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ChEMBL ligand: CHEMBL1539 (Fanasil, Fanasulf, J21.373J, NSC-759319, RO 4-4393, RO-4-4393, RO-44393, Sulfadoxin, Sulfadoxine, Sulfadoxinum, Sulforthamidine, Sulphadoxine, Sulphormethoxine, WR-4073) |
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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 falciparum (target type: ORGANISM) [ChEMBL: CHEMBL364] | ||||||||
ChEMBL | Antimicrobial activity against Plasmodium falciparum | F | 4.43 | pIC50 | 37000 | nM | IC50 | Bioorg Med Chem (2010) 18: 2225-2231 [PMID:20185316] |
ChEMBL | Antiplasmodial activity against chloroquine and sulfadoxine-resistant and mefloquine-sensitive Plasmodium falciparum W2 infected in human erythrocytes by anti-HRP2 assay | F | 4.81 | pIC50 | >15500 | nM | IC50 | Bioorg Med Chem (2015) 23: 5979-5984 [PMID:26190461] |
ChEMBL | Antimalarial activity against chloroquine/sulfadoxine-resistant Plasmodium falciparum W2 infected in human A+ erythrocytes assessed as reduction in parasite growth after 72 hrs by HRP2 detection based ELISA | F | 4.82 | pIC50 | 15000 | nM | IC50 | Bioorg Med Chem (2016) 24: 4492-4498 [PMID:27485600] |
ChEMBL | Antimalarial activity against chloroquine-sensitive Plasmodium falciparum W2 by [3H]hypoxanthine uptake | F | 5.21 | pIC50 | 6100 | nM | IC50 | J Med Chem (2009) 52: 952-963 [PMID:19191586] |
ChEMBL | Antimalarial activity against chloroquine-resistant Plasmodium falciparum D6 by [3H]hypoxanthine uptake | F | 7.4 | pIC50 | 40 | nM | IC50 | J Med Chem (2009) 52: 952-963 [PMID:19191586] |
ChEMBL | Antimalarial activity Plasmodium falciparum 3D7 | F | 7.52 | pEC50 | 30 | nM | EC50 | Bioorg Med Chem Lett (2010) 20: 4027-4031 [PMID:20610151] |
Plasmodium falciparum hydroxymethyldihydropterin pyrophosphokinase-dihydropteroate synthase in Plasmodium falciparum K1 [GtoPdb: 3065] | ||||||||
GtoPdb | Parasite growth inhibition assay | - | 6.65 | pIC50 | 223 | nM | IC50 | Mol Microbiol (1997) 23: 979-86 [PMID:9076734] |
Plasmodium falciparum hydroxymethyldihydropterin pyrophosphokinase-dihydropteroate synthase in Plasmodium falciparum 3D7 [GtoPdb: 3065] [UniProtKB: Q8IAU3] | ||||||||
GtoPdb | Parasite growth inhibition assay | - | 7.14 | pIC50 | 73 | nM | IC50 | Mol Microbiol (1997) 23: 979-86 [PMID:9076734] |
Plasmodium falciparum hydroxymethyldihydropterin pyrophosphokinase-dihydropteroate synthase in Plasmodium falciparum Dd2 [GtoPdb: 3065] | ||||||||
GtoPdb | Parasite growth inhibition assay | - | 5.4 | pIC50 | 3970 | nM | IC50 | Mol Microbiol (1997) 23: 979-86 [PMID:9076734] |
Plasmodium falciparum hydroxymethyldihydropterin pyrophosphokinase-dihydropteroate synthase in Plasmodium falciparum HB3 [GtoPdb: 3065] | ||||||||
GtoPdb | Parasite growth inhibition assay | - | 8.4 | pIC50 | 4 | nM | IC50 | Mol Microbiol (1997) 23: 979-86 [PMID:9076734] |
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]