Compile Data Set for Download or QSAR
Found 111 with Last Name = 'thomsen' and Initial = 'b'
TargetNeuropeptide Y receptor type 5(Homo sapiens (Human))
Taisho Pharmaceutical Co. Ltd

Curated by ChEMBL
LigandPNGBDBM50166561(CHEMBL195380 | Naphthalene-1-sulfonic acid {4-[(4-...)copy SMILEScopy InChI
Affinity DataIC50: 1.30nMAssay Description:Inhibitory activity against constitutively activated human Neuropeptide Y receptor Y5 stransiently expressed in COS-1 cells using [125I]-PYYMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z89BXQPubMed
TargetNeuropeptide Y receptor type 5(Homo sapiens (Human))
Taisho Pharmaceutical Co. Ltd

Curated by ChEMBL
LigandPNGBDBM50166554(CHEMBL192266 | N-{4-[(4-Amino-quinazolin-2-ylamino...)copy SMILEScopy InChI
Affinity DataIC50: 1.60nMAssay Description:Inhibitory activity against constitutively activated human Neuropeptide Y receptor Y5 stransiently expressed in COS-1 cells using [125I]-PYYMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z89BXQPubMed
TargetMelanin-concentrating hormone receptor 1(Homo sapiens (Human))
Taisho Pharmaceutical Co. Ltd.

Curated by ChEMBL
LigandPNGBDBM50170193(CHEMBL360081 | N-[4-(4-Dimethylamino-quinazolin-2-...)copy SMILEScopy InChI
Affinity DataIC50: 2nMAssay Description:Inhibitory activity against human CA-MCH-R1 (Melanin-concentrating hormone receptor 1) by using [125I](Phe13,Tyr19)MCH as radioligand expressed in HE...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23R0TM4PubMed
TargetNeuropeptide Y receptor type 5(Homo sapiens (Human))
Taisho Pharmaceutical Co. Ltd

Curated by ChEMBL
LigandPNGBDBM50166552(4-Bromo-N-{4-[(4-dimethylamino-quinazolin-2-ylamin...)copy SMILEScopy InChI
Affinity DataIC50: 2.5nMAssay Description:Inhibitory activity against constitutively activated human Neuropeptide Y receptor Y5 stransiently expressed in COS-1 cells using [125I]-PYYMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z89BXQPubMed
TargetNeuropeptide Y receptor type 5(Homo sapiens (Human))
Taisho Pharmaceutical Co. Ltd

Curated by ChEMBL
LigandPNGBDBM50170189(4-Bromo-N-{4-[(4-dimethylamino-quinazolin-2-ylamin...)copy SMILEScopy InChI
Affinity DataIC50: 2.70nMAssay Description:Inhibitory activity against neuropeptide Y receptor type 5 by using [125I]PYY as radioligand expressed in COS-1 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23R0TM4PubMed
TargetNeuropeptide Y receptor type 5(Homo sapiens (Human))
Taisho Pharmaceutical Co. Ltd

Curated by ChEMBL
LigandPNGBDBM50166555(4-Bromo-N-{4-[(4-dimethylamino-quinazolin-2-ylamin...)copy SMILEScopy InChI
Affinity DataIC50: 2.70nMAssay Description:Inhibitory activity against constitutively activated human Neuropeptide Y receptor Y5 stransiently expressed in COS-1 cells using [125I]-PYYMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z89BXQPubMed
TargetMelanin-concentrating hormone receptor 1(Homo sapiens (Human))
Taisho Pharmaceutical Co. Ltd.

Curated by ChEMBL
LigandPNGBDBM50170191(CHEMBL182150 | N-((cis)-4-(4-(dimethylamino)quinaz...)copy SMILEScopy InChI
Affinity DataIC50: 3.40nMAssay Description:Inhibitory activity against human CA-MCH-R1 (Melanin-concentrating hormone receptor 1) by using [125I](Phe13,Tyr19)MCH as radioligand expressed in HE...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23R0TM4PubMed
TargetMelanin-concentrating hormone receptor 1(Homo sapiens (Human))
Taisho Pharmaceutical Co. Ltd.

Curated by ChEMBL
LigandPNGBDBM50170180(3-Chloro-N-[4-(4-dimethylamino-quinazolin-2-ylamin...)copy SMILEScopy InChI
Affinity DataIC50: 4.5nMAssay Description:Inhibitory activity against human CA-MCH-R1 (Melanin-concentrating hormone receptor 1) by using [125I](Phe13,Tyr19)MCH as radioligand expressed in HE...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23R0TM4PubMed
TargetMelanin-concentrating hormone receptor 1(Homo sapiens (Human))
Taisho Pharmaceutical Co. Ltd.

Curated by ChEMBL
LigandPNGBDBM50170179(CHEMBL180962 | N-[4-(4-Dimethylamino-quinazolin-2-...)copy SMILEScopy InChI
Affinity DataIC50: 4.60nMAssay Description:Inhibitory activity against human CA-MCH-R1 (Melanin-concentrating hormone receptor 1) by using [125I](Phe13,Tyr19)MCH as radioligand expressed in HE...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23R0TM4PubMed
TargetMelanin-concentrating hormone receptor 1(Homo sapiens (Human))
Taisho Pharmaceutical Co. Ltd.

Curated by ChEMBL
LigandPNGBDBM50170192(CHEMBL181466 | cis-N*2*-{4-[(4-Bromo-2-trifluorome...)copy SMILEScopy InChI
Affinity DataIC50: 4.90nMAssay Description:Inhibitory activity against human CA-MCH-R1 (Melanin-concentrating hormone receptor 1) by using [125I](Phe13,Tyr19)MCH as radioligand expressed in HE...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23R0TM4PubMed
TargetNeuropeptide Y receptor type 5(Homo sapiens (Human))
Taisho Pharmaceutical Co. Ltd

Curated by ChEMBL
LigandPNGBDBM50166559(Butane-1-sulfonic acid {4-[(4-dimethylamino-quinaz...)copy SMILEScopy InChI
Affinity DataIC50: 4.90nMAssay Description:Inhibitory activity against constitutively activated human Neuropeptide Y receptor Y5 stransiently expressed in COS-1 cells using [125I]-PYYMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z89BXQPubMed
TargetMelanin-concentrating hormone receptor 1(Homo sapiens (Human))
Taisho Pharmaceutical Co. Ltd.

Curated by ChEMBL
LigandPNGBDBM50170182(3,4-Dichloro-N-[4-(4-dimethylamino-quinazolin-2-yl...)copy SMILEScopy InChI
Affinity DataIC50: 5nMAssay Description:Inhibitory activity against human CA-MCH-R1 (Melanin-concentrating hormone receptor 1) by using [125I](Phe13,Tyr19)MCH as radioligand expressed in HE...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23R0TM4PubMed
TargetAlpha-2A adrenergic receptor(Homo sapiens (Human))
Taisho Pharmaceutical Co. Ltd

Curated by ChEMBL
LigandPNGBDBM50166551(CHEMBL194173 | N*2*-[1-(4-Bromo-2-trifluoromethoxy...)copy SMILEScopy InChI
Affinity DataIC50: 5.60nMAssay Description:Inhibitory activity against constitutively activated human Alpha-2A adrenergic receptor transiently expressed in COS-1 cells using [3H]-MK912More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z89BXQPubMed
TargetMelanin-concentrating hormone receptor 1(Homo sapiens (Human))
Taisho Pharmaceutical Co. Ltd.

Curated by ChEMBL
LigandPNGBDBM50170176(3-Bromo-N-[4-(4-dimethylamino-quinazolin-2-ylamino...)copy SMILEScopy InChI
Affinity DataIC50: 5.90nMAssay Description:Inhibitory activity against human CA-MCH-R1 (Melanin-concentrating hormone receptor 1) by using [125I](Phe13,Tyr19)MCH as radioligand expressed in HE...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23R0TM4PubMed
TargetMelanin-concentrating hormone receptor 1(Homo sapiens (Human))
Taisho Pharmaceutical Co. Ltd.

Curated by ChEMBL
LigandPNGBDBM50170200(CHEMBL181383 | N-[4-(4-Dimethylamino-quinazolin-2-...)copy SMILEScopy InChI
Affinity DataIC50: 6.80nMAssay Description:Inhibitory activity against human CA-MCH-R1 (Melanin-concentrating hormone receptor 1) by using [125I](Phe13,Tyr19)MCH as radioligand expressed in HE...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23R0TM4PubMed
TargetAlpha-2A adrenergic receptor(Homo sapiens (Human))
Taisho Pharmaceutical Co. Ltd

Curated by ChEMBL
LigandPNGBDBM50166555(4-Bromo-N-{4-[(4-dimethylamino-quinazolin-2-ylamin...)copy SMILEScopy InChI
Affinity DataIC50: 7.70nMAssay Description:Inhibitory activity against constitutively activated human Alpha-2A adrenergic receptor transiently expressed in COS-1 cells using [3H]-MK912More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z89BXQPubMed
TargetAlpha-2A adrenergic receptor(Homo sapiens (Human))
Taisho Pharmaceutical Co. Ltd

Curated by ChEMBL
LigandPNGBDBM50170189(4-Bromo-N-{4-[(4-dimethylamino-quinazolin-2-ylamin...)copy SMILEScopy InChI
Affinity DataIC50: 7.70nMAssay Description:Inhibitory activity against alpha-2A adrenergic receptor by using [3H]MK-912 as radioligand expressed in COS-1 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23R0TM4PubMed
TargetMelanin-concentrating hormone receptor 1(Homo sapiens (Human))
Taisho Pharmaceutical Co. Ltd.

Curated by ChEMBL
LigandPNGBDBM50170199(CHEMBL361442 | N-[4-(4-Dimethylamino-quinazolin-2-...)copy SMILEScopy InChI
Affinity DataIC50: 9.40nMAssay Description:Inhibitory activity against human CA-MCH-R1 (Melanin-concentrating hormone receptor 1) by using [125I](Phe13,Tyr19)MCH as radioligand expressed in HE...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23R0TM4PubMed
TargetMelanin-concentrating hormone receptor 1(Homo sapiens (Human))
Taisho Pharmaceutical Co. Ltd.

Curated by ChEMBL
LigandPNGBDBM50170198(CHEMBL362193 | N-[4-(4-Dimethylamino-quinazolin-2-...)copy SMILEScopy InChI
Affinity DataIC50: 9.5nMAssay Description:Inhibitory activity against human CA-MCH-R1 (Melanin-concentrating hormone receptor 1) by using [125I](Phe13,Tyr19)MCH as radioligand expressed in HE...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23R0TM4PubMed
TargetAlpha-2A adrenergic receptor(Homo sapiens (Human))
Taisho Pharmaceutical Co. Ltd

Curated by ChEMBL
LigandPNGBDBM50170194(CHEMBL367355 | trans-4-Bromo-N-{4-[(4-dimethylamin...)copy SMILEScopy InChI
Affinity DataIC50: 9.90nMAssay Description:Inhibitory activity against alpha-2A adrenergic receptor by using [3H]MK-912 as radioligand expressed in COS-1 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23R0TM4PubMed
TargetMelanin-concentrating hormone receptor 1(Homo sapiens (Human))
Taisho Pharmaceutical Co. Ltd.

Curated by ChEMBL
LigandPNGBDBM50170195(3-Cyano-N-[4-(4-dimethylamino-quinazolin-2-ylamino...)copy SMILEScopy InChI
Affinity DataIC50: 10nMAssay Description:Inhibitory activity against human CA-MCH-R1 (Melanin-concentrating hormone receptor 1) by using [125I](Phe13,Tyr19)MCH as radioligand expressed in HE...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23R0TM4PubMed
TargetMelanin-concentrating hormone receptor 1(Homo sapiens (Human))
Taisho Pharmaceutical Co. Ltd.

Curated by ChEMBL
LigandPNGBDBM50170183(CHEMBL181632 | N-[4-(4-Dimethylamino-quinazolin-2-...)copy SMILEScopy InChI
Affinity DataIC50: 15nMAssay Description:Inhibitory activity against human CA-MCH-R1 (Melanin-concentrating hormone receptor 1) by using [125I](Phe13,Tyr19)MCH as radioligand expressed in HE...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23R0TM4PubMed
TargetAlpha-2A adrenergic receptor(Homo sapiens (Human))
Taisho Pharmaceutical Co. Ltd

Curated by ChEMBL
LigandPNGBDBM50166552(4-Bromo-N-{4-[(4-dimethylamino-quinazolin-2-ylamin...)copy SMILEScopy InChI
Affinity DataIC50: 21nMAssay Description:Inhibitory activity against constitutively activated human Alpha-2A adrenergic receptor transiently expressed in COS-1 cells using [3H]-MK912More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z89BXQPubMed
TargetAlpha-2A adrenergic receptor(Homo sapiens (Human))
Taisho Pharmaceutical Co. Ltd

Curated by ChEMBL
LigandPNGBDBM50170177(CHEMBL360117 | trans-4-Bromo-N-{4-[(4-dimethylamin...)copy SMILEScopy InChI
Affinity DataIC50: 31nMAssay Description:Inhibitory activity against alpha-2A adrenergic receptor by using [3H]MK-912 as radioligand expressed in COS-1 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23R0TM4PubMed
TargetNeuropeptide Y receptor type 5(Homo sapiens (Human))
Taisho Pharmaceutical Co. Ltd

Curated by ChEMBL
LigandPNGBDBM50166563(4-Bromo-N-[4-(4-dimethylamino-quinazolin-2-ylamino...)copy SMILEScopy InChI
Affinity DataIC50: 31nMAssay Description:Inhibitory activity against constitutively activated human Neuropeptide Y receptor Y5 stransiently expressed in COS-1 cells using [125I]-PYYMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z89BXQPubMed
TargetAlpha-2A adrenergic receptor(Homo sapiens (Human))
Taisho Pharmaceutical Co. Ltd

Curated by ChEMBL
LigandPNGBDBM50170187(CHEMBL181727 | trans-4-Bromo-N-{4-[(4-dimethylamin...)copy SMILEScopy InChI
Affinity DataIC50: 34nMAssay Description:Inhibitory activity against alpha-2A adrenergic receptor by using [3H]MK-912 as radioligand expressed in COS-1 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23R0TM4PubMed
TargetMelanin-concentrating hormone receptor 1(Homo sapiens (Human))
Taisho Pharmaceutical Co. Ltd.

Curated by ChEMBL
LigandPNGBDBM50170175(CHEMBL178084 | cis-N*2*-[4-(4-Bromo-2-trifluoromet...)copy SMILEScopy InChI
Affinity DataIC50: 35nMAssay Description:Inhibitory activity against human CA-MCH-R1 (Melanin-concentrating hormone receptor 1) by using [125I](Phe13,Tyr19)MCH as radioligand expressed in HE...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23R0TM4PubMed
TargetMelanin-concentrating hormone receptor 1(Homo sapiens (Human))
Taisho Pharmaceutical Co. Ltd.

Curated by ChEMBL
LigandPNGBDBM50170185(CHEMBL360159 | N-[4-(4-Dimethylamino-quinazolin-2-...)copy SMILEScopy InChI
Affinity DataIC50: 38nMAssay Description:Inhibitory activity against human CA-MCH-R1 (Melanin-concentrating hormone receptor 1) by using [125I](Phe13,Tyr19)MCH as radioligand expressed in HE...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23R0TM4PubMed
TargetNeuropeptide Y receptor type 5(Homo sapiens (Human))
Taisho Pharmaceutical Co. Ltd

Curated by ChEMBL
LigandPNGBDBM50166564(CHEMBL195123 | N-{4-[(4-Dimethylamino-quinazolin-2...)copy SMILEScopy InChI
Affinity DataIC50: 41nMAssay Description:Inhibitory activity against constitutively activated human Neuropeptide Y receptor Y5 stransiently expressed in COS-1 cells using [125I]-PYYMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z89BXQPubMed
TargetAlpha-2A adrenergic receptor(Homo sapiens (Human))
Taisho Pharmaceutical Co. Ltd

Curated by ChEMBL
LigandPNGBDBM50170196(CHEMBL182235 | trans-N*2*-(4-{[(4-Bromo-2-trifluor...)copy SMILEScopy InChI
Affinity DataIC50: 44nMAssay Description:Inhibitory activity against alpha-2A adrenergic receptor by using [3H]MK-912 as radioligand expressed in COS-1 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23R0TM4PubMed
TargetAlpha-2A adrenergic receptor(Homo sapiens (Human))
Taisho Pharmaceutical Co. Ltd

Curated by ChEMBL
LigandPNGBDBM50166563(4-Bromo-N-[4-(4-dimethylamino-quinazolin-2-ylamino...)copy SMILEScopy InChI
Affinity DataIC50: 47nMAssay Description:Inhibitory activity against constitutively activated human Alpha-2A adrenergic receptor transiently expressed in COS-1 cells using [3H]-MK912More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z89BXQPubMed
TargetAlpha-2A adrenergic receptor(Homo sapiens (Human))
Taisho Pharmaceutical Co. Ltd

Curated by ChEMBL
LigandPNGBDBM50170182(3,4-Dichloro-N-[4-(4-dimethylamino-quinazolin-2-yl...)copy SMILEScopy InChI
Affinity DataIC50: 47nMAssay Description:Inhibitory activity against alpha-2A adrenergic receptor by using [3H]MK-912 as radioligand expressed in COS-1 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23R0TM4PubMed
TargetAlpha-2A adrenergic receptor(Homo sapiens (Human))
Taisho Pharmaceutical Co. Ltd

Curated by ChEMBL
LigandPNGBDBM50170184(4-Bromo-N-[4-(4-dimethylamino-quinazolin-2-ylamino...)copy SMILEScopy InChI
Affinity DataIC50: 57nMAssay Description:Inhibitory activity against alpha-2A adrenergic receptor by using [3H]MK-912 as radioligand expressed in COS-1 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23R0TM4PubMed
TargetAlpha-2A adrenergic receptor(Homo sapiens (Human))
Taisho Pharmaceutical Co. Ltd

Curated by ChEMBL
LigandPNGBDBM50166565(4-Bromo-N-[4-(quinazolin-2-ylamino)-cyclohexyl]-2-...)copy SMILEScopy InChI
Affinity DataIC50: 57nMAssay Description:Inhibitory activity against constitutively activated human Alpha-2A adrenergic receptor transiently expressed in COS-1 cells using [3H]-MK912More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z89BXQPubMed
TargetAlpha-2A adrenergic receptor(Homo sapiens (Human))
Taisho Pharmaceutical Co. Ltd

Curated by ChEMBL
LigandPNGBDBM50166559(Butane-1-sulfonic acid {4-[(4-dimethylamino-quinaz...)copy SMILEScopy InChI
Affinity DataIC50: 58nMAssay Description:Inhibitory activity against constitutively activated human Alpha-2A adrenergic receptor transiently expressed in COS-1 cells using [3H]-MK912More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z89BXQPubMed
TargetAlpha-2A adrenergic receptor(Homo sapiens (Human))
Taisho Pharmaceutical Co. Ltd

Curated by ChEMBL
LigandPNGBDBM50170183(CHEMBL181632 | N-[4-(4-Dimethylamino-quinazolin-2-...)copy SMILEScopy InChI
Affinity DataIC50: 60nMAssay Description:Inhibitory activity against alpha-2A adrenergic receptor by using [3H]MK-912 as radioligand expressed in COS-1 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23R0TM4PubMed
TargetAlpha-2A adrenergic receptor(Homo sapiens (Human))
Taisho Pharmaceutical Co. Ltd

Curated by ChEMBL
LigandPNGBDBM50170176(3-Bromo-N-[4-(4-dimethylamino-quinazolin-2-ylamino...)copy SMILEScopy InChI
Affinity DataIC50: 63nMAssay Description:Inhibitory activity against alpha-2A adrenergic receptor by using [3H]MK-912 as radioligand expressed in COS-1 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23R0TM4PubMed
TargetAlpha-2A adrenergic receptor(Homo sapiens (Human))
Taisho Pharmaceutical Co. Ltd

Curated by ChEMBL
LigandPNGBDBM50170193(CHEMBL360081 | N-[4-(4-Dimethylamino-quinazolin-2-...)copy SMILEScopy InChI
Affinity DataIC50: 71nMAssay Description:Inhibitory activity against alpha-2A adrenergic receptor by using [3H]MK-912 as radioligand expressed in COS-1 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23R0TM4PubMed
TargetAlpha-2A adrenergic receptor(Homo sapiens (Human))
Taisho Pharmaceutical Co. Ltd

Curated by ChEMBL
LigandPNGBDBM50170180(3-Chloro-N-[4-(4-dimethylamino-quinazolin-2-ylamin...)copy SMILEScopy InChI
Affinity DataIC50: 76nMAssay Description:Inhibitory activity against alpha-2A adrenergic receptor by using [3H]MK-912 as radioligand expressed in COS-1 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23R0TM4PubMed
TargetNeuropeptide Y receptor type 5(Homo sapiens (Human))
Taisho Pharmaceutical Co. Ltd

Curated by ChEMBL
LigandPNGBDBM50166562(4-Bromo-N-[4-(quinazolin-2-ylaminomethyl)-cyclohex...)copy SMILEScopy InChI
Affinity DataIC50: 78nMAssay Description:Inhibitory activity against constitutively activated human Neuropeptide Y receptor Y5 stransiently expressed in COS-1 cells using [125I]-PYYMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z89BXQPubMed
TargetMelanin-concentrating hormone receptor 1(Homo sapiens (Human))
Taisho Pharmaceutical Co. Ltd.

Curated by ChEMBL
LigandPNGBDBM50170181(CHEMBL181393 | cis-4-Bromo-N-[4-(4-dimethylamino-q...)copy SMILEScopy InChI
Affinity DataIC50: 79nMAssay Description:Inhibitory activity against human CA-MCH-R1 (Melanin-concentrating hormone receptor 1) by using [125I](Phe13,Tyr19)MCH as radioligand expressed in HE...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23R0TM4PubMed
TargetMelanin-concentrating hormone receptor 1(Homo sapiens (Human))
Taisho Pharmaceutical Co. Ltd.

Curated by ChEMBL
LigandPNGBDBM50166565(4-Bromo-N-[4-(quinazolin-2-ylamino)-cyclohexyl]-2-...)copy SMILEScopy InChI
Affinity DataIC50: 83nMAssay Description:Inhibitory activity against mutated constitutively activated human Melanin concentrating hormone receptor 1 (CA-MCH-R1) stably expressed in HEK293 ce...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z89BXQPubMed
TargetMelanin-concentrating hormone receptor 1(Homo sapiens (Human))
Taisho Pharmaceutical Co. Ltd.

Curated by ChEMBL
LigandPNGBDBM50170184(4-Bromo-N-[4-(4-dimethylamino-quinazolin-2-ylamino...)copy SMILEScopy InChI
Affinity DataIC50: 83nMAssay Description:Inhibitory activity against human CA-MCH-R1 (Melanin-concentrating hormone receptor 1) by using [125I](Phe13,Tyr19)MCH as radioligand expressed in HE...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23R0TM4PubMed
TargetAlpha-2A adrenergic receptor(Homo sapiens (Human))
Taisho Pharmaceutical Co. Ltd

Curated by ChEMBL
LigandPNGBDBM50166564(CHEMBL195123 | N-{4-[(4-Dimethylamino-quinazolin-2...)copy SMILEScopy InChI
Affinity DataIC50: 86nMAssay Description:Inhibitory activity against constitutively activated human Alpha-2A adrenergic receptor transiently expressed in COS-1 cells using [3H]-MK912More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z89BXQPubMed
TargetAlpha-2A adrenergic receptor(Homo sapiens (Human))
Taisho Pharmaceutical Co. Ltd

Curated by ChEMBL
LigandPNGBDBM50166561(CHEMBL195380 | Naphthalene-1-sulfonic acid {4-[(4-...)copy SMILEScopy InChI
Affinity DataIC50: 97nMAssay Description:Inhibitory activity against constitutively activated human Alpha-2A adrenergic receptor transiently expressed in COS-1 cells using [3H]-MK912More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z89BXQPubMed
TargetAlpha-2A adrenergic receptor(Homo sapiens (Human))
Taisho Pharmaceutical Co. Ltd

Curated by ChEMBL
LigandPNGBDBM50170200(CHEMBL181383 | N-[4-(4-Dimethylamino-quinazolin-2-...)copy SMILEScopy InChI
Affinity DataIC50: 97nMAssay Description:Inhibitory activity against alpha-2A adrenergic receptor by using [3H]MK-912 as radioligand expressed in COS-1 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23R0TM4PubMed
TargetAlpha-2A adrenergic receptor(Homo sapiens (Human))
Taisho Pharmaceutical Co. Ltd

Curated by ChEMBL
LigandPNGBDBM50166554(CHEMBL192266 | N-{4-[(4-Amino-quinazolin-2-ylamino...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:Inhibitory activity against constitutively activated human Alpha-2A adrenergic receptor transiently expressed in COS-1 cells using [3H]-MK912More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z89BXQPubMed
TargetAlpha-2A adrenergic receptor(Homo sapiens (Human))
Taisho Pharmaceutical Co. Ltd

Curated by ChEMBL
LigandPNGBDBM50170179(CHEMBL180962 | N-[4-(4-Dimethylamino-quinazolin-2-...)copy SMILEScopy InChI
Affinity DataIC50: 110nMAssay Description:Inhibitory activity against alpha-2A adrenergic receptor by using [3H]MK-912 as radioligand expressed in COS-1 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23R0TM4PubMed
TargetAlpha-2A adrenergic receptor(Homo sapiens (Human))
Taisho Pharmaceutical Co. Ltd

Curated by ChEMBL
LigandPNGBDBM50166560(4-Bromo-N-[4-(4-dimethylamino-quinazolin-2-ylamino...)copy SMILEScopy InChI
Affinity DataIC50: 110nMAssay Description:Inhibitory activity against constitutively activated human Alpha-2A adrenergic receptor transiently expressed in COS-1 cells using [3H]-MK912More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z89BXQPubMed
TargetNeuropeptide Y receptor type 5(Homo sapiens (Human))
Taisho Pharmaceutical Co. Ltd

Curated by ChEMBL
LigandPNGBDBM50170178(4-Bromo-N-[4-(4-dimethylamino-quinazolin-2-ylamino...)copy SMILEScopy InChI
Affinity DataIC50: 120nMAssay Description:Inhibitory activity against neuropeptide Y receptor type 5 by using [125I]PYY as radioligand expressed in COS-1 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23R0TM4PubMed
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