BDBM10520 9-{[7-(1,2,3,4-tetrahydroacridin-9-ylsulfanyl)heptyl]sulfanyl}-1,2,3,4-tetrahydroacridine::tacrine homobivalent compound 3d

SMILES C(CCCSc1c2CCCCc2nc2ccccc12)CCCSc1c2CCCCc2nc2ccccc12

InChI Key InChIKey=IKDHJGMFECPDDI-UHFFFAOYSA-N

Data  2 KI  2 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 10520   

TargetCarboxylic ester hydrolase(Equus caballus (Horse))
Universita Degli Studi Di Siena

LigandPNGBDBM10520(9-{[7-(1,2,3,4-tetrahydroacridin-9-ylsulfanyl)hept...)
Affinity DataKi:  380nM ΔG°:  -8.75kcal/molepH: 8.0 T: 2°CAssay Description:Inhibition of enzyme activity was measured over a substrate concentration range of 0.01-30 mM and at least six inhibitor concentrations to determine ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universita Degli Studi Di Siena

LigandPNGBDBM10520(9-{[7-(1,2,3,4-tetrahydroacridin-9-ylsulfanyl)hept...)
Affinity DataKi: >1.00E+4nM ΔG°: >-6.82kcal/molepH: 8.0 T: 2°CAssay Description:Inhibition of enzyme activity was measured over a substrate concentration range of 0.01-30 mM and at least six inhibitor concentrations to determine ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM10520(9-{[7-(1,2,3,4-tetrahydroacridin-9-ylsulfanyl)hept...)
Affinity DataIC50:  380nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Bos taurus (bovine))
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM10520(9-{[7-(1,2,3,4-tetrahydroacridin-9-ylsulfanyl)hept...)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of fetal bovine serum AChE using acetylthiocholine iodide as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed