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BDBM50209292 CHEMBL3884793

SMILES: COc1ccc(OC)c(c1)[C@H]1[C@@H](C(=O)N1c1ccc(cc1)S(N)(=O)=O)c1ccccc1

InChI Key: InChIKey=GJEOIPWOOVXMSD-VXKWHMMOSA-N

Data: 4 KI

Find this compound or compounds like it in BindingDB or PDB:
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Similarity at least:  must be >=0.5
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50209292   
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 2


(Homo sapiens (Human))
BDBM50209292
PNG
(CHEMBL3884793)
Show SMILES COc1ccc(OC)c(c1)[C@H]1[C@@H](C(=O)N1c1ccc(cc1)S(N)(=O)=O)c1ccccc1 |r|
Show InChI InChI=1S/C23H22N2O5S/c1-29-17-10-13-20(30-2)19(14-17)22-21(15-6-4-3-5-7-15)23(26)25(22)16-8-11-18(12-9-16)31(24,27)28/h3-14,21-22H,1-2H3,(H2,24,27,28)/t21-,22-/m0/s1
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Article
PubMed
0.760n/an/an/an/an/an/an/an/a



National Institute of Pharmaceutical Education and Research (NIPER)

Curated by ChEMBL


Assay Description
Inhibition of human recombinant carbonic anhydrase-2 using CO2 as substrate preincubated for 10 mins by stopped-flow CO2 hydrase assay


Bioorg Med Chem 25: 539-544 (2017)


Article DOI: 10.1016/j.bmc.2016.11.027
BindingDB Entry DOI: 10.7270/Q2G73GQQ
More data for this
Ligand-Target Pair
Carbonic anhydrase 7


(Homo sapiens (Human))
BDBM50209292
PNG
(CHEMBL3884793)
Show SMILES COc1ccc(OC)c(c1)[C@H]1[C@@H](C(=O)N1c1ccc(cc1)S(N)(=O)=O)c1ccccc1 |r|
Show InChI InChI=1S/C23H22N2O5S/c1-29-17-10-13-20(30-2)19(14-17)22-21(15-6-4-3-5-7-15)23(26)25(22)16-8-11-18(12-9-16)31(24,27)28/h3-14,21-22H,1-2H3,(H2,24,27,28)/t21-,22-/m0/s1
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Article
PubMed
9.10n/an/an/an/an/an/an/an/a



National Institute of Pharmaceutical Education and Research (NIPER)

Curated by ChEMBL


Assay Description
Inhibition of human recombinant carbonic anhydrase-7 using CO2 as substrate preincubated for 10 mins by stopped-flow CO2 hydrase assay


Bioorg Med Chem 25: 539-544 (2017)


Article DOI: 10.1016/j.bmc.2016.11.027
BindingDB Entry DOI: 10.7270/Q2G73GQQ
More data for this
Ligand-Target Pair
Carbonic anhydrase 4


(Homo sapiens (Human))
BDBM50209292
PNG
(CHEMBL3884793)
Show SMILES COc1ccc(OC)c(c1)[C@H]1[C@@H](C(=O)N1c1ccc(cc1)S(N)(=O)=O)c1ccccc1 |r|
Show InChI InChI=1S/C23H22N2O5S/c1-29-17-10-13-20(30-2)19(14-17)22-21(15-6-4-3-5-7-15)23(26)25(22)16-8-11-18(12-9-16)31(24,27)28/h3-14,21-22H,1-2H3,(H2,24,27,28)/t21-,22-/m0/s1
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Article
PubMed
36n/an/an/an/an/an/an/an/a



National Institute of Pharmaceutical Education and Research (NIPER)

Curated by ChEMBL


Assay Description
Inhibition of human recombinant carbonic anhydrase-4 using CO2 as substrate preincubated for 10 mins by stopped-flow CO2 hydrase assay


Bioorg Med Chem 25: 539-544 (2017)


Article DOI: 10.1016/j.bmc.2016.11.027
BindingDB Entry DOI: 10.7270/Q2G73GQQ
More data for this
Ligand-Target Pair
Carbonic anhydrase 1


(Homo sapiens (Human))
BDBM50209292
PNG
(CHEMBL3884793)
Show SMILES COc1ccc(OC)c(c1)[C@H]1[C@@H](C(=O)N1c1ccc(cc1)S(N)(=O)=O)c1ccccc1 |r|
Show InChI InChI=1S/C23H22N2O5S/c1-29-17-10-13-20(30-2)19(14-17)22-21(15-6-4-3-5-7-15)23(26)25(22)16-8-11-18(12-9-16)31(24,27)28/h3-14,21-22H,1-2H3,(H2,24,27,28)/t21-,22-/m0/s1
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Article
PubMed
61n/an/an/an/an/an/an/an/a



National Institute of Pharmaceutical Education and Research (NIPER)

Curated by ChEMBL


Assay Description
Inhibition of human recombinant carbonic anhydrase-1 using CO2 as substrate preincubated for 10 mins by stopped-flow CO2 hydrase assay


Bioorg Med Chem 25: 539-544 (2017)


Article DOI: 10.1016/j.bmc.2016.11.027
BindingDB Entry DOI: 10.7270/Q2G73GQQ
More data for this
Ligand-Target Pair