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10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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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.
ASN007 (ERK-IN-3) is a potent and orally active inhibitor of ERK . ASN007 inhibits ERK1/2 with low single-digit nM IC 50 values. ASN007 can be used for the research of cancers driven by RAS mutations
In Vitro
ASN007 (ERK-IN-3) inhibits the phosphorylation of ERK1/2 substrates such as RSK1, FRA1, and Elk1 in various cell lines. ASN007 showes single-digit nanomolar antiproliferative activity that is selective for MAPK-pathway dependent cancer cell lines. MCE has not independently confirmed the accuracy of these methods. They are for reference only.
In Vivo
ASN007 (ERK-IN-3) (daily p.o.) inhibits tumor growth in multiple BRAF and KRAS mutant xenograft models in mice and was well tolerated at efficacious doses . MCE has not independently confirmed the accuracy of these methods. They are for reference only.
IC50& Target:ERK1 ERK2
| ALogP | 2.3 |
|---|
| 異性体SMILES | CC1=CN=C(N=C1N2C=C(N=C2)C(=O)N[C@H](CN)C3=CC(=CC(=C3)Cl)F)NC4CCOCC4 |
|---|---|
| PubChem CID | 124122366 |
| MeSH用語 | ASN007;ERK-IN-3;N-((1S)-2-amino-1-(3-chloro-5-fluorophenyl)ethyl)-1-(5-methyl-2-(oxan-4-ylamino)pyrimidin-4-yl)imidazole-4-carboxamide |
| 分子量 | 473.93 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
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