Compile Data Set for Download or QSAR
Found 112 with Last Name = 'campo' and Initial = 'b'
TargetAcetylcholinesterase(Homo sapiens (Human))
Southwest Research Institute

Curated by ChEMBL
LigandPNGBDBM50009661(CHEMBL3235218)copy SMILEScopy InChI
Affinity DataKi:  588nMAssay Description:Inhibition of human AChE using acetylthiocholine as substrate after 4 hrs by robotic spectrophotometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q280545WPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Southwest Research Institute

Curated by ChEMBL
LigandPNGBDBM50009659(CHEMBL3235216)copy SMILEScopy InChI
Affinity DataKi:  1.49E+3nMAssay Description:Inhibition of human AChE using acetylthiocholine as substrate after 4 hrs by robotic spectrophotometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q280545WPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Southwest Research Institute

Curated by ChEMBL
LigandPNGBDBM50009660(CHEMBL3235217)copy SMILEScopy InChI
Affinity DataKi:  3.08E+3nMAssay Description:Inhibition of human AChE using acetylthiocholine as substrate after 4 hrs by robotic spectrophotometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q280545WPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Southwest Research Institute

Curated by ChEMBL
LigandPNGBDBM50009658(CHEMBL3235215)copy SMILEScopy InChI
Affinity DataKi:  6.22E+3nMAssay Description:Inhibition of human AChE using acetylthiocholine as substrate after 4 hrs by robotic spectrophotometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q280545WPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Southwest Research Institute

Curated by ChEMBL
LigandPNGBDBM50009664(CHEMBL3235221)copy SMILEScopy InChI
Affinity DataKi:  3.12E+4nMAssay Description:Inhibition of human AChE using acetylthiocholine as substrate after 4 hrs by robotic spectrophotometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q280545WPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Southwest Research Institute

Curated by ChEMBL
LigandPNGBDBM50009670(CHEMBL3235227)copy SMILEScopy InChI
Affinity DataKi:  5.52E+4nMAssay Description:Inhibition of human AChE using acetylthiocholine as substrate after 4 hrs by robotic spectrophotometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q280545WPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Southwest Research Institute

Curated by ChEMBL
LigandPNGBDBM50009694(CHEMBL3235232)copy SMILEScopy InChI
Affinity DataKi:  1.37E+5nMAssay Description:Inhibition of human AChE using acetylthiocholine as substrate after 4 hrs by robotic spectrophotometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q280545WPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Southwest Research Institute

Curated by ChEMBL
LigandPNGBDBM50009663(CHEMBL3235220)copy SMILEScopy InChI
Affinity DataKi:  1.44E+5nMAssay Description:Inhibition of human AChE using acetylthiocholine as substrate after 4 hrs by robotic spectrophotometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q280545WPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Southwest Research Institute

Curated by ChEMBL
LigandPNGBDBM50009667(CHEMBL3235224)copy SMILEScopy InChI
Affinity DataKi:  1.59E+5nMAssay Description:Inhibition of human AChE using acetylthiocholine as substrate after 4 hrs by robotic spectrophotometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q280545WPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Southwest Research Institute

Curated by ChEMBL
LigandPNGBDBM50009662(CHEMBL3235219 | US9162983, C)copy SMILEScopy InChI
Affinity DataKi:  1.80E+5nMAssay Description:Inhibition of human AChE using acetylthiocholine as substrate after 4 hrs by robotic spectrophotometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q280545WPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Southwest Research Institute

Curated by ChEMBL
LigandPNGBDBM50009715(CHEMBL3235235)copy SMILEScopy InChI
Affinity DataKi:  1.99E+5nMAssay Description:Inhibition of human AChE using acetylthiocholine as substrate after 4 hrs by robotic spectrophotometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q280545WPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Southwest Research Institute

Curated by ChEMBL
LigandPNGBDBM50009665(CHEMBL3235222)copy SMILEScopy InChI
Affinity DataKi:  1.99E+5nMAssay Description:Inhibition of human AChE using acetylthiocholine as substrate after 4 hrs by robotic spectrophotometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q280545WPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Southwest Research Institute

Curated by ChEMBL
LigandPNGBDBM50009675(CHEMBL3235230)copy SMILEScopy InChI
Affinity DataKi:  2.33E+5nMAssay Description:Inhibition of human AChE using acetylthiocholine as substrate after 4 hrs by robotic spectrophotometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q280545WPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Southwest Research Institute

Curated by ChEMBL
LigandPNGBDBM50009650(CHEMBL3235207)copy SMILEScopy InChI
Affinity DataKi:  2.34E+5nMAssay Description:Inhibition of human AChE using acetylthiocholine as substrate after 4 hrs by robotic spectrophotometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q280545WPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Southwest Research Institute

Curated by ChEMBL
LigandPNGBDBM50009713(CHEMBL3235234)copy SMILEScopy InChI
Affinity DataKi:  2.66E+5nMAssay Description:Inhibition of human AChE using acetylthiocholine as substrate after 4 hrs by robotic spectrophotometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q280545WPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Southwest Research Institute

Curated by ChEMBL
LigandPNGBDBM50009671(CHEMBL3235228)copy SMILEScopy InChI
Affinity DataKi:  2.86E+5nMAssay Description:Inhibition of human AChE using acetylthiocholine as substrate after 4 hrs by robotic spectrophotometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q280545WPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Southwest Research Institute

Curated by ChEMBL
LigandPNGBDBM50009669(CHEMBL3235226)copy SMILEScopy InChI
Affinity DataKi:  2.98E+5nMAssay Description:Inhibition of human AChE using acetylthiocholine as substrate after 4 hrs by robotic spectrophotometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q280545WPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Southwest Research Institute

Curated by ChEMBL
LigandPNGBDBM50009673(CHEMBL3235229)copy SMILEScopy InChI
Affinity DataKi:  3.45E+5nMAssay Description:Inhibition of human AChE using acetylthiocholine as substrate after 4 hrs by robotic spectrophotometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q280545WPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Southwest Research Institute

Curated by ChEMBL
LigandPNGBDBM50009692(CHEMBL3235231)copy SMILEScopy InChI
Affinity DataKi:  5.51E+5nMAssay Description:Inhibition of human AChE using acetylthiocholine as substrate after 4 hrs by robotic spectrophotometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q280545WPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Southwest Research Institute

Curated by ChEMBL
LigandPNGBDBM50009655(CHEMBL3235212)copy SMILEScopy InChI
Affinity DataKi:  5.95E+5nMAssay Description:Inhibition of human AChE using acetylthiocholine as substrate after 4 hrs by robotic spectrophotometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q280545WPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Southwest Research Institute

Curated by ChEMBL
LigandPNGBDBM50009652(CHEMBL3235209)copy SMILEScopy InChI
Affinity DataKi:  7.33E+5nMAssay Description:Inhibition of human AChE using acetylthiocholine as substrate after 4 hrs by robotic spectrophotometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q280545WPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Southwest Research Institute

Curated by ChEMBL
LigandPNGBDBM50009668(CHEMBL3235225)copy SMILEScopy InChI
Affinity DataKi:  1.61E+6nMAssay Description:Inhibition of human AChE using acetylthiocholine as substrate after 4 hrs by robotic spectrophotometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q280545WPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Southwest Research Institute

Curated by ChEMBL
LigandPNGBDBM50009654(CHEMBL3235211)copy SMILEScopy InChI
Affinity DataKi:  1.63E+6nMAssay Description:Inhibition of human AChE using acetylthiocholine as substrate after 4 hrs by robotic spectrophotometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q280545WPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Southwest Research Institute

Curated by ChEMBL
LigandPNGBDBM50009656(CHEMBL3235213)copy SMILEScopy InChI
Affinity DataKi:  1.93E+6nMAssay Description:Inhibition of human AChE using acetylthiocholine as substrate after 4 hrs by robotic spectrophotometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q280545WPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Southwest Research Institute

Curated by ChEMBL
LigandPNGBDBM50009666(CHEMBL3235223)copy SMILEScopy InChI
Affinity DataKi:  1.93E+6nMAssay Description:Inhibition of human AChE using acetylthiocholine as substrate after 4 hrs by robotic spectrophotometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q280545WPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Southwest Research Institute

Curated by ChEMBL
LigandPNGBDBM50009651(CHEMBL3235208 | US9162983, E)copy SMILEScopy InChI
Affinity DataKi:  2.30E+6nMAssay Description:Inhibition of human AChE using acetylthiocholine as substrate after 4 hrs by robotic spectrophotometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q280545WPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Southwest Research Institute

Curated by ChEMBL
LigandPNGBDBM50009648(CHEMBL3235205)copy SMILEScopy InChI
Affinity DataKi:  2.43E+6nMAssay Description:Inhibition of human AChE using acetylthiocholine as substrate after 4 hrs by robotic spectrophotometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q280545WPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Southwest Research Institute

Curated by ChEMBL
LigandPNGBDBM50009711(CHEMBL3235233)copy SMILEScopy InChI
Affinity DataKi:  2.52E+6nMAssay Description:Inhibition of human AChE using acetylthiocholine as substrate after 4 hrs by robotic spectrophotometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q280545WPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Southwest Research Institute

Curated by ChEMBL
LigandPNGBDBM50009657(CHEMBL3235214)copy SMILEScopy InChI
Affinity DataKi:  2.67E+6nMAssay Description:Inhibition of human AChE using acetylthiocholine as substrate after 4 hrs by robotic spectrophotometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q280545WPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Southwest Research Institute

Curated by ChEMBL
LigandPNGBDBM50009649(CHEMBL3235206)copy SMILEScopy InChI
Affinity DataKi:  3.18E+6nMAssay Description:Inhibition of human AChE using acetylthiocholine as substrate after 4 hrs by robotic spectrophotometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q280545WPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Southwest Research Institute

Curated by ChEMBL
LigandPNGBDBM50009653(CHEMBL3235210)copy SMILEScopy InChI
Affinity DataKi:  9.50E+7nMAssay Description:Inhibition of human AChE using acetylthiocholine as substrate after 4 hrs by robotic spectrophotometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q280545WPubMed
TargetSerine/threonine-protein kinase haspin(Homo sapiens (Human))TBA
LigandPNGBDBM50603974(CHEMBL5201904)copy SMILES
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H70KXTPubMed
TargetSerine/threonine-protein kinase haspin(Homo sapiens (Human))TBA
LigandPNGBDBM50603992(CHEMBL5179988)copy SMILES
Affinity DataIC50: 11nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H70KXTPubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
University of Liverpool

Curated by ChEMBL
LigandPNGBDBM151585(US11739089, Compound Ketoconazole | US8987315, Ket...)copy SMILEScopy InChI
Affinity DataIC50: 13nMAssay Description:Inhibition of CYP3A4 in human liver microsomes assessed as testosterone 6beta-hydroxylation after 4 to 40 mins in presence of NADPH by LCMS analysisMore data for this Ligand-Target Pair
TargetCytochrome P450 3A4(Homo sapiens (Human))
University of Liverpool

Curated by ChEMBL
LigandPNGBDBM151585(US11739089, Compound Ketoconazole | US8987315, Ket...)copy SMILEScopy InChI
Affinity DataIC50: 22nMAssay Description:Inhibition of CYP3A4 in human liver microsomes assessed as midazolam 1'-hydroxylation after 4 to 40 mins in presence of NADPH by LCMS analysisMore data for this Ligand-Target Pair
TargetCytochrome P450 2D6(Homo sapiens (Human))
University of Liverpool

Curated by ChEMBL
LigandPNGBDBM50121975((6-Methoxy-quinolin-4-yl)-(5-vinyl-1-aza-bicyclo[2...)copy SMILEScopy InChI
Affinity DataIC50: 25nMAssay Description:Inhibition of CYP2D6 in human liver microsomes assessed as dextromethorphan O-demethylation after 4 to 40 mins in presence of NADPH by LCMS analysisMore data for this Ligand-Target Pair
TargetSerine/threonine-protein kinase haspin(Homo sapiens (Human))TBA
LigandPNGBDBM50603978(CHEMBL5187817)copy SMILES
Affinity DataIC50: 32nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H70KXTPubMed
TargetSerine/threonine-protein kinase haspin(Homo sapiens (Human))TBA
LigandPNGBDBM50603989(CHEMBL5192443)copy SMILES
Affinity DataIC50: 45nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H70KXTPubMed
TargetSerine/threonine-protein kinase haspin(Homo sapiens (Human))TBA
LigandPNGBDBM50603986(CHEMBL5187610)copy SMILES
Affinity DataIC50: 78nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H70KXTPubMed
TargetSerine/threonine-protein kinase haspin(Homo sapiens (Human))TBA
LigandPNGBDBM50603988(CHEMBL5170360)copy SMILES
Affinity DataIC50: 140nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H70KXTPubMed
TargetSerine/threonine-protein kinase haspin(Homo sapiens (Human))TBA
LigandPNGBDBM50603984(CHEMBL5195201)copy SMILES
Affinity DataIC50: 200nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H70KXTPubMed
TargetCytochrome P450 2C19(Homo sapiens (Human))
University of Liverpool

Curated by ChEMBL
LigandPNGBDBM50273689(CHEMBL4128999)copy SMILEScopy InChI
Affinity DataIC50: 480nMAssay Description:Inhibition of CYP2C19 in human liver microsomes assessed as (S)-mephenytoin 4'-hydroxylation after 4 to 40 mins in presence of NADPH by LCMS analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K076SBPubMed
TargetSerine/threonine-protein kinase haspin(Homo sapiens (Human))TBA
LigandPNGBDBM50603985(CHEMBL5207627)copy SMILES
Affinity DataIC50: 690nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H70KXTPubMed
TargetCytochrome P450 2C9(Homo sapiens (Human))
University of Liverpool

Curated by ChEMBL
LigandPNGBDBM50090677(4-Amino-N-(2-phenyl-2H-pyrazol-3-yl)-benzenesulfon...)copy SMILEScopy InChI
Affinity DataIC50: 720nMAssay Description:Inhibition of CYP2C9 in human liver microsomes assessed as tolbutamide methylhydroxylation after 4 to 40 mins in presence of NADPH by LCMS analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K076SBPubMedDrugBank
TargetSerine/threonine-protein kinase haspin(Homo sapiens (Human))TBA
LigandPNGBDBM50603979(CHEMBL5204715)copy SMILES
Affinity DataIC50: 770nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H70KXTPubMed
TargetSerine/threonine-protein kinase haspin(Homo sapiens (Human))TBA
LigandPNGBDBM50603976(CHEMBL5200247)copy SMILES
Affinity DataIC50: 1.28E+3nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H70KXTPubMed
TargetSerine/threonine-protein kinase haspin(Homo sapiens (Human))TBA
LigandPNGBDBM50603983(CHEMBL5181699)copy SMILES
Affinity DataIC50: 1.33E+3nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H70KXTPubMed
TargetSerine/threonine-protein kinase haspin(Homo sapiens (Human))TBA
LigandPNGBDBM50603977(CHEMBL5189523)copy SMILES
Affinity DataIC50: 1.74E+3nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H70KXTPubMed
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