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35 similar compounds to monomer 50274853

Compile data set for download or QSAR
Wt: 265.3
BDBM75834
Wt: 269.2
BDBM119123
Wt: 246.3
BDBM50092285
Wt: 221.2
BDBM50092271
Purchase
Wt: 237.2
BDBM50092273
Purchase
Wt: 313.3
BDBM50202147
Wt: 327.4
BDBM50202152
Wt: 343.4
BDBM50202153
Wt: 327.4
BDBM50202165
Wt: 369.5
BDBM50202173
Wt: 347.8
BDBM50202175
Wt: 381.3
BDBM50202177
Wt: 239.2
BDBM50241154
Purchase
Wt: 235.3
BDBM50241156
Purchase
Wt: 251.3
BDBM50241157
Purchase
Displayed 1 to 15 (of 35 total )  |  Next  |  Last  >>

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 26 hits for monomerid = 75834,119123,50092285,50092271,50092273,50202147,50202152,50202153,50202165,50202173,50202175,50202177,50241154,50241156,50241157   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kcal/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
insulin-degrading enzyme isoform 1 precursor


(Homo sapiens)
BDBM75834
PNG
(5-(4-hydroxy-3,5-dimethyl-benzylidene)-2-thioxo-th...)
Show SMILES Cc1cc(C=C2SC(S)=NC2=O)cc(C)c1O
Show InChI InChI=1S/C12H11NO2S2/c1-6-3-8(4-7(2)10(6)14)5-9-11(15)13-12(16)17-9/h3-5,14H,1-2H3,(H,13,15,16)
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n/an/a>5.60E+4n/an/an/an/an/an/a



The Scripps Research Institute Molecular Screening Center

Curated by PubChem BioAssay


Assay Description
Source (MLPCN Center Name): The Scripps Research Institute Molecular Screening Center (SRIMSC) Center Affiliation: The Scripps Research Institute (TS...


PubChem Bioassay (2010)


BindingDB Entry DOI: 10.7270/Q2416VHJ
More data for this
Ligand-Target Pair
Beta-lactamase TEM


(Enterobacter cloacae)
BDBM50092271
PNG
((Z)-5-Benzylidene-2-thioxothiazolidin-4-one | (Z)-...)
Show SMILES SC1=NC(=O)C(S1)=Cc1ccccc1
Show InChI InChI=1S/C10H7NOS2/c12-9-8(14-10(13)11-9)6-7-4-2-1-3-5-7/h1-6H,(H,11,12,13)
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n/an/a>7.00E+5n/an/an/an/an/an/a



The R. W. Johnson Pharmaceutical Research Institute

Curated by ChEMBL


Assay Description
Inhibitory activity against class A Beta-lactamase TEM isolated from Enterobacter coli


Bioorg Med Chem Lett 10: 2179-82 (2001)


Article DOI: 10.1016/s0960-894x(00)00444-3
BindingDB Entry DOI: 10.7270/Q2T15456
More data for this
Ligand-Target Pair
MurE


(Staphylococcus aureus)
BDBM119123
PNG
(MurD/E/F inhibitor (compound 69))
Show SMILES Oc1ccc(C=C2SC(S)=NC2=O)c(O)c1O
Show InChI InChI=1S/C10H7NO4S2/c12-5-2-1-4(7(13)8(5)14)3-6-9(15)11-10(16)17-6/h1-3,12-14H,(H,11,15,16)
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n/an/a 6.00E+3n/an/an/an/an/an/a



University of Ljubljana, A?kerceva 7, 1000 Ljubljana, Slovenia





Bioorg Chem 55: 2-15 (2014)


Article DOI: 10.1016/j.bioorg.2014.03.008
BindingDB Entry DOI: 10.7270/Q2ZG6QWR
More data for this
Ligand-Target Pair
MurF


(Escherichia coli)
BDBM119123
PNG
(MurD/E/F inhibitor (compound 69))
Show SMILES Oc1ccc(C=C2SC(S)=NC2=O)c(O)c1O
Show InChI InChI=1S/C10H7NO4S2/c12-5-2-1-4(7(13)8(5)14)3-6-9(15)11-10(16)17-6/h1-3,12-14H,(H,11,15,16)
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n/an/a 2.00E+3n/an/an/an/an/an/a



University of Ljubljana, A?kerceva 7, 1000 Ljubljana, Slovenia





Bioorg Chem 55: 2-15 (2014)


Article DOI: 10.1016/j.bioorg.2014.03.008
BindingDB Entry DOI: 10.7270/Q2ZG6QWR
More data for this
Ligand-Target Pair
A disintegrin and metalloproteinase with thrombospondin motifs 5 (ADAMTS-5)


(Homo sapiens (Human))
BDBM50202147
PNG
(5-(3-phenoxybenzylidene)-2-thioxothiazolidin-4-one...)
Show SMILES SC1=NC(=O)C(S1)=Cc1cccc(Oc2ccccc2)c1
Show InChI InChI=1S/C16H11NO2S2/c18-15-14(21-16(20)17-15)10-11-5-4-8-13(9-11)19-12-6-2-1-3-7-12/h1-10H,(H,17,18,20)
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n/an/a>2.20E+4n/an/an/an/an/an/a



Wyeth Research

Curated by ChEMBL


Assay Description
Inhibition of ADAMTS5


Bioorg Med Chem Lett 17: 1185-8 (2007)


Article DOI: 10.1016/j.bmcl.2006.12.027
BindingDB Entry DOI: 10.7270/Q2PN95BB
More data for this
Ligand-Target Pair
A disintegrin and metalloproteinase with thrombospondin motifs 5 (ADAMTS-5)


(Homo sapiens (Human))
BDBM50202175
PNG
(5-(3-(4-chlorophenoxy)benzylidene)-2-thioxothiazol...)
Show SMILES SC1=NC(=O)C(S1)=Cc1cccc(Oc2ccc(Cl)cc2)c1
Show InChI InChI=1S/C16H10ClNO2S2/c17-11-4-6-12(7-5-11)20-13-3-1-2-10(8-13)9-14-15(19)18-16(21)22-14/h1-9H,(H,18,19,21)
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n/an/a 4.90E+3n/an/an/an/an/an/a



Wyeth Research

Curated by ChEMBL


Assay Description
Inhibition of ADAMTS5


Bioorg Med Chem Lett 17: 1185-8 (2007)


Article DOI: 10.1016/j.bmcl.2006.12.027
BindingDB Entry DOI: 10.7270/Q2PN95BB
More data for this
Ligand-Target Pair
A disintegrin and metalloproteinase with thrombospondin motifs 5 (ADAMTS-5)


(Homo sapiens (Human))
BDBM50202153
PNG
(5-(3-(4-methoxyphenoxy)benzylidene)-2-thioxothiazo...)
Show SMILES COc1ccc(Oc2cccc(C=C3SC(S)=NC3=O)c2)cc1
Show InChI InChI=1S/C17H13NO3S2/c1-20-12-5-7-13(8-6-12)21-14-4-2-3-11(9-14)10-15-16(19)18-17(22)23-15/h2-10H,1H3,(H,18,19,22)
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n/an/a 1.62E+4n/an/an/an/an/an/a



Wyeth Research

Curated by ChEMBL


Assay Description
Inhibition of ADAMTS5


Bioorg Med Chem Lett 17: 1185-8 (2007)


Article DOI: 10.1016/j.bmcl.2006.12.027
BindingDB Entry DOI: 10.7270/Q2PN95BB
More data for this
Ligand-Target Pair
A disintegrin and metalloproteinase with thrombospondin motifs 5 (ADAMTS-5)


(Homo sapiens (Human))
BDBM50202165
PNG
(5-(3-(p-tolyloxy)benzylidene)-2-thioxothiazolidin-...)
Show SMILES Cc1ccc(Oc2cccc(C=C3SC(S)=NC3=O)c2)cc1
Show InChI InChI=1S/C17H13NO2S2/c1-11-5-7-13(8-6-11)20-14-4-2-3-12(9-14)10-15-16(19)18-17(21)22-15/h2-10H,1H3,(H,18,19,21)
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n/an/a 1.48E+4n/an/an/an/an/an/a



Wyeth Research

Curated by ChEMBL


Assay Description
Inhibition of ADAMTS5


Bioorg Med Chem Lett 17: 1185-8 (2007)


Article DOI: 10.1016/j.bmcl.2006.12.027
BindingDB Entry DOI: 10.7270/Q2PN95BB
More data for this
Ligand-Target Pair
A disintegrin and metalloproteinase with thrombospondin motifs 5 (ADAMTS-5)


(Homo sapiens (Human))
BDBM50202173
PNG
(5-(3-(4-tert-butylphenoxy)benzylidene)-2-thioxothi...)
Show SMILES CC(C)(C)c1ccc(Oc2cccc(C=C3SC(S)=NC3=O)c2)cc1
Show InChI InChI=1S/C20H19NO2S2/c1-20(2,3)14-7-9-15(10-8-14)23-16-6-4-5-13(11-16)12-17-18(22)21-19(24)25-17/h4-12H,1-3H3,(H,21,22,24)
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n/an/a 1.70E+3n/an/an/an/an/an/a



Wyeth Research

Curated by ChEMBL


Assay Description
Inhibition of ADAMTS5


Bioorg Med Chem Lett 17: 1185-8 (2007)


Article DOI: 10.1016/j.bmcl.2006.12.027
BindingDB Entry DOI: 10.7270/Q2PN95BB
More data for this
Ligand-Target Pair
A disintegrin and metalloproteinase with thrombospondin motifs 5 (ADAMTS-5)


(Homo sapiens (Human))
BDBM50202177
PNG
(5-(3-(4-(trifluoromethyl)phenoxy)benzylidene)-2-th...)
Show SMILES FC(F)(F)c1ccc(Oc2cccc(C=C3SC(S)=NC3=O)c2)cc1
Show InChI InChI=1S/C17H10F3NO2S2/c18-17(19,20)11-4-6-12(7-5-11)23-13-3-1-2-10(8-13)9-14-15(22)21-16(24)25-14/h1-9H,(H,21,22,24)
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n/an/a 5.30E+3n/an/an/an/an/an/a



Wyeth Research

Curated by ChEMBL


Assay Description
Inhibition of ADAMTS5


Bioorg Med Chem Lett 17: 1185-8 (2007)


Article DOI: 10.1016/j.bmcl.2006.12.027
BindingDB Entry DOI: 10.7270/Q2PN95BB
More data for this
Ligand-Target Pair
A disintegrin and metalloproteinase with thrombospondin motifs 5 (ADAMTS-5)


(Homo sapiens (Human))
BDBM50202152
PNG
(5-(3-(benzyloxy)benzylidene)-2-thioxothiazolidin-4...)
Show SMILES SC1=NC(=O)C(S1)=Cc1cccc(OCc2ccccc2)c1
Show InChI InChI=1S/C17H13NO2S2/c19-16-15(22-17(21)18-16)10-13-7-4-8-14(9-13)20-11-12-5-2-1-3-6-12/h1-10H,11H2,(H,18,19,21)
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n/an/a 2.01E+4n/an/an/an/an/an/a



Wyeth Research

Curated by ChEMBL


Assay Description
Inhibition of ADAMTS5


Bioorg Med Chem Lett 17: 1185-8 (2007)


Article DOI: 10.1016/j.bmcl.2006.12.027
BindingDB Entry DOI: 10.7270/Q2PN95BB
More data for this
Ligand-Target Pair
Arylamine N-acetyltransferase 1


(Homo sapiens)
BDBM50092273
PNG
((Z)-5-(2'-Hydroxybenzylidene)-2-thioxothiazolidin-...)
Show SMILES Oc1ccccc1C=C1SC(S)=NC1=O
Show InChI InChI=1S/C10H7NO2S2/c12-7-4-2-1-3-6(7)5-8-9(13)11-10(14)15-8/h1-5,12H,(H,11,13,14)
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n/an/a 1.10E+3n/an/an/an/an/an/a



University of Oxford

Curated by ChEMBL


Assay Description
Inhibition of human recombinant NAT1 assessed as hydrolysis of acetyl coA using PABA as substrate by Ellman's method


Bioorg Med Chem 17: 905-18 (2009)


Article DOI: 10.1016/j.bmc.2008.11.032
BindingDB Entry DOI: 10.7270/Q2PZ58Q3
More data for this
Ligand-Target Pair
Arylamine N-acetyltransferase 1


(Homo sapiens)
BDBM50241157
PNG
((Z)-5-(4'-Methoxybenzylidene)-2-thioxothiazolidin-...)
Show SMILES COc1ccc(C=C2SC(S)=NC2=O)cc1
Show InChI InChI=1S/C11H9NO2S2/c1-14-8-4-2-7(3-5-8)6-9-10(13)12-11(15)16-9/h2-6H,1H3,(H,12,13,15)
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n/an/a>3.00E+4n/an/an/an/an/an/a



University of Oxford

Curated by ChEMBL


Assay Description
Inhibition of human recombinant NAT1 assessed as hydrolysis of acetyl coA using PABA as substrate by Ellman's method


Bioorg Med Chem 17: 905-18 (2009)


Article DOI: 10.1016/j.bmc.2008.11.032
BindingDB Entry DOI: 10.7270/Q2PZ58Q3
More data for this
Ligand-Target Pair
Arylamine N-acetyltransferase 1


(Homo sapiens)
BDBM50241156
PNG
((Z)-5-(4'-Methylbenzylidene)-2-thioxothiazolidin-4...)
Show SMILES Cc1ccc(C=C2SC(S)=NC2=O)cc1
Show InChI InChI=1S/C11H9NOS2/c1-7-2-4-8(5-3-7)6-9-10(13)12-11(14)15-9/h2-6H,1H3,(H,12,13,14)
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n/an/a>3.00E+4n/an/an/an/an/an/a



University of Oxford

Curated by ChEMBL


Assay Description
Inhibition of human recombinant NAT1 assessed as hydrolysis of acetyl coA using PABA as substrate by Ellman's method


Bioorg Med Chem 17: 905-18 (2009)


Article DOI: 10.1016/j.bmc.2008.11.032
BindingDB Entry DOI: 10.7270/Q2PZ58Q3
More data for this
Ligand-Target Pair
Arylamine N-acetyltransferase 1


(Homo sapiens)
BDBM50241154
PNG
((Z)-5-(4'-Fluorobenzylidene)-2-thioxothiazolidin-4...)
Show SMILES Fc1ccc(C=C2SC(S)=NC2=O)cc1
Show InChI InChI=1S/C10H6FNOS2/c11-7-3-1-6(2-4-7)5-8-9(13)12-10(14)15-8/h1-5H,(H,12,13,14)
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n/an/a 1.29E+4n/an/an/an/an/an/a



University of Oxford

Curated by ChEMBL


Assay Description
Inhibition of human recombinant NAT1 assessed as hydrolysis of acetyl coA using PABA as substrate by Ellman's method


Bioorg Med Chem 17: 905-18 (2009)


Article DOI: 10.1016/j.bmc.2008.11.032
BindingDB Entry DOI: 10.7270/Q2PZ58Q3
More data for this
Ligand-Target Pair
Arylamine N-acetyltransferase 1


(Homo sapiens)
BDBM50092271
PNG
((Z)-5-Benzylidene-2-thioxothiazolidin-4-one | (Z)-...)
Show SMILES SC1=NC(=O)C(S1)=Cc1ccccc1
Show InChI InChI=1S/C10H7NOS2/c12-9-8(14-10(13)11-9)6-7-4-2-1-3-5-7/h1-6H,(H,11,12,13)
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n/an/a 1.30E+4n/an/an/an/an/an/a



University of Oxford

Curated by ChEMBL


Assay Description
Inhibition of human recombinant NAT1 assessed as hydrolysis of acetyl coA using PABA as substrate by Ellman's method


Bioorg Med Chem 17: 905-18 (2009)


Article DOI: 10.1016/j.bmc.2008.11.032
BindingDB Entry DOI: 10.7270/Q2PZ58Q3
More data for this
Ligand-Target Pair
Aldose reductase (ALR2)


(Bos taurus (Cattle))
BDBM50202147
PNG
(5-(3-phenoxybenzylidene)-2-thioxothiazolidin-4-one...)
Show SMILES SC1=NC(=O)C(S1)=Cc1cccc(Oc2ccccc2)c1
Show InChI InChI=1S/C16H11NO2S2/c18-15-14(21-16(20)17-15)10-11-5-4-8-13(9-11)19-12-6-2-1-3-7-12/h1-10H,(H,17,18,20)
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n/an/a 2.94E+3n/an/an/an/an/an/a



University of Messina

Curated by ChEMBL


Assay Description
Inhibition of bovine lens aldose reductase assessed as inhibition of NDAPH oxidation by non-linear regression analysis


Bioorg Med Chem Lett 21: 200-3 (2010)


Article DOI: 10.1016/j.bmcl.2010.11.041
BindingDB Entry DOI: 10.7270/Q2ZP46C4
More data for this
Ligand-Target Pair
Aldose reductase (ALR2)


(Bos taurus (Cattle))
BDBM50241157
PNG
((Z)-5-(4'-Methoxybenzylidene)-2-thioxothiazolidin-...)
Show SMILES COc1ccc(C=C2SC(S)=NC2=O)cc1
Show InChI InChI=1S/C11H9NO2S2/c1-14-8-4-2-7(3-5-8)6-9-10(13)12-11(15)16-9/h2-6H,1H3,(H,12,13,15)
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n/an/a 5.23E+3n/an/an/an/an/an/a



University of Messina

Curated by ChEMBL


Assay Description
Inhibition of bovine lens aldose reductase assessed as inhibition of NDAPH oxidation by non-linear regression analysis


Bioorg Med Chem Lett 21: 200-3 (2010)


Article DOI: 10.1016/j.bmcl.2010.11.041
BindingDB Entry DOI: 10.7270/Q2ZP46C4
More data for this
Ligand-Target Pair
Tyrosinase


(Agaricus bisporus (Common mushroom))
BDBM50092273
PNG
((Z)-5-(2'-Hydroxybenzylidene)-2-thioxothiazolidin-...)
Show SMILES Oc1ccccc1C=C1SC(S)=NC1=O
Show InChI InChI=1S/C10H7NO2S2/c12-7-4-2-1-3-6(7)5-8-9(13)11-10(14)15-8/h1-5,12H,(H,11,13,14)
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n/an/a 9.55E+6n/an/an/an/an/an/a



Shaoyang University

Curated by ChEMBL


Assay Description
Inhibition of diphenolase activity of mushroom tyrosinase preincubated with compound for 10 mins before addition of L-DOPA as substrate by spectropho...


Bioorg Med Chem Lett 21: 2376-9 (2011)


Article DOI: 10.1016/j.bmcl.2011.02.076
BindingDB Entry DOI: 10.7270/Q2SF2WG1
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Electrophorus electricus (Electric eel))
BDBM50092271
PNG
((Z)-5-Benzylidene-2-thioxothiazolidin-4-one | (Z)-...)
Show SMILES SC1=NC(=O)C(S1)=Cc1ccccc1
Show InChI InChI=1S/C10H7NOS2/c12-9-8(14-10(13)11-9)6-7-4-2-1-3-5-7/h1-6H,(H,11,12,13)
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n/an/a>1.00E+5n/an/an/an/an/an/a



The University of Adelaide

Curated by ChEMBL


Assay Description
Inhibition of Electrophorus electricus acetylcholinesterase preincubated for 15 mins by spectrophotometry


Bioorg Med Chem 19: 7453-63 (2011)


Article DOI: 10.1016/j.bmc.2011.10.042
BindingDB Entry DOI: 10.7270/Q2WQ0468
More data for this
Ligand-Target Pair
Beta-lactamase


(Enterobacter cloacae)
BDBM50092271
PNG
((Z)-5-Benzylidene-2-thioxothiazolidin-4-one | (Z)-...)
Show SMILES SC1=NC(=O)C(S1)=Cc1ccccc1
Show InChI InChI=1S/C10H7NOS2/c12-9-8(14-10(13)11-9)6-7-4-2-1-3-5-7/h1-6H,(H,11,12,13)
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n/an/a 4.55E+5n/an/an/an/an/an/a



The R. W. Johnson Pharmaceutical Research Institute

Curated by ChEMBL


Assay Description
Inhibitory activity against class C Beta-lactamase isolated from Enterobacter cloacae


Bioorg Med Chem Lett 10: 2179-82 (2001)


Article DOI: 10.1016/s0960-894x(00)00444-3
BindingDB Entry DOI: 10.7270/Q2T15456
More data for this
Ligand-Target Pair
Beta-lactamase


(Enterobacter cloacae)
BDBM50092273
PNG
((Z)-5-(2'-Hydroxybenzylidene)-2-thioxothiazolidin-...)
Show SMILES Oc1ccccc1C=C1SC(S)=NC1=O
Show InChI InChI=1S/C10H7NO2S2/c12-7-4-2-1-3-6(7)5-8-9(13)11-10(14)15-8/h1-5,12H,(H,11,13,14)
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n/an/a 3.35E+5n/an/an/an/an/an/a



The R. W. Johnson Pharmaceutical Research Institute

Curated by ChEMBL


Assay Description
Inhibitory activity against class C Beta-lactamase isolated from Enterobacter cloacae


Bioorg Med Chem Lett 10: 2179-82 (2001)


Article DOI: 10.1016/s0960-894x(00)00444-3
BindingDB Entry DOI: 10.7270/Q2T15456
More data for this
Ligand-Target Pair
Beta-lactamase TEM


(Enterobacter cloacae)
BDBM50092273
PNG
((Z)-5-(2'-Hydroxybenzylidene)-2-thioxothiazolidin-...)
Show SMILES Oc1ccccc1C=C1SC(S)=NC1=O
Show InChI InChI=1S/C10H7NO2S2/c12-7-4-2-1-3-6(7)5-8-9(13)11-10(14)15-8/h1-5,12H,(H,11,13,14)
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n/an/a>7.00E+5n/an/an/an/an/an/a



The R. W. Johnson Pharmaceutical Research Institute

Curated by ChEMBL


Assay Description
Inhibitory activity against class A Beta-lactamase TEM isolated from Enterobacter coli


Bioorg Med Chem Lett 10: 2179-82 (2001)


Article DOI: 10.1016/s0960-894x(00)00444-3
BindingDB Entry DOI: 10.7270/Q2T15456
More data for this
Ligand-Target Pair
Beta-lactamase


(Enterobacter cloacae)
BDBM50092285
PNG
(4-[4-Oxo-2-thioxo-thiazolidin-(5Z)-ylidenemethyl]-...)
Show SMILES SC1=NC(=O)C(S1)=Cc1ccc(cc1)C#N
Show InChI InChI=1S/C11H6N2OS2/c12-6-8-3-1-7(2-4-8)5-9-10(14)13-11(15)16-9/h1-5H,(H,13,14,15)
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n/an/a 5.00E+5n/an/an/an/an/an/a



The R. W. Johnson Pharmaceutical Research Institute

Curated by ChEMBL


Assay Description
Inhibitory activity against class C Beta-lactamase isolated from Enterobacter cloacae


Bioorg Med Chem Lett 10: 2179-82 (2001)


Article DOI: 10.1016/s0960-894x(00)00444-3
BindingDB Entry DOI: 10.7270/Q2T15456
More data for this
Ligand-Target Pair
Beta-lactamase TEM


(Enterobacter cloacae)
BDBM50092285
PNG
(4-[4-Oxo-2-thioxo-thiazolidin-(5Z)-ylidenemethyl]-...)
Show SMILES SC1=NC(=O)C(S1)=Cc1ccc(cc1)C#N
Show InChI InChI=1S/C11H6N2OS2/c12-6-8-3-1-7(2-4-8)5-9-10(14)13-11(15)16-9/h1-5H,(H,13,14,15)
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n/an/a>7.00E+5n/an/an/an/an/an/a



The R. W. Johnson Pharmaceutical Research Institute

Curated by ChEMBL


Assay Description
Inhibitory activity against class A Beta-lactamase TEM isolated from Enterobacter coli


Bioorg Med Chem Lett 10: 2179-82 (2001)


Article DOI: 10.1016/s0960-894x(00)00444-3
BindingDB Entry DOI: 10.7270/Q2T15456
More data for this
Ligand-Target Pair
MurD


(Escherichia coli (strain K12))
BDBM119123
PNG
(MurD/E/F inhibitor (compound 69))
Show SMILES Oc1ccc(C=C2SC(S)=NC2=O)c(O)c1O
Show InChI InChI=1S/C10H7NO4S2/c12-5-2-1-4(7(13)8(5)14)3-6-9(15)11-10(16)17-6/h1-3,12-14H,(H,11,15,16)
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n/an/a 2.00E+3n/an/an/an/an/an/a



University of Ljubljana, A?kerceva 7, 1000 Ljubljana, Slovenia





Bioorg Chem 55: 2-15 (2014)


Article DOI: 10.1016/j.bioorg.2014.03.008
BindingDB Entry DOI: 10.7270/Q2ZG6QWR
More data for this
Ligand-Target Pair