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Found 6 Enz. Inhib. hit(s) with Target = 'D(1A) dopamine receptor' and Ligand = 'BDBM86282'
TargetD(1A) dopamine receptor(RAT)
Harvard University

Curated by PDSP Ki Database
LigandPNGBDBM86282(6-Chloro-1-phenyl-2,3,4,5-tetrahydro-1H-benzo[d]az...)
Affinity DataKi:  1.90nMMore data for this Ligand-Target Pair
TargetD(1A) dopamine receptor(Homo sapiens (Human))
Northeastern University

Curated by ChEMBL
LigandPNGBDBM86282(6-Chloro-1-phenyl-2,3,4,5-tetrahydro-1H-benzo[d]az...)
Affinity DataKi:  7nMAssay Description:The compound was evaluated for the dissociation constant for inhibiting the binding of [3H]-SCH- 23390 at dopamine receptor D1More data for this Ligand-Target Pair
TargetD(1A) dopamine receptor(Homo sapiens (Human))
Northeastern University

Curated by ChEMBL
LigandPNGBDBM86282(6-Chloro-1-phenyl-2,3,4,5-tetrahydro-1H-benzo[d]az...)
Affinity DataKi:  15nMAssay Description:Displacement of [3H]-SCH23390 from wild type human D1R expressed in HEK293 cell membranes incubated for 90 mins by scintillation counting based compe...More data for this Ligand-Target Pair
TargetD(1A) dopamine receptor(Homo sapiens (Human))
Northeastern University

Curated by ChEMBL
LigandPNGBDBM86282(6-Chloro-1-phenyl-2,3,4,5-tetrahydro-1H-benzo[d]az...)
Affinity DataEC50:  360nMAssay Description:Agonist activity at wild type human D1R expressed in HEK293 cells assessed as effect on beta-arrestin2 recruitment by PRESTO-Tango beta-arrestin2 rec...More data for this Ligand-Target Pair
TargetD(1A) dopamine receptor(Homo sapiens (Human))
Northeastern University

Curated by ChEMBL
LigandPNGBDBM86282(6-Chloro-1-phenyl-2,3,4,5-tetrahydro-1H-benzo[d]az...)
Affinity DataEC50:  4.70nMAssay Description:Agonist activity at wild type human D1R expressed in HEK293 cells assessed as effect on cAMP accumulation incubated for 10 mins by Gs-cAMP Glosensor ...More data for this Ligand-Target Pair
TargetD(1A) dopamine receptor(Homo sapiens (Human))
Northeastern University

Curated by ChEMBL
LigandPNGBDBM86282(6-Chloro-1-phenyl-2,3,4,5-tetrahydro-1H-benzo[d]az...)
Affinity DataEC50:  9.50E+3nMAssay Description:Agonist activity at recombinant human D1 receptor expressed in CHOK1 cells assessed as induction of beta arrestin2 recruitment measured after 30 mins...More data for this Ligand-Target Pair