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BDBM50174271 4-(piperazin-1-yl)-1H-indole::CHEMBL200234

SMILES: C1CN(CCN1)c1cccc2[nH]ccc12

InChI Key: InChIKey=YZKSXUIOKWQABW-UHFFFAOYSA-N

Data: 2 KI

PDB links: 1 PDB ID matches this monomer.

Find this compound or compounds like it in BindingDB or PDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50174271   
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
Beta-1 adrenergic receptor


(Homo sapiens (Human))
BDBM50174271
PNG
(4-(piperazin-1-yl)-1H-indole | CHEMBL200234)
Show SMILES C1CN(CCN1)c1cccc2[nH]ccc12
Show InChI InChI=1S/C12H15N3/c1-2-11-10(4-5-14-11)12(3-1)15-8-6-13-7-9-15/h1-5,13-14H,6-9H2
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Similars

Article
PubMed
68n/an/an/an/an/an/an/an/a



Pfizer Inc.

Curated by ChEMBL


Assay Description
Binding affinity to beta1 adrenergic receptor (unknown origin)


J Med Chem 56: 3444-5 (2013)


Article DOI: 10.1021/jm400561w
BindingDB Entry DOI: 10.7270/Q23N24RC
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 6


(Homo sapiens (Human))
BDBM50174271
PNG
(4-(piperazin-1-yl)-1H-indole | CHEMBL200234)
Show SMILES C1CN(CCN1)c1cccc2[nH]ccc12
Show InChI InChI=1S/C12H15N3/c1-2-11-10(4-5-14-11)12(3-1)15-8-6-13-7-9-15/h1-5,13-14H,6-9H2
Reactome pathway
KEGG

UniProtKB/SwissProt

DrugBank
antibodypedia
GoogleScholar
AffyNet 
Purchase

CHEMBL
MMDB
PC cid
PC sid
PDB
UniChem

Patents


Similars

Article
PubMed
2.70E+3n/an/an/an/an/an/an/an/a



Virginia Commonwealth University

Curated by ChEMBL


Assay Description
Displacement of [3H]LSD from human 5HT6 receptor expressed in HEK293 cells


Bioorg Med Chem Lett 15: 5298-302 (2005)


Article DOI: 10.1016/j.bmcl.2005.08.059
BindingDB Entry DOI: 10.7270/Q2ZW1KGZ
More data for this
Ligand-Target Pair