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SMILES: C[C@@H](NC(=O)c1ccc(NC(=O)c2[nH]c(C)c(Cl)c2Cl)c(OC2CCN(CC2)C(=O)OC(C)(C)C)c1)C(O)=O

InChI Key: InChIKey=WUCKMZXHDIJUHE-UHFFFAOYSA-N

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50249821   
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
DNA gyrase subunit A/B


(Escherichia coli (strain K12))
BDBM50249821
PNG
(CHEMBL4756218)
Show SMILES C[C@@H](NC(=O)c1ccc(NC(=O)c2[nH]c(C)c(Cl)c2Cl)c(OC2CCN(CC2)C(=O)OC(C)(C)C)c1)C(O)=O |r|
Show InChI InChI=1S/C18H15N3O3S/c1-12-9-18(22)21(2)17-8-5-14(10-16(12)17)20-25(23,24)15-6-3-13(11-19)4-7-15/h3-10,20H,1-2H3
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Patents


Similars

n/an/a 71n/an/an/an/an/an/a


TBA

Assay Description
Evaluated for the percent binding affinity against H1 receptor by an H1 histamine-mediated bronchospasm


Citation and Details
More data for this
Ligand-Target Pair