Compile Data Set for Download or QSAR
Found 116 with Last Name = 'unlu' and Initial = 's'
TargetAcetylcholinesterase(Homo sapiens (Human))
NOBEL ILAÇ SANAYII VE TICARET A.S.

US Patent
LigandPNGBDBM8960((+/-)-2-[(1-benzylpiperidin-4-yl)methyl]-5,6-dimet...)copy SMILEScopy InChI
Affinity DataIC50: 8nMAssay Description:The potential of the compounds of the present invention to inhibit acetylcholinesterase and butyrylcholinesterase enzymes were tested according to th...More data for this Ligand-Target Pair
TargetAcetylcholinesterase(Homo sapiens (Human))
NOBEL ILAÇ SANAYII VE TICARET A.S.

US Patent
LigandPNGBDBM8960((+/-)-2-[(1-benzylpiperidin-4-yl)methyl]-5,6-dimet...)copy SMILEScopy InChI
Affinity DataIC50: 8nMAssay Description:Inhibition of human recombinant AChE using acetylthiocholine iodide substrate incubated for 15 mins by spectrophotometry based Ellman's methodMore data for this Ligand-Target Pair
TargetAcetylcholinesterase(Homo sapiens (Human))
NOBEL ILAÇ SANAYII VE TICARET A.S.

US Patent
LigandPNGBDBM10404((1S,12S,14R)-9-methoxy-4-methyl-11-oxa-4-azatetrac...)copy SMILEScopy InChI
Affinity DataIC50: 700nMAssay Description:Inhibition of human recombinant AChE using acetylthiocholine iodide substrate incubated for 15 mins by spectrophotometry based Ellman's methodMore data for this Ligand-Target Pair
TargetAcetylcholinesterase(Homo sapiens (Human))
NOBEL ILAÇ SANAYII VE TICARET A.S.

US Patent
LigandPNGBDBM10404((1S,12S,14R)-9-methoxy-4-methyl-11-oxa-4-azatetrac...)copy SMILEScopy InChI
Affinity DataIC50: 700nMAssay Description:The potential of the compounds of the present invention to inhibit acetylcholinesterase and butyrylcholinesterase enzymes were tested according to th...More data for this Ligand-Target Pair
TargetAcetylcholinesterase(Homo sapiens (Human))
NOBEL ILAÇ SANAYII VE TICARET A.S.

US Patent
LigandPNGBDBM50024874(CHEMBL3335066)copy SMILEScopy InChI
Affinity DataIC50: 800nMAssay Description:Inhibition of human recombinant AChE using acetylthiocholine iodide substrate incubated for 15 mins by spectrophotometry based Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2RKBPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
NOBEL ILAÇ SANAYII VE TICARET A.S.

US Patent
LigandPNGBDBM50024893(CHEMBL3335048)copy SMILEScopy InChI
Affinity DataIC50: 900nMAssay Description:Inhibition of human recombinant AChE using acetylthiocholine iodide substrate incubated for 15 mins by spectrophotometry based Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2RKBPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
NOBEL ILAÇ SANAYII VE TICARET A.S.

US Patent
LigandPNGBDBM50024881(CHEMBL3335060)copy SMILEScopy InChI
Affinity DataIC50: 900nMAssay Description:Inhibition of human recombinant AChE using acetylthiocholine iodide substrate incubated for 15 mins by spectrophotometry based Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2RKBPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
NOBEL ILAÇ SANAYII VE TICARET A.S.

US Patent
LigandPNGBDBM50024891(CHEMBL3335050)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of human recombinant AChE using acetylthiocholine iodide substrate incubated for 15 mins by spectrophotometry based Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2RKBPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
NOBEL ILAÇ SANAYII VE TICARET A.S.

US Patent
LigandPNGBDBM50024872(CHEMBL3335068)copy SMILEScopy InChI
Affinity DataIC50: 1.10E+3nMAssay Description:Inhibition of human recombinant AChE using acetylthiocholine iodide substrate incubated for 15 mins by spectrophotometry based Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2RKBPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
NOBEL ILAÇ SANAYII VE TICARET A.S.

US Patent
LigandPNGBDBM50024900(CHEMBL3335029)copy SMILEScopy InChI
Affinity DataIC50: 1.30E+3nMAssay Description:Inhibition of human recombinant AChE using acetylthiocholine iodide substrate incubated for 15 mins by spectrophotometry based Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2RKBPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
NOBEL ILAÇ SANAYII VE TICARET A.S.

US Patent
LigandPNGBDBM50024890(CHEMBL3335051)copy SMILEScopy InChI
Affinity DataIC50: 1.70E+3nMAssay Description:Inhibition of human recombinant AChE using acetylthiocholine iodide substrate incubated for 15 mins by spectrophotometry based Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2RKBPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
NOBEL ILAÇ SANAYII VE TICARET A.S.

US Patent
LigandPNGBDBM50024898(CHEMBL3335031)copy SMILEScopy InChI
Affinity DataIC50: 2.10E+3nMAssay Description:Inhibition of human recombinant AChE using acetylthiocholine iodide substrate incubated for 15 mins by spectrophotometry based Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2RKBPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
NOBEL ILAÇ SANAYII VE TICARET A.S.

US Patent
LigandPNGBDBM50024897(CHEMBL3335032)copy SMILEScopy InChI
Affinity DataIC50: 2.70E+3nMAssay Description:Inhibition of human recombinant AChE using acetylthiocholine iodide substrate incubated for 15 mins by spectrophotometry based Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2RKBPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
NOBEL ILAÇ SANAYII VE TICARET A.S.

US Patent
LigandPNGBDBM50024862(CHEMBL3335019)copy SMILEScopy InChI
Affinity DataIC50: 2.80E+3nMAssay Description:Inhibition of human recombinant AChE using acetylthiocholine iodide substrate incubated for 15 mins by spectrophotometry based Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2RKBPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
NOBEL ILAÇ SANAYII VE TICARET A.S.

US Patent
LigandPNGBDBM294221((±)-3-(1-(dimethylamino)ethyl)-1-methoxy-6H-benzo[...)copy SMILEScopy InChI
Affinity DataIC50: 2.80E+3nMAssay Description:The potential of the compounds of the present invention to inhibit acetylcholinesterase and butyrylcholinesterase enzymes were tested according to th...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q24Q7X1CUS Patent
TargetAcetylcholinesterase(Homo sapiens (Human))
NOBEL ILAÇ SANAYII VE TICARET A.S.

US Patent
LigandPNGBDBM50024953(CHEMBL3335025)copy SMILEScopy InChI
Affinity DataIC50: 2.80E+3nMAssay Description:Inhibition of human recombinant AChE using acetylthiocholine iodide substrate incubated for 15 mins by spectrophotometry based Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2RKBPubMed
TargetCholinesterase(Homo sapiens (Human))
Eastern Mediterranean University

Curated by ChEMBL
LigandPNGBDBM50024893(CHEMBL3335048)copy SMILEScopy InChI
Affinity DataIC50: 3.10E+3nMAssay Description:Inhibition of human recombinant BuChE using butyrylthiocholine iodide substrate incubated for 15 mins by spectrophotometry based Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2RKBPubMed
TargetCholinesterase(Homo sapiens (Human))
Eastern Mediterranean University

Curated by ChEMBL
LigandPNGBDBM50024874(CHEMBL3335066)copy SMILEScopy InChI
Affinity DataIC50: 3.70E+3nMAssay Description:Inhibition of human recombinant BuChE using butyrylthiocholine iodide substrate incubated for 15 mins by spectrophotometry based Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2RKBPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
NOBEL ILAÇ SANAYII VE TICARET A.S.

US Patent
LigandPNGBDBM50024876(CHEMBL3335064)copy SMILEScopy InChI
Affinity DataIC50: 4.10E+3nMAssay Description:Inhibition of human recombinant AChE using acetylthiocholine iodide substrate incubated for 15 mins by spectrophotometry based Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2RKBPubMed
TargetCholinesterase(Homo sapiens (Human))
Eastern Mediterranean University

Curated by ChEMBL
LigandPNGBDBM294223((±)-3-(1-(dimethylamino)ethyl)-1-hydroxy-6H-benzo[...)copy SMILEScopy InChI
Affinity DataIC50: 4.20E+3nMAssay Description:The potential of the compounds of the present invention to inhibit acetylcholinesterase and butyrylcholinesterase enzymes were tested according to th...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q24Q7X1CUS Patent
TargetCholinesterase(Homo sapiens (Human))
Eastern Mediterranean University

Curated by ChEMBL
LigandPNGBDBM50024957(CHEMBL3335021)copy SMILEScopy InChI
Affinity DataIC50: 4.20E+3nMAssay Description:Inhibition of human recombinant BuChE using butyrylthiocholine iodide substrate incubated for 15 mins by spectrophotometry based Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2RKBPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
NOBEL ILAÇ SANAYII VE TICARET A.S.

US Patent
LigandPNGBDBM50024896(CHEMBL3335046)copy SMILEScopy InChI
Affinity DataIC50: 4.30E+3nMAssay Description:Inhibition of human recombinant AChE using acetylthiocholine iodide substrate incubated for 15 mins by spectrophotometry based Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2RKBPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
NOBEL ILAÇ SANAYII VE TICARET A.S.

US Patent
LigandPNGBDBM50024895(CHEMBL3335047)copy SMILEScopy InChI
Affinity DataIC50: 4.90E+3nMAssay Description:Inhibition of human recombinant AChE using acetylthiocholine iodide substrate incubated for 15 mins by spectrophotometry based Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2RKBPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
NOBEL ILAÇ SANAYII VE TICARET A.S.

US Patent
LigandPNGBDBM50024933(CHEMBL3335026)copy SMILEScopy InChI
Affinity DataIC50: 6.00E+3nMAssay Description:Inhibition of human recombinant AChE using acetylthiocholine iodide substrate incubated for 15 mins by spectrophotometry based Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2RKBPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
NOBEL ILAÇ SANAYII VE TICARET A.S.

US Patent
LigandPNGBDBM50024892(CHEMBL3335049)copy SMILEScopy InChI
Affinity DataIC50: 6.20E+3nMAssay Description:Inhibition of human recombinant AChE using acetylthiocholine iodide substrate incubated for 15 mins by spectrophotometry based Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2RKBPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
NOBEL ILAÇ SANAYII VE TICARET A.S.

US Patent
LigandPNGBDBM50024887(CHEMBL3335054)copy SMILEScopy InChI
Affinity DataIC50: 6.40E+3nMAssay Description:Inhibition of human recombinant AChE using acetylthiocholine iodide substrate incubated for 15 mins by spectrophotometry based Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2RKBPubMed
TargetCholinesterase(Homo sapiens (Human))
Eastern Mediterranean University

Curated by ChEMBL
LigandPNGBDBM50024872(CHEMBL3335068)copy SMILEScopy InChI
Affinity DataIC50: 6.50E+3nMAssay Description:Inhibition of human recombinant BuChE using butyrylthiocholine iodide substrate incubated for 15 mins by spectrophotometry based Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2RKBPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
NOBEL ILAÇ SANAYII VE TICARET A.S.

US Patent
LigandPNGBDBM50024885(CHEMBL3335056)copy SMILEScopy InChI
Affinity DataIC50: 6.70E+3nMAssay Description:Inhibition of human recombinant AChE using acetylthiocholine iodide substrate incubated for 15 mins by spectrophotometry based Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2RKBPubMed
TargetCholinesterase(Homo sapiens (Human))
Eastern Mediterranean University

Curated by ChEMBL
LigandPNGBDBM8960((+/-)-2-[(1-benzylpiperidin-4-yl)methyl]-5,6-dimet...)copy SMILEScopy InChI
Affinity DataIC50: 7.10E+3nMAssay Description:Inhibition of human recombinant BuChE using butyrylthiocholine iodide substrate incubated for 15 mins by spectrophotometry based Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2RKBPubMed
TargetCholinesterase(Homo sapiens (Human))
Eastern Mediterranean University

Curated by ChEMBL
LigandPNGBDBM8960((+/-)-2-[(1-benzylpiperidin-4-yl)methyl]-5,6-dimet...)copy SMILEScopy InChI
Affinity DataIC50: 7.10E+3nMAssay Description:The potential of the compounds of the present invention to inhibit acetylcholinesterase and butyrylcholinesterase enzymes were tested according to th...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q24Q7X1CUS Patent
TargetAcetylcholinesterase(Homo sapiens (Human))
NOBEL ILAÇ SANAYII VE TICARET A.S.

US Patent
LigandPNGBDBM50024899(CHEMBL3335030)copy SMILEScopy InChI
Affinity DataIC50: 7.30E+3nMAssay Description:Inhibition of human recombinant AChE using acetylthiocholine iodide substrate incubated for 15 mins by spectrophotometry based Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2RKBPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
NOBEL ILAÇ SANAYII VE TICARET A.S.

US Patent
LigandPNGBDBM50024864(CHEMBL3335018)copy SMILEScopy InChI
Affinity DataIC50: 7.90E+3nMAssay Description:Inhibition of human recombinant AChE using acetylthiocholine iodide substrate incubated for 15 mins by spectrophotometry based Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2RKBPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
NOBEL ILAÇ SANAYII VE TICARET A.S.

US Patent
LigandPNGBDBM294220((S)-3-(1-(dimethylamino)ethyl)-6H-benzo[c]chromen-...)copy SMILEScopy InChI
Affinity DataIC50: 7.90E+3nMAssay Description:The potential of the compounds of the present invention to inhibit acetylcholinesterase and butyrylcholinesterase enzymes were tested according to th...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q24Q7X1CUS Patent
TargetAcetylcholinesterase(Homo sapiens (Human))
NOBEL ILAÇ SANAYII VE TICARET A.S.

US Patent
LigandPNGBDBM50024924(CHEMBL3335027)copy SMILEScopy InChI
Affinity DataIC50: 8.10E+3nMAssay Description:Inhibition of human recombinant AChE using acetylthiocholine iodide substrate incubated for 15 mins by spectrophotometry based Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2RKBPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
NOBEL ILAÇ SANAYII VE TICARET A.S.

US Patent
LigandPNGBDBM50024868(CHEMBL3335071)copy SMILEScopy InChI
Affinity DataIC50: 8.20E+3nMAssay Description:Inhibition of human recombinant AChE using acetylthiocholine iodide substrate incubated for 15 mins by spectrophotometry based Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2RKBPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
NOBEL ILAÇ SANAYII VE TICARET A.S.

US Patent
LigandPNGBDBM50024871(CHEMBL3335069)copy SMILEScopy InChI
Affinity DataIC50: 8.30E+3nMAssay Description:Inhibition of human recombinant AChE using acetylthiocholine iodide substrate incubated for 15 mins by spectrophotometry based Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2RKBPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
NOBEL ILAÇ SANAYII VE TICARET A.S.

US Patent
LigandPNGBDBM50024879(CHEMBL3335062)copy SMILEScopy InChI
Affinity DataIC50: 8.50E+3nMAssay Description:Inhibition of human recombinant AChE using acetylthiocholine iodide substrate incubated for 15 mins by spectrophotometry based Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2RKBPubMed
TargetCholinesterase(Homo sapiens (Human))
Eastern Mediterranean University

Curated by ChEMBL
LigandPNGBDBM294226((±)-1-(1-(dimethylamino)ethyl)-6-oxo-6H-benzo[c]ch...)copy SMILEScopy InChI
Affinity DataIC50: 8.50E+3nMAssay Description:The potential of the compounds of the present invention to inhibit acetylcholinesterase and butyrylcholinesterase enzymes were tested according to th...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q24Q7X1CUS Patent
TargetCholinesterase(Homo sapiens (Human))
Eastern Mediterranean University

Curated by ChEMBL
LigandPNGBDBM50024954(CHEMBL3335024)copy SMILEScopy InChI
Affinity DataIC50: 8.50E+3nMAssay Description:Inhibition of human recombinant BuChE using butyrylthiocholine iodide substrate incubated for 15 mins by spectrophotometry based Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2RKBPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
NOBEL ILAÇ SANAYII VE TICARET A.S.

US Patent
LigandPNGBDBM50024886(CHEMBL3335055)copy SMILEScopy InChI
Affinity DataIC50: 8.70E+3nMAssay Description:Inhibition of human recombinant AChE using acetylthiocholine iodide substrate incubated for 15 mins by spectrophotometry based Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2RKBPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
NOBEL ILAÇ SANAYII VE TICARET A.S.

US Patent
LigandPNGBDBM50024889(CHEMBL3335052)copy SMILEScopy InChI
Affinity DataIC50: 9.20E+3nMAssay Description:Inhibition of human recombinant AChE using acetylthiocholine iodide substrate incubated for 15 mins by spectrophotometry based Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2RKBPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
NOBEL ILAÇ SANAYII VE TICARET A.S.

US Patent
LigandPNGBDBM50024865(CHEMBL3335017)copy SMILEScopy InChI
Affinity DataIC50: 1.09E+4nMAssay Description:Inhibition of human recombinant AChE using acetylthiocholine iodide substrate incubated for 15 mins by spectrophotometry based Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2RKBPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
NOBEL ILAÇ SANAYII VE TICARET A.S.

US Patent
LigandPNGBDBM294219((±)-3-(1-(dimethylamino)ethyl)-6H-benzo[c]chromen-...)copy SMILEScopy InChI
Affinity DataIC50: 1.09E+4nMAssay Description:The potential of the compounds of the present invention to inhibit acetylcholinesterase and butyrylcholinesterase enzymes were tested according to th...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q24Q7X1CUS Patent
TargetCholinesterase(Homo sapiens (Human))
Eastern Mediterranean University

Curated by ChEMBL
LigandPNGBDBM11682(2,3-dihydroxybutanedioic acid; 3-[(1S)-1-(dimethyl...)copy SMILEScopy InChI
Affinity DataIC50: 1.10E+4nMAssay Description:The potential of the compounds of the present invention to inhibit acetylcholinesterase and butyrylcholinesterase enzymes were tested according to th...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q24Q7X1CUS PatentDrugBank
TargetCholinesterase(Homo sapiens (Human))
Eastern Mediterranean University

Curated by ChEMBL
LigandPNGBDBM50024866(CHEMBL151763)copy SMILEScopy InChI
Affinity DataIC50: 1.10E+4nMAssay Description:Inhibition of human recombinant BuChE using butyrylthiocholine iodide substrate incubated for 15 mins by spectrophotometry based Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2RKBPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
NOBEL ILAÇ SANAYII VE TICARET A.S.

US Patent
LigandPNGBDBM50024880(CHEMBL3335061)copy SMILEScopy InChI
Affinity DataIC50: 1.14E+4nMAssay Description:Inhibition of human recombinant AChE using acetylthiocholine iodide substrate incubated for 15 mins by spectrophotometry based Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2RKBPubMed
TargetCholinesterase(Homo sapiens (Human))
Eastern Mediterranean University

Curated by ChEMBL
LigandPNGBDBM50024881(CHEMBL3335060)copy SMILEScopy InChI
Affinity DataIC50: 1.21E+4nMAssay Description:Inhibition of human recombinant BuChE using butyrylthiocholine iodide substrate incubated for 15 mins by spectrophotometry based Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2RKBPubMed
TargetCholinesterase(Homo sapiens (Human))
Eastern Mediterranean University

Curated by ChEMBL
LigandPNGBDBM294225((±)-3-(1-(dimethylamino)ethyl)-6-oxo-6H-benzo[c]ch...)copy SMILEScopy InChI
Affinity DataIC50: 1.27E+4nMAssay Description:The potential of the compounds of the present invention to inhibit acetylcholinesterase and butyrylcholinesterase enzymes were tested according to th...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q24Q7X1CUS Patent
TargetCholinesterase(Homo sapiens (Human))
Eastern Mediterranean University

Curated by ChEMBL
LigandPNGBDBM50024955(CHEMBL3335023)copy SMILEScopy InChI
Affinity DataIC50: 1.27E+4nMAssay Description:Inhibition of human recombinant BuChE using butyrylthiocholine iodide substrate incubated for 15 mins by spectrophotometry based Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2RKBPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
NOBEL ILAÇ SANAYII VE TICARET A.S.

US Patent
LigandPNGBDBM50024888(CHEMBL3335053)copy SMILEScopy InChI
Affinity DataIC50: 1.37E+4nMAssay Description:Inhibition of human recombinant AChE using acetylthiocholine iodide substrate incubated for 15 mins by spectrophotometry based Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2RKBPubMed
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