RY764 [Ligand Id: 1337] activity data from GtoPdb and ChEMBL

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ChEMBL ligand: CHEMBL364346
  • MC2 receptor/Melanocortin receptor 2 in Human [ChEMBL: CHEMBL1965] [GtoPdb: 283] [UniProtKB: Q01718]
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  • MC3 receptor/Melanocortin receptor 3 in Human [ChEMBL: CHEMBL4644] [GtoPdb: 284] [UniProtKB: P41968]
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  • MC4 receptor/Melanocortin receptor 4 in Human [ChEMBL: CHEMBL259] [GtoPdb: 285] [UniProtKB: P32245]
  • MC4 receptor/Melanocortin receptor 4 in Mouse [ChEMBL: CHEMBL3719] [GtoPdb: 285] [UniProtKB: P56450]
  • MC4 receptor/Melanocortin receptor 4 in Rat [ChEMBL: CHEMBL2700] [GtoPdb: 285] [UniProtKB: P70596]
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  • MC5 receptor/Melanocortin receptor 5 in Human [ChEMBL: CHEMBL4608] [GtoPdb: 286] [UniProtKB: P33032]
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DB Assay description Assay Type Standard value Standard parameter Original value Original units Original parameter Reference
MC2 receptor/Melanocortin receptor 2 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL1965] [GtoPdb: 283] [UniProtKB: Q01718]
ChEMBL Inhibition concentration (binding affinity) against human melanocortin receptor 2 by displacement of [125I]NDP-alpha-MSH from the human receptors expressed in CHO cells B 5 pIC50 >10000 nM IC50 Bioorg Med Chem Lett (2005) 15: 3501-3505 [PMID:15982875]
MC3 receptor/Melanocortin receptor 3 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL4644] [GtoPdb: 284] [UniProtKB: P41968]
ChEMBL Inhibition concentration (binding affinity) against human melanocortin receptor 3 by displacement of [125I]NDP-alpha-MSH from the human receptors expressed in CHO cells B 6.03 pIC50 942 nM IC50 Bioorg Med Chem Lett (2005) 15: 3501-3505 [PMID:15982875]
MC4 receptor/Melanocortin receptor 4 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL259] [GtoPdb: 285] [UniProtKB: P32245]
ChEMBL Inhibition concentration (binding affinity) against human melanocortin receptor 4 by displacement of [125I]NDP-alpha-MSH from the human receptors expressed in CHO cells B 5.1 pIC50 8000 nM IC50 Bioorg Med Chem Lett (2005) 15: 3501-3505 [PMID:15982875]
ChEMBL Inhibition concentration (binding affinity) against dog melanocortin receptor 4 by displacement of [125I]NDP-alpha-MSH from the human receptors expressed in CHO cells B 5.15 pIC50 7000 nM IC50 Bioorg Med Chem Lett (2005) 15: 3501-3505 [PMID:15982875]
ChEMBL Inhibition concentration (binding affinity) against human melanocortin receptor 4 by displacement of [125I]NDP-alpha-MSH from the human receptors expressed in CHO cells B 8.1 pIC50 8 nM IC50 Bioorg Med Chem Lett (2005) 15: 3501-3505 [PMID:15982875]
GtoPdb - - 8.1 pIC50 - - - Bioorg Med Chem Lett (2005) 15: 3501-5 [PMID:15982875]
ChEMBL Effective concentration (binding affinity) exhibited against human melanocortin receptor 4 by radio labeled ligand assay (Displacement of [125I]NDP-alpha-MSH from the human receptors expressed in CHO cells) F 4.96 pEC50 11000 nM EC50 Bioorg Med Chem Lett (2005) 15: 3501-3505 [PMID:15982875]
ChEMBL Concentration of compound at 50% maximum cAMP accumulation in human melanocortin receptor (hMC4R) F 4.96 pEC50 11000 nM EC50 Bioorg Med Chem Lett (2005) 15: 3501-3505 [PMID:15982875]
ChEMBL Concentration of compound at 50% maximum cAMP accumulation in dog melanocortin receptor (dMC4R) F 4.96 pEC50 11000 nM EC50 Bioorg Med Chem Lett (2005) 15: 3501-3505 [PMID:15982875]
ChEMBL Effective concentration (binding affinity) exhibited against human melanocortin receptor 4 by radio labeled ligand assay (Displacement of [125I]NDP-alpha-MSH from the human receptors expressed in CHO cells) F 7.96 pEC50 11 nM EC50 Bioorg Med Chem Lett (2005) 15: 3501-3505 [PMID:15982875]
MC4 receptor/Melanocortin receptor 4 in Mouse (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL3719] [GtoPdb: 285] [UniProtKB: P56450]
ChEMBL Inhibition concentration (binding affinity) against mouse melanocortin receptor 4 by displacement of [125I]NDP-alpha-MSH from the human receptors expressed in CHO cells B 5.52 pIC50 3000 nM IC50 Bioorg Med Chem Lett (2005) 15: 3501-3505 [PMID:15982875]
ChEMBL Concentration of compound at 50% maximum cAMP accumulation in mouse melanocortin receptor (mMC4R) F 5.22 pEC50 6000 nM EC50 Bioorg Med Chem Lett (2005) 15: 3501-3505 [PMID:15982875]
MC4 receptor/Melanocortin receptor 4 in Rat (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL2700] [GtoPdb: 285] [UniProtKB: P70596]
ChEMBL Inhibition concentration (binding affinity) against rat melanocortin receptor 4 by displacement of [125I]NDP-alpha-MSH from the human receptors expressed in CHO cells B 5.52 pIC50 3000 nM IC50 Bioorg Med Chem Lett (2005) 15: 3501-3505 [PMID:15982875]
ChEMBL Concentration of compound at 50% maximum cAMP accumulation in rat melanocortin receptor (rMC4R) F 5.3 pEC50 5000 nM EC50 Bioorg Med Chem Lett (2005) 15: 3501-3505 [PMID:15982875]
MC5 receptor/Melanocortin receptor 5 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL4608] [GtoPdb: 286] [UniProtKB: P33032]
ChEMBL Inhibition concentration (binding affinity) against human melanocortin receptor 5 by displacement of [125I]NDP-alpha-MSH from the human receptors expressed in CHO cells B 6.02 pIC50 945 nM IC50 Bioorg Med Chem Lett (2005) 15: 3501-3505 [PMID:15982875]
ChEMBL Effective concentration (binding affinity) exhibited against human melanocortin receptor 5 by radio labeled ligand assay (Displacement of [125I]NDP-alpha-MSH from the human receptors expressed in CHO cells) F 6.07 pEC50 850 nM EC50 Bioorg Med Chem Lett (2005) 15: 3501-3505 [PMID:15982875]

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]