GDC-0623
GDC-0623, also known as G-868, is an orally active, selective MEK inhibitor with potential antineoplastic activity. MEK inhibitor GDC-0623 specifically inhibits mitogen-activated protein kinase kinase (MEK or MAP/ERK kinase), resulting in inhibition of growth factor-mediated cell signaling and tumor cell proliferation. MEK is a key component of the RAS/RAF/MEK/ERK signaling pathway that regulates cell growth; constitutive activation of this pathway has been implicated in many cancers. Check for active clinical trials or closed clinical trials using this agent. (NCI Thesaurus) . (In Vitro) :GDC-0623 (RG 7421) and G-573 are able to prevent MEK phosphorylation by CRAF in vitro, and able to block MEK phosphorylation by BRAF (V600E) . GDC-0623 (RG 7421) is potent, ATP-uncompetitive inhibitors of MEK1 but shows distinct shifts in cellular activity compared with the other two inhibitors, only 6-fold half-maximum effective concentration (EC50) decreases. (In Vivo) :GDC-0623 (RG 7421) (40 mg/kg, p.o.) shows percent tumour growth inhibition (%TGI) in MiaPaCa-2 xenograft model. GDC-0623 (RG 7421) and G-573 show superior antitumour activity compared to GDC-0623 (RG 7421) in all three KRAS models.
Product Specifications
CAS Number
1168091-68-6
Product Name Alternative
GDC0623 | GDC-0632 | GDC 0632 | G868 | G 868 | G-868
Purity
>98% (HPLC)
Solubility
DMSO : ≥ 30 mg/mL. 65.76 mM
Smiles
OCCONC (=O) C1=C (NC2=C (F) C=C (I) C=C2) N2C=NC=C2C=C1
Molecular Formula
C16H14FIN4O3
Molecular Weight
456.21
Storage Conditions
Storage temperature: -20°C. Stability: ≥ 2 years
Notes
For research use only.
Other Product Names
5- ((2-fluoro-4-iodophenyl) amino) -N- (2-hydroxyethoxy) imidazo[1,5-a]pyridine-6-carboxamide
Available Sizes
Frequently Asked Questions
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