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GDC-0879

SIGMA/SML1953 - ≥98% (HPLC)

Synonym: 1H-Inden-1-one, 2,3-dihydro-5-[1-(2-hydroxyethyl)-3-(4-pyridinyl)-1H-pyrazol-4-yl]-, oxime; 2,3-Dihydro-5-[1-(2-hydroxyethyl)-3-(4-pyridinyl)-1H-pyrazol-4-yl]-1H-inden-1-one oxime; 2-[4-[(1E)-1-(Hydroxyimino)-2,3-dihydro-1H-inden-5-yl]-3-(pyridine-4-yl)-1H-pyrazol-1-yl]ethan-1-ol; 5-(1-(2-Hydroxyethyl)-3-(pyridin-4-yl)-1H-pyrazol-4-yl)-2,3-dihydro-1H-inden-1-one oxime; AR00341677; GDC0879

CAS Number: 905281-76-7
Empirical Formula (Hill Notation): C19H18N4O2
Molecular Weight: 334.37
MDL Number: MFCD16875916
Linear Formula: C19H18N4O2
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-SML1953-5MG 5 mg
$123.00
1/EA
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45-SML1953-25MG 25 mg
$496.00
1/EA
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assay ≥98% (HPLC)
color white to beige
form powder
InChI 1S/C19H18N4O2/c24-10-9-23-12-17(19(21-23)13-5-7-20-8-6-13)15-1-3-16-14(11-15)2-4-18(16)22-25/h1,3,5-8,11-12,24-25H,2,4,9-10H2/b22-18+
InChI key DEZZLWQELQORIU-RELWKKBWSA-N
Quality Level 100 
SMILES string OCCN(N=C1C2=CC=NC=C2)C=C1C3=CC=C4C(CC/C4=NO)=C3
solubility DMSO: 2 mg/mL, clear (warmed)
storage temp. 2-8°C
Biochem/physiol Actions: GDC-0879 (AR00341677) is an orally active, ATP site-targeting, highly potent Raf inhibitor (IC50 against V600E B-Raf-catalyzed MEK phophorylation = 0.13 nM with 4 μM ATP; IC50 against pERK in V600E B-Raf-expressing cells = 29 nM/Colo205, 59 nM/A375, 63 nM/Malme-3M) with great selectivity over >200 protein kinases (IC50 >1 μM). Oral administration is shown to effectively suppress Colo205 and A375 xenografts-derived tumor growth and pMEK1 in mice in vivo (35 mg/kg bid; 50-200 mg/kg qd or bid). Paradoxically, GDC-0879 also induces wild-type and enhances V600E B-Raf dimerization in an allosteric manner independent of kinase activity inhibition, resulting in selective anti-proliferation activity against V600E B-Raf cancer cells, but not in KRAS mutant or RAS/WT Raf cells, where GDC-0879 induces formation of B–C and A–B heterodimers and downstream signaling activation.
Biochem/physiol Actions: Orally active potent Raf inhibitor with V600E B-Raf-selective anticancer activity, while enhancing Raf signaling in KRAS mutant or RAS/WT Raf cells.
RIDADR NONH for all modes of transport
WGK Germany WGK 3
Flash Point(F) Not applicable
Flash Point(C) Not applicable
Purity ≥98% (HPLC)
Storage Temp. 2-8°C
UNSPSC 12352200

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