ZINC12409120 structure
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Common Name | ZINC12409120 | ||
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CAS Number | 1010888-06-8 | Molecular Weight | 344.37 | |
Density | N/A | Boiling Point | N/A | |
Molecular Formula | C20H16N4O2 | Melting Point | N/A | |
MSDS | N/A | Flash Point | N/A |
Use of ZINC12409120ZINC12409120 is a high selective ERK inhibitor. ZINC12409120 acts on disrupting FGF23:α-Klotho interaction to inhibit ERK activity with an IC50 of 5.0 μM[1]. |
Name | ZINC12409120 |
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Description | ZINC12409120 is a high selective ERK inhibitor. ZINC12409120 acts on disrupting FGF23:α-Klotho interaction to inhibit ERK activity with an IC50 of 5.0 μM[1]. |
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Related Catalog | |
Target |
ERK:5 μM (IC50) |
In Vitro | FGF23 induces hypophosphatemia, mediated by ternary complex formed by FGF23, the FGF receptor (FGFR), and α-Klotho[1]. ZINC12409120 (1 nM-0.1 mM; 5 h) inhibits ERK reporter activities mediated by FGF23 (1 μM), with an IC50 of 5 μM[1]. ZINC12409120 (10 μM; 5 h) specificaly inhibits ERK activity mediated by FGF23:α-Klotho instead of EGF-mediated ERK activation, and exhibits no inhibitory effect on EGFR tyrosine kinase or EGF/EGFR interaction[1]. ZINC12409120 has an half-life of 8.4 h, predicted by pkCSM64 (http://biosig.unimelb.edu.au/pkcsm/)[1]. Cell Proliferation Assay[1] Cell Line: Human embryonic kidney (HEK) 293T cells Concentration: 1 nM-0.1 mM Incubation Time: 5 hours Result: Inhibited FGF23-mediated ERK reporter activity in a dose-dependent manner, with an IC50 of 5 μM. And reduced FGF23-mediated ERK activities by 70%, as well. |
References |
Molecular Formula | C20H16N4O2 |
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Molecular Weight | 344.37 |