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BDBM50415655 CHEMBL1078529

SMILES: N#CNC(NCCSc1ccccc1)=NCCCc1cnc[nH]1

InChI Key: InChIKey=AAOBJKVPHPJNIH-UHFFFAOYSA-N

Data: 2 EC50

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   Substructure
Similarity at least:  must be >=0.5
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50415655   
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
Histamine H4 receptor


(Homo sapiens (Human))
BDBM50415655
PNG
(CHEMBL1078529)
Show SMILES N#CNC(NCCSc1ccccc1)=NCCCc1cnc[nH]1 |w:14.15|
Show InChI InChI=1S/C16H20N6S/c17-12-21-16(19-8-4-5-14-11-18-13-22-14)20-9-10-23-15-6-2-1-3-7-15/h1-3,6-7,11,13H,4-5,8-10H2,(H,18,22)(H2,19,20,21)
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CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 1.29E+3n/an/an/an/a



University of Regensburg

Curated by ChEMBL


Assay Description
Agonist activity at human histamine H4 receptor expressed in Sf9 cells coexpressing RGS19 protein by steady-state GTPase assay


J Med Chem 52: 6297-313 (2009)


Article DOI: 10.1021/jm900526h
BindingDB Entry DOI: 10.7270/Q2PN96VG
More data for this
Ligand-Target Pair
Histamine H2 Receptor


(Homo sapiens (Human))
BDBM50415655
PNG
(CHEMBL1078529)
Show SMILES N#CNC(NCCSc1ccccc1)=NCCCc1cnc[nH]1 |w:14.15|
Show InChI InChI=1S/C16H20N6S/c17-12-21-16(19-8-4-5-14-11-18-13-22-14)20-9-10-23-15-6-2-1-3-7-15/h1-3,6-7,11,13H,4-5,8-10H2,(H,18,22)(H2,19,20,21)
Reactome pathway
KEGG

UniProtKB/SwissProt

DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 7.24E+3n/an/an/an/a



University of Regensburg

Curated by ChEMBL


Assay Description
Agonist activity at human histamine H2 receptor expressed in Sf9 cells coexpressing GsalphaS protein by steady-state GTPase assay


J Med Chem 52: 6297-313 (2009)


Article DOI: 10.1021/jm900526h
BindingDB Entry DOI: 10.7270/Q2PN96VG
More data for this
Ligand-Target Pair