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ChEMBL ligand: CHEMBL269671 |
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DB | Assay description | Assay Type | Standard value | Standard parameter | Original value | Original units | Original parameter | Reference |
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Plasmodium berghei (target type: ORGANISM) [ChEMBL: CHEMBL612653] | ||||||||
ChEMBL | Antimalarial activity against sporozoite stage of Plasmodium berghei yoelii infected in human HepG2 cells | F | 4.92 | pIC50 | 12000 | nM | IC50 | J. Med. Chem. (2016) 59: 264-281 [PMID:26640981] |
Plasmodium falciparum (target type: ORGANISM) [ChEMBL: CHEMBL364] | ||||||||
ChEMBL | Antimalarial activity against chloroquine resistant Plasmodium falciparum W2 after 72 hrs by LDH assay | F | 6.85 | pIC50 | 140 | nM | IC50 | Bioorg. Med. Chem. Lett. (2016) 26: 2084-2087 [PMID:26965857] |
ChEMBL | Antimalarial activity against chloroquine-sensitive Plasmodium falciparum D6 after 48 hrs by LDH release assay | F | 7.03 | pIC50 | 94 | nM | IC50 | Eur J Med Chem (2018) 143: 866-880 [PMID:29223887] |
ChEMBL | Antimalarial activity against chloroquine-resistant Plasmodium falciparum W2 after 48 hrs by LDH release assay | F | 7.03 | pIC50 | 94 | nM | IC50 | Eur J Med Chem (2018) 143: 866-880 [PMID:29223887] |
ChEMBL | Antiplasmodial activity against chloroquine-susceptible blood forms of Plasmodium falciparum 3D7 infected in human erythrocytes measured after 48 hrs by SYBR green1 staining based fluorescence assay | F | 7.13 | pIC50 | 74 | nM | IC50 | Bioorg Med Chem (2018) 26: 3837-3844 [PMID:29983285] |
ChEMBL | Antimalarial activity against chloroquine-sensitive Plasmodium falciparum D6 infected in red blood cells after 72 hrs by Malstat reagent based LDH assay | F | 7.35 | pIC50 | 45 | nM | IC50 | Eur J Med Chem (2017) 129: 175-185 [PMID:28222317] |
ChEMBL | Antiplasmodial activity against chloroquine-resistant Plasmodium falciparum W2 after 48 hrs by YOYO-1 dye-based flow cytometry | F | 7.49 | pIC50 | 32.1 | nM | IC50 | Eur J Med Chem (2017) 138: 993-1001 [PMID:28756265] |
ChEMBL | Antiplasmodial activity against chloroquine-sensitive Plasmodium falciparum D10 infected in human A positive erythrocyte assessed as inhibition of parasite growth after 72 hrs by parasite lactate dehydrogenase assay | F | 7.54 | pIC50 | 29 | nM | IC50 | MedChemComm (2015) 6: 357-362 |
ChEMBL | Antimalarial activity against Plasmodium falciparum K1 infected in human erythrocytes after 72 hrs by lactate dehydrogenase assay | F | 7.6 | pIC50 | 25 | nM | IC50 | J Nat Prod (2017) 80: 3120-3127 [PMID:29182338] |
ChEMBL | Antiplasmodial activity against chloroquine-sensitive Plasmodium falciparum D6 infected in human RBC assessed as decrease in parasite viability after 72 hrs by LDH assay | F | 7.6 | pIC50 | 25 | nM | IC50 | Eur J Med Chem (2017) 126: 675-686 [PMID:27936446] |
ChEMBL | Antimalarial activity against chloroquine-resistant Plasmodium falciparum W2 infected in red blood cells after 72 hrs by Malstat reagent based LDH assay | F | 7.64 | pIC50 | 23 | nM | IC50 | Eur J Med Chem (2017) 129: 175-185 [PMID:28222317] |
ChEMBL | Antimalarial activity against chloroquine-sensitive Plasmodium falciparum 3D7 infected in human type A+ erythrocytes after 24 hrs by [3H]-hypoxanthine incorporation assay | F | 7.72 | pIC50 | 19 | nM | IC50 | Eur J Med Chem (2017) 139: 22-47 [PMID:28800458] |
ChEMBL | Antimalarial activity against chloroquine-resistant Plasmodium falciparum W2 infected in human type A+ erythrocytes after 24 hrs by [3H]-hypoxanthine incorporation assay | F | 7.72 | pIC50 | 19 | nM | IC50 | Eur J Med Chem (2017) 139: 22-47 [PMID:28800458] |
ChEMBL | Antiplasmodial activity against chloroquine-resistant Plasmodium falciparum W2 infected in human erythrocytes | F | 7.79 | pIC50 | 16.3 | nM | IC50 | Bioorg Med Chem Lett (2018) 28: 265-272 |
ChEMBL | Antimalarial activity against chloroquine-resistant Plasmodium falciparum W2 infected in human erythrocytes assessed as parasite growth inhibition after 48 hrs by YOYO1 probe-based flow cytometric method | F | 7.82 | pIC50 | 15 | nM | IC50 | Bioorg Med Chem Lett (2017) 27: 1693-1697 [PMID:28318947] |
ChEMBL | Antiplasmodial activity against synchronized ring stage of chloroquine-resistant Plasmodium falciparum INDO infected in human erythrocytes after 48 hrs by SYBR Green 1 dye based fluorescence assay | F | 7.82 | pIC50 | 15 | nM | IC50 | Eur J Med Chem (2018) 155: 623-638 [PMID:29929118] |
ChEMBL | Antiplasmodial activity against synchronized ring stage of chloroquine-sensitive Plasmodium falciparum 3D7 infected in human erythrocytes after 48 hrs by SYBR Green 1 dye based fluorescence assay | F | 7.82 | pIC50 | 15 | nM | IC50 | Eur J Med Chem (2018) 155: 623-638 [PMID:29929118] |
ChEMBL | Antiplasmodial activity against chloroquine-resistant Plasmodium falciparum W2 infected in human RBC assessed as decrease in parasite viability after 72 hrs by LDH assay | F | 7.85 | pIC50 | 14 | nM | IC50 | Eur J Med Chem (2017) 126: 675-686 [PMID:27936446] |
ChEMBL | Antimalarial activity against mutidrug resistant Plasmodium falciparum TM91C235 after 48 hrs by [3H]hypoxanthine incorporation assay | F | 7.89 | pIC50 | 13 | nM | IC50 | J. Med. Chem. (2016) 59: 264-281 [PMID:26640981] |
ChEMBL | Antiplasmodial activity against synchronized ring stage of chloroquine-resistant Plasmodium falciparum Dd2 infected in human erythrocytes after 48 hrs by SYBR Green 1 dye based fluorescence assay | F | 7.89 | pIC50 | 13 | nM | IC50 | Eur J Med Chem (2018) 155: 623-638 [PMID:29929118] |
ChEMBL | Antiplasmodial activity against chloroquine-resistant ring stage Plasmodium falciparum Dd2 after 72 hrs by SYBR green 1 dye based assay | F | 7.92 | pIC50 | 12.1 | nM | IC50 | Bioorg Med Chem Lett (2018) 28: 40-42 [PMID:29162457] |
ChEMBL | Antiplasmodial activity against chloroquine-resistant Plasmodium falciparum W2 infected in human A positive erythrocyte assessed as inhibition of parasite growth after 72 hrs by parasite lactate dehydrogenase assay | F | 7.92 | pIC50 | 12 | nM | IC50 | MedChemComm (2015) 6: 357-362 |
ChEMBL | Antiplasmodial activity against ring-stage chloroquine-resistant Plasmodium falciparum Dd2 assessed as reduction in parasite viability after 72 hrs by SYBR Green I dye-based assay | F | 7.92 | pIC50 | 12 | nM | IC50 | Bioorg Med Chem Lett (2018) 28: 3368-3371 [PMID:30219526] |
ChEMBL | Growth inhibition of Plasmodium falciparum 3D7 asynchronous cultures by PicoGreen dye based assay | F | 7.98 | pIC50 | 10.4 | nM | IC50 | J Med Chem (2018) 61: 8847-8858 [PMID:30192536] |
ChEMBL | Antiplasmodial activity against asexual erythrocyte stage of chloroquine-resistant Plasmodium falciparum W2 infected in human red blood cells after 48 hrs by lactate dehydrogenase assay | F | 8 | pIC50 | 10 | nM | IC50 | J Nat Prod (2017) 80: 1750-1757 [PMID:28557449] |
ChEMBL | Antimalarial activity against chloroquine/mefloquine-resistant Plasmodium falciparum Dd2 measured after 72 hrs by SYBR green1 dye based fluorescence assay | F | 8.05 | pIC50 | 9 | nM | IC50 | J Nat Prod (2018) 81: 475-483 [PMID:29048892] |
ChEMBL | Antimalarial activity against Plasmodium falciparum Dd2 incubated for 72 hours by DAPI-staining based confocal imaging analysis | F | 8.05 | pIC50 | 9 | nM | IC50 | Bioorg. Med. Chem. Lett. (2016) 26: 3326-3329 [PMID:27212070] |
ChEMBL | Antiplasmodial activity against chloroquine/mefloquine-resistant Plasmodium falciparum Dd2 incubated for 72 hrs by SYBR green 1 dye based fluorescence assay | F | 8.05 | pIC50 | 9 | nM | IC50 | Bioorg Med Chem (2017) 25: 4203-4211 [PMID:28648491] |
ChEMBL | Antimalarial activity against Plasmodium falciparum Dd2 ring stage parasite assessed as decrease in parasite viability after 72 hrs by SYBR green 1 dye based assay | F | 8.07 | pIC50 | 8.5 | nM | IC50 | J Nat Prod (2018) 81: 1260-1265 [PMID:29738243] |
ChEMBL | Antiplasmodial activity against ring-stage of chloroquine-resistant/mefloquine-sensitive Plasmodium falciparum W2 assessed as parasite growth inhibition after 48 hrs by YOYO-1 dye-based flow cytometric method | F | 8.15 | pIC50 | 7 | nM | IC50 | Eur J Med Chem (2018) 143: 150-156 [PMID:29174811] |
ChEMBL | Antimalarial activity against chloroquine-resistant Plasmodium falciparum W2 after 48 hrs by [3H]hypoxanthine incorporation assay | F | 8.15 | pIC50 | 7 | nM | IC50 | J. Med. Chem. (2016) 59: 264-281 [PMID:26640981] |
ChEMBL | Antiplasmodial activity against Plasmodium falciparum Dd2 after 72 hrs by SYBR Green I dye-based assay | F | 8.15 | pIC50 | 7 | nM | IC50 | J Nat Prod (2017) 80: 1639-1647 [PMID:28463001] |
ChEMBL | Antiplasmodial activity against Plasmodium falciparum Dd2 incubated under low oxygen conditions after 72 hrs by SYBR green assay | F | 8.21 | pIC50 | 6.2 | nM | IC50 | Bioorg. Med. Chem. (2016) 24: 2544-2548 [PMID:27112454] |
ChEMBL | Antimalarial activity against chloroquine-resistant Plasmodium falciparum W2 infected in human erythrocytes after 48 hrs by YOYO-1 dye based flow cytometric analysis | F | 8.22 | pIC50 | 6 | nM | IC50 | J Med Chem (2017) 60: 5889-5908 [PMID:28635296] |
ChEMBL | Antiplasmodial activity against chloroquine-sensitive Plasmodium falciparum 3D7 incubated for 72 hrs by SYBR green 1 dye based fluorescence assay | F | 8.23 | pIC50 | 5.9 | nM | IC50 | Bioorg Med Chem (2017) 25: 4203-4211 [PMID:28648491] |
ChEMBL | Antimalarial activity against mid-ring stage of Plasmodium falciparum Fab9 infected in human O-positive erythrocytes after 72 hrs by SYBR Green I dye-based fluorescence assay | F | 8.28 | pIC50 | 5.2 | nM | IC50 | Bioorg Med Chem (2017) 25: 6467-6478 [PMID:29111368] |
ChEMBL | Antimalarial activity against mid-ring stage of multidrug-sensitive Plasmodium falciparum 3D7 infected in human O-positive erythrocytes after 72 hrs by SYBR Green I dye-based fluorescence assay | F | 8.39 | pIC50 | 4.1 | nM | IC50 | Bioorg Med Chem (2017) 25: 6467-6478 [PMID:29111368] |
ChEMBL | Antiplasmodial activity against Plasmodium falciparum 3D7 erythrocytic stage assessed as reduction in parasitic LDH activity measured after 48 hrs by colorimetric method | F | 8.4 | pIC50 | 4 | nM | IC50 | J Nat Prod (2017) 80: 1404-1410 [PMID:28368118] |
ChEMBL | Antiplasmodial activity against asexual erythrocyte stage of chloroquine-sensitive Plasmodium falciparum 3D7 infected in human red blood cells after 48 hrs by lactate dehydrogenase assay | F | 8.4 | pIC50 | 4 | nM | IC50 | J Nat Prod (2017) 80: 1750-1757 [PMID:28557449] |
ChEMBL | Antimalarial activity against chloroquine-resistant Plasmodium falciparum Dd2 assessed as parasite growth inhibition after 72 hrs by SYBR Green 1 assay | F | 8.4 | pIC50 | 4 | nM | IC50 | J Nat Prod (2017) 80: 96-107 [PMID:27997206] |
ChEMBL | Antimalarial activity against mid-ring stage of Plasmodium falciparum GB4 infected in human O-positive erythrocytes after 72 hrs by SYBR Green I dye-based fluorescence assay | F | 8.66 | pIC50 | 2.2 | nM | IC50 | Bioorg Med Chem (2017) 25: 6467-6478 [PMID:29111368] |
ChEMBL | Antiparasitic activity against Plasmodium falciparum W2 after 48 hrs by YOYO-1 probe-based flow cytometry | F | 7.64 | pEC50 | 23 | nM | EC50 | J Med Chem (2017) 60: 6911-6923 [PMID:28763614] |
ChEMBL | Antimalarial activity against synchronous culture of Plasmodium falciparum 3D7 ring stage parasite infected in human erythrocytes incubated for 3 hrs followed by compound wash out and measured after 24 hrs by NanoGlo-reagent based bioluminescence assay | F | 7.89 | pEC50 | 13 | nM | EC50 | J Med Chem (2017) 60: 1171-1188 [PMID:28080063] |
ChEMBL | Antiplasmodial activity against chloroquine resistant Plasmodium falciparum W2 erythrocytic ring stage after 48 hrs using hypoxanthine by flow cytometric analysis | F | 8 | pEC50 | 10 | nM | EC50 | Eur J Med Chem (2018) 149: 69-78 [PMID:29499488] |
ChEMBL | Antiplasmodium activity against Plasmodium falciparum W2 by flow cytometry | F | 8.03 | pEC50 | 9.3 | nM | EC50 | ACS Med. Chem. Lett. (2015) 6: 1145-1149 [PMID:26617969] |
ChEMBL | Antimalarial activity against Plasmodium falciparum 3D7 asexual blood stage infected in human erythrocytes incubated for 72 hrs by LDH assay | F | 8.1 | pEC50 | 8 | nM | EC50 | J Med Chem (2017) 60: 1171-1188 [PMID:28080063] |
ChEMBL | Antimalarial activity against chloroquine and mefloquine resistant Plasmodium falciparum W2mef infected in human erythrocytes incubated for 72 hrs by LDH assay | F | 8.22 | pEC50 | 6 | nM | EC50 | J Med Chem (2017) 60: 1171-1188 [PMID:28080063] |
ChEMBL | Antimalarial activity against synchronous culture of Plasmodium falciparum 3D7 ring stage parasite infected in human erythrocytes incubated for 6 hrs followed by compound wash out and measured after 24 hrs by NanoGlo-reagent based bioluminescence assay | F | 8.3 | pEC50 | 5 | nM | EC50 | J Med Chem (2017) 60: 1171-1188 [PMID:28080063] |
ChEMBL | Antimalarial activity against synchronous culture of Plasmodium falciparum 3D7 ring stage parasite infected in human erythrocytes incubated for 24 hrs followed by compound wash out and measured after 24 hrs by NanoGlo-reagent based bioluminescence assay | F | 8.7 | pEC50 | 2 | nM | EC50 | J Med Chem (2017) 60: 1171-1188 [PMID:28080063] |
Plasmodium falciparum 3D7 (target type: ORGANISM) [ChEMBL: CHEMBL2366922] | ||||||||
ChEMBL | Antimalarial activity against Plasmodium falciparum 3D7 incubated for 72 hours by DAPI-staining based confocal imaging analysis | F | 8.11 | pIC50 | 7.75 | nM | IC50 | Bioorg. Med. Chem. Lett. (2016) 26: 3326-3329 [PMID:27212070] |
Plasmodium falciparum D6 (target type: ORGANISM) [ChEMBL: CHEMBL2367107] | ||||||||
ChEMBL | Antimalarial activity against chloroquine sensitive Plasmodium falciparum D6 after 72 hrs by LDH assay | F | 7.15 | pIC50 | 71 | nM | IC50 | Bioorg. Med. Chem. Lett. (2016) 26: 2084-2087 [PMID:26965857] |
ChEMBL | Antimalarial activity against chloroquine-susceptible Plasmodium falciparum D6 after 48 hrs by [3H]hypoxanthine incorporation assay | F | 8.05 | pIC50 | 9 | nM | IC50 | J. Med. Chem. (2016) 59: 264-281 [PMID:26640981] |
Plasmodium falciparum (isolate K1 / Thailand) in Plasmodium falciparum K1 (target type: ORGANISM) [ChEMBL: CHEMBL612856] | ||||||||
ChEMBL | Antiplasmodial activity against chloroquine/pyrimethamine resistant Plasmodium falciparum K1 infected in human red blood cells after 48 hrs by [3H]hypoxanthine incorporation assay | F | 8.19 | pIC50 | 6.4 | nM | IC50 | Bioorg. Med. Chem. (2016) 24: 3781-3789 [PMID:27344215] |
ChEMBL | Antiplasmodial activity against erythrocytic stage of chloroquine/pyrimethamine-resistant Plasmodium falciparum K1 assessed as reduction in [3H]hypoxanthine incorporation after 48 hrs by liquid scintillation counting method | F | 8.19 | pIC50 | 6.4 | nM | IC50 | Bioorg Med Chem (2017) 25: 2251-2259 [PMID:28279559] |
ChEMBL data shown on this page come from version 27:
Gaulton A, Hersey A, Nowotka M, Bento AP, Chambers J, Mendez D, Mutowo P, Atkinson F, Bellis LJ, CibriƔn-Uhalte E, Davies M, Dedman N, Karlsson A, MagariƱos MP, Overington JP, Papadatos G, Smit I, Leach AR. (2017) 'The ChEMBL database in 2017.' Nucleic Acids Res., 45(D1). DOI: 10.1093/nar/gkw1074. [PMCID:5210557]