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BDBM50086253 CHEMBL3425763

SMILES: C(c1ccccc1)c1cc2CCNCCc2cn1

InChI Key: InChIKey=RJSBTQXSGIHBAJ-UHFFFAOYSA-N

Data: 1 KI  1 EC50

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 = 50086253   
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
5-hydroxytryptamine receptor 2C


(Homo sapiens (Human))
BDBM50086253
PNG
(CHEMBL3425763)
Show SMILES C(c1ccccc1)c1cc2CCNCCc2cn1
Show InChI InChI=1S/C16H18N2/c1-2-4-13(5-3-1)10-16-11-14-6-8-17-9-7-15(14)12-18-16/h1-5,11-12,17H,6-10H2
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CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
35n/an/an/an/an/an/an/an/a



University of Cambridge

Curated by ChEMBL


Assay Description
Inhibition of Cy3B conjugated serotonin analogue binding to human recombinant 5-HT2C receptor expressed in Swiss mouse 3T3 cell membranes after 60 mi...


ACS Med Chem Lett 6: 329-33 (2015)


Article DOI: 10.1021/ml500507v
BindingDB Entry DOI: 10.7270/Q29K4CZW
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 2B


(Homo sapiens (Human))
BDBM50086253
PNG
(CHEMBL3425763)
Show SMILES C(c1ccccc1)c1cc2CCNCCc2cn1
Show InChI InChI=1S/C16H18N2/c1-2-4-13(5-3-1)10-16-11-14-6-8-17-9-7-15(14)12-18-16/h1-5,11-12,17H,6-10H2
Reactome pathway
KEGG

UniProtKB/SwissProt

DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 27n/an/an/an/a



University of Cambridge

Curated by ChEMBL


Assay Description
Agonist activity at human recombinant 5-HT2B receptor expressed in CHOK1 cells assessed as induction of Ca2+ mobilization after 1 hr by FLIPR assay


ACS Med Chem Lett 6: 329-33 (2015)


Article DOI: 10.1021/ml500507v
BindingDB Entry DOI: 10.7270/Q29K4CZW
More data for this
Ligand-Target Pair