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Formula | C21H18ClFN6O2 |
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Molecular Weight | 439.85 | CAS No. | 1453848-26-4 | |
Solubility (25°C)* | In vitro | DMSO | 87 mg/mL (197.79 mM) | |
Ethanol | 87 mg/mL (197.79 mM) | |||
Water | Insoluble | |||
* <1 mg/ml means slightly soluble or insoluble. * Please note that Selleck tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations. * Room temperature shipping (Stability testing shows this product can be shipped without any cooling measures.) |
Description | Ravoxertinib (GDC-0994) is a potent, orally available and highly selective ERK1/2 inhibitor with IC50 of 1.1 nM and 0.3 nM, respectively. Phase 1. | ||||
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Targets |
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In vitro | GDC-0994 potently inhibits phospho-p90RSK in tumor cells. [1] |
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In vivo | GDC-0994 (p.o.) results in significant single-agent activity in multiple in vivo cancer models, including KRAS-mutant and BRAF-mutant human xenograft tumors in mice. [1] In vivo, GDC-0994 (p.o.) inhibits both ERK phosphorylation and activation of ERK-mediated signal transduction pathways, and subsequently prevents ERK-dependent tumor cell proliferation and survival. [2] |
Animal Study: |
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Data from [Data independently produced by , , Blood, 2018, 131(18):2047-2059]
Data from [Data independently produced by , , Biochim Biophys Acta, 2015, 1852(12):2671-7]
Data from [Data independently produced by , , Biochem Biophys Res Commun, 2017, 486(4):1062-1068]
Data from [Data independently produced by , , Cell Immunol, 2017, 314:63-72]
Tumour-selective activity of RAS-GTP inhibition in pancreatic cancer [ Nature, 2024, 629(8013):927-936] | PubMed: 38588697 |
Targeting ERK-MYD88 interaction leads to ERK dysregulation and immunogenic cancer cell death [ Nat Commun, 2024, 15(1):7037] | PubMed: 39147750 |
Myeloid cells coordinately induce glioma cell-intrinsic and cell-extrinsic pathways for chemoresistance via GP130 signaling [ Cell Rep Med, 2024, S2666-3791(24)00372-0] | PubMed: 39053460 |
Conformation selection by ATP-competitive inhibitors and allosteric communication in ERK2 [ Elife, 2024, 12RP91507] | PubMed: 38537148 |
The ERK inhibitor GDC-0994 selectively inhibits growth of BRAF mutant cancer cells [ Transl Oncol, 2024, 45:101991] | PubMed: 38728872 |
HER3 V104 mutations regulate cell signaling, growth, and drug sensitivity in cancer [ Mol Carcinog, 2024, 10.1002/mc.23743] | PubMed: 38751013 |
DUSP22 Ameliorates Endothelial-to-Mesenchymal Transition in HUVECs through Smad2/3 and MAPK Signaling Pathways [ Cardiovasc Ther, 2024, 2024:5583961] | PubMed: 38495810 |
Transcriptional and chromatin profiling of human blood innate lymphoid cell subsets sheds light on HIV-1 pathogenesis [ EMBO J, 2023, e114153.] | PubMed: 37382276 |
Tetrandrine synergizes with MAPK inhibitors in treating KRAS-mutant pancreatic ductal adenocarcinoma via collaboratively modulating the TRAIL-death receptor axis [ Pharmacol Res, 2023, 197:106955] | PubMed: 37820855 |
High-Throughput Functional Evaluation of MAP2K1 Variants in Cancer [ Mol Cancer Ther, 2023, 22(2):227-239] | PubMed: 36442478 |
RETURN POLICY
Selleck Chemical’s Unconditional Return Policy ensures a smooth online shopping experience for our customers. If you are in any way unsatisfied with your purchase, you may return any item(s) within 7 days of receiving it. In the event of product quality issues, either protocol related or product related problems, you may return any item(s) within 365 days from the original purchase date. Please follow the instructions below when returning products.
SHIPPING AND STORAGE
Selleck products are transported at room temperature. If you receive the product at room temperature, please rest assured, the Selleck Quality Inspection Department has conducted experiments to verify that the normal temperature placement of one month will not affect the biological activity of powder products. After collecting, please store the product according to the requirements described in the datasheet. Most Selleck products are stable under the recommended conditions.
NOT FOR HUMAN, VETERINARY DIAGNOSTIC OR THERAPEUTIC USE.