null

SMILES CN1CCCN(CC1)C(=S)[C@@H]1CCCN1C(=O)NCc1ccc(cc1C)C(=O)N1Cc2cccn2Cc2ccccc12

InChI Key InChIKey=XTIWITBMTVGYLG-PMERELPUSA-N

  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 = 50307111   

TargetVasopressin V1a receptor(Homo sapiens (Human))
UMR 7200 CNRS/Universit£ de Strasbourg

Curated by ChEMBL
LigandPNGBDBM50307111((2S)-N-[2-Methyl-4-(5H-pyrrolo[2,1-c][1,4]benzodia...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+3nMAssay Description:Displacement of [3H]AVP from human vasopressin V1a receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FX7BD4PubMed
TargetOxytocin receptor(Homo sapiens (Human))
UMR 7200 CNRS/Universit£ de Strasbourg

Curated by ChEMBL
LigandPNGBDBM50307111((2S)-N-[2-Methyl-4-(5H-pyrrolo[2,1-c][1,4]benzodia...)copy SMILEScopy InChI
Affinity DataKi:  2.50E+3nMAssay Description:Displacement of [3H]AVP from human oxytocin receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FX7BD4PubMed
TargetVasopressin V2 receptor(Homo sapiens (Human))
UMR 7200 CNRS/Universit£ de Strasbourg

Curated by ChEMBL
LigandPNGBDBM50307111((2S)-N-[2-Methyl-4-(5H-pyrrolo[2,1-c][1,4]benzodia...)copy SMILEScopy InChI
Affinity DataKi:  3.40E+3nMAssay Description:Displacement of [3H]AVP from human vasopressin V2 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FX7BD4PubMed