Co-Target(s) Information
Target General Information | Top | ||||
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Target ID | T87023 | Target Info | |||
Target Name | Platelet-activating factor receptor (PTAFR) | ||||
Synonyms |
PTAFR; PAF-R
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Target Type | Successful Target | ||||
Gene Name | PTAFR | ||||
Biochemical Class | GPCR rhodopsin | ||||
UniProt ID |
Co-Targets of This Target | Top | |||||
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Co-Target Name | Histamine H1 receptor (H1R) | Successful Target | ||||
UniProt ID | HRH1_HUMAN | |||||
Gene Name | HRH1 | |||||
Synonyms |
HH1R; H1R
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Representative Drug(s) | RUPATADINE | Drug Info | IC50 = 3.9 nM | Click to Show More | [1] | |
2 | PegCNTF | Drug Info | IC50 = 100 nM | [1] | ||
Co-Target Name | Cytochrome P450 2B6 (CYP2B6) | Literature-reported Target | ||||
UniProt ID | CP2B6_HUMAN | |||||
Gene Name | CYP2B6 | |||||
Synonyms |
Cytochrome P450 IIB1; CYPIIB6; 1,4-cineole 2-exo-monooxygenase
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Representative Drug(s) | Ticlopidine | Drug Info | Ki = 200 nM | [2] |
References | Top | ||||
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REF 1 | Designed multiple ligands. An emerging drug discovery paradigm. J Med Chem. 2005 Oct 20;48(21):6523-43. | ||||
REF 2 | Cytochrome p450 enzymes mechanism based inhibitors: common sub-structures and reactivity. Curr Drug Metab. 2005 Oct;6(5):413-54. |
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