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BDBM50330337 CHEMBL1276394::Ethyl1-(3-iodophenyl)-5-phenyl-3-(5-sulfamoyl-1,3,4-thiadiazol-2-ylcarbamoyl)-1H-pyrazole-4-carboxylate

SMILES: CCOC(=O)c1c(nn(c1-c1ccccc1)-c1cccc(I)c1)C(=O)Nc1nnc(s1)S(N)(=O)=O

InChI Key: InChIKey=CTOWPVTYZJLDOC-UHFFFAOYSA-N

Data: 2 KI  4 IC50

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 6 hits for monomerid = 50330337   
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))
BDBM50330337
PNG
(CHEMBL1276394 | Ethyl1-(3-iodophenyl)-5-phenyl-3-(...)
Show SMILES CCOC(=O)c1c(nn(c1-c1ccccc1)-c1cccc(I)c1)C(=O)Nc1nnc(s1)S(N)(=O)=O
Show InChI InChI=1S/C21H17IN6O5S2/c1-2-33-19(30)15-16(18(29)24-20-25-26-21(34-20)35(23,31)32)27-28(14-10-6-9-13(22)11-14)17(15)12-7-4-3-5-8-12/h3-11H,2H2,1H3,(H2,23,31,32)(H,24,25,29)
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70n/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
More data for this
Ligand-Target Pair
Carbonic anhydrase 1


(Homo sapiens (Human))
BDBM50330337
PNG
(CHEMBL1276394 | Ethyl1-(3-iodophenyl)-5-phenyl-3-(...)
Show SMILES CCOC(=O)c1c(nn(c1-c1ccccc1)-c1cccc(I)c1)C(=O)Nc1nnc(s1)S(N)(=O)=O
Show InChI InChI=1S/C21H17IN6O5S2/c1-2-33-19(30)15-16(18(29)24-20-25-26-21(34-20)35(23,31)32)27-28(14-10-6-9-13(22)11-14)17(15)12-7-4-3-5-8-12/h3-11H,2H2,1H3,(H2,23,31,32)(H,24,25,29)
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90n/an/an/an/an/an/an/an/a



Dumlupinar University

Curated by ChEMBL


Assay Description
Inhibition of human carbonic anhydrase 1 by Lineweaver-Burk plot analysis


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


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


(Homo sapiens (Human))
BDBM50330337
PNG
(CHEMBL1276394 | Ethyl1-(3-iodophenyl)-5-phenyl-3-(...)
Show SMILES CCOC(=O)c1c(nn(c1-c1ccccc1)-c1cccc(I)c1)C(=O)Nc1nnc(s1)S(N)(=O)=O
Show InChI InChI=1S/C21H17IN6O5S2/c1-2-33-19(30)15-16(18(29)24-20-25-26-21(34-20)35(23,31)32)27-28(14-10-6-9-13(22)11-14)17(15)12-7-4-3-5-8-12/h3-11H,2H2,1H3,(H2,23,31,32)(H,24,25,29)
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n/an/a 50n/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
More data for this
Ligand-Target Pair
Carbonic anhydrase 1


(Homo sapiens (Human))
BDBM50330337
PNG
(CHEMBL1276394 | Ethyl1-(3-iodophenyl)-5-phenyl-3-(...)
Show SMILES CCOC(=O)c1c(nn(c1-c1ccccc1)-c1cccc(I)c1)C(=O)Nc1nnc(s1)S(N)(=O)=O
Show InChI InChI=1S/C21H17IN6O5S2/c1-2-33-19(30)15-16(18(29)24-20-25-26-21(34-20)35(23,31)32)27-28(14-10-6-9-13(22)11-14)17(15)12-7-4-3-5-8-12/h3-11H,2H2,1H3,(H2,23,31,32)(H,24,25,29)
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n/an/a 110n/an/an/an/an/an/a



Dumlupinar University

Curated by ChEMBL


Assay Description
Inhibition of human carbonic anhydrase 1 hydratase activity by spectrophotometry


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


Article DOI: 10.1016/j.ejmech.2010.07.041
More data for this
Ligand-Target Pair
Carbonic anhydrase 1


(Homo sapiens (Human))
BDBM50330337
PNG
(CHEMBL1276394 | Ethyl1-(3-iodophenyl)-5-phenyl-3-(...)
Show SMILES CCOC(=O)c1c(nn(c1-c1ccccc1)-c1cccc(I)c1)C(=O)Nc1nnc(s1)S(N)(=O)=O
Show InChI InChI=1S/C21H17IN6O5S2/c1-2-33-19(30)15-16(18(29)24-20-25-26-21(34-20)35(23,31)32)27-28(14-10-6-9-13(22)11-14)17(15)12-7-4-3-5-8-12/h3-11H,2H2,1H3,(H2,23,31,32)(H,24,25,29)
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n/an/a 50n/an/an/an/an/an/a



Dumlupinar University

Curated by ChEMBL


Assay Description
Inhibition of human carbonic anhydrase 1 esterase activity by spectrophotometry


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


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


(Homo sapiens (Human))
BDBM50330337
PNG
(CHEMBL1276394 | Ethyl1-(3-iodophenyl)-5-phenyl-3-(...)
Show SMILES CCOC(=O)c1c(nn(c1-c1ccccc1)-c1cccc(I)c1)C(=O)Nc1nnc(s1)S(N)(=O)=O
Show InChI InChI=1S/C21H17IN6O5S2/c1-2-33-19(30)15-16(18(29)24-20-25-26-21(34-20)35(23,31)32)27-28(14-10-6-9-13(22)11-14)17(15)12-7-4-3-5-8-12/h3-11H,2H2,1H3,(H2,23,31,32)(H,24,25,29)
PDB
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Reactome pathway
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PC sid
UniChem
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PubMed
n/an/a 130n/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
More data for this
Ligand-Target Pair