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ChEMBL ligand: CHEMBL419792 (Pnu-95666, PNU-95666E, Sumanirol, Sumanirole) |
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DB | Assay description | Assay Type | Standard value | Standard parameter | Original value | Original units | Original parameter | Reference |
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D2 receptor/Dopamine D2 receptor in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL217] [GtoPdb: 215] [UniProtKB: P14416] | ||||||||
ChEMBL | Displacement of [3H]N-methylspiperone from human D2 receptor transfected in HEK293 cells measured after 60 mins by liquid scintillation counter | B | 4.79 | pKi | 16300 | nM | Ki | J Med Chem (2016) 59: 2973-2988 [PMID:27035329] |
ChEMBL | Displacement of [3H]-methylscopolamine from human dopamine D2 receptor expressed in HEK293 cell membranes incubated for 90 mins by microbeta scintillation counting analysis | B | 4.79 | pKi | 16300 | nM | Ki | J Med Chem (2021) 64: 16088-16105 [PMID:34699207] |
ChEMBL | Displacement of [3H]-(R)-(+)7-OH-DPAT from human dopamine D2 receptor expressed in HEK293 cell membranes incubated for 90 mins by microbeta scintillation counting analysis | B | 7.09 | pKi | 80.6 | nM | Ki | J Med Chem (2021) 64: 16088-16105 [PMID:34699207] |
ChEMBL | Displacement of [3H]-(R)-(+)-7-OH-DPAT from human dopamine D2 receptor expressed in HEK293 cell membranes after 90 mins by micro beta scintillation counting analysis | B | 7.33 | pKi | 46.3 | nM | Ki | J Med Chem (2017) 60: 2890-2907 [PMID:28300398] |
ChEMBL | Displacement of [3H]7-OH-DPAT from human D2 receptor transfected in HEK293 cells measured after 60 mins by liquid scintillation counter | B | 7.77 | pKi | 17.1 | nM | Ki | J Med Chem (2016) 59: 2973-2988 [PMID:27035329] |
ChEMBL | Binding affinity towards Dopamine receptor D2 by displacement of [3H]U-86170. | B | 8.05 | pKi | 9 | nM | Ki | J Med Chem (1997) 40: 639-646 [PMID:9057850] |
GtoPdb | - | - | 8.1 | pKi | 9 | nM | Ki | J Pharmacol Exp Ther (2005) 314: 1248-56 [PMID:15980060] |
ChEMBL | Agonist activity at human dopamine D2 receptor expressed in HEK293 cells coexpressing renilla luciferase-fused Galphai1/GFP10-fused Ggamma2 by BRET assay | B | 6.26 | pEC50 | 543.3 | nM | EC50 | J Med Chem (2017) 60: 2890-2907 [PMID:28300398] |
ChEMBL | Agonist activity at renilla luciferase-tagged human dopamine D2 receptor expressed in HEK293 cells coexpressing mVenus-fused beta-arrestin 2 assessed as induction of beta-arrestin 2 recruitment by BRET assay | B | 6.3 | pEC50 | 501.2 | nM | EC50 | J Med Chem (2017) 60: 2890-2907 [PMID:28300398] |
ChEMBL | In vitro effective concentration tested on HEK293 cells co-transfected with human Dopamine receptor D2 using FLIPR assay | F | 6.78 | pEC50 | 165 | nM | EC50 | J Med Chem (2004) 47: 3853-3864 [PMID:15239663] |
ChEMBL | Agonist activity at human dopamine D2 receptor expressed in HEK293 cells coexpressing renilla luciferase-fused GalphaoA/GFP10-fused Ggamma2 by BRET assay | B | 7.13 | pEC50 | 74.8 | nM | EC50 | J Med Chem (2017) 60: 2890-2907 [PMID:28300398] |
ChEMBL | Agonist activity at recombinant human D2 receptor expressing in CHOp cells assessed as receptor mediated stimulation of mitogenesis measured as [3H]thymidine incorporation after 24 hrs by scintillation spectrometry | B | 7.19 | pEC50 | 64.7 | nM | EC50 | J Med Chem (2016) 59: 2973-2988 [PMID:27035329] |
ChEMBL | Agonist activity at human D2 receptor transfected in HEK293T cells by BRET based G0 activation assay | B | 7.22 | pEC50 | 60.1 | nM | EC50 | J Med Chem (2016) 59: 2973-2988 [PMID:27035329] |
ChEMBL | Agonist activity at human dopamine D2 receptor expressed in HEK293 cells assessed as cAMP inhibition by BRET assay | F | 7.49 | pEC50 | 32.2 | nM | EC50 | J Med Chem (2017) 60: 2890-2907 [PMID:28300398] |
ChEMBL | Agonist activity at recombinant human D2 receptor expressing in CHO cells assessed as receptor mediated stimulation of mitogenesis measured as [3H]thymidine incorporation by beta plate counter | B | 8.34 | pEC50 | 4.6 | nM | EC50 | J Med Chem (2016) 59: 2973-2988 [PMID:27035329] |
D2 receptor/Dopamine D2 receptor in Rat (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL339] [GtoPdb: 215] [UniProtKB: P61169] | ||||||||
ChEMBL | In vitro effective concentration tested on HEK293 cells co-transfected with ferret Dopamine receptor D2 using FLIPR assay | F | 7.46 | pEC50 | 35 | nM | EC50 | J Med Chem (2004) 47: 3853-3864 [PMID:15239663] |
ChEMBL | In vitro effective concentration tested on HEK293 cells co-transfected with rat Dopamine receptor D2 using FLIPR assay | F | 7.97 | pEC50 | 10.8 | nM | EC50 | J Med Chem (2004) 47: 3853-3864 [PMID:15239663] |
D3 receptor/Dopamine D3 receptor in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL234] [GtoPdb: 216] [UniProtKB: P35462] | ||||||||
ChEMBL | Displacement of [3H]N-methylspiperone from human D3 receptor transfected in HEK293 cells measured after 60 mins by liquid scintillation counter | B | 5.2 | pKi | 6330 | nM | Ki | J Med Chem (2016) 59: 2973-2988 [PMID:27035329] |
ChEMBL | Displacement of [3H]-methylscopolamine from human dopamine D3 receptor expressed in HEK293 cell membranes incubated for 90 mins by microbeta scintillation counting analysis | B | 5.2 | pKi | 6330 | nM | Ki | J Med Chem (2021) 64: 16088-16105 [PMID:34699207] |
ChEMBL | Binding affinity towards Dopamine receptor D3 by displacement of [3H](+)-7-OH-DPAT. | B | 5.63 | pKi | 2333 | nM | Ki | J Med Chem (1997) 40: 639-646 [PMID:9057850] |
ChEMBL | Displacement of [3H]-(R)-(+)7-OH-DPAT from human dopamine D3 receptor expressed in HEK293 cell membranes incubated for 90 mins by microbeta scintillation counting analysis | B | 6.11 | pKi | 784 | nM | Ki | J Med Chem (2021) 64: 16088-16105 [PMID:34699207] |
ChEMBL | Displacement of [3H]-(R)-(+)-7-OH-DPAT from human dopamine D3 receptor expressed in HEK293 cell membranes after 90 mins by micro beta scintillation counting analysis | B | 6.24 | pKi | 573 | nM | Ki | J Med Chem (2017) 60: 2890-2907 [PMID:28300398] |
ChEMBL | Displacement of [3H]7-OH-DPAT from human D3 receptor transfected in HEK293 cells measured after 60 mins by liquid scintillation counter | B | 6.26 | pKi | 546 | nM | Ki | J Med Chem (2016) 59: 2973-2988 [PMID:27035329] |
ChEMBL | Agonist activity at recombinant human D3 receptor expressing in CHOp cells assessed as receptor mediated stimulation of mitogenesis measured as [3H]thymidine incorporation after 24 hrs by scintillation spectrometry | B | 6.17 | pEC50 | 669 | nM | EC50 | J Med Chem (2016) 59: 2973-2988 [PMID:27035329] |
ChEMBL | Agonist activity at human D3 receptor transfected in HEK293T cells by BRET based G0 activation assay | B | 6.73 | pEC50 | 186 | nM | EC50 | J Med Chem (2016) 59: 2973-2988 [PMID:27035329] |
5-HT1A receptor/Serotonin 1a (5-HT1a) receptor in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL214] [GtoPdb: 1] [UniProtKB: P08908] | ||||||||
ChEMBL | Binding affinity towards Serotonin 5-hydroxytryptamine 1A receptor by displacement of [3H]-(+)-8-OH-DPAT. | B | 7.14 | pKi | 73 | nM | Ki | J Med Chem (1997) 40: 639-646 [PMID:9057850] |
ChEMBL data shown on this page come from version 34:
Zdrazil B, Felix E, Hunter F, Manners EJ, Blackshaw J, Corbett S, de Veij M, Ioannidis H, Lopez DM, Mosquera JF, Magarinos MP, Bosc N, Arcila R, Kizilören T, Gaulton A, Bento AP, Adasme MF, Monecke P, Landrum GA, Leach AR. (2024). The ChEMBL Database in 2023: a drug discovery platform spanning multiple bioactivity data types and time periods. Nucleic Acids Res., 52(D1). DOI: 10.1093/nar/gkad1004. [EPMCID:10767899] [PMID:37933841]
Davies M, Nowotka M, Papadatos G, Dedman N, Gaulton A, Atkinson F, Bellis L, Overington JP. (2015) 'ChEMBL web services: streamlining access to drug discovery data and utilities.' Nucleic Acids Res., 43(W1). DOI: 10.1093/nar/gkv352. [EPMCID:25883136]