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ChEMBL ligand: CHEMBL274990 (SC-58125) |
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DB | Assay description | Assay Type | Standard value | Standard parameter | Original value | Original units | Original parameter | Reference |
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COX-1 /Cyclooxygenase-1 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL221] [GtoPdb: 1375] [UniProtKB: P23219] | ||||||||
ChEMBL | Inhibition of human Prostaglandin G/H synthase 1 at 10 ug/mL expressed as the mean percent inhibition of control PGE-2 production | B | 4 | pIC50 | >100000 | nM | IC50 | J Med Chem (1997) 40: 980-989 [PMID:9083488] |
ChEMBL | In vitro inhibition of prostaglandin G/H synthase 1. | B | 4 | pIC50 | >100000 | nM | IC50 | J Med Chem (1995) 38: 4570-4578 [PMID:7473585] |
ChEMBL | Tested for inhibition against Prostaglandin G/H synthase 1 | B | 4 | pIC50 | >100000 | nM | IC50 | J Med Chem (1994) 37: 3878-3881 [PMID:7966148] |
ChEMBL | In vitro inhibitory concentration against recombinant human COX-1 (Cyclooxygenase-1) | B | 4 | pIC50 | >100000 | nM | IC50 | Bioorg Med Chem Lett (1997) 7: 2121-2124 |
ChEMBL | Inhibitory activity against human recombinant Prostaglandin G/H synthase 1 expressed in microsomes taken from baculovirus infected Sf9 cells | B | 4.3 | pIC50 | >50000 | nM | IC50 | Bioorg Med Chem Lett (1996) 6: 87-92 |
ChEMBL | Inhibition of human COX1 expressed in african green monkey COS cells assessed as inhibition of arachidonic acid-stimulated PGE2 production by enzyme immunoassay | B | 4.49 | pIC50 | 32000 | nM | IC50 | Bioorg Med Chem Lett (2009) 19: 4509-4514 [PMID:19523822] |
ChEMBL | IC50 value against Prostaglandin G/H synthase 1 of human platelet rich plasma | B | 4.7 | pIC50 | >20000 | nM | IC50 | J Med Chem (1999) 42: 1161-1169 [PMID:10197960] |
ChEMBL | IC50 against Prostaglandin G/H synthase 1 from human platelet rich plasma | B | 4.7 | pIC50 | >20000 | nM | IC50 | J Med Chem (1999) 42: 1151-1160 [PMID:10197959] |
Cyclooxygenase-1 in Sheep (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL2949] [UniProtKB: P05979] | ||||||||
ChEMBL | IC50 value against ovine Prostaglandin G/H synthase 1 | B | 4.7 | pIC50 | >20000 | nM | IC50 | J Med Chem (1999) 42: 1161-1169 [PMID:10197960] |
COX-2 /Cyclooxygenase-2 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL230] [GtoPdb: 1376] [UniProtKB: P35354] | ||||||||
ChEMBL | Inhibition of COX-2 (unknown origin) | B | 5.96 | pIC50 | 1100 | nM | IC50 | Bioorg Med Chem Lett (2016) 26: 1516-1520 [PMID:26898334] |
ChEMBL | IC50 against recombinant human Prostaglandin G/H synthase 2 | B | 6.51 | pIC50 | 310 | nM | IC50 | J Med Chem (1999) 42: 1151-1160 [PMID:10197959] |
ChEMBL | Inhibition of recombinant human prostaglandin G/H synthase 2 (COX-2) | B | 6.51 | pIC50 | 310 | nM | IC50 | J Med Chem (1999) 42: 1161-1169 [PMID:10197960] |
ChEMBL | Inhibitory activity against human recombinant Prostaglandin G/H synthase 2 expressed in microsomes taken from baculovirus infected Sf9 cells | B | 6.7 | pIC50 | 200 | nM | IC50 | Bioorg Med Chem Lett (1996) 6: 87-92 |
ChEMBL | Inhibition of human cyclooxygenase-2 (hCOX-2) enzyme. | B | 7 | pIC50 | 100 | nM | IC50 | Bioorg Med Chem Lett (1999) 9: 1167-1170 [PMID:10328306] |
ChEMBL | Inhibition of human Prostaglandin G/H synthase 2 | B | 7 | pIC50 | 100 | nM | IC50 | J Med Chem (2001) 44: 3223-3230 [PMID:11563921] |
ChEMBL | In vitro inhibitory concentration against human Prostaglandin G/H synthase 2 | B | 7 | pIC50 | 100 | nM | IC50 | Bioorg Med Chem Lett (1997) 7: 2121-2124 |
ChEMBL | In vitro inhibitory concentration required to block human recombinant prostaglandin G/H synthase 2 (COX-2) | B | 7 | pIC50 | 100 | nM | IC50 | J Med Chem (1997) 40: 1347-1365 [PMID:9135032] |
ChEMBL | Tested for inhibition against Prostaglandin G/H synthase 2 | B | 7.05 | pIC50 | 90 | nM | IC50 | J Med Chem (1994) 37: 3878-3881 [PMID:7966148] |
ChEMBL | Inhibition of human Prostaglandin G/H synthase 2 at 10 ug/mL expressed as the mean percent inhibition of control PGE-2 production | B | 7.05 | pIC50 | 90 | nM | IC50 | J Med Chem (1997) 40: 980-989 [PMID:9083488] |
ChEMBL | Inhibition of human COX2 expressed in african green monkey COS cells assessed as inhibition of arachidonic acid-stimulated PGE2 production by enzyme immunoassay | B | 7.18 | pIC50 | 66 | nM | IC50 | Bioorg Med Chem Lett (2009) 19: 4509-4514 [PMID:19523822] |
ChEMBL | In vitro inhibition of prostaglandin G/H synthase 2 (COX-2). | B | 7.3 | pIC50 | 50 | nM | IC50 | J Med Chem (1995) 38: 4570-4578 [PMID:7473585] |
GtoPdb | - | - | 7.39 | pIC50 | - | - | - | J Biol Chem (1996) 271: 15810-4 [PMID:8663121] |
COX-2 /Cyclooxygenase-2 in Mouse (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL4321] [GtoPdb: 1376] [UniProtKB: Q05769] | ||||||||
ChEMBL | IC50 value was determined against Prostaglandin G/H synthase 2 of J7744A.1 cell lines. | B | 7.15 | pIC50 | 70 | nM | IC50 | J Med Chem (1999) 42: 1151-1160 [PMID:10197959] |
ChEMBL | IC50 value against Prostaglandin G/H synthase 2 of murine J774A.1 cell line | B | 7.15 | pIC50 | 70 | nM | IC50 | J Med Chem (1999) 42: 1161-1169 [PMID:10197960] |
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]