Inhibitor
Cat.No. | Name | Information |
---|---|---|
M58476 | SGK1-IN-4 | SGK1-IN-4 is a highly selective, orally active SGK1 inhibitor. SGK1-IN-4 can be used for the research of osteoarthritis. |
M11404 | EMD638683 | EMD638683 is a highly selective SGK1 inhibitor with an IC50 value of 3 μM. |
M5325 | GSK 650394 | GSK650394 is a serum- and glucocorticoid-regulated kinase-1 inhibitor with IC50 of 62 nM and 103 nM for SGK1 and SGK2, respectively. |
M56791 | SGK1-IN-3 | SGK1-IN-3 is a potent and orally active inhibitor of SGK1. |
M29542 | HaloPROTAC-E | HaloPROTAC-E is a novel HaloPROTAC potent degrader, inducing reversible degradation of two endosomally localized proteins, SGK3 and VPS34, with a DC50 of 3-10 nM, remarkably selective inducing only degradation of the Halo tagged endogenous VPS34 complex (VPS34, VPS15, Beclin1, and ATG14). |
M28400 | SGK1-IN-2 | SGK1-IN-2 (14h) is a selective SGK1 (serum and glucocorticoid regulated kinase 1) inhibitor, with an IC50 of 5 nM at 10 μM ATP concentration. |
M28315 | SI-113 | SI-113 is a SGK1 inhibitor, with an IC50 of 600 nM. SI113 induces autophagy. |
M14535 | EMD638683 R-Form | EMD638683 R-Form is the R-form of EMD638683. EMD638683 is a highly selective SGK1 inhibitor with IC50 of 3 μM. |
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