

EC Number	Inhibitors	Comment	Organism	Structure
3.1.1.8	chlorogenic acid	30.8% inhibition at 1 mM	Homo sapiens
3.1.1.8	galanthamine	80.3% inhibition at 1 mM	Homo sapiens
3.1.1.8	gallic acid	48.8% inhibition at 1 mM	Homo sapiens
3.1.1.8	genistein	65.7% inhibition at 1 mM	Homo sapiens
3.1.1.8	luteolin 7-O-rutinoside	54.9% inhibition at 1 mM	Homo sapiens
3.1.1.8	additional information	no inhibition of BChE by caffeic, gallic, and quinic acids, and biochanin A, apigenin, kaempferol-3-O-galactoside, and diosmin	Homo sapiens
3.1.1.8	naringin	13.7% inhibition at 1 mM	Homo sapiens
3.1.1.8	quercetin	48.8% inhibition at 1 mM	Homo sapiens
3.1.1.8	silibinin	51.4% inhibition at 1 mM	Homo sapiens
3.1.1.8	silymarin	43.2% inhibition at 1 mM	Homo sapiens

Organism

EC Number	Organism	UniProt	Comment	Textmining
3.1.1.8	Homo sapiens	-	-	-

Synonyms

EC Number	Synonyms	Comment	Organism
3.1.1.8	BChE	-	Homo sapiens
3.1.1.8	butyrylcholinesterase	-	Homo sapiens

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Release 2023.1 (January 2023)