BindingDB logo
myBDB logout
Compile Data Set for Download or QSAR

Found 4 hits Enz. Inhib. hit(s) with Target = 'Carbonic anhydrase 2' and Ligand = 'BDBM50288900'   
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))
BDBM50288900
PNG
((2-{2-[2-(4-Sulfamoyl-benzoylamino)-acetylamino]-a...)
Show SMILES NS(=O)(=O)c1ccc(cc1)C(=O)NCC(=O)NCC(=O)NCC(=O)NCC(O)=O
Show InChI InChI=1S/C15H19N5O8S/c16-29(27,28)10-3-1-9(2-4-10)15(26)20-7-13(23)18-5-11(21)17-6-12(22)19-8-14(24)25/h1-4H,5-8H2,(H,17,21)(H,18,23)(H,19,22)(H,20,26)(H,24,25)(H2,16,27,28)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
Article
n/an/an/an/an/an/a 2.50E+5n/an/a



TBA

Curated by ChEMBL


Assay Description
Kinetic constant for binding human carbonic anhydrase II (Kon=Kd x Koff)


Bioorg Med Chem Lett 6: 559-564 (1996)


Article DOI: 10.1016/0960-894X(96)00069-8
More data for this
Ligand-Target Pair
Carbonic anhydrase 2


(Homo sapiens (Human))
BDBM50288900
PNG
((2-{2-[2-(4-Sulfamoyl-benzoylamino)-acetylamino]-a...)
Show SMILES NS(=O)(=O)c1ccc(cc1)C(=O)NCC(=O)NCC(=O)NCC(=O)NCC(O)=O
Show InChI InChI=1S/C15H19N5O8S/c16-29(27,28)10-3-1-9(2-4-10)15(26)20-7-13(23)18-5-11(21)17-6-12(22)19-8-14(24)25/h1-4H,5-8H2,(H,17,21)(H,18,23)(H,19,22)(H,20,26)(H,24,25)(H2,16,27,28)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
Article
n/an/an/a 390n/an/an/an/an/a



TBA

Curated by ChEMBL




Bioorg Med Chem Lett 6: 559-564 (1996)


Article DOI: 10.1016/0960-894X(96)00069-8
More data for this
Ligand-Target Pair
Carbonic anhydrase 2


(Homo sapiens (Human))
BDBM50288900
PNG
((2-{2-[2-(4-Sulfamoyl-benzoylamino)-acetylamino]-a...)
Show SMILES NS(=O)(=O)c1ccc(cc1)C(=O)NCC(=O)NCC(=O)NCC(=O)NCC(O)=O
Show InChI InChI=1S/C15H19N5O8S/c16-29(27,28)10-3-1-9(2-4-10)15(26)20-7-13(23)18-5-11(21)17-6-12(22)19-8-14(24)25/h1-4H,5-8H2,(H,17,21)(H,18,23)(H,19,22)(H,20,26)(H,24,25)(H2,16,27,28)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
Article
n/an/an/a 360n/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Dissociation constant against human carbonic anhydrase II at 37 degree centigrade


Bioorg Med Chem Lett 6: 559-564 (1996)


Article DOI: 10.1016/0960-894X(96)00069-8
More data for this
Ligand-Target Pair
Carbonic anhydrase 2


(Homo sapiens (Human))
BDBM50288900
PNG
((2-{2-[2-(4-Sulfamoyl-benzoylamino)-acetylamino]-a...)
Show SMILES NS(=O)(=O)c1ccc(cc1)C(=O)NCC(=O)NCC(=O)NCC(=O)NCC(O)=O
Show InChI InChI=1S/C15H19N5O8S/c16-29(27,28)10-3-1-9(2-4-10)15(26)20-7-13(23)18-5-11(21)17-6-12(22)19-8-14(24)25/h1-4H,5-8H2,(H,17,21)(H,18,23)(H,19,22)(H,20,26)(H,24,25)(H2,16,27,28)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
Article
n/an/an/an/an/a 0.0900n/an/an/a



TBA

Curated by ChEMBL


Assay Description
Kinetic constant for binding human carbonic anhydrase II (Kon=Kd x Koff)


Bioorg Med Chem Lett 6: 559-564 (1996)


Article DOI: 10.1016/0960-894X(96)00069-8
More data for this
Ligand-Target Pair