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BDBM50314534 CHEMBL1090030::N-4-(Aminosulfonyl)phenethyl-S-(2,3,4,6-tetra-O-acetyl-1-thio-beta-D-glucopyranosyl)sulfonamide

SMILES: CC(=O)OC[C@H]1O[C@H]([C@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H]1OC(C)=O)S(=O)(=O)NCCc1ccc(cc1)S(N)(=O)=O

InChI Key: InChIKey=NINWXMVJOLDJPK-BDHVOXNPSA-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 = 50314534   
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 12


(Homo sapiens (Human))
BDBM50314534
PNG
(CHEMBL1090030 | N-4-(Aminosulfonyl)phenethyl-S-(2,...)
Show SMILES CC(=O)OC[C@H]1O[C@H]([C@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H]1OC(C)=O)S(=O)(=O)NCCc1ccc(cc1)S(N)(=O)=O |r|
Show InChI InChI=1S/C22H30N2O13S2/c1-12(25)33-11-18-19(34-13(2)26)20(35-14(3)27)21(36-15(4)28)22(37-18)39(31,32)24-10-9-16-5-7-17(8-6-16)38(23,29)30/h5-8,18-22,24H,9-11H2,1-4H3,(H2,23,29,30)/t18-,19-,20+,21-,22+/m1/s1
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9.5n/an/an/an/an/an/an/an/a



Griffith University

Curated by ChEMBL


Assay Description
Inhibition of human recombinant CA12 by stopped flow CO2 hydration assay


J Med Chem 53: 2913-26 (2010)


Article DOI: 10.1021/jm901888x
BindingDB Entry DOI: 10.7270/Q2DN460W
More data for this
Ligand-Target Pair
Carbonic anhydrase 2


(Homo sapiens (Human))
BDBM50314534
PNG
(CHEMBL1090030 | N-4-(Aminosulfonyl)phenethyl-S-(2,...)
Show SMILES CC(=O)OC[C@H]1O[C@H]([C@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H]1OC(C)=O)S(=O)(=O)NCCc1ccc(cc1)S(N)(=O)=O |r|
Show InChI InChI=1S/C22H30N2O13S2/c1-12(25)33-11-18-19(34-13(2)26)20(35-14(3)27)21(36-15(4)28)22(37-18)39(31,32)24-10-9-16-5-7-17(8-6-16)38(23,29)30/h5-8,18-22,24H,9-11H2,1-4H3,(H2,23,29,30)/t18-,19-,20+,21-,22+/m1/s1
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15.4n/an/an/an/an/an/an/an/a



Griffith University

Curated by ChEMBL


Assay Description
Inhibition of human recombinant CA2 by stopped flow CO2 hydration assay


J Med Chem 53: 2913-26 (2010)


Article DOI: 10.1021/jm901888x
BindingDB Entry DOI: 10.7270/Q2DN460W
More data for this
Ligand-Target Pair
3D
3D Structure (docked)
Carbonic anhydrase 1


(Homo sapiens (Human))
BDBM50314534
PNG
(CHEMBL1090030 | N-4-(Aminosulfonyl)phenethyl-S-(2,...)
Show SMILES CC(=O)OC[C@H]1O[C@H]([C@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H]1OC(C)=O)S(=O)(=O)NCCc1ccc(cc1)S(N)(=O)=O |r|
Show InChI InChI=1S/C22H30N2O13S2/c1-12(25)33-11-18-19(34-13(2)26)20(35-14(3)27)21(36-15(4)28)22(37-18)39(31,32)24-10-9-16-5-7-17(8-6-16)38(23,29)30/h5-8,18-22,24H,9-11H2,1-4H3,(H2,23,29,30)/t18-,19-,20+,21-,22+/m1/s1
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90n/an/an/an/an/an/an/an/a



Griffith University

Curated by ChEMBL


Assay Description
Inhibition of human recombinant CA1 by stopped flow CO2 hydration assay


J Med Chem 53: 2913-26 (2010)


Article DOI: 10.1021/jm901888x
BindingDB Entry DOI: 10.7270/Q2DN460W
More data for this
Ligand-Target Pair
Carbonic anhydrase 9


(Homo sapiens (Human))
BDBM50314534
PNG
(CHEMBL1090030 | N-4-(Aminosulfonyl)phenethyl-S-(2,...)
Show SMILES CC(=O)OC[C@H]1O[C@H]([C@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H]1OC(C)=O)S(=O)(=O)NCCc1ccc(cc1)S(N)(=O)=O |r|
Show InChI InChI=1S/C22H30N2O13S2/c1-12(25)33-11-18-19(34-13(2)26)20(35-14(3)27)21(36-15(4)28)22(37-18)39(31,32)24-10-9-16-5-7-17(8-6-16)38(23,29)30/h5-8,18-22,24H,9-11H2,1-4H3,(H2,23,29,30)/t18-,19-,20+,21-,22+/m1/s1
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PC cid
PC sid
UniChem
Article
PubMed
95n/an/an/an/an/an/an/an/a



Griffith University

Curated by ChEMBL


Assay Description
Inhibition of human recombinant CA9 by stopped flow CO2 hydration assay


J Med Chem 53: 2913-26 (2010)


Article DOI: 10.1021/jm901888x
BindingDB Entry DOI: 10.7270/Q2DN460W
More data for this
Ligand-Target Pair