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Compile Data Set for Download or QSAR

Found 3 hits Enz. Inhib. hit(s) with Target = 'Carbonic anhydrase 2' and Ligand = 'BDBM50330332'   
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
Carbonic anhydrase 2


(Homo sapiens (Human))
BDBM50330332
PNG
(CHEMBL1276022 | Diethyl 2-(2-(3-(4-(ethoxycarbonyl...)
Show SMILES [#6]-[#6]-[#8]-[#6](=O)-[#6](=[#7]\[#7]-c1cccc(c1)-n1nc(-[#6](=O)-[#7]-c2nnc(s2)S([#7])(=O)=O)c(-[#6](=O)-[#8]-[#6]-[#6])c1-c1ccccc1)\[#6](=O)-[#8]-[#6]-[#6]
Show InChI InChI=1S/C28H28N8O9S2/c1-4-43-24(38)19-20(23(37)30-27-33-34-28(46-27)47(29,41)42)35-36(22(19)16-11-8-7-9-12-16)18-14-10-13-17(15-18)31-32-21(25(39)44-5-2)26(40)45-6-3/h7-15,31H,4-6H2,1-3H3,(H2,29,41,42)(H,30,33,37)
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50n/an/an/an/an/an/an/an/a



Dumlupinar University

Curated by ChEMBL


Assay Description
Inhibition of human carbonic anhydrase 2 by Lineweaver-Burk plot analysis


Eur J Med Chem 45: 4769-73 (2010)


Article DOI: 10.1016/j.ejmech.2010.07.041
BindingDB Entry DOI: 10.7270/Q2X06796
More data for this
Ligand-Target Pair
Carbonic anhydrase 2


(Homo sapiens (Human))
BDBM50330332
PNG
(CHEMBL1276022 | Diethyl 2-(2-(3-(4-(ethoxycarbonyl...)
Show SMILES [#6]-[#6]-[#8]-[#6](=O)-[#6](=[#7]\[#7]-c1cccc(c1)-n1nc(-[#6](=O)-[#7]-c2nnc(s2)S([#7])(=O)=O)c(-[#6](=O)-[#8]-[#6]-[#6])c1-c1ccccc1)\[#6](=O)-[#8]-[#6]-[#6]
Show InChI InChI=1S/C28H28N8O9S2/c1-4-43-24(38)19-20(23(37)30-27-33-34-28(46-27)47(29,41)42)35-36(22(19)16-11-8-7-9-12-16)18-14-10-13-17(15-18)31-32-21(25(39)44-5-2)26(40)45-6-3/h7-15,31H,4-6H2,1-3H3,(H2,29,41,42)(H,30,33,37)
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n/an/a 60n/an/an/an/an/an/a



Dumlupinar University

Curated by ChEMBL


Assay Description
Inhibition of human carbonic anhydrase 2 hydratase activity by spectrophotometry


Eur J Med Chem 45: 4769-73 (2010)


Article DOI: 10.1016/j.ejmech.2010.07.041
BindingDB Entry DOI: 10.7270/Q2X06796
More data for this
Ligand-Target Pair
Carbonic anhydrase 2


(Homo sapiens (Human))
BDBM50330332
PNG
(CHEMBL1276022 | Diethyl 2-(2-(3-(4-(ethoxycarbonyl...)
Show SMILES [#6]-[#6]-[#8]-[#6](=O)-[#6](=[#7]\[#7]-c1cccc(c1)-n1nc(-[#6](=O)-[#7]-c2nnc(s2)S([#7])(=O)=O)c(-[#6](=O)-[#8]-[#6]-[#6])c1-c1ccccc1)\[#6](=O)-[#8]-[#6]-[#6]
Show InChI InChI=1S/C28H28N8O9S2/c1-4-43-24(38)19-20(23(37)30-27-33-34-28(46-27)47(29,41)42)35-36(22(19)16-11-8-7-9-12-16)18-14-10-13-17(15-18)31-32-21(25(39)44-5-2)26(40)45-6-3/h7-15,31H,4-6H2,1-3H3,(H2,29,41,42)(H,30,33,37)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
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PC cid
PC sid
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Article
PubMed
n/an/a 140n/an/an/an/an/an/a



Dumlupinar University

Curated by ChEMBL


Assay Description
Inhibition of human carbonic anhydrase 2 esterase activity by spectrophotometry


Eur J Med Chem 45: 4769-73 (2010)


Article DOI: 10.1016/j.ejmech.2010.07.041
BindingDB Entry DOI: 10.7270/Q2X06796
More data for this
Ligand-Target Pair