BDBM50145565 1,2,3,4,8,9,10,11,12,13-decahydrocycloocta[b][1,4]diazepino[6,7,1-hi]indole::CHEMBL89738

SMILES C1Cn2c3CCCCCCc3c3cccc(CN1)c23

InChI Key InChIKey=FEOKYCHGJRHIDE-UHFFFAOYSA-N

Data  4 KI  1 EC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50145565   

Target5-hydroxytryptamine receptor 2C(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50145565(1,2,3,4,8,9,10,11,12,13-decahydrocycloocta[b][1,4]...)
Affinity DataKi:  13nMAssay Description:Agonistic binding affinity against human 5-hydroxytryptamine 2C receptor in CHO cells using [125I]- DOI More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 2A(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50145565(1,2,3,4,8,9,10,11,12,13-decahydrocycloocta[b][1,4]...)
Affinity DataKi:  36nMAssay Description:Agonistic binding affinity of the compound against human 5-hydroxytryptamine 2A receptor in CHO cells using 8-OH-DPA radioligandMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetD(1A) dopamine receptor(RAT)
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50145565(1,2,3,4,8,9,10,11,12,13-decahydrocycloocta[b][1,4]...)
Affinity DataKi:  665nMAssay Description:Binding affinity of the compound against dopamine receptor D1AMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 2B(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50145565(1,2,3,4,8,9,10,11,12,13-decahydrocycloocta[b][1,4]...)
Affinity DataKi: >5.00E+3nMAssay Description:Binding affinity of the compound against 5-hydroxytryptamine 1A receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed