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BAY-293

SIGMA/SML2703 - ≥98% (HPLC)

Synonym: 6,7-Dimethoxy-2-methyl-N-[(R)-1-(4-{2-[(methylamino)methyl]phenyl}thien-2-yl)ethyl]quinazolin-4-amine; BAY 293; BAY293

CAS Number: 2244904-70-7
Empirical Formula (Hill Notation): C25H28N4O2S
Molecular Weight: 448.58
Linear Formula: C25H28N4O2S
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-SML2703-5MG 5 mg
$143.00
1/EA
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45-SML2703-25MG 25 mg
$457.00
1/EA
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assay ≥98% (HPLC)
color white to beige
form powder
optical activity [α]/D -85.0 to -103.0°, c = 1.0 in DMSO
Quality Level 100 
SMILES string C[C@H](C1=CC(C2=CC=CC=C2CNC)=CS1)NC3=C4C=C(C(OC)=CC4=NC(C)=N3)OC
solubility DMSO: 2 mg/mL, clear
storage temp. −20°C
Biochem/physiol Actions: BAY-293 selectively inhibits SOS1-mediated KRAS activation (IC50 = 52 nM; 50 nM wt or G12C hKRAS & 10 nM SOS1cat) via direct SOS1 binding, blocking SOS1-KRAS interaction (IC50 = 21 nM; 10 nM hSOS1cat & 5 nM hKRAS G12C) without affecting (IC50 >20 μM) CRAF RBD-KRAS interaction, KRAS G12C activation by SOS2, Cdc42 activation by DBS, or EGFR kinase activity. BAY-293 downregulates cellular active RAS (IC50 = 200 nM/Calu-1, 410 nM/HeLa) and downstream ERK phosphorylation (K-562, 150 nM/Calu-1) with good target selectivity as assessed over 358 kinases (<37% inhibition at 1 μM) and a panel of 77 GPCRs, transporters, nuclear receptors and enzymes.
WGK Germany WGK 3
Flash Point(F) Not applicable
Flash Point(C) Not applicable
Purity ≥98% (HPLC)
Storage Temp. −20°C
UNSPSC 12352200

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