SGC-CK2-1
Modify Date: 2024-01-05 17:03:41
SGC-CK2-1 structure
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Common Name | SGC-CK2-1 | ||
|---|---|---|---|---|
| CAS Number | 2470424-39-4 | Molecular Weight | 375.43 | |
| Density | N/A | Boiling Point | N/A | |
| Molecular Formula | C20H21N7O | Melting Point | N/A | |
| MSDS | N/A | Flash Point | N/A | |
Use of SGC-CK2-1SGC-CK2-1 is a highly potent, ATP-competitive, and cell-active CK2 chemical probe with exclusive selectivity for both human CK2 isoforms, with IC50s of 36 and 16 nM for CK2α and CK2α′respectively in the nanoBRET assay. SGC-CK2-1 can be used for the research of neurodegenerative diseases[1][2]. |
| Name | SGC-CK2-1 |
|---|
| Description | SGC-CK2-1 is a highly potent, ATP-competitive, and cell-active CK2 chemical probe with exclusive selectivity for both human CK2 isoforms, with IC50s of 36 and 16 nM for CK2α and CK2α′respectively in the nanoBRET assay. SGC-CK2-1 can be used for the research of neurodegenerative diseases[1][2]. |
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| Related Catalog | |
| Target |
CK2α:36 nM (IC50) CK2α':16 nM (IC50) |
| In Vitro | SGC-CK2-1 inhibits CSNK2A2 and CSNK2A1 with IC50s value of 2.3 and 4.2 nM[1]. SGC-CK2-1 inhibits DYRK2 with the IC50 value of 3.7 μM[1]. SGC-CK2-1 inhibits blood U-937, MV4-11, MOLM-13, OCI-LY19, OCI-AML5 cells with IC50s of 120, 690, 750, 760 and 810 nM, respectively. SGC-CK2-1 inhibits Head/Neck Detroit562 cells with an IC50 of 550 nM. SGC-CK2-1 inhibits Lung NCI-H2286 cells with an IC50 of 550 nM. SGC-CK2-1 inhibits Brain SK-N-MC cells with an IC50 of 730 nM. SGC-CK2-1 inhibits Breast BT-20 cells with an IC50 of 810 nM. SGC-CK2-1 inhibits Skin A375 cells with an IC50 of 830 nM. SGC-CK2-1 inhibits Stomach SNU-1 cells with an IC50 of 860 nM. SGC-CK2-1 inhibits Duodenum Hutu 80 cells with an IC50 of 920 nM[1]. |
| References |
| Molecular Formula | C20H21N7O |
|---|---|
| Molecular Weight | 375.43 |