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BDBM50387160 4-ureidophenyl sulfamate ring derivative 3ay::CHEMBL2047841

SMILES: NS(=O)(=O)Oc1ccc(NC(=O)NCCc2cccs2)cc1

InChI Key: InChIKey=JHMZUJGRFILZST-UHFFFAOYSA-N

Data: 9 KI

Find this compound or compounds like it in BindingDB or PDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 9 hits for monomerid = 50387160   
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 1


(Homo sapiens (Human))
BDBM50387160
PNG
(4-ureidophenyl sulfamate ring derivative 3ay | CHE...)
Show SMILES NS(=O)(=O)Oc1ccc(NC(=O)NCCc2cccs2)cc1
Show InChI InChI=1S/C13H15N3O4S2/c14-22(18,19)20-11-5-3-10(4-6-11)16-13(17)15-8-7-12-2-1-9-21-12/h1-6,9H,7-8H2,(H2,14,18,19)(H2,15,16,17)
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1n/an/an/an/an/an/an/an/a



Romanian Academy

Curated by ChEMBL


Assay Description
Inhibition of human carbonic anhydrase-1


Bioorg Med Chem 21: 1404-9 (2013)


Article DOI: 10.1016/j.bmc.2012.11.004
BindingDB Entry DOI: 10.7270/Q2XW4M4Q
More data for this
Ligand-Target Pair
Carbonic anhydrase 2


(Homo sapiens (Human))
BDBM50387160
PNG
(4-ureidophenyl sulfamate ring derivative 3ay | CHE...)
Show SMILES NS(=O)(=O)Oc1ccc(NC(=O)NCCc2cccs2)cc1
Show InChI InChI=1S/C13H15N3O4S2/c14-22(18,19)20-11-5-3-10(4-6-11)16-13(17)15-8-7-12-2-1-9-21-12/h1-6,9H,7-8H2,(H2,14,18,19)(H2,15,16,17)
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2.30n/an/an/an/an/an/an/an/a



Romanian Academy

Curated by ChEMBL


Assay Description
Inhibition of human carbonic anhydrase-2


Bioorg Med Chem 21: 1404-9 (2013)


Article DOI: 10.1016/j.bmc.2012.11.004
BindingDB Entry DOI: 10.7270/Q2XW4M4Q
More data for this
Ligand-Target Pair
Carbonic anhydrase 12


(Homo sapiens (Human))
BDBM50387160
PNG
(4-ureidophenyl sulfamate ring derivative 3ay | CHE...)
Show SMILES NS(=O)(=O)Oc1ccc(NC(=O)NCCc2cccs2)cc1
Show InChI InChI=1S/C13H15N3O4S2/c14-22(18,19)20-11-5-3-10(4-6-11)16-13(17)15-8-7-12-2-1-9-21-12/h1-6,9H,7-8H2,(H2,14,18,19)(H2,15,16,17)
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3n/an/an/an/an/an/an/an/a



Ecole Nationale Sup£rieure de Chimie de Montpellier

Curated by ChEMBL


Assay Description
Inhibition of human carbonic anhydrase 12 preincubated for 15 mins measured for 10 to 100 sec using phenol red indicator-based stopped flow assay


Bioorg Med Chem Lett 22: 4681-5 (2012)


Article DOI: 10.1016/j.bmcl.2012.05.083
BindingDB Entry DOI: 10.7270/Q20866C2
More data for this
Ligand-Target Pair
Carbonic anhydrase 9


(Homo sapiens (Human))
BDBM50387160
PNG
(4-ureidophenyl sulfamate ring derivative 3ay | CHE...)
Show SMILES NS(=O)(=O)Oc1ccc(NC(=O)NCCc2cccs2)cc1
Show InChI InChI=1S/C13H15N3O4S2/c14-22(18,19)20-11-5-3-10(4-6-11)16-13(17)15-8-7-12-2-1-9-21-12/h1-6,9H,7-8H2,(H2,14,18,19)(H2,15,16,17)
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3.70n/an/an/an/an/an/an/an/a



Romanian Academy

Curated by ChEMBL


Assay Description
Inhibition of human carbonic anhydrase-9


Bioorg Med Chem 21: 1404-9 (2013)


Article DOI: 10.1016/j.bmc.2012.11.004
BindingDB Entry DOI: 10.7270/Q2XW4M4Q
More data for this
Ligand-Target Pair
Carbonic anhydrase 12


(Homo sapiens (Human))
BDBM50387160
PNG
(4-ureidophenyl sulfamate ring derivative 3ay | CHE...)
Show SMILES NS(=O)(=O)Oc1ccc(NC(=O)NCCc2cccs2)cc1
Show InChI InChI=1S/C13H15N3O4S2/c14-22(18,19)20-11-5-3-10(4-6-11)16-13(17)15-8-7-12-2-1-9-21-12/h1-6,9H,7-8H2,(H2,14,18,19)(H2,15,16,17)
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4.20n/an/an/an/an/an/an/an/a



Romanian Academy

Curated by ChEMBL


Assay Description
Inhibition of human carbonic anhydrase-12


Bioorg Med Chem 21: 1404-9 (2013)


Article DOI: 10.1016/j.bmc.2012.11.004
BindingDB Entry DOI: 10.7270/Q2XW4M4Q
More data for this
Ligand-Target Pair
Carbonic anhydrase 9


(Homo sapiens (Human))
BDBM50387160
PNG
(4-ureidophenyl sulfamate ring derivative 3ay | CHE...)
Show SMILES NS(=O)(=O)Oc1ccc(NC(=O)NCCc2cccs2)cc1
Show InChI InChI=1S/C13H15N3O4S2/c14-22(18,19)20-11-5-3-10(4-6-11)16-13(17)15-8-7-12-2-1-9-21-12/h1-6,9H,7-8H2,(H2,14,18,19)(H2,15,16,17)
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9n/an/an/an/an/an/an/an/a



Birla Institute of Technology





J Enzyme Inhib Med Chem 29: 571-81 (2014)


BindingDB Entry DOI: 10.7270/Q2NC5ZCQ
More data for this
Ligand-Target Pair
Carbonic anhydrase 9


(Homo sapiens (Human))
BDBM50387160
PNG
(4-ureidophenyl sulfamate ring derivative 3ay | CHE...)
Show SMILES NS(=O)(=O)Oc1ccc(NC(=O)NCCc2cccs2)cc1
Show InChI InChI=1S/C13H15N3O4S2/c14-22(18,19)20-11-5-3-10(4-6-11)16-13(17)15-8-7-12-2-1-9-21-12/h1-6,9H,7-8H2,(H2,14,18,19)(H2,15,16,17)
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9n/an/an/an/an/an/an/an/a



Ecole Nationale Sup£rieure de Chimie de Montpellier

Curated by ChEMBL


Assay Description
Inhibition of human carbonic anhydrase 9 preincubated for 15 mins measured for 10 to 100 sec using phenol red indicator-based stopped flow assay


Bioorg Med Chem Lett 22: 4681-5 (2012)


Article DOI: 10.1016/j.bmcl.2012.05.083
BindingDB Entry DOI: 10.7270/Q20866C2
More data for this
Ligand-Target Pair
Carbonic anhydrase 2


(Homo sapiens (Human))
BDBM50387160
PNG
(4-ureidophenyl sulfamate ring derivative 3ay | CHE...)
Show SMILES NS(=O)(=O)Oc1ccc(NC(=O)NCCc2cccs2)cc1
Show InChI InChI=1S/C13H15N3O4S2/c14-22(18,19)20-11-5-3-10(4-6-11)16-13(17)15-8-7-12-2-1-9-21-12/h1-6,9H,7-8H2,(H2,14,18,19)(H2,15,16,17)
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236n/an/an/an/an/an/an/an/a



Ecole Nationale Sup£rieure de Chimie de Montpellier

Curated by ChEMBL


Assay Description
Inhibition of human carbonic anhydrase 2 preincubated for 15 mins measured for 10 to 100 sec using phenol red indicator-based stopped flow assay


Bioorg Med Chem Lett 22: 4681-5 (2012)


Article DOI: 10.1016/j.bmcl.2012.05.083
BindingDB Entry DOI: 10.7270/Q20866C2
More data for this
Ligand-Target Pair
Carbonic anhydrase 1


(Homo sapiens (Human))
BDBM50387160
PNG
(4-ureidophenyl sulfamate ring derivative 3ay | CHE...)
Show SMILES NS(=O)(=O)Oc1ccc(NC(=O)NCCc2cccs2)cc1
Show InChI InChI=1S/C13H15N3O4S2/c14-22(18,19)20-11-5-3-10(4-6-11)16-13(17)15-8-7-12-2-1-9-21-12/h1-6,9H,7-8H2,(H2,14,18,19)(H2,15,16,17)
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4.30E+3n/an/an/an/an/an/an/an/a



Ecole Nationale Sup£rieure de Chimie de Montpellier

Curated by ChEMBL


Assay Description
Inhibition of human carbonic anhydrase 1 preincubated for 15 mins measured for 10 to 100 sec using phenol red indicator-based stopped flow assay


Bioorg Med Chem Lett 22: 4681-5 (2012)


Article DOI: 10.1016/j.bmcl.2012.05.083
BindingDB Entry DOI: 10.7270/Q20866C2
More data for this
Ligand-Target Pair