BindingDB logo
myBDB logout
Compile Data Set for Download or QSAR

Found 3 hits of ki for monomerid = 50084534   
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))
BDBM50084534
PNG
(2,6-Diethyl-4-phenyl-1-{[2-(5-sulfamoyl-[1,3,4]thi...)
Show SMILES CCc1cc(cc(CC)[n+]1CC(=O)NCCC(=O)Nc1nnc(s1)S(N)(=O)=O)-c1ccccc1
Show InChI InChI=1S/C22H26N6O4S2/c1-3-17-12-16(15-8-6-5-7-9-15)13-18(4-2)28(17)14-20(30)24-11-10-19(29)25-21-26-27-22(33-21)34(23,31)32/h5-9,12-13H,3-4,10-11,14H2,1-2H3,(H3-,23,24,25,26,29,30,31,32)/p+1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

PubMed
4n/an/an/an/an/an/an/an/a



Università degli Studi

Curated by ChEMBL


Assay Description
Inhibitory activity against human carbonic anhydrase II (CA2)


J Med Chem 43: 292-300 (2000)


BindingDB Entry DOI: 10.7270/Q22806T7
More data for this
Ligand-Target Pair
Carbonic anhydrase 4


(Bos taurus (bovine))
BDBM50084534
PNG
(2,6-Diethyl-4-phenyl-1-{[2-(5-sulfamoyl-[1,3,4]thi...)
Show SMILES CCc1cc(cc(CC)[n+]1CC(=O)NCCC(=O)Nc1nnc(s1)S(N)(=O)=O)-c1ccccc1
Show InChI InChI=1S/C22H26N6O4S2/c1-3-17-12-16(15-8-6-5-7-9-15)13-18(4-2)28(17)14-20(30)24-11-10-19(29)25-21-26-27-22(33-21)34(23,31)32/h5-9,12-13H,3-4,10-11,14H2,1-2H3,(H3-,23,24,25,26,29,30,31,32)/p+1
Reactome pathway
KEGG

UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

PubMed
19n/an/an/an/an/an/an/an/a



Università degli Studi

Curated by ChEMBL


Assay Description
Inhibitory activity against bovine carbonic anhydrase IV (CA4), isolated from bovine lung microsomes


J Med Chem 43: 292-300 (2000)


BindingDB Entry DOI: 10.7270/Q22806T7
More data for this
Ligand-Target Pair
Carbonic anhydrase 1


(Homo sapiens (Human))
BDBM50084534
PNG
(2,6-Diethyl-4-phenyl-1-{[2-(5-sulfamoyl-[1,3,4]thi...)
Show SMILES CCc1cc(cc(CC)[n+]1CC(=O)NCCC(=O)Nc1nnc(s1)S(N)(=O)=O)-c1ccccc1
Show InChI InChI=1S/C22H26N6O4S2/c1-3-17-12-16(15-8-6-5-7-9-15)13-18(4-2)28(17)14-20(30)24-11-10-19(29)25-21-26-27-22(33-21)34(23,31)32/h5-9,12-13H,3-4,10-11,14H2,1-2H3,(H3-,23,24,25,26,29,30,31,32)/p+1
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

PubMed
41n/an/an/an/an/an/an/an/a



Università degli Studi

Curated by ChEMBL


Assay Description
Inhibitory activity against human carbonic anhydrase I (CA1)


J Med Chem 43: 292-300 (2000)


BindingDB Entry DOI: 10.7270/Q22806T7
More data for this
Ligand-Target Pair