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ChEMBL ligand: CHEMBL175543 (MRS-3558, MRS-5358) |
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DB | Assay description | Assay Type | Standard value | Standard parameter | Original value | Original units | Original parameter | Reference |
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A1 receptor/Adenosine A1 receptor in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL226] [GtoPdb: 18] [UniProtKB: P30542] | ||||||||
ChEMBL | Inhibition of [3H]R-PIA binding to human Adenosine A1 receptor expressed in CHO cells | B | 6.59 | pKi | 260 | nM | Ki | J Med Chem (2005) 48: 1745-1758 [PMID:15771421] |
ChEMBL | Displacement of radioligand from human adenosine A1 receptor expressed in CHO cells | B | 6.59 | pKi | 260 | nM | Ki | Bioorg Med Chem Lett (2008) 18: 2813-2819 [PMID:18424135] |
ChEMBL | Displacement of [3H]CCPA form human adenosine A1 receptor expressed in CHO cells | B | 6.59 | pKi | 260 | nM | Ki | Bioorg Med Chem (2008) 16: 8546-8556 [PMID:18752961] |
ChEMBL | Displacement of [3H]R-PIA from human recombinant adenosine A1 receptor expressed in CHO cells after 60 mins by liquid scintillation counting | B | 6.59 | pKi | 260 | nM | Ki | J Med Chem (2012) 55: 4847-4860 [PMID:22559880] |
ChEMBL | Displacement of [3H]CCPA from human recombinant adenosine A1 receptor expressed in CHO cells after 60 mins by gamma counter | B | 6.59 | pKi | 260 | nM | Ki | J Med Chem (2012) 55: 5676-5703 [PMID:22468757] |
GtoPdb | - | - | 6.59 | pKi | 260 | nM | Ki | Nat Rev Drug Discov (2006) 5: 247-64 [PMID:16518376] |
A1 receptor/Adenosine A1 receptor in Mouse (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL3688] [GtoPdb: 18] [UniProtKB: Q60612] | ||||||||
GtoPdb | - | - | 7.8 | pKi | 15.8 | nM | Ki | . A3 Adenosine Receptors from Cell Biology to Pharmacology and Therapeutics (2010) |
ChEMBL | Displacement of [125I]N6-(4-amino-3-iodobenzyl)adenosine-5'-N-methyl-uronamide from mouse recombinant adenosine A1 receptor expressed in HEK293 cells | B | 7.82 | pKi | 15.3 | nM | Ki | Bioorg Med Chem Lett (2008) 18: 2813-2819 [PMID:18424135] |
A1 receptor in Rat [GtoPdb: 18] [UniProtKB: P25099] | ||||||||
GtoPdb | - | - | 6.98 | pKi | 105 | nM | Ki | . A3 Adenosine Receptors from Cell Biology to Pharmacology and Therapeutics (2010) |
A2A receptor/Adenosine A2a receptor in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL251] [GtoPdb: 19] [UniProtKB: P29274] | ||||||||
GtoPdb | - | - | 5.63 | pKi | 2330 | nM | Ki | Nat Rev Drug Discov (2006) 5: 247-64 [PMID:16518376] |
ChEMBL | Inhibition of [3H]-CGS- 21680 binding to human Adenosine A2A receptor expressed in CHO cells | B | 5.64 | pKi | 2300 | nM | Ki | J Med Chem (2005) 48: 1745-1758 [PMID:15771421] |
ChEMBL | Displacement of radioligand from human adenosine A2A receptor expressed in HEK293 cells | B | 5.64 | pKi | 2300 | nM | Ki | Bioorg Med Chem Lett (2008) 18: 2813-2819 [PMID:18424135] |
ChEMBL | Displacement of [3H]R-PIA form human adenosine A2A receptor expressed in HEK cells | B | 5.64 | pKi | 2300 | nM | Ki | Bioorg Med Chem (2008) 16: 8546-8556 [PMID:18752961] |
ChEMBL | Displacement of [3H]CGS21680 from human recombinant adenosine A2A receptor expressed in HEK293 cells after 60 mins by liquid scintillation counting | B | 5.64 | pKi | 2300 | nM | Ki | J Med Chem (2012) 55: 4847-4860 [PMID:22559880] |
ChEMBL | Displacement of [3H]CGS21680 from human recombinant adenosine A2A receptor expressed in CHO cells after 60 mins by gamma counter | B | 5.64 | pKi | 2300 | nM | Ki | J Med Chem (2012) 55: 5676-5703 [PMID:22468757] |
A2A receptor/Adenosine A2a receptor in Mouse (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL2115] [GtoPdb: 19] [UniProtKB: Q60613] | ||||||||
GtoPdb | - | - | 4.98 | pKi | 10400 | nM | Ki | . A3 Adenosine Receptors from Cell Biology to Pharmacology and Therapeutics (2010) |
ChEMBL | Displacement of [3H]2-[p-(2-carboxyethyl)phenyl-ethylamino]-5'-N-ethylcarboxamidoadenosine from mouse recombinant adenosine A2A receptor expressed in HEK293 cells | B | 4.98 | pKi | 10400 | nM | Ki | Bioorg Med Chem Lett (2008) 18: 2813-2819 [PMID:18424135] |
A2A receptor in Rat [GtoPdb: 19] [UniProtKB: P30543] | ||||||||
GtoPdb | - | - | 5.97 | pKi | 1080 | nM | Ki | . A3 Adenosine Receptors from Cell Biology to Pharmacology and Therapeutics (2010) |
A2B receptor/Adenosine A2b receptor in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL255] [GtoPdb: 20] [UniProtKB: P29275] | ||||||||
GtoPdb | - | - | 5 | pKi | >10000 | nM | Ki | Nat Rev Drug Discov (2006) 5: 247-64 [PMID:16518376] |
ChEMBL | Activation of human adenosine A2B receptor | B | 5 | pEC50 | >=10000 | nM | EC50 | Bioorg Med Chem Lett (2008) 18: 2813-2819 [PMID:18424135] |
A3 receptor/Adenosine A3 receptor in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL256] [GtoPdb: 21] [UniProtKB: P0DMS8] | ||||||||
ChEMBL | Inhibition of [125I]-AB-MECA binding to human Adenosine A3 receptor expressed in CHO cells | B | 9.54 | pKi | 0.29 | nM | Ki | J Med Chem (2005) 48: 1745-1758 [PMID:15771421] |
ChEMBL | Displacement of radioligand from human adenosine A3 receptor expressed in CHO cells | B | 9.54 | pKi | 0.29 | nM | Ki | Bioorg Med Chem Lett (2008) 18: 2813-2819 [PMID:18424135] |
ChEMBL | Displacement of [3H]CGS21680 form human adenosine A3 receptor expressed in CHO cells | B | 9.54 | pKi | 0.29 | nM | Ki | Bioorg Med Chem (2008) 16: 8546-8556 [PMID:18752961] |
ChEMBL | Displacement of [3H]I-AB-MECA from human recombinant adenosine A3 receptor expressed in CHO cells after 60 mins by gamma counting | B | 9.54 | pKi | 0.29 | nM | Ki | J Med Chem (2012) 55: 4847-4860 [PMID:22559880] |
ChEMBL | Displacement of [125I]I-AB-MECA from human recombinant adenosine A3 receptor expressed in CHO cells after 60 mins by gamma counter | B | 9.54 | pKi | 0.29 | nM | Ki | J Med Chem (2012) 55: 5676-5703 [PMID:22468757] |
GtoPdb | - | - | 9.54 | pKi | 0.29 | nM | Ki | Nat Rev Drug Discov (2006) 5: 247-64 [PMID:16518376] |
A3 receptor/Adenosine A3 receptor in Mouse (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL1075269] [GtoPdb: 21] [UniProtKB: Q61618] | ||||||||
ChEMBL | Displacement of [125I]N6-(-amino-3-iodobenzyl)adenosine-5'-N-methyl-uronamide from mouse recombinant adenosine A3 receptor expressed in HEK293 cells | B | 8.83 | pKi | 1.49 | nM | Ki | Bioorg Med Chem Lett (2008) 18: 2813-2819 [PMID:18424135] |
GtoPdb | - | - | 8.83 | pKi | 1.49 | nM | Ki | . A3 Adenosine Receptors from Cell Biology to Pharmacology and Therapeutics (2010) |
A3 receptor/Adenosine A3 receptor in Rat (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL3360] [GtoPdb: 21] [UniProtKB: P28647] | ||||||||
GtoPdb | - | - | 9 | pKi | 1 | nM | Ki | . A3 Adenosine Receptors from Cell Biology to Pharmacology and Therapeutics (2010) |
ChEMBL | Inhibition of [125I]AB-MECA binding to rat Adenosine A3 receptor expressed in CHO cells | B | 9 | pKi | 1 | nM | Ki | J Med Chem (2005) 48: 1745-1758 [PMID:15771421] |
ChEMBL | Displacement of [125I]I-AB-MECA from human rat adenosine A3 receptor expressed in CHO cells after 60 mins by gamma counter | B | 9 | pKi | 1 | nM | Ki | J Med Chem (2012) 55: 5676-5703 [PMID:22468757] |
5-HT2B receptor/Serotonin 2b (5-HT2b) receptor in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL1833] [GtoPdb: 7] [UniProtKB: P41595] | ||||||||
ChEMBL | Antagonist activity at human 5-HT2BR expressed in Flp-In HEK cells assessed as inhibition of 5-HT-induced calcium mobilization preincubated for 5 to 10 mins followed 5-HT addition by Fluo-4 dye based FLIPR assay | F | 5.49 | pIC50 | 3260 | nM | IC50 | J Med Chem (2016) 59: 11006-11026 [PMID:27933810] |
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]