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 About 13 results found for searched term "SGK" (0.114 seconds)

Cat.No.  Name Target
M10382 PROTAC SGK3 degrader-1 PROTAC
SGK3-PROTAC1
PROTAC SGK3 degrader-1 (SGK3-PROTAC1) is a potent SGK3 degrader, it is a PROTAC conjugate of the 308-R SGK inhibitor with the VH032 VHL binding ligand, targeting SGK3.
M28400 SGK1-IN-2  SGK
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.
M50485 SGKtide Others
SGKtide is used as an SGK(Serum and glucocorticoid-inducible kinase) substrate.
M56791 SGK1-IN-3  SGK
SGK1-IN-3 is a potent and orally active inhibitor of SGK1.
M4708 Herbacetin Others
Herbacetin is a natural flavonoid found in flaxseed and has a variety of pharmacological activities, including antioxidant, anti-inflammatory and anticancer effects. Herbacetin is an Ornithine decarboxylase (ODC) allosteric inhibitor that binds directly to Asp44, Asp243 and Glu384 on ODC. It is also an SGK1 inhibitor.
M5325 GSK 650394 SGK
GSK650394 is a serum- and glucocorticoid-regulated kinase-1 inhibitor with IC50 of 62 nM and 103 nM for SGK1 and SGK2, respectively.
M5533 Corticosterone GCR
17-Deoxycortisol; 11β,21-Dihydroxyprogesterone; Kendall's compound B
Corticosterone (17-Deoxycortisol) is an orally active and adrenal cortex-produced glucocorticoid, which plays an important role in regulating neuronal functions of the limbic system. Corticosterone increases the Rab-mediated AMPAR membrane traffic via SGK-induced phosphorylation of GDI.
M7683 CKI-7 dihydrochloride Casein Kinase
CKI-7 is a CK1 inhibitor; also inhibits SGK, S6K1 and MSK1.
M11404 EMD638683 SGK
EMD638683 is a highly selective SGK1 inhibitor with an IC50 value of 3 μM.
M14535 EMD638683 R-Form SGK
EMD638683 R-Form is the R-form of EMD638683. EMD638683 is a highly selective SGK1 inhibitor with IC50 of 3 μM.
M28315 SI-113  SGK
SI-113 is a SGK1 inhibitor, with an IC50 of 600 nM. SI113 induces autophagy.
M29542 HaloPROTAC-E  SGK
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).
M45282 CKI-7 free base Casein Kinase
CKI-7 free base is a potent and ATP-competitive casein kinase 1 (CK1) inhibitor with an IC50 of 6 μM and a Ki of 8.5 μM. In addition, CKI-7 free base selectively inhibits Cdc7 kinase, SGK, S6K1 and MSK1.



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