BDBM50187891 2-[(1E,3E)-5-[(2E)-1-[5-({2-[(Z)-[(cyanoamino)({3-[3-(piperidin-1-ylmethyl)phenoxy]propyl}amino)methylidene]amino]ethyl}carbamoyl)pentyl]-3,3-dimethyl-2,3-dihydro-1H-indol-2-ylidene]penta-1,3-dien-1-yl]-3,3-dimethyl-1-(4-sulfonatobutyl)-3H-indol-1-ium::CHEMBL213357

SMILES CC1(C)C(=CC=CC=CC2=[N+](CCCCS(=O)(=O)[O-])c3ccccc3C2(C)C)N(CCCCCC(=O)NCCN=C(NC#N)NCCCOc2cccc(CN3CCCCC3)c2)c2ccccc21

InChI Key InChIKey=GFJYCIFKTFCPQN-UHFFFAOYSA-N

Data  2 EC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50187891   

TargetHistamine H2 receptor(Guinea pig)
The University of Kansas

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50187891BDBM50187891(2-[(1E,3E)-5-[(2E)-1-[5-({2-[(Z)-[(cyanoamino)({3-...)
Affinity DataEC50:  90nMAssay Description:Agonist activity at guinea pig H2RMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H2 receptor(Human)
The University of Kansas

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50187891BDBM50187891(2-[(1E,3E)-5-[(2E)-1-[5-({2-[(Z)-[(cyanoamino)({3-...)
Affinity DataEC50:  160nMAssay Description:Agonist activity at human H2RMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed