Compile Data Set for Download or QSAR
Found 92 with Last Name = 'pike' and Initial = 'aj'
TargetMuscarinic acetylcholine receptor M1(RAT)
Novo Nordisk CNS Division

Curated by ChEMBL
LigandPNGBDBM50006582(1-Methyl-5-(4-propylsulfanyl-[1,2,5]thiadiazol-3-y...)copy SMILEScopy InChI
Affinity DataIC50: 0.900nMAssay Description:In vitro binding affinity against muscarinic acetylcholine receptor M1 from rat hippocampus, using [3H]-oxotremorine-M (Oxo-M) as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22J69THPubMed
TargetMuscarinic acetylcholine receptor M1(RAT)
Novo Nordisk CNS Division

Curated by ChEMBL
LigandPNGBDBM50006572(5-(4-Butylsulfanyl-[1,2,5]thiadiazol-3-yl)-1-methy...)copy SMILEScopy InChI
Affinity DataIC50: 1.30nMAssay Description:In vitro binding affinity against muscarinic acetylcholine receptor M1 from rat hippocampus, using [3H]-pirenzepine (Pz) as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22J69THPubMed
TargetMuscarinic acetylcholine receptor M1(RAT)
Novo Nordisk CNS Division

Curated by ChEMBL
LigandPNGBDBM50006572(5-(4-Butylsulfanyl-[1,2,5]thiadiazol-3-yl)-1-methy...)copy SMILEScopy InChI
Affinity DataIC50: 1.30nMAssay Description:In vitro binding affinity against muscarinic acetylcholine receptor M1 from rat hippocampus, using [3H]-pirenzepine (Pz) as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22J69THPubMed
TargetMuscarinic acetylcholine receptor M1(RAT)
Novo Nordisk CNS Division

Curated by ChEMBL
LigandPNGBDBM50003351(3-(4-butoxy-1,2,5-thiadiazol-3-yl)-1-methyl-1,2,5,...)copy SMILEScopy InChI
Affinity DataIC50: 1.40nMAssay Description:In vitro binding affinity against muscarinic acetylcholine receptor M1 from rat hippocampus, using [3H]-oxotremorine-M (Oxo-M) as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22J69THPubMed
TargetMuscarinic acetylcholine receptor M1(RAT)
Novo Nordisk CNS Division

Curated by ChEMBL
LigandPNGBDBM50003351(3-(4-butoxy-1,2,5-thiadiazol-3-yl)-1-methyl-1,2,5,...)copy SMILEScopy InChI
Affinity DataIC50: 1.40nMAssay Description:In vitro binding affinity against muscarinic acetylcholine receptor M1 from rat hippocampus, using [3H]-oxotremorine-M (Oxo-M) as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22J69THPubMed
TargetMuscarinic acetylcholine receptor M1(RAT)
Novo Nordisk CNS Division

Curated by ChEMBL
LigandPNGBDBM50003369(1-Methyl-5-(4-propoxy-[1,2,5]thiadiazol-3-yl)-1,2,...)copy SMILEScopy InChI
Affinity DataIC50: 1.60nMAssay Description:In vitro binding affinity against muscarinic acetylcholine receptor M1 from rat hippocampus, using [3H]-pirenzepine (Pz) as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22J69THPubMed
TargetMuscarinic acetylcholine receptor M1(RAT)
Novo Nordisk CNS Division

Curated by ChEMBL
LigandPNGBDBM50006580(1-Methyl-5-(4-methylsulfanyl-[1,2,5]thiadiazol-3-y...)copy SMILEScopy InChI
Affinity DataIC50: 2.30nMAssay Description:In vitro binding affinity against muscarinic acetylcholine receptor M1 from rat hippocampus, using [3H]-oxotremorine-M (Oxo-M) as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22J69THPubMed
TargetMuscarinic acetylcholine receptor M1(RAT)
Novo Nordisk CNS Division

Curated by ChEMBL
LigandPNGBDBM50003366(1-Methyl-5-(4-pentyloxy-[1,2,5]thiadiazol-3-yl)-1,...)copy SMILEScopy InChI
Affinity DataIC50: 4nMAssay Description:In vitro binding affinity against muscarinic acetylcholine receptor M1 from rat hippocampus, using [3H]-pirenzepine (Pz) as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22J69THPubMed
TargetMuscarinic acetylcholine receptor M1(RAT)
Novo Nordisk CNS Division

Curated by ChEMBL
LigandPNGBDBM50003366(1-Methyl-5-(4-pentyloxy-[1,2,5]thiadiazol-3-yl)-1,...)copy SMILEScopy InChI
Affinity DataIC50: 4nMAssay Description:In vitro binding affinity against muscarinic acetylcholine receptor M1 from rat hippocampus, using [3H]-pirenzepine (Pz) as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22J69THPubMed
TargetMuscarinic acetylcholine receptor M1(RAT)
Novo Nordisk CNS Division

Curated by ChEMBL
LigandPNGBDBM50006582(1-Methyl-5-(4-propylsulfanyl-[1,2,5]thiadiazol-3-y...)copy SMILEScopy InChI
Affinity DataIC50: 4nMAssay Description:In vitro binding affinity against muscarinic acetylcholine receptor M1 from rat hippocampus, using [3H]-pirenzepine (Pz) as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22J69THPubMed
TargetMuscarinic acetylcholine receptor M1(RAT)
Novo Nordisk CNS Division

Curated by ChEMBL
LigandPNGBDBM50003363(1-Methyl-5-(4-pentylsulfanyl-[1,2,5]thiadiazol-3-y...)copy SMILEScopy InChI
Affinity DataIC50: 4.80nMAssay Description:In vitro binding affinity against M1 receptor from rat hippocampus, using [3H]-oxotremorine-M (Oxo-M) as radioligand.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22J69THPubMed
TargetMuscarinic acetylcholine receptor M1(RAT)
Novo Nordisk CNS Division

Curated by ChEMBL
LigandPNGBDBM50003363(1-Methyl-5-(4-pentylsulfanyl-[1,2,5]thiadiazol-3-y...)copy SMILEScopy InChI
Affinity DataIC50: 4.80nMAssay Description:In vitro binding affinity against muscarinic acetylcholine receptor M1 from rat hippocampus, using [3H]-pirenzepine (Pz) as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22J69THPubMed
TargetMuscarinic acetylcholine receptor M1(RAT)
Novo Nordisk CNS Division

Curated by ChEMBL
LigandPNGBDBM50003365(3-(3-(ethoxy)-1,2,5-thiadiazol-4-yl)-1,2,5,6-tetra...)copy SMILEScopy InChI
Affinity DataIC50: 5.70nMAssay Description:In vitro binding affinity against muscarinic acetylcholine receptor M1 from rat hippocampus, using [3H]-oxotremorine-M (Oxo-M) as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22J69THPubMed
TargetMuscarinic acetylcholine receptor M1(RAT)
Novo Nordisk CNS Division

Curated by ChEMBL
LigandPNGBDBM50003356(5-(4-Heptyloxy-[1,2,5]thiadiazol-3-yl)-1-methyl-1,...)copy SMILEScopy InChI
Affinity DataIC50: 6.20nMAssay Description:In vitro binding affinity against muscarinic acetylcholine receptor M1 from rat hippocampus, using [3H]-oxotremorine-M (Oxo-M) as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22J69THPubMed
TargetMuscarinic acetylcholine receptor M1(RAT)
Novo Nordisk CNS Division

Curated by ChEMBL
LigandPNGBDBM50003355(5-(4-Hexylsulfanyl-[1,2,5]thiadiazol-3-yl)-1-methy...)copy SMILEScopy InChI
Affinity DataIC50: 6.5nMAssay Description:In vitro binding affinity against muscarinic acetylcholine receptor M1 from rat hippocampus, using [3H]-pirenzepine (Pz) as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22J69THPubMed
TargetMuscarinic acetylcholine receptor M1(RAT)
Novo Nordisk CNS Division

Curated by ChEMBL
LigandPNGBDBM50003355(5-(4-Hexylsulfanyl-[1,2,5]thiadiazol-3-yl)-1-methy...)copy SMILEScopy InChI
Affinity DataIC50: 6.5nMAssay Description:In vitro binding affinity against Muscarinic acetylcholine receptor M1 from rat hippocampus, using [3H]-oxotremorine-M (Oxo-M) as radioligand.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22J69THPubMed
TargetMuscarinic acetylcholine receptor M1(RAT)
Novo Nordisk CNS Division

Curated by ChEMBL
LigandPNGBDBM50006598(1-Methyl-5-[4-(1-methyl-pentyloxy)-[1,2,5]thiadiaz...)copy SMILEScopy InChI
Affinity DataIC50: 6.90nMAssay Description:In vitro binding affinity against Muscarinic acetylcholine receptor M1 from rat hippocampus, using [3H]-pirenzepine (Pz) as radioligand.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22J69THPubMed
TargetMuscarinic acetylcholine receptor M1(RAT)
Novo Nordisk CNS Division

Curated by ChEMBL
LigandPNGBDBM50003359(5-(4-Hexyloxy-[1,2,5]thiadiazol-3-yl)-1-methyl-1,2...)copy SMILEScopy InChI
Affinity DataIC50: 7nMAssay Description:In vitro binding affinity against muscarinic acetylcholine receptor M1 from rat hippocampus, using [3H]-oxotremorine-M (Oxo-M) as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22J69THPubMed
TargetMuscarinic acetylcholine receptor M1(RAT)
Novo Nordisk CNS Division

Curated by ChEMBL
LigandPNGBDBM50006598(1-Methyl-5-[4-(1-methyl-pentyloxy)-[1,2,5]thiadiaz...)copy SMILEScopy InChI
Affinity DataIC50: 7nMAssay Description:In vitro binding affinity against muscarinic acetylcholine receptor M1 from rat hippocampus, using [3H]-pirenzepine (Pz) as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22J69THPubMed
TargetMuscarinic acetylcholine receptor M1(RAT)
Novo Nordisk CNS Division

Curated by ChEMBL
LigandPNGBDBM50003359(5-(4-Hexyloxy-[1,2,5]thiadiazol-3-yl)-1-methyl-1,2...)copy SMILEScopy InChI
Affinity DataIC50: 7nMAssay Description:In vitro binding affinity against muscarinic acetylcholine receptor M1 from rat hippocampus, using [3H]-pirenzepine (Pz) as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22J69THPubMed
TargetMuscarinic acetylcholine receptor M1(RAT)
Novo Nordisk CNS Division

Curated by ChEMBL
LigandPNGBDBM50006592(1-Methyl-5-[4-(4-methyl-pentyloxy)-[1,2,5]thiadiaz...)copy SMILEScopy InChI
Affinity DataIC50: 8nMAssay Description:In vitro binding affinity against muscarinic acetylcholine receptor M1 from rat hippocampus, using [3H]-oxotremorine-M (Oxo-M) as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22J69THPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50368782(Bexlosteride | CHEMBL24955 | LY-191704)copy SMILEScopy InChI
Affinity DataIC50: 8nMAssay Description:In vitro inhibition of DHT production in Hs 68 (human genital fibroblast) cells.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2T43TQXPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50031890((10R,13S)-17-tert-Butylcarbamoyl-10,13-dimethyl-2,...)copy SMILEScopy InChI
Affinity DataIC50: 8nMAssay Description:Compound was tested for inhibition of Type II 5-alpha-reductase in Human Prostate Homogenates (HPH)More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2T43TQXPubMed
TargetMuscarinic acetylcholine receptor M1(RAT)
Novo Nordisk CNS Division

Curated by ChEMBL
LigandPNGBDBM50006577(1-Methyl-5-[4-(3-methyl-pentyloxy)-[1,2,5]thiadiaz...)copy SMILEScopy InChI
Affinity DataIC50: 8.40nMAssay Description:In vitro binding affinity against muscarinic acetylcholine receptor M1 from rat hippocampus, using [3H]-pirenzepine (Pz) as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22J69THPubMed
TargetMuscarinic acetylcholine receptor M1(RAT)
Novo Nordisk CNS Division

Curated by ChEMBL
LigandPNGBDBM50006577(1-Methyl-5-[4-(3-methyl-pentyloxy)-[1,2,5]thiadiaz...)copy SMILEScopy InChI
Affinity DataIC50: 8.40nMAssay Description:In vitro binding affinity against muscarinic acetylcholine receptor M1 from rat hippocampus, using [3H]-pirenzepine (Pz) as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22J69THPubMed
TargetMuscarinic acetylcholine receptor M1(RAT)
Novo Nordisk CNS Division

Curated by ChEMBL
LigandPNGBDBM50006587(1-Methyl-5-[4-(2-methyl-pentyloxy)-[1,2,5]thiadiaz...)copy SMILEScopy InChI
Affinity DataIC50: 9nMAssay Description:In vitro binding affinity against muscarinic acetylcholine receptor M1 from rat hippocampus, using [3H]-pirenzepine (Pz) as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22J69THPubMed
TargetMuscarinic acetylcholine receptor M1(RAT)
Novo Nordisk CNS Division

Curated by ChEMBL
LigandPNGBDBM50006587(1-Methyl-5-[4-(2-methyl-pentyloxy)-[1,2,5]thiadiaz...)copy SMILEScopy InChI
Affinity DataIC50: 9nMAssay Description:In vitro binding affinity against muscarinic acetylcholine receptor M1 from rat hippocampus, using [3H]-pirenzepine (Pz) as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22J69THPubMed
TargetMuscarinic acetylcholine receptor M1(RAT)
Novo Nordisk CNS Division

Curated by ChEMBL
LigandPNGBDBM50006592(1-Methyl-5-[4-(4-methyl-pentyloxy)-[1,2,5]thiadiaz...)copy SMILEScopy InChI
Affinity DataIC50: 9.70nMAssay Description:In vitro binding affinity against muscarinic acetylcholine receptor M1 from rat hippocampus, using [3H]-pirenzepine (Pz) as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22J69THPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50334788((17beta-(N-tert-butylcarbamoyl)-4-aza-5alpha-andro...)copy SMILEScopy InChI
Affinity DataIC50: 10nMAssay Description:Compound was tested for inhibition of Type II 5-alpha-reductase in Human Prostate Homogenates (HPH).More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2T43TQXPubMedDrugBank
TargetMuscarinic acetylcholine receptor M1(RAT)
Novo Nordisk CNS Division

Curated by ChEMBL
LigandPNGBDBM50003358(5-(4-Chloro-[1,2,5]thiadiazol-3-yl)-1-methyl-1,2,3...)copy SMILEScopy InChI
Affinity DataIC50: 10.8nMAssay Description:In vitro binding affinity against muscarinic acetylcholine receptor M1 from rat hippocampus, using [3H]-oxotremorine-M (Oxo-M) as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22J69THPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50044878(4,8-Dimethyl-1,4,4a,5,6,10b-hexahydro-2H-benzo[f]q...)copy SMILEScopy InChI
Affinity DataIC50: 11nMAssay Description:In vitro inhibition of DHT production in Hs 68 (human genital fibroblast) cells.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2T43TQXPubMed
TargetMuscarinic acetylcholine receptor M1(RAT)
Novo Nordisk CNS Division

Curated by ChEMBL
LigandPNGBDBM50003358(5-(4-Chloro-[1,2,5]thiadiazol-3-yl)-1-methyl-1,2,3...)copy SMILEScopy InChI
Affinity DataIC50: 11nMAssay Description:In vitro binding affinity against muscarinic acetylcholine receptor M1 from rat hippocampus, using [3H]-oxotremorine-M (Oxo-M) as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22J69THPubMed
TargetMuscarinic acetylcholine receptor M1(RAT)
Novo Nordisk CNS Division

Curated by ChEMBL
LigandPNGBDBM50006595(5-(4-Heptylsulfanyl-[1,2,5]thiadiazol-3-yl)-1-meth...)copy SMILEScopy InChI
Affinity DataIC50: 12nMAssay Description:In vitro binding affinity against muscarinic acetylcholine receptor M1 from rat hippocampus, using [3H]-pirenzepine (Pz) as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22J69THPubMed
TargetMuscarinic acetylcholine receptor M1(RAT)
Novo Nordisk CNS Division

Curated by ChEMBL
LigandPNGBDBM50003356(5-(4-Heptyloxy-[1,2,5]thiadiazol-3-yl)-1-methyl-1,...)copy SMILEScopy InChI
Affinity DataIC50: 12nMAssay Description:In vitro binding affinity against muscarinic acetylcholine receptor M1 from rat hippocampus, using [3H]-pirenzepine (Pz) as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22J69THPubMed
TargetMuscarinic acetylcholine receptor M1(RAT)
Novo Nordisk CNS Division

Curated by ChEMBL
LigandPNGBDBM50006595(5-(4-Heptylsulfanyl-[1,2,5]thiadiazol-3-yl)-1-meth...)copy SMILEScopy InChI
Affinity DataIC50: 12nMAssay Description:In vitro binding affinity against muscarinic acetylcholine receptor M1 from rat hippocampus, using [3H]-oxotremorine-M (Oxo-M) as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22J69THPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50044879((4aR,10bR)-8-Chloro-4,10b-dimethyl-1,4,4a,5,6,10b-...)copy SMILEScopy InChI
Affinity DataIC50: 17nMAssay Description:In vitro inhibition of DHT production in Hs 68 (human genital fibroblast) cells.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2T43TQXPubMed
TargetMuscarinic acetylcholine receptor M1(RAT)
Novo Nordisk CNS Division

Curated by ChEMBL
LigandPNGBDBM50003369(1-Methyl-5-(4-propoxy-[1,2,5]thiadiazol-3-yl)-1,2,...)copy SMILEScopy InChI
Affinity DataIC50: 18nMAssay Description:In vitro binding affinity against muscarinic acetylcholine receptor M1 from rat hippocampus, using [3H]-pirenzepine (Pz) as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22J69THPubMed
TargetMuscarinic acetylcholine receptor M1(RAT)
Novo Nordisk CNS Division

Curated by ChEMBL
LigandPNGBDBM50006574(5-(4-Ethylsulfanyl-[1,2,5]thiadiazol-3-yl)-1-methy...)copy SMILEScopy InChI
Affinity DataIC50: 18nMAssay Description:In vitro binding affinity against muscarinic acetylcholine receptor M1 from rat hippocampus, using [3H]-pirenzepine (Pz) as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22J69THPubMed
TargetMuscarinic acetylcholine receptor M1(RAT)
Novo Nordisk CNS Division

Curated by ChEMBL
LigandPNGBDBM50006574(5-(4-Ethylsulfanyl-[1,2,5]thiadiazol-3-yl)-1-methy...)copy SMILEScopy InChI
Affinity DataIC50: 18nMAssay Description:In vitro binding affinity against muscarinic acetylcholine receptor M1 from rat hippocampus, using [3H]-oxotremorine-M (Oxo-M) as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22J69THPubMed
TargetMuscarinic acetylcholine receptor M1(RAT)
Novo Nordisk CNS Division

Curated by ChEMBL
LigandPNGBDBM50003361(5-(4-Methoxy-[1,2,5]thiadiazol-3-yl)-1-methyl-1,2,...)copy SMILEScopy InChI
Affinity DataIC50: 22nMAssay Description:In vitro binding affinity against muscarinic acetylcholine receptor M1 from rat hippocampus, using [3H]-oxotremorine-M (Oxo-M) as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22J69THPubMed
TargetMuscarinic acetylcholine receptor M1(RAT)
Novo Nordisk CNS Division

Curated by ChEMBL
LigandPNGBDBM50003361(5-(4-Methoxy-[1,2,5]thiadiazol-3-yl)-1-methyl-1,2,...)copy SMILEScopy InChI
Affinity DataIC50: 22nMAssay Description:In vitro binding affinity against Muscarinic acetylcholine receptor M1 from rat hippocampus, using [3H]-pirenzepine (Pz) as radioligand.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22J69THPubMed
TargetMuscarinic acetylcholine receptor M1(RAT)
Novo Nordisk CNS Division

Curated by ChEMBL
LigandPNGBDBM50004656((2-Carbamoyloxy-ethyl)-trimethyl-ammonium | (2-Car...)copy SMILEScopy InChI
Affinity DataIC50: 23nMAssay Description:In vitro binding affinity against Muscarinic acetylcholine receptor M1 from rat hippocampus, using [3H]-oxotremorine-M (Oxo-M) as radioligand.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22J69THPubMed
TargetMuscarinic acetylcholine receptor M1(RAT)
Novo Nordisk CNS Division

Curated by ChEMBL
LigandPNGBDBM50006579(5-(4-Butoxy-furazan-3-yl)-1-methyl-1,2,3,6-tetrahy...)copy SMILEScopy InChI
Affinity DataIC50: 24nMAssay Description:In vitro binding affinity against muscarinic acetylcholine receptor M1 from rat hippocampus, using [3H]-oxotremorine-M (Oxo-M) as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22J69THPubMed
TargetMuscarinic acetylcholine receptor M1(RAT)
Novo Nordisk CNS Division

Curated by ChEMBL
LigandPNGBDBM50006575(5-[4-(Hexane-1-sulfonyl)-[1,2,5]thiadiazol-3-yl]-1...)copy SMILEScopy InChI
Affinity DataIC50: 29nMAssay Description:In vitro binding affinity against muscarinic acetylcholine receptor M1 from rat hippocampus, using [3H]-pirenzepine (Pz) as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22J69THPubMed
TargetMuscarinic acetylcholine receptor M1(RAT)
Novo Nordisk CNS Division

Curated by ChEMBL
LigandPNGBDBM50006575(5-[4-(Hexane-1-sulfonyl)-[1,2,5]thiadiazol-3-yl]-1...)copy SMILEScopy InChI
Affinity DataIC50: 29nMAssay Description:In vitro binding affinity against muscarinic acetylcholine receptor M1 from rat hippocampus, using [3H]-oxotremorine-M (Oxo-M) as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22J69THPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50044881(8-Chloro-4-methyl-1,4,5,6-tetrahydro-2H-benzo[f]qu...)copy SMILEScopy InChI
Affinity DataIC50: 30nMAssay Description:In vitro inhibition of DHT production in Hs 68 (human genital fibroblast) cells.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2T43TQXPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50044891(8-Fluoro-4-methyl-1,4,4a,5,6,10b-hexahydro-2H-benz...)copy SMILEScopy InChI
Affinity DataIC50: 35nMAssay Description:In vitro inhibition of DHT production in Hs 68 (human genital fibroblast) cells.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2T43TQXPubMed
TargetMuscarinic acetylcholine receptor M1(RAT)
Novo Nordisk CNS Division

Curated by ChEMBL
LigandPNGBDBM50006588(1-Methyl-5-(4-octyloxy-[1,2,5]thiadiazol-3-yl)-1,2...)copy SMILEScopy InChI
Affinity DataIC50: 40nMAssay Description:In vitro binding affinity against muscarinic acetylcholine receptor M1 from rat hippocampus, using [3H]-pirenzepine (Pz) as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22J69THPubMed
TargetMuscarinic acetylcholine receptor M1(RAT)
Novo Nordisk CNS Division

Curated by ChEMBL
LigandPNGBDBM50006588(1-Methyl-5-(4-octyloxy-[1,2,5]thiadiazol-3-yl)-1,2...)copy SMILEScopy InChI
Affinity DataIC50: 40nMAssay Description:In vitro binding affinity against muscarinic acetylcholine receptor M1 from rat hippocampus, using [3H]-pirenzepine (Pz) as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22J69THPubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50044885((4aS,10bR)-8-Chloro-4-methyl-1,4,4a,5,6,10b-hexahy...)copy SMILEScopy InChI
Affinity DataIC50: 41nMAssay Description:In vitro inhibition of DHT production in Hs 68 (human genital fibroblast) cells.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2T43TQXPubMed
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