10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
GW779439X is a pyrazolopyridazine identified in an inhibitor of the S. aureus PASTA kinase Stk1 . GW779439X potentiates the activity of β-lactam antibiotics against various MRSA and MSSA isolates, some even crossing the breakpoint from resistant to sensitive. GW779439X is an AURKA inhibitor and induces apoptosis by the caspases 3/7 pathway MRSA:methicillin-resistant S. aureus ; MSSA: methicillin-sensitive S. aureus
In Vitro
GW779439X (2 μM) biochemically inhibits Stk1. GW779439X (5 μM) potentiates ceftaroline activity against a ceftaroline-resistant MRSA strain. GW779439X is able to potentiate the activity of oxacillin against various S. aureus isolates, including both MRSA and MSSA isolates, but the potentiation is clearly strongest in PBP2A-containing strains. GW779439X has growth inhibition effects on the AGP-01 cell line (IC 50 = 0.57 μM). GW779439X (1μM) significantly blockS the cell cycle at the G0/G1 phase and sub-G1 phase. GW779439X (1μM; 72 hours; AGP-01 cells) significantly decreases expression levels of genes involved in proliferation progression ( c-MYC , NRAS , and CDC25A ) and increases expression levels of genes involved in cell cycle blocking ( CDKN1A and TP53 ) [2 . MCE has not independently confirmed the accuracy of these methods. They are for reference only.
IC50& Target:Aurora A|Stk1|apoptosis
| Isomeric SMILES | CN1CCN(CC1)C2=C(C=C(C=C2)NC3=NC=CC(=N3)C4=C5C=CC=NN5N=C4)C(F)(F)F |
|---|---|
| PubChem CID | 10173796 |
| Molecular Weight | 454.46 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
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