null

SMILES CO\N=C1\C[C@H](N(C1)C(=O)c1ccc(cc1)-c1ccccc1C)C(=O)NC[C@@H](O)c1ccccc1

InChI Key InChIKey=IBXGJPAYWMFXSF-UEEONYLUSA-N

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

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 10 hits for monomerid = 50326713   

TargetOxytocin receptor(Homo sapiens (Human))
LCG Bioscience

Curated by PDSP Ki Database
LigandPNGBDBM50326713((2S,4Z)-N-[(2S)-2-hydroxy-2-phenylethyl]-4-(methox...)copy SMILEScopy InChI
Affinity DataKi:  17nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MC8XKTPubMed
TargetOxytocin receptor(Homo sapiens (Human))
LCG Bioscience

Curated by PDSP Ki Database
LigandPNGBDBM50326713((2S,4Z)-N-[(2S)-2-hydroxy-2-phenylethyl]-4-(methox...)copy SMILEScopy InChI
Affinity DataKi:  28nMAssay Description:Displacement of [3H]-oxytocin from oxytocin receptor in human uterus tissueMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20R9PMZPubMed
TargetOxytocin receptor(Homo sapiens (Human))
LCG Bioscience

Curated by PDSP Ki Database
LigandPNGBDBM50326713((2S,4Z)-N-[(2S)-2-hydroxy-2-phenylethyl]-4-(methox...)copy SMILEScopy InChI
Affinity DataKi:  28nMAssay Description:Displacement of [3H]-oxytocin from human oxytocin receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20R9PMZPubMed
TargetOxytocin receptor(RAT)
DrugMolDesign

Curated by ChEMBL
LigandPNGBDBM50326713((2S,4Z)-N-[(2S)-2-hydroxy-2-phenylethyl]-4-(methox...)copy SMILEScopy InChI
Affinity DataKi:  135nMAssay Description:Displacement of [3H]-oxytocin from rat oxytocin receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20R9PMZPubMed
TargetOxytocin receptor(RAT)
DrugMolDesign

Curated by ChEMBL
LigandPNGBDBM50326713((2S,4Z)-N-[(2S)-2-hydroxy-2-phenylethyl]-4-(methox...)copy SMILEScopy InChI
Affinity DataKi:  135nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MC8XKTPubMed
TargetVasopressin V1a receptor(Homo sapiens (Human))
DrugMolDesign

Curated by ChEMBL
LigandPNGBDBM50326713((2S,4Z)-N-[(2S)-2-hydroxy-2-phenylethyl]-4-(methox...)copy SMILEScopy InChI
Affinity DataKi:  170nMAssay Description:Displacement of [3H]-vasopressin from human vasopressin V1a receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20R9PMZPubMed
TargetVasopressin V1a receptor(Homo sapiens (Human))
DrugMolDesign

Curated by ChEMBL
LigandPNGBDBM50326713((2S,4Z)-N-[(2S)-2-hydroxy-2-phenylethyl]-4-(methox...)copy SMILEScopy InChI
Affinity DataKi:  170nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MC8XKTPubMed
TargetVasopressin V2 receptor(Homo sapiens (Human))
DrugMolDesign

Curated by ChEMBL
LigandPNGBDBM50326713((2S,4Z)-N-[(2S)-2-hydroxy-2-phenylethyl]-4-(methox...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMAssay Description:Displacement of [3H]-vasopressin from human vasopressin V2 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20R9PMZPubMed
TargetVasopressin V1b receptor(Homo sapiens (Human))
LCG Bioscience

Curated by PDSP Ki Database
LigandPNGBDBM50326713((2S,4Z)-N-[(2S)-2-hydroxy-2-phenylethyl]-4-(methox...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MC8XKTPubMed
TargetVasopressin V2 receptor(Homo sapiens (Human))
DrugMolDesign

Curated by ChEMBL
LigandPNGBDBM50326713((2S,4Z)-N-[(2S)-2-hydroxy-2-phenylethyl]-4-(methox...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MC8XKTPubMed