AMPK-IN-3 structure
|
Common Name | AMPK-IN-3 | ||
---|---|---|---|---|
CAS Number | 2417674-27-0 | Molecular Weight | 451.56 | |
Density | N/A | Boiling Point | N/A | |
Molecular Formula | C25H33N5O3 | Melting Point | N/A | |
MSDS | N/A | Flash Point | N/A |
Use of AMPK-IN-3AMPK-IN-3 (compound 67) is a potent and selective AMPK inhibitor with IC50s of 60.7, 107 and 3820 nM for AMPK (α2), AMPK (α1) and KDR, respectively. AMPK-IN-3 inhibits AMPK does not affect cell viability or cause significant cytotoxicity in K562 cells. AMPK-IN-3 can be used in study of cancer[1]. |
Name | AMPK-IN-3 |
---|
Description | AMPK-IN-3 (compound 67) is a potent and selective AMPK inhibitor with IC50s of 60.7, 107 and 3820 nM for AMPK (α2), AMPK (α1) and KDR, respectively. AMPK-IN-3 inhibits AMPK does not affect cell viability or cause significant cytotoxicity in K562 cells. AMPK-IN-3 can be used in study of cancer[1]. |
---|---|
Related Catalog | |
Target |
AMPK (α2):60.7 nM (IC50) AMPK (α1):107 nM (IC50) KDR:3820 nM (IC50) |
In Vitro | AMPK-IN-3 (100 nM) shows inhibition values for AMPK(α2), FLT1, JAK1 JH2-pseudokinase and AMPK(α1) for 64%, 43%, 41% and 29%, respectively[1]. AMPK-IN-3 (0.195313, 0.78125, 3.125, 12.5, 50 µM; 2 h) decreases the level of p-ACC in K562 cells[1]. AMPK-IN-3 (1-100 µM; 24, 48, 72 h) shows potent inhibition of cellular AMPK activity but not affect cell viability[1]. Cell Viability Assay[1] Cell Line: K562 cells Concentration: 0.195313, 0.78125, 3.125, 12.5, 50 µM Incubation Time: 2 h Result: Decreased cellular levels of p-ACC(Ser79) in K562 cells. Cell Viability Assay[1] Cell Line: K562 cells Concentration: 1-100 µM Incubation Time: 24, 48, 72 h Result: Showed no measurable impact on cell viability in K562 cells cultured under hypoxic conditions for 72 hours. |
References |
Molecular Formula | C25H33N5O3 |
---|---|
Molecular Weight | 451.56 |