BDBM50364974 CHEMBL1950736

SMILES O=c1ccc(n[nH]1)-c1ccc(OC2CCN(CC2)C2CCC2)nc1

InChI Key InChIKey=PNDGEZRNHBDFPU-UHFFFAOYSA-N

Data  2 KI  1 IC50

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50364974   

TargetHistamine H3 receptor(Homo sapiens (Human))
Cephalon

Curated by ChEMBL

LigandBDBM50364974(CHEMBL1950736)Copy SMILESCopy InChI

Affinity DataKi:  6.30nMAssay Description:Displacement of [3H]NAMH from human histamine H3 receptor expressed in CHO cellsMore data for this Ligand-Target Pair

Target InfoPDBReactome pathwayKEGG
UniProtKB/SwissProt
DrugBankantibodypediaGoogleScholar

Ligand InfoCHEMBLPC cidPC sidPatentsSimilars

In DepthDetails ArticlePubMed
Copy BDB DOI

TargetHistamine H3 receptor(Rattus norvegicus (rat))
Cephalon

Curated by ChEMBL

LigandBDBM50364974(CHEMBL1950736)Copy SMILESCopy InChI

Affinity DataKi:  19nMAssay Description:Displacement of [3H]NAMH from rat histamine H3 receptor expressed in CHO cellsMore data for this Ligand-Target Pair

Target InfoPDBReactome pathwayKEGG
UniProtKB/SwissProt
GoogleScholar

Ligand InfoCHEMBLPC cidPC sidPatentsSimilars

In DepthDetails ArticlePubMed
Copy BDB DOI

TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Cephalon

Curated by ChEMBL

LigandBDBM50364974(CHEMBL1950736)Copy SMILESCopy InChI

Affinity DataIC50:  9.00E+3nMAssay Description:Inhibition of human Erg by patch clamp assayMore data for this Ligand-Target Pair

Target InfoPDBMMDBReactome pathwayKEGG
UniProtKB/SwissProt
B.MOADDrugBankantibodypediaGoogleScholar

Ligand InfoCHEMBLPC cidPC sidPatentsSimilars

In DepthDetails ArticlePubMed
Copy BDB DOI