BDBM50013634 24-(1H-5-imidazolylmethyl)-16-(1H-3-indolylmethyl)-13-[1-methyl-(1S)-propyl]perhydrodipyrido[1,2-a:1,2-d]pyrrolo[1,2-j][1,4,7,10,13,16]hexaazacyclooctadecine-6,12,15,18,23,26-hexaone::CHEMBL52176

SMILES CC[C@H](C)[C@@H]1NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H]2CCCN2C(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H]2CCCCN2C(=O)[C@@H]2CCCCN2C1=O

InChI Key InChIKey=WCNGAVKBHXZVJO-UHFFFAOYSA-N

Data  3 KI

  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 3 hits for monomerid = 50013634   

TargetOxytocin receptor(Rat)
Merck Sharp & Dohme Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50013634(CHEMBL52176 | 24-(1H-5-imidazolylmethyl)-16-(1H-3-...)
Affinity DataKi:  7.80nMAssay Description:Inhibition of [3H]- oxytocin binding to rat uterine Oxytocin receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetVasopressin V2 receptor(Rat)
Merck Sharp & Dohme Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50013634(CHEMBL52176 | 24-(1H-5-imidazolylmethyl)-16-(1H-3-...)
Affinity DataKi:  1.80E+3nMAssay Description:Inhibition of [3H]arginine vasopressin binding to rat kidney medulla Vasopressin V2 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetVasopressin V1a/V1b receptor(Rat)
Merck Sharp & Dohme Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50013634(CHEMBL52176 | 24-(1H-5-imidazolylmethyl)-16-(1H-3-...)
Affinity DataKi:  2.20E+3nMAssay Description:Inhibition of [3H]arginine vasopressin binding to rat liver Vasopressin V1 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed