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3 similar compounds to monomer 50209855

Compile data set for download or QSAR
Wt: 424.9
BDBM50209856
Wt: 370.4
BDBM50209858
Wt: 401.2
BDBM50234561

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 8 hits for monomerid = 50209856,50209858,50234561   
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
Carbonic anhydrase


(Homo sapiens (Human))
BDBM50209858
PNG
(CHEMBL3884577)
Show SMILES Cc1ccc(cc1)-c1cn2nc(sc2n1)-c1ccc(cc1)S(N)(=O)=O
Show InChI InChI=1S/C17H14N4O2S2/c1-11-2-4-12(5-3-11)15-10-21-17(19-15)24-16(20-21)13-6-8-14(9-7-13)25(18,22)23/h2-10H,1H3,(H2,18,22,23)
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3.30n/an/an/an/an/an/an/an/a



Kurukshetra University

Curated by ChEMBL


Assay Description
Inhibition of recombinant human membrane bound carbonic anhydrase 12 by stopped-flow CO2 hydration assay


Bioorg Med Chem 25: 1286-1293 (2017)


Article DOI: 10.1016/j.bmc.2016.12.047
BindingDB Entry DOI: 10.7270/Q2222WSR
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 1A (5-HT1A)


(Homo sapiens (Human))
BDBM50209856
PNG
(CHEMBL3885178)
Show SMILES Cc1nc2ccccc2c(=O)n1CCCCCN1CCN(CC1)c1ccc(Cl)cc1
Show InChI InChI=1S/C24H29ClN4O/c1-19-26-23-8-4-3-7-22(23)24(30)29(19)14-6-2-5-13-27-15-17-28(18-16-27)21-11-9-20(25)10-12-21/h3-4,7-12H,2,5-6,13-18H2,1H3
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100n/an/an/an/an/an/an/an/a



Universit£ di Catania

Curated by ChEMBL


Assay Description
Displacement of [3H]-8-OH-DPAT from recombinant human 5-HT1A receptor expressed in CHOK1 cell membranes after 1 hr by liquid scintillation counting m...


Bioorg Med Chem 25: 1250-1259 (2017)


Article DOI: 10.1016/j.bmc.2016.12.039
BindingDB Entry DOI: 10.7270/Q25T3NH5
More data for this
Ligand-Target Pair
Carbonic anhydrase 2


(Homo sapiens (Human))
BDBM50209858
PNG
(CHEMBL3884577)
Show SMILES Cc1ccc(cc1)-c1cn2nc(sc2n1)-c1ccc(cc1)S(N)(=O)=O
Show InChI InChI=1S/C17H14N4O2S2/c1-11-2-4-12(5-3-11)15-10-21-17(19-15)24-16(20-21)13-6-8-14(9-7-13)25(18,22)23/h2-10H,1H3,(H2,18,22,23)
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240n/an/an/an/an/an/an/an/a



Kurukshetra University

Curated by ChEMBL


Assay Description
Inhibition of recombinant human erythrocyte cytosolic carbonic anhydrase 2 by stopped-flow CO2 hydration assay


Bioorg Med Chem 25: 1286-1293 (2017)


Article DOI: 10.1016/j.bmc.2016.12.047
BindingDB Entry DOI: 10.7270/Q2222WSR
More data for this
Ligand-Target Pair
Carbonic anhydrase 1


(Homo sapiens (Human))
BDBM50209858
PNG
(CHEMBL3884577)
Show SMILES Cc1ccc(cc1)-c1cn2nc(sc2n1)-c1ccc(cc1)S(N)(=O)=O
Show InChI InChI=1S/C17H14N4O2S2/c1-11-2-4-12(5-3-11)15-10-21-17(19-15)24-16(20-21)13-6-8-14(9-7-13)25(18,22)23/h2-10H,1H3,(H2,18,22,23)
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243n/an/an/an/an/an/an/an/a



Kurukshetra University

Curated by ChEMBL


Assay Description
Inhibition of recombinant human erythrocyte cytosolic carbonic anhydrase 1 by stopped-flow CO2 hydration assay


Bioorg Med Chem 25: 1286-1293 (2017)


Article DOI: 10.1016/j.bmc.2016.12.047
BindingDB Entry DOI: 10.7270/Q2222WSR
More data for this
Ligand-Target Pair
Carbonic anhydrase 9


(Homo sapiens (Human))
BDBM50209858
PNG
(CHEMBL3884577)
Show SMILES Cc1ccc(cc1)-c1cn2nc(sc2n1)-c1ccc(cc1)S(N)(=O)=O
Show InChI InChI=1S/C17H14N4O2S2/c1-11-2-4-12(5-3-11)15-10-21-17(19-15)24-16(20-21)13-6-8-14(9-7-13)25(18,22)23/h2-10H,1H3,(H2,18,22,23)
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275n/an/an/an/an/an/an/an/a



Kurukshetra University

Curated by ChEMBL


Assay Description
Inhibition of recombinant human membrane bound carbonic anhydrase 9 by stopped-flow CO2 hydration assay


Bioorg Med Chem 25: 1286-1293 (2017)


Article DOI: 10.1016/j.bmc.2016.12.047
BindingDB Entry DOI: 10.7270/Q2222WSR
More data for this
Ligand-Target Pair
5-Hydroxytryptamine receptor 7 (5-HT7)


(Homo sapiens (Human))
BDBM50209856
PNG
(CHEMBL3885178)
Show SMILES Cc1nc2ccccc2c(=O)n1CCCCCN1CCN(CC1)c1ccc(Cl)cc1
Show InChI InChI=1S/C24H29ClN4O/c1-19-26-23-8-4-3-7-22(23)24(30)29(19)14-6-2-5-13-27-15-17-28(18-16-27)21-11-9-20(25)10-12-21/h3-4,7-12H,2,5-6,13-18H2,1H3
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327n/an/an/an/an/an/an/an/a



Universit£ di Catania

Curated by ChEMBL


Assay Description
Displacement of [3H]-5-HT from recombinant human 5-HT7A receptor expressed in CHOK1 cell membranes after 40 mins by liquid scintillation counting met...


Bioorg Med Chem 25: 1250-1259 (2017)


Article DOI: 10.1016/j.bmc.2016.12.039
BindingDB Entry DOI: 10.7270/Q25T3NH5
More data for this
Ligand-Target Pair
Alpha-galactosidase A


(Homo sapiens (Human))
BDBM50234561
PNG
(CHEMBL4090087)
Show SMILES COc1ccc(Br)cc1\C=C\C(=O)NC[C@H]1N[C@H](CO)[C@H](O)[C@@H]1O
Show InChI InChI=1S/C16H21BrN2O5/c1-24-13-4-3-10(17)6-9(13)2-5-14(21)18-7-11-15(22)16(23)12(8-20)19-11/h2-6,11-12,15-16,19-20,22-23H,7-8H2,1H3,(H,18,21)/b5-2+/t11-,12-,15-,16+/m1/s1
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n/an/a 3.00E+3n/an/an/an/an/an/a



National Cheng-Kung University

Curated by ChEMBL


Assay Description
Inhibition of recombinant human alpha GAL-A using 4-methylumbelliferyl alpha-D-galactopyranoside as substrate at pH 7 after 15 mins by fluorescence a...


Eur J Med Chem 126: 1-6 (2017)


Article DOI: 10.1016/j.ejmech.2016.10.004
More data for this
Ligand-Target Pair
Alpha-galactosidase A


(Homo sapiens (Human))
BDBM50234561
PNG
(CHEMBL4090087)
Show SMILES COc1ccc(Br)cc1\C=C\C(=O)NC[C@H]1N[C@H](CO)[C@H](O)[C@@H]1O
Show InChI InChI=1S/C16H21BrN2O5/c1-24-13-4-3-10(17)6-9(13)2-5-14(21)18-7-11-15(22)16(23)12(8-20)19-11/h2-6,11-12,15-16,19-20,22-23H,7-8H2,1H3,(H,18,21)/b5-2+/t11-,12-,15-,16+/m1/s1
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n/an/a 3.28E+4n/an/an/an/an/an/a



National Cheng-Kung University

Curated by ChEMBL


Assay Description
Inhibition of recombinant human alpha GAL-A using 4-methylumbelliferyl alpha-D-galactopyranoside as substrate at pH 4.6 after 15 mins by fluorescence...


Eur J Med Chem 126: 1-6 (2017)


Article DOI: 10.1016/j.ejmech.2016.10.004
More data for this
Ligand-Target Pair