BDBM50021323 3-(1-Allyl-3-methyl-piperidin-3-yl)-phenol::3-(1-Allyl-3-methyl-piperidin-3-yl)-phenol:hydrochloricacid::CHEMBL151270

SMILES CC1(CCCN(CC=C)C1)c1cccc(O)c1

InChI Key InChIKey=PDNXCHZQJQBVIV-UHFFFAOYSA-N

Data  10 Kd

  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 10 hits for monomerid = 50021323   

TargetKappa-type opioid receptor(Rattus norvegicus (rat))
TBA

Curated by ChEMBL
LigandPNGBDBM50021323(3-(1-Allyl-3-methyl-piperidin-3-yl)-phenol | 3-(1-...)
Affinity DataKd:  137nMAssay Description:Opioid receptor affinity against Opioid receptor kappa 1 by using the curve-fitting program LIGANDMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMu-type opioid receptor(Rattus norvegicus (rat))
TBA

Curated by ChEMBL
LigandPNGBDBM50021323(3-(1-Allyl-3-methyl-piperidin-3-yl)-phenol | 3-(1-...)
Affinity DataKd:  370nMAssay Description:Mu2 opioid receptor affinity against the receptor site model site 2 (mu2) by using the curve-fitting program LIGANDMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDelta-type opioid receptor(Rattus norvegicus (rat))
TBA

Curated by ChEMBL
LigandPNGBDBM50021323(3-(1-Allyl-3-methyl-piperidin-3-yl)-phenol | 3-(1-...)
Affinity DataKd:  4.00E+3nMAssay Description:Opioid receptor affinity against the Opioid receptor delta 1 by using the curve-fitting program LIGANDMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMu-type opioid receptor(Rattus norvegicus (rat))
TBA

Curated by ChEMBL
LigandPNGBDBM50021323(3-(1-Allyl-3-methyl-piperidin-3-yl)-phenol | 3-(1-...)
Affinity DataKd:  370nMAssay Description:Opioid receptor mu 1 affinity against the receptor site model site 1 (mu1) by using the curve-fitting program LIGANDMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMu-type opioid receptor(Rattus norvegicus (rat))
TBA

Curated by ChEMBL
LigandPNGBDBM50021323(3-(1-Allyl-3-methyl-piperidin-3-yl)-phenol | 3-(1-...)
Affinity DataKd:  24nMAssay Description:Opioid receptor mu 1 affinity against the receptor site model site 1 (mu1) by using the curve-fitting program LIGANDMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDelta-type opioid receptor(Rattus norvegicus (rat))
TBA

Curated by ChEMBL
LigandPNGBDBM50021323(3-(1-Allyl-3-methyl-piperidin-3-yl)-phenol | 3-(1-...)
Affinity DataKd:  4.00E+3nMAssay Description:Opioid receptor affinity against the Opioid receptor delta 1 by using the curve-fitting program LIGANDMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50021323(3-(1-Allyl-3-methyl-piperidin-3-yl)-phenol | 3-(1-...)
Affinity DataKd:  3.70E+3nMAssay Description:Opioid receptor affinity against the receptor site model site 5 by using the curve-fitting program LIGANDMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50021323(3-(1-Allyl-3-methyl-piperidin-3-yl)-phenol | 3-(1-...)
Affinity DataKd:  3.70E+3nMAssay Description:Opioid receptor affinity against the receptor site model site 5 by using the curve-fitting program LIGANDMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetKappa-type opioid receptor(Rattus norvegicus (rat))
TBA

Curated by ChEMBL
LigandPNGBDBM50021323(3-(1-Allyl-3-methyl-piperidin-3-yl)-phenol | 3-(1-...)
Affinity DataKd:  137nMAssay Description:Opioid receptor affinity against Opioid receptor kappa 1 by using the curve-fitting program LIGANDMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMu-type opioid receptor(Rattus norvegicus (rat))
TBA

Curated by ChEMBL
LigandPNGBDBM50021323(3-(1-Allyl-3-methyl-piperidin-3-yl)-phenol | 3-(1-...)
Affinity DataKd:  100nMAssay Description:Opioid receptor mu 1 affinity against the receptor site model site 1 (mu1) by using the curve-fitting program LIGANDMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed