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Ravoxertinib

SKU: orb1300705

Description

Ravoxertinib

Research Area

Signal Transduction

Images & Validation

Key Properties

CAS Number1453848-26-4
MW440.86
Purity99.87% (May vary between batches)
FormulaC21H18ClFN6O2
SMILESCn1nccc1Nc1nccc(n1)-c1ccn([C@H](CO)c2ccc(Cl)c(F)c2)c(=O)c1
TargetERK
Solubility10% DMSO+40% PEG300+5% Tween 80+45% Saline:2 mg/mL (4.54 mM);Ethanol:81 mg/mL (183.73 mM);DMSO:245 mg/mL (555.73 mM)

Bioactivity

Target IC50
ERK1:1.1 nM|ERK2:0.3 nM|p-RSK:12 nM
In Vivo
GDC-0994 (p.o.) inhibits intracellular ERK phosphorylation and activation of ERK-mediated signaling pathways, subsequently impeding the proliferation and survival of ERK-dependent tumor cells. In in vitro cancer models, GDC-0994 (p.o.) demonstrates significant single-dose efficacy, including against BRAF and KRAS mutant human xenograft tumors in mice.
In Vitro
GDC-0994 significantly inhibits phospho-p90RSK in tumor cells.

Storage & Handling

Storagestore at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Expiration Date12 months from date of receipt.
DisclaimerFor research use only

Alternative Names

Ravoxertinib, inhibit, ERK1, ERK2, ERK, Extracellular signal regulated kinases, Inhibitor, GDC-0994, GDC0994, GDC 0994

Similar Products

  • GDC-0994 [orb1226241]

    >98% (HPLC)

    1453848-26-4

    440.864

    C21H18ClFN6O2

    1 g, 500 mg, 200 mg, 100 mg, 5 mg, 10 mg, 25 mg, 2 mg, 50 mg
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Key Properties

No computed properties available.

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Protocol Information

Ravoxertinib (orb1300705)

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% DMSO +
%+
% Tween 80 +
%

Available Sizes

Select a size below

1 mg
$ 80.00
2 mg
$ 90.00
5 mg
$ 120.00
1 ml x 10 mM (in DMSO)
$ 130.00
10 mg
$ 140.00
25 mg
$ 220.00
50 mg
$ 340.00
100 mg
$ 490.00
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