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Compile Data Set for Download or QSAR

Found 353 hits with Last Name = 'guan' and Initial = 'q'   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kJ/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Cholinesterase


(Homo sapiens (Human))
BDBM50599186
PNG
(CHEMBL5201089)
Show SMILES CCN(CC)Cc1ccccc1CNC(=O)c1cc(C)cc(NC(=O)c2ccc(F)cc2)c1
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0.0940n/an/an/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00944
BindingDB Entry DOI: 10.7270/Q2HX1HP4
More data for this
Ligand-Target Pair
Cholinesterase


(Homo sapiens (Human))
BDBM50599167
PNG
(CHEMBL5195228)
Show SMILES CCN(CC)Cc1ccccc1CNC(=O)c1cccc(NC(=O)c2ccc(F)cc2)c1
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0.610n/an/an/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00944
BindingDB Entry DOI: 10.7270/Q2HX1HP4
More data for this
Ligand-Target Pair
Xanthine dehydrogenase/oxidase


(Bos taurus (Bovine))
BDBM50057015
PNG
(CHEMBL3331617)
Show SMILES Cc1nc([se]c1C(O)=O)-c1ccc(OCC=C)c(c1)C#N
Show InChI InChI=1S/C15H12N2O3Se/c1-3-6-20-12-5-4-10(7-11(12)8-16)14-17-9(2)13(21-14)15(18)19/h3-5,7H,1,6H2,2H3,(H,18,19)
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0.900n/an/an/an/an/an/an/an/a



Shenyang Pharmaceutical University

Curated by ChEMBL


Assay Description
Mixed-type inhibition of bovine xanthine oxidase assessed as inhibition of uric acid formation by Lineweaver-Burk plot


Eur J Med Chem 85: 508-16 (2014)


Article DOI: 10.1016/j.ejmech.2014.08.014
BindingDB Entry DOI: 10.7270/Q2HX1F9C
More data for this
Ligand-Target Pair
Xanthine dehydrogenase/oxidase


(Bos taurus (Bovine))
BDBM50057015
PNG
(CHEMBL3331617)
Show SMILES Cc1nc([se]c1C(O)=O)-c1ccc(OCC=C)c(c1)C#N
Show InChI InChI=1S/C15H12N2O3Se/c1-3-6-20-12-5-4-10(7-11(12)8-16)14-17-9(2)13(21-14)15(18)19/h3-5,7H,1,6H2,2H3,(H,18,19)
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2.30n/an/an/an/an/an/an/an/a



Shenyang Pharmaceutical University

Curated by ChEMBL


Assay Description
Mixed-type inhibition of bovine xanthine oxidase assessed as inhibition of uric acid formation by secondary Lineweaver-Burk plot


Eur J Med Chem 85: 508-16 (2014)


Article DOI: 10.1016/j.ejmech.2014.08.014
BindingDB Entry DOI: 10.7270/Q2HX1F9C
More data for this
Ligand-Target Pair
Cholinesterase


(Homo sapiens (Human))
BDBM8958
PNG
(10-(2-diethylaminopropyl)phenothiazine | CHEMBL120...)
Show SMILES CCN(CC)C(C)CN1c2ccccc2Sc2ccccc12
Show InChI InChI=1S/C19H24N2S/c1-4-20(5-2)15(3)14-21-16-10-6-8-12-18(16)22-19-13-9-7-11-17(19)21/h6-13,15H,4-5,14H2,1-3H3
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20n/an/an/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00944
BindingDB Entry DOI: 10.7270/Q2HX1HP4
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Cocaine esterase


(Homo sapiens (Human))
BDBM50552232
PNG
(CHEMBL4776624)
Show SMILES COc1cc(\C=C2/Cc3ccc(cc3C2=O)N2CCCC2)ccc1O
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68n/an/an/an/an/an/an/an/a


TBA

Assay Description
Mixed inhibition of hCES2A in human liver microsome assessed as reduction in fluorescein diacetate hydrolysis preincubated for 10 mins followed by su...


Citation and Details

Article DOI: 10.1016/j.ejmech.2020.112856
BindingDB Entry DOI: 10.7270/Q2NZ8CB7
More data for this
Ligand-Target Pair
Cocaine esterase


(Homo sapiens (Human))
BDBM50571105
PNG
(CHEMBL4851375)
Show SMILES Cc1ccc(CC2C(=O)N(N=C2c2ccc(C)cc2)C2CCCCC2)cc1 |c:10|
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90n/an/an/an/an/an/an/an/a


TBA

Assay Description
Non-competitive inhibition of CES2 in human liver microsomes using fluorescein diacetate as substrate by Lineweaver-Burk plot based Michelis-Menten e...


Citation and Details

Article DOI: 10.1016/j.bmc.2021.116187
BindingDB Entry DOI: 10.7270/Q2SN0DQP
More data for this
Ligand-Target Pair
Pancreatic triacylglycerol lipase


(Sus scrofa (Pig))
BDBM50552240
PNG
(CHEMBL4780197)
Show SMILES COc1cc(\C=C2/Cc3ccc(cc3C2=O)N(CCCCCCCCCCCCO)CCCCCCCCCCCCO)ccc1O
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120n/an/an/an/an/an/an/an/a


TBA

Assay Description
Mixed type inhibition of porcine pancreatic lipase using 4MUO as substrate by Lineweaver-Burk plot analysis


Citation and Details

Article DOI: 10.1016/j.bmc.2020.115853
BindingDB Entry DOI: 10.7270/Q2DV1PJS
More data for this
Ligand-Target Pair
Cholinesterase


(Homo sapiens (Human))
BDBM50599195
PNG
(CHEBI:51246 | CHEMBL332935)
Show SMILES CC[N+](C)(CC)CCC[n+]1c(-c2ccccc2)c2cc(N)ccc2c2ccc(N)cc12
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PDB
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430n/an/an/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00944
BindingDB Entry DOI: 10.7270/Q2HX1HP4
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Cholinesterase


(Homo sapiens (Human))
BDBM50100134
PNG
(2-(4-Dimethylamino-phenyl)-3,6-dimethyl-benzothiaz...)
Show SMILES CN(C)c1ccc(cc1)-c1sc2cc(C)ccc2[n+]1C
Show InChI InChI=1S/C17H19N2S/c1-12-5-10-15-16(11-12)20-17(19(15)4)13-6-8-14(9-7-13)18(2)3/h5-11H,1-4H3/q+1
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800n/an/an/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00944
BindingDB Entry DOI: 10.7270/Q2HX1HP4
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Cocaine esterase


(Homo sapiens (Human))
BDBM50017698
PNG
(4-(4-(4-chlorophenyl)-4-hydroxypiperidin-1-yl)-N,N...)
Show SMILES CN(C)C(=O)C(CCN1CCC(O)(CC1)c1ccc(Cl)cc1)(c1ccccc1)c1ccccc1
Show InChI InChI=1S/C29H33ClN2O2/c1-31(2)27(33)29(24-9-5-3-6-10-24,25-11-7-4-8-12-25)19-22-32-20-17-28(34,18-21-32)23-13-15-26(30)16-14-23/h3-16,34H,17-22H2,1-2H3
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1.50E+3n/an/an/an/an/an/an/an/a


TBA

Assay Description
Inhibition of human CES2A using 4-methylumbelliferone as a substrate


Citation and Details

Article DOI: 10.1016/j.ejmech.2020.112856
BindingDB Entry DOI: 10.7270/Q2NZ8CB7
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))
BDBM50599186
PNG
(CHEMBL5201089)
Show SMILES CCN(CC)Cc1ccccc1CNC(=O)c1cc(C)cc(NC(=O)c2ccc(F)cc2)c1
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n/an/a 0.0210n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00944
BindingDB Entry DOI: 10.7270/Q2HX1HP4
More data for this
Ligand-Target Pair
Cholinesterase


(Homo sapiens (Human))
BDBM50599186
PNG
(CHEMBL5201089)
Show SMILES CCN(CC)Cc1ccccc1CNC(=O)c1cc(C)cc(NC(=O)c2ccc(F)cc2)c1
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n/an/a 0.0390n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00944
BindingDB Entry DOI: 10.7270/Q2HX1HP4
More data for this
Ligand-Target Pair
Cholinesterase


(Homo sapiens (Human))
BDBM50599167
PNG
(CHEMBL5195228)
Show SMILES CCN(CC)Cc1ccccc1CNC(=O)c1cccc(NC(=O)c2ccc(F)cc2)c1
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n/an/a 0.0800n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00944
BindingDB Entry DOI: 10.7270/Q2HX1HP4
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))
BDBM50599172
PNG
(CHEMBL5181960)
Show SMILES CCN(CC)Cc1ccccc1CNC(=O)c1cccc(NC(=O)c2ccc(Br)cc2)c1
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n/an/a 0.0870n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00944
BindingDB Entry DOI: 10.7270/Q2HX1HP4
More data for this
Ligand-Target Pair
Cholinesterase


(Homo sapiens (Human))
BDBM50599173
PNG
(CHEMBL5200785)
Show SMILES CCN(CC)Cc1ccccc1CNC(=O)c1cccc(NC(=O)c2ccc(I)cc2)c1
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n/an/a 0.110n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00944
BindingDB Entry DOI: 10.7270/Q2HX1HP4
More data for this
Ligand-Target Pair
Cholinesterase


(Homo sapiens (Human))
BDBM50599172
PNG
(CHEMBL5181960)
Show SMILES CCN(CC)Cc1ccccc1CNC(=O)c1cccc(NC(=O)c2ccc(Br)cc2)c1
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n/an/a 0.130n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00944
BindingDB Entry DOI: 10.7270/Q2HX1HP4
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))
BDBM50599154
PNG
(CHEMBL5185039)
Show SMILES CCN(CC)Cc1ccccc1CNC(=O)c1cccc(NC(=O)c2cccs2)c1
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n/an/a 0.130n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00944
BindingDB Entry DOI: 10.7270/Q2HX1HP4
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))
BDBM50599188
PNG
(CHEMBL5184944)
Show SMILES CCN(CC)Cc1ccccc1CNC(=O)c1cccc(NC(=O)c2ccc(F)cc2)c1C
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n/an/a 0.140n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00944
BindingDB Entry DOI: 10.7270/Q2HX1HP4
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))
BDBM50599167
PNG
(CHEMBL5195228)
Show SMILES CCN(CC)Cc1ccccc1CNC(=O)c1cccc(NC(=O)c2ccc(F)cc2)c1
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n/an/a 0.150n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00944
BindingDB Entry DOI: 10.7270/Q2HX1HP4
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))
BDBM50599191
PNG
(CHEMBL5184728)
Show SMILES CCN(CC)Cc1ccccc1CNC(=O)c1cc(Cl)cc(NC(=O)c2ccc(F)cc2)c1
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n/an/a 0.160n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00944
BindingDB Entry DOI: 10.7270/Q2HX1HP4
More data for this
Ligand-Target Pair
Cholinesterase


(Homo sapiens (Human))
BDBM50599191
PNG
(CHEMBL5184728)
Show SMILES CCN(CC)Cc1ccccc1CNC(=O)c1cc(Cl)cc(NC(=O)c2ccc(F)cc2)c1
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n/an/a 0.220n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00944
BindingDB Entry DOI: 10.7270/Q2HX1HP4
More data for this
Ligand-Target Pair
Cholinesterase


(Homo sapiens (Human))
BDBM50599188
PNG
(CHEMBL5184944)
Show SMILES CCN(CC)Cc1ccccc1CNC(=O)c1cccc(NC(=O)c2ccc(F)cc2)c1C
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n/an/a 0.260n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00944
BindingDB Entry DOI: 10.7270/Q2HX1HP4
More data for this
Ligand-Target Pair
Cholinesterase


(Homo sapiens (Human))
BDBM50599164
PNG
(CHEMBL5201951)
Show SMILES CCN(CC)Cc1ccccc1CNC(=O)c1cccc(NC(=O)c2ccco2)c1
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n/an/a 0.260n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00944
BindingDB Entry DOI: 10.7270/Q2HX1HP4
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))
BDBM50599160
PNG
(CHEMBL5173939)
Show SMILES CN(C)Cc1ccccc1CNC(=O)c1cccc(NC(=O)c2cccs2)c1
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n/an/a 0.290n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00944
BindingDB Entry DOI: 10.7270/Q2HX1HP4
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))
BDBM50599173
PNG
(CHEMBL5200785)
Show SMILES CCN(CC)Cc1ccccc1CNC(=O)c1cccc(NC(=O)c2ccc(I)cc2)c1
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n/an/a 0.340n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00944
BindingDB Entry DOI: 10.7270/Q2HX1HP4
More data for this
Ligand-Target Pair
Cholinesterase


(Homo sapiens (Human))
BDBM50599154
PNG
(CHEMBL5185039)
Show SMILES CCN(CC)Cc1ccccc1CNC(=O)c1cccc(NC(=O)c2cccs2)c1
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n/an/a 0.350n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00944
BindingDB Entry DOI: 10.7270/Q2HX1HP4
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))
BDBM50599185
PNG
(CHEMBL5199323)
Show SMILES CCN(CC)Cc1ccccc1CNC(=O)c1ccc(C)c(NC(=O)c2ccc(F)cc2)c1
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n/an/a 0.380n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00944
BindingDB Entry DOI: 10.7270/Q2HX1HP4
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))
BDBM50599182
PNG
(CHEMBL5197490)
Show SMILES CCN(CC)Cc1ccccc1CNC(=O)c1cc(Br)cc(NC(=O)c2ccc(F)cc2)c1
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n/an/a 0.420n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00944
BindingDB Entry DOI: 10.7270/Q2HX1HP4
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))
BDBM50599161
PNG
(CHEMBL5208367)
Show SMILES CCCN(CCC)Cc1ccccc1CNC(=O)c1cccc(NC(=O)c2cccs2)c1
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n/an/a 0.450n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00944
BindingDB Entry DOI: 10.7270/Q2HX1HP4
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))
BDBM50599170
PNG
(CHEMBL5201163)
Show SMILES CCN(CC)Cc1ccccc1CNC(=O)c1cccc(NC(=O)c2c(F)c(F)c(F)c(F)c2F)c1
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n/an/a 0.480n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00944
BindingDB Entry DOI: 10.7270/Q2HX1HP4
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))
BDBM50599190
PNG
(CHEMBL5191236)
Show SMILES CCN(CC)Cc1ccccc1CNC(=O)c1cc(F)cc(NC(=O)c2ccc(F)cc2)c1
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n/an/a 0.550n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00944
BindingDB Entry DOI: 10.7270/Q2HX1HP4
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))
BDBM50599175
PNG
(CHEMBL5188290)
Show SMILES CCN(CC)Cc1ccccc1CNC(=O)c1cccc(NC(=O)c2ccc(OC)cc2)c1
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n/an/a 0.550n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00944
BindingDB Entry DOI: 10.7270/Q2HX1HP4
More data for this
Ligand-Target Pair
Cholinesterase


(Homo sapiens (Human))
BDBM50599182
PNG
(CHEMBL5197490)
Show SMILES CCN(CC)Cc1ccccc1CNC(=O)c1cc(Br)cc(NC(=O)c2ccc(F)cc2)c1
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n/an/a 0.580n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00944
BindingDB Entry DOI: 10.7270/Q2HX1HP4
More data for this
Ligand-Target Pair
Cholinesterase


(Homo sapiens (Human))
BDBM50599190
PNG
(CHEMBL5191236)
Show SMILES CCN(CC)Cc1ccccc1CNC(=O)c1cc(F)cc(NC(=O)c2ccc(F)cc2)c1
PDB
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n/an/a 0.610n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00944
BindingDB Entry DOI: 10.7270/Q2HX1HP4
More data for this
Ligand-Target Pair
Cholinesterase


(Homo sapiens (Human))
BDBM50599161
PNG
(CHEMBL5208367)
Show SMILES CCCN(CCC)Cc1ccccc1CNC(=O)c1cccc(NC(=O)c2cccs2)c1
PDB
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n/an/a 0.670n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00944
BindingDB Entry DOI: 10.7270/Q2HX1HP4
More data for this
Ligand-Target Pair
Cholinesterase


(Homo sapiens (Human))
BDBM50599160
PNG
(CHEMBL5173939)
Show SMILES CN(C)Cc1ccccc1CNC(=O)c1cccc(NC(=O)c2cccs2)c1
PDB
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n/an/a 0.75n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00944
BindingDB Entry DOI: 10.7270/Q2HX1HP4
More data for this
Ligand-Target Pair
Cholinesterase


(Homo sapiens (Human))
BDBM50599171
PNG
(CHEMBL5198895)
Show SMILES CCN(CC)Cc1ccccc1CNC(=O)c1cccc(NC(=O)c2ccc(Cl)cc2)c1
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n/an/a 0.760n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00944
BindingDB Entry DOI: 10.7270/Q2HX1HP4
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))
BDBM50599164
PNG
(CHEMBL5201951)
Show SMILES CCN(CC)Cc1ccccc1CNC(=O)c1cccc(NC(=O)c2ccco2)c1
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n/an/a 0.790n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00944
BindingDB Entry DOI: 10.7270/Q2HX1HP4
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))
BDBM50599189
PNG
(CHEMBL5183552)
Show SMILES CCN(CC)Cc1ccccc1CNC(=O)c1cc(NC(=O)c2ccc(F)cc2)cc(OC)c1
PDB

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n/an/a 0.820n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00944
BindingDB Entry DOI: 10.7270/Q2HX1HP4
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))
BDBM50599166
PNG
(CHEMBL5195383)
Show SMILES CCN(CC)Cc1ccccc1CNC(=O)c1cccc(NC(=O)c2ccccc2)c1
PDB

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n/an/a 0.960n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00944
BindingDB Entry DOI: 10.7270/Q2HX1HP4
More data for this
Ligand-Target Pair
Cholinesterase


(Homo sapiens (Human))
BDBM50599166
PNG
(CHEMBL5195383)
Show SMILES CCN(CC)Cc1ccccc1CNC(=O)c1cccc(NC(=O)c2ccccc2)c1
PDB
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n/an/a 0.980n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00944
BindingDB Entry DOI: 10.7270/Q2HX1HP4
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))
BDBM50599171
PNG
(CHEMBL5198895)
Show SMILES CCN(CC)Cc1ccccc1CNC(=O)c1cccc(NC(=O)c2ccc(Cl)cc2)c1
PDB

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n/an/a 1n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00944
BindingDB Entry DOI: 10.7270/Q2HX1HP4
More data for this
Ligand-Target Pair
Cholinesterase


(Homo sapiens (Human))
BDBM50599193
PNG
(CHEMBL5185696)
Show SMILES CCN(CC)Cc1ccccc1CNC(=O)c1cc(NC(=O)c2ccc(F)cc2)cc(c1)[N+]([O-])=O
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Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00944
BindingDB Entry DOI: 10.7270/Q2HX1HP4
More data for this
Ligand-Target Pair
Cholinesterase


(Homo sapiens (Human))
BDBM50599175
PNG
(CHEMBL5188290)
Show SMILES CCN(CC)Cc1ccccc1CNC(=O)c1cccc(NC(=O)c2ccc(OC)cc2)c1
PDB
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n/an/a 1n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00944
BindingDB Entry DOI: 10.7270/Q2HX1HP4
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))
BDBM50599178
PNG
(CHEMBL5190491)
Show SMILES CCN(CC)Cc1ccccc1CNC(=O)c1cccc(c1)C(=O)Nc1cccs1
PDB

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n/an/a 1.20n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00944
BindingDB Entry DOI: 10.7270/Q2HX1HP4
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))
BDBM50599193
PNG
(CHEMBL5185696)
Show SMILES CCN(CC)Cc1ccccc1CNC(=O)c1cc(NC(=O)c2ccc(F)cc2)cc(c1)[N+]([O-])=O
PDB

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n/an/a 1.30n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00944
BindingDB Entry DOI: 10.7270/Q2HX1HP4
More data for this
Ligand-Target Pair
Cholinesterase


(Homo sapiens (Human))
BDBM50599170
PNG
(CHEMBL5201163)
Show SMILES CCN(CC)Cc1ccccc1CNC(=O)c1cccc(NC(=O)c2c(F)c(F)c(F)c(F)c2F)c1
PDB
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n/an/a 1.30n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00944
BindingDB Entry DOI: 10.7270/Q2HX1HP4
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))
BDBM50599194
PNG
(CHEMBL5174951)
Show SMILES CCN(CC)Cc1ccccc1CNC(=O)c1cc(NC(=O)c2ccc(F)cc2)cc(c1)C(F)(F)F
PDB

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n/an/a 1.40n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00944
BindingDB Entry DOI: 10.7270/Q2HX1HP4
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))
BDBM50599187
PNG
(CHEMBL5208374)
Show SMILES CCN(CC)Cc1ccccc1CNC(=O)c1cc(NC(=O)c2ccc(F)cc2)ccc1C
PDB

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n/an/a 1.40n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00944
BindingDB Entry DOI: 10.7270/Q2HX1HP4
More data for this
Ligand-Target Pair
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