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Compound was evaluated for inhibition of human ACHE in an vitro cell free assay measured by absorbance method
Assay data:31 Active, 15 Activity ≤ 1 µM, 927 Tested
SummaryCompounds, ActiveCompounds, activity ≤ 1 µMPubMed CitationRelated BioAssays by Target
Inhibition of Torpedo californica eel AChE using acetylthiocholine/DTNB as substrate preincubated for 10 mins followed by substrate addition measured every 30 secs for 30 mins by Ellmans method
Assay data:55 Active, 3 Activity ≤ 1 nM, 47 Activity ≤ 1 µM, 58 Tested
SummaryCompounds, ActiveCompounds, activity ≤ 1 µMRelated BioAssays by Target
qHTS Validation Assay for Inhibitors of HP1-beta Chromodomain Interactions with Methylated Histone Tails
Assay data:186 Active, 3 Activity ≤ 1 nM, 104 Activity ≤ 1 µM, 1280 Tested
SummaryCompounds, ActiveCompounds, activity ≤ 1 µMPubMed CitationRelated BioAssays by DepositorRelated BioAssays by Same ProjectRelated BioAssays by Target
Concentration required to inhibit hydrolytic activity of bovine erythrocyte acetylcholinesterase by 50%
Assay data:4 Active, 2 Activity ≤ 1 µM, 9 Tested
qHTS Assay for Antagonists of Acetylcholine Muscarinic M1 Receptor: Kinetic Measurement of Intracellular Calcium Response
Assay data:161 Active, 270 Activity ≤ 1 µM, 1279 Tested
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