BindingDB logo
myBDB logout

PubMed code 25221658

Compile data set for download or QSAR
Found 6 hits of Enzyme Inhibition Constant Data   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kJ/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
D(3) dopamine receptor


(Homo sapiens (Human))
BDBM50026746
PNG
(CHEMBL3335471)
Show SMILES NCC(=O)N[C@H]1CC[C@H](CCN2CCN(CC2)c2cc(cc(c2)C(F)(F)F)C#N)CC1 |r,wU:5.4,wD:8.8,(44.7,-19.21,;43.93,-20.55,;42.39,-20.55,;41.62,-21.88,;41.62,-19.21,;40.08,-19.21,;39.31,-20.55,;37.77,-20.55,;37,-19.21,;35.46,-19.21,;34.69,-17.88,;33.15,-17.88,;32.38,-19.21,;30.84,-19.21,;30.07,-17.88,;30.84,-16.54,;32.38,-16.54,;28.53,-17.88,;27.76,-19.21,;26.22,-19.21,;25.45,-17.88,;26.22,-16.54,;27.76,-16.54,;25.45,-15.21,;26.22,-13.88,;23.91,-15.21,;24.68,-13.88,;25.45,-20.55,;24.68,-21.88,;37.77,-17.88,;39.31,-17.88,)|
Show InChI InChI=1S/C22H30F3N5O/c23-22(24,25)18-11-17(14-26)12-20(13-18)30-9-7-29(8-10-30)6-5-16-1-3-19(4-2-16)28-21(31)15-27/h11-13,16,19H,1-10,15,27H2,(H,28,31)/t16-,19-
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
0.620n/an/an/an/an/an/an/an/a



Gedeon Richter Plc

Curated by ChEMBL


Assay Description
Displacement of [3H]-raclopride from human D3 receptor expressed in CHO-K1 cells after 120 mins by scintillation counting analysis


ACS Med Chem Lett 5: 1010-4 (2014)


Article DOI: 10.1021/ml500201u
BindingDB Entry DOI: 10.7270/Q2CC128M
More data for this
Ligand-Target Pair
D(3) dopamine receptor


(Homo sapiens (Human))
BDBM50026747
PNG
(CHEMBL3335472)
Show SMILES NS(=O)(=O)N[C@H]1CC[C@H](CCN2CCN(CC2)c2cc(cc(c2)C(F)(F)F)C#N)CC1 |r,wU:5.4,wD:8.8,(31.51,-21.3,;30.02,-21.7,;30.02,-23.24,;28.69,-22.47,;29.25,-20.36,;27.71,-20.36,;26.94,-21.7,;25.4,-21.7,;24.63,-20.36,;23.09,-20.36,;22.32,-19.03,;20.78,-19.03,;20.01,-20.36,;18.47,-20.36,;17.7,-19.03,;18.47,-17.7,;20.01,-17.7,;16.16,-19.03,;15.39,-20.36,;13.85,-20.36,;13.08,-19.03,;13.85,-17.7,;15.39,-17.7,;13.08,-16.36,;12.31,-15.02,;13.85,-15.02,;11.54,-16.36,;13.08,-21.7,;12.31,-23.03,;25.4,-19.03,;26.94,-19.03,)|
Show InChI InChI=1S/C20H28F3N5O2S/c21-20(22,23)17-11-16(14-24)12-19(13-17)28-9-7-27(8-10-28)6-5-15-1-3-18(4-2-15)26-31(25,29)30/h11-13,15,18,26H,1-10H2,(H2,25,29,30)/t15-,18-
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
0.670n/an/an/an/an/an/an/an/a



Gedeon Richter Plc

Curated by ChEMBL


Assay Description
Displacement of [3H]-raclopride from human D3 receptor expressed in CHO-K1 cells after 120 mins by scintillation counting analysis


ACS Med Chem Lett 5: 1010-4 (2014)


Article DOI: 10.1021/ml500201u
BindingDB Entry DOI: 10.7270/Q2CC128M
More data for this
Ligand-Target Pair
D(3) dopamine receptor


(Homo sapiens (Human))
BDBM50026745
PNG
(CHEMBL3335470)
Show SMILES NC(=O)N[C@H]1CC[C@H](CCN2CCN(CC2)c2cc(cc(c2)C(F)(F)F)C#N)CC1 |r,wU:4.3,wD:7.7,(20.37,-9.78,;21.14,-8.45,;22.68,-8.45,;20.37,-7.12,;18.83,-7.12,;18.06,-8.45,;16.52,-8.45,;15.75,-7.12,;14.21,-7.12,;13.44,-5.78,;11.9,-5.78,;11.13,-7.12,;9.59,-7.12,;8.82,-5.78,;9.59,-4.45,;11.13,-4.45,;7.28,-5.78,;6.51,-7.12,;4.97,-7.12,;4.2,-5.78,;4.97,-4.45,;6.51,-4.45,;4.2,-3.12,;4.97,-1.78,;2.66,-3.12,;3.43,-1.78,;4.2,-8.45,;3.43,-9.78,;16.52,-5.78,;18.06,-5.78,)|
Show InChI InChI=1S/C21H28F3N5O/c22-21(23,24)17-11-16(14-25)12-19(13-17)29-9-7-28(8-10-29)6-5-15-1-3-18(4-2-15)27-20(26)30/h11-13,15,18H,1-10H2,(H3,26,27,30)/t15-,18-
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
0.75n/an/an/an/an/an/an/an/a



Gedeon Richter Plc

Curated by ChEMBL


Assay Description
Displacement of [3H]-raclopride from human D3 receptor expressed in CHO-K1 cells after 120 mins by scintillation counting analysis


ACS Med Chem Lett 5: 1010-4 (2014)


Article DOI: 10.1021/ml500201u
BindingDB Entry DOI: 10.7270/Q2CC128M
More data for this
Ligand-Target Pair
D(2) dopamine receptor


(Homo sapiens (Human))
BDBM50026746
PNG
(CHEMBL3335471)
Show SMILES NCC(=O)N[C@H]1CC[C@H](CCN2CCN(CC2)c2cc(cc(c2)C(F)(F)F)C#N)CC1 |r,wU:5.4,wD:8.8,(44.7,-19.21,;43.93,-20.55,;42.39,-20.55,;41.62,-21.88,;41.62,-19.21,;40.08,-19.21,;39.31,-20.55,;37.77,-20.55,;37,-19.21,;35.46,-19.21,;34.69,-17.88,;33.15,-17.88,;32.38,-19.21,;30.84,-19.21,;30.07,-17.88,;30.84,-16.54,;32.38,-16.54,;28.53,-17.88,;27.76,-19.21,;26.22,-19.21,;25.45,-17.88,;26.22,-16.54,;27.76,-16.54,;25.45,-15.21,;26.22,-13.88,;23.91,-15.21,;24.68,-13.88,;25.45,-20.55,;24.68,-21.88,;37.77,-17.88,;39.31,-17.88,)|
Show InChI InChI=1S/C22H30F3N5O/c23-22(24,25)18-11-17(14-26)12-20(13-18)30-9-7-29(8-10-30)6-5-16-1-3-19(4-2-16)28-21(31)15-27/h11-13,16,19H,1-10,15,27H2,(H,28,31)/t16-,19-
PDB

Reactome pathway
KEGG

UniProtKB/SwissProt

DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
5.40n/an/an/an/an/an/an/an/a



Gedeon Richter Plc

Curated by ChEMBL


Assay Description
Displacement of [3H]-raclopride from human D2long receptor expressed in HEK293Galpha15 cells after 120 mins by scintillation counting analysis


ACS Med Chem Lett 5: 1010-4 (2014)


Article DOI: 10.1021/ml500201u
BindingDB Entry DOI: 10.7270/Q2CC128M
More data for this
Ligand-Target Pair
D(2) dopamine receptor


(Homo sapiens (Human))
BDBM50026745
PNG
(CHEMBL3335470)
Show SMILES NC(=O)N[C@H]1CC[C@H](CCN2CCN(CC2)c2cc(cc(c2)C(F)(F)F)C#N)CC1 |r,wU:4.3,wD:7.7,(20.37,-9.78,;21.14,-8.45,;22.68,-8.45,;20.37,-7.12,;18.83,-7.12,;18.06,-8.45,;16.52,-8.45,;15.75,-7.12,;14.21,-7.12,;13.44,-5.78,;11.9,-5.78,;11.13,-7.12,;9.59,-7.12,;8.82,-5.78,;9.59,-4.45,;11.13,-4.45,;7.28,-5.78,;6.51,-7.12,;4.97,-7.12,;4.2,-5.78,;4.97,-4.45,;6.51,-4.45,;4.2,-3.12,;4.97,-1.78,;2.66,-3.12,;3.43,-1.78,;4.2,-8.45,;3.43,-9.78,;16.52,-5.78,;18.06,-5.78,)|
Show InChI InChI=1S/C21H28F3N5O/c22-21(23,24)17-11-16(14-25)12-19(13-17)29-9-7-28(8-10-29)6-5-15-1-3-18(4-2-15)27-20(26)30/h11-13,15,18H,1-10H2,(H3,26,27,30)/t15-,18-
PDB

Reactome pathway
KEGG

UniProtKB/SwissProt

DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
30n/an/an/an/an/an/an/an/a



Gedeon Richter Plc

Curated by ChEMBL


Assay Description
Displacement of [3H]-raclopride from human D2long receptor expressed in HEK293Galpha15 cells after 120 mins by scintillation counting analysis


ACS Med Chem Lett 5: 1010-4 (2014)


Article DOI: 10.1021/ml500201u
BindingDB Entry DOI: 10.7270/Q2CC128M
More data for this
Ligand-Target Pair
D(2) dopamine receptor


(Homo sapiens (Human))
BDBM50026747
PNG
(CHEMBL3335472)
Show SMILES NS(=O)(=O)N[C@H]1CC[C@H](CCN2CCN(CC2)c2cc(cc(c2)C(F)(F)F)C#N)CC1 |r,wU:5.4,wD:8.8,(31.51,-21.3,;30.02,-21.7,;30.02,-23.24,;28.69,-22.47,;29.25,-20.36,;27.71,-20.36,;26.94,-21.7,;25.4,-21.7,;24.63,-20.36,;23.09,-20.36,;22.32,-19.03,;20.78,-19.03,;20.01,-20.36,;18.47,-20.36,;17.7,-19.03,;18.47,-17.7,;20.01,-17.7,;16.16,-19.03,;15.39,-20.36,;13.85,-20.36,;13.08,-19.03,;13.85,-17.7,;15.39,-17.7,;13.08,-16.36,;12.31,-15.02,;13.85,-15.02,;11.54,-16.36,;13.08,-21.7,;12.31,-23.03,;25.4,-19.03,;26.94,-19.03,)|
Show InChI InChI=1S/C20H28F3N5O2S/c21-20(22,23)17-11-16(14-24)12-19(13-17)28-9-7-27(8-10-28)6-5-15-1-3-18(4-2-15)26-31(25,29)30/h11-13,15,18,26H,1-10H2,(H2,25,29,30)/t15-,18-
PDB

Reactome pathway
KEGG

UniProtKB/SwissProt

DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
37n/an/an/an/an/an/an/an/a



Gedeon Richter Plc

Curated by ChEMBL


Assay Description
Displacement of [3H]-raclopride from human D2long receptor expressed in HEK293Galpha15 cells after 120 mins by scintillation counting analysis


ACS Med Chem Lett 5: 1010-4 (2014)


Article DOI: 10.1021/ml500201u
BindingDB Entry DOI: 10.7270/Q2CC128M
More data for this
Ligand-Target Pair
* indicates data uncertainty>20%