Co-Target(s) Information
Target General Information | Top | ||||
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Target ID | T34949 | Target Info | |||
Target Name | Voltage-gated calcium channel alpha Cav2.1 (CACNA1A) | ||||
Synonyms |
Voltage-gated calcium channel alpha subunit Cav2.1; Voltage-dependent P/Q-type calcium channel; RBA-I; RAT brain class A; Calcium channel, L type, alpha-1 polypeptide, isoform 4; Calcium channel, L type, alpha-1 polypeptide isoform 4; CACNA1A; Brain calcium channel I; BI
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Target Type | Successful Target | ||||
Gene Name | CACNA1A | ||||
Biochemical Class | Voltage-gated ion channel | ||||
UniProt ID |
Co-Targets of This Target | Top | |||||
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Co-Target Name | Cytochrome P450 2J2 (CYP2J2) | Co-Target | ||||
UniProt ID | CP2J2_HUMAN | |||||
Gene Name | CYP2J2 | |||||
Synonyms |
Albendazole monooxygenase (hydroxylating); Albendazole monooxygenase (sulfoxide-forming); Arachidonic acid epoxygenase; Hydroperoxy icosatetraenoate isomerase; CYPIIJ2
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Representative Drug(s) | Flunarizine | Drug Info | Ki = 100 nM | [1] | ||
Co-Target Name | Brain sodium channel alpha (Types I, II, III) | Co-Target | ||||
UniProt ID | SCN1A_HUMAN; SCN2A_HUMAN; SCN3A_HUMAN | |||||
Gene Name | SCN1A; SCN2A; SCN3A | |||||
Representative Drug(s) | Flunarizine | Drug Info | IC50 = 600 nM | [2] |
References | Top | ||||
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REF 1 | Discovery and characterization of novel, potent, and selective cytochrome P450 2J2 inhibitors. Drug Metab Dispos. 2013 Jan;41(1):60-71. | ||||
REF 2 | [3H]Batrachotoxinin A 20 alpha-benzoate binding to voltage-sensitive sodium channels: a rapid and quantitative assay for local anesthetic activity in a variety of drugs. J Med Chem. 1985 Mar;28(3):381-8. |
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