null

SMILES CCN(CC)c1nc(C)c(s1)C(=S)Nc1cc(ccc1Cl)[N+]([O-])=O

InChI Key InChIKey=DKCVZWQRTVXRGB-UHFFFAOYSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 67287   

TargetBeta-galactosidase(Escherichia coli)
Burnham Center for Chemical Genomics

Curated by PubChem BioAssay
LigandPNGBDBM67287(MLS000770828 | N-(2-chloranyl-5-nitro-phenyl)-2-(d...)copy SMILEScopy InChI
Affinity DataEC50:  2.48E+4nMAssay Description:Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute(SBMRI, San Diego, C...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2SN07DKPCBioAssay
TargetApelin receptor(Homo sapiens (Human))
Sanford-Burnham Center for Chemical Genomics

Curated by PubChem BioAssay
LigandPNGBDBM67287(MLS000770828 | N-(2-chloranyl-5-nitro-phenyl)-2-(d...)copy SMILEScopy InChI
Affinity DataIC50: 5.55E+3nMAssay Description:Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford- Sanford-Burnham Medical Research Institute(SBMRI, San...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2MK6BBZPCBioAssay