Co-Target(s) Information
Target General Information | Top | ||||
---|---|---|---|---|---|
Target ID | T76937 | Target Info | |||
Target Name | Voltage-gated sodium channel alpha Nav1.3 (SCN3A) | ||||
Synonyms |
Voltage-gated sodium channel subunit alpha Nav1.3; Voltage-gated sodium channel subtype III; Sodium channel protein, brain III subunit alpha; Sodium channel protein type III subunit alpha; Sodium channel protein type 3 subunit alpha; Sodium channel protein brain III subunit alpha; NAC3; KIAA1356
Click to Show/Hide
|
||||
Target Type | Successful Target | ||||
Gene Name | SCN3A | ||||
Biochemical Class | Voltage-gated ion channel | ||||
UniProt ID |
Co-Targets of This Target | Top | |||||
---|---|---|---|---|---|---|
Co-Target Name | Voltage-gated potassium channel Kv11.1 (KCNH2) | Successful Target | ||||
UniProt ID | KCNH2_HUMAN | |||||
Gene Name | KCNH2 | |||||
Synonyms |
hERG1; hERG-1; Voltage-gated potassium channel subunit Kv11.1; Potassium voltage-gated channel subfamily H member 2; HERG K+ channel; HERG; H-ERG; Ether-a-go-go-related protein 1; Ether-a-go-go-related gene potassium channel 1; Ether-a-go-go related protein 1; Ether-a-go-go related gene potassium channel 1; Eag related protein 1; Eag homolog; ERG-1; ERG
Click to Show/Hide
|
|||||
Representative Drug(s) | LIDOFLAZINE | Drug Info | IC50 = 15.85 nM | [1] | ||
Co-Target Name | Solute carrier family 29 member 1 (SLC29A1) | Successful Target | ||||
UniProt ID | S29A1_HUMAN | |||||
Gene Name | SLC29A1 | |||||
Synonyms |
SLC29A1; Nucleoside transporter, es-type; Nucleoside transporter 1; Equilibrative nitrobenzylmercaptopurine riboside-sensitive nucleoside transporter; Equilibrative NBMPR-sensitive nucleoside transporter; ENT1
Click to Show/Hide
|
|||||
Representative Drug(s) | LIDOFLAZINE | Drug Info | Ki = 279.9 nM | [2] |
References | Top | ||||
---|---|---|---|---|---|
REF 1 | A discriminant model constructed by the support vector machine method for HERG potassium channel inhibitors. Bioorg Med Chem Lett. 2005 Jun 2;15(11):2886-90. | ||||
REF 2 | Synthesis, flow cytometric evaluation, and identification of highly potent dipyridamole analogues as equilibrative nucleoside transporter 1 inhibit... J Med Chem. 2007 Aug 9;50(16):3906-20. |
If You Find Any Error in Data or Bug in Web Service, Please Kindly Report It to Dr. Zhou and Dr. Zhang.