Co-Target(s) Information
Target General Information | Top | ||||
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Target ID | T01318 | Target Info | |||
Target Name | Plasmodium Dihydroorotate dehydrogenase (Malaria DHOdehase) | ||||
Synonyms |
PFF0160c; Mitochondrially bound dihydroorotate-ubiqui oxidoreductase; Dihydroorotate oxidase of Plasmodium falciparum; Dihydroorotate dehydrogenase of Plasmodium falciparum; DHOdehase of Plasmodium falciparum; DHODase; DHODH of Plasmodium falciparum; DHOD
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Target Type | Successful Target | ||||
Gene Name | Malaria DHOdehase | ||||
Biochemical Class | CH-CH donor oxidoreductase | ||||
UniProt ID |
Co-Targets of This Target | Top | |||||
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Co-Target Name | Indoleamine 2,3-dioxygenase 1 (IDO1) | Successful Target | ||||
UniProt ID | I23O1_HUMAN | |||||
Gene Name | IDO1 | |||||
Synonyms |
Indoleamine-pyrrole 2,3-dioxygenase; INDO; IDO-1; IDO
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Representative Drug(s) | Avastin+/-Tarceva | Drug Info | IC50 = 1000 nM | [1] | ||
Co-Target Name | Cytochrome P450 1A2 (CYP1A2) | Co-Target | ||||
UniProt ID | CP1A2_HUMAN | |||||
Gene Name | CYP1A2 | |||||
Synonyms |
Cholesterol 25-hydroxylase; Hydroperoxy icosatetraenoate dehydratase; CYPIA2; Cytochrome P(3)450; Cytochrome P450 4; Cytochrome P450-P3
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Representative Drug(s) | Leflunomide | Drug Info | IC50 = 500 nM | [2] |
References | Top | ||||
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REF 1 | Indoleamine 2,3-dioxygenase is the anticancer target for a novel series of potent naphthoquinone-based inhibitors. J Med Chem. 2008 Mar 27;51(6):1706-18. | ||||
REF 2 | DrugMatrix in vitro pharmacology data. National Toxicology Program |
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