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BDBM368162 3-(2-Aminobenzo[d]thiazol-4-yl)-6-(((3 S,5S)-5-(hydroxymethyl)pyrrolidin-3-yl) sulfonyl)-2-(2H-tetrazol-5-yl)benzenesulfonamide::US10227331, Example 349

SMILES: Nc1nc2c(cccc2s1)-c1ccc(c(c1-c1nn[nH]n1)S(N)(=O)=O)S(=O)(=O)[C@@H]1CN[C@H](CO)C1

InChI Key:

Data: 3 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 3 hits for monomerid = 368162   
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
Metallo-beta-lactamase type 2


(Serratia marcescens)
BDBM368162
PNG
(3-(2-Aminobenzo[d]thiazol-4-yl)-6-(((3 S,5S)-5-(hy...)
Show SMILES Nc1nc2c(cccc2s1)-c1ccc(c(c1-c1nn[nH]n1)S(N)(=O)=O)S(=O)(=O)[C@@H]1CN[C@H](CO)C1 |r|
PDB

UniProtKB/SwissProt
UniProtKB/TrEMBL

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 0.220n/an/an/an/an/an/a



Abbott Laboratories



Assay Description
The Class B enzyme activities were measured in the presence of the test inhibitor in a fluorescence assay against a commercially available substrate ...


J Med Chem 51: 1231-41 (2008)


BindingDB Entry DOI: 10.7270/Q2Z60RCD
More data for this
Ligand-Target Pair
VIM-1


(Pseudomonas aeruginosa)
BDBM368162
PNG
(3-(2-Aminobenzo[d]thiazol-4-yl)-6-(((3 S,5S)-5-(hy...)
Show SMILES Nc1nc2c(cccc2s1)-c1ccc(c(c1-c1nn[nH]n1)S(N)(=O)=O)S(=O)(=O)[C@@H]1CN[C@H](CO)C1 |r|
PDB

UniProtKB/TrEMBL

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 0.452n/an/an/an/an/an/a



Abbott Laboratories



Assay Description
The Class B enzyme activities were measured in the presence of the test inhibitor in a fluorescence assay against a commercially available substrate ...


J Med Chem 51: 1231-41 (2008)


BindingDB Entry DOI: 10.7270/Q2Z60RCD
More data for this
Ligand-Target Pair
Beta-lactamase NDM-1


(Klebsiella pneumoniae)
BDBM368162
PNG
(3-(2-Aminobenzo[d]thiazol-4-yl)-6-(((3 S,5S)-5-(hy...)
Show SMILES Nc1nc2c(cccc2s1)-c1ccc(c(c1-c1nn[nH]n1)S(N)(=O)=O)S(=O)(=O)[C@@H]1CN[C@H](CO)C1 |r|
PDB

UniProtKB/SwissProt
UniProtKB/TrEMBL

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 0.0660n/an/an/an/an/an/a



Abbott Laboratories



Assay Description
The Class B enzyme activities were measured in the presence of the test inhibitor in a fluorescence assay against a commercially available substrate ...


J Med Chem 51: 1231-41 (2008)


BindingDB Entry DOI: 10.7270/Q2Z60RCD
More data for this
Ligand-Target Pair