3103654-99-2

EGFR-IN-201 Chemical Structure
3103654-99-2

Chemical Structure

EGFR-IN-201

  • CAS No.: 3103654-99-2
  • Formula:C17H16N4O2S
  • Molecular Weight:340.40

InChIKey: PFNZZAPTKBOKGP-SKGUUVROSA-N

SMILES: COC1=CC=C(/C=C2C(N/C(S/2)=N\N=C(C)\C3=CC=CN3)=O)C=C1

Biological Activity: EGFR-IN-201 is a potent EGFR inhibitor, with an IC50 of 0.091 μM against wild-type EGFR; for mutant EGFR variants, the IC50 values of EGFRT790M, EGFRL858R and EGFRC797S are 0.147 μM, 0.221 μM and 0.703 μM, respectively. EGFR-IN-201 inhibits EGFR downstream signaling proteins AKT1 (IC50 = 0.225 μg/mL) and ERK1 (IC50 = 0.705 μg/mL). EGFR-IN-201 induces G0/G1 cell cycle arrest, apoptosis and low-level necrosis in cancer cells. EGFR-IN-201 is applicable to research on cancers such as colon cancer[1].

Cat. No. Product Name Purity Description Pricing
HY-181659
EGFR-IN-201 EGFR-IN-201 is a potent EGFR inhibitor, with an IC50 of 0.091 μM against wild-type EGFR; for mutant EGFR variants, the IC50 values of EGFRT790M, EGFRL858R and EGFRC797S are 0.147 μM, 0.221 μM and 0.703 μM, respectively. EGFR-IN-201 inhibits EGFR downstream signaling proteins AKT1 (IC50 = 0.225 μg/mL) and ERK1 (IC50 = 0.705 μg/mL). EGFR-IN-201 induces G0/G1 cell cycle arrest, apoptosis and low-level necrosis in cancer cells. EGFR-IN-201 is applicable to research on cancers such as colon cancer.
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