الصفحة الرئيسية>>Signaling Pathways>> Tyrosine Kinase>> EGFR>>EMI56

EMI56

رقم الكتالوجGC62420

يُظهر EMI56 ، وهو مشتق من EMI1 ، فاعلية أكبر تجاه EGFR المتحولة أكثر من EMI1يثبط EMI56 الطفرات الثلاثية EGFR

Products are for research use only. Not for human use. We do not sell to patients.

EMI56 التركيب الكيميائي

Cas No.: 2414374-41-5

الحجم السعر المخزون الكميّة
10mM (in 1mL DMSO)
347٫00
متوفر
5 mg
315٫00
متوفر
10 mg
495٫00
متوفر
25 mg
855٫00
متوفر
50 mg
1305٫00
متوفر
100 mg
2025٫00
متوفر

Tel:(909) 407-4943 Email: sales@glpbio.com

مراجعات العميل

بناء على آراء العملاء.

  • GlpBio Citations

    GlpBio Citations
  • Bioactive Compounds Premium Provider

    Bioactive Compounds Premium Provider

Sample solution is provided at 25 µL, 10mM.

Description Chemical Properties Product Documents

EMI56, the derivative of EMI1, displays greater potency toward mutant EGFR than EMI1. EMI56 inhibits EGFR triple mutants[1].

EMI56 inhibits EGFR ex19del/T790M/C797S and EGFR L858R/T790M/C797S. EMI56 can be used in the research of mutant EGFR-associated, drug-resistant non-small-cell lung cancer (NSCLC)[1].EMI56 (10, 15, 20 μM; 2 h of treatment) strongly inhibits total EGFR levels, activation and downstream signaling in PC9 EGFR ex19del/T790M/C797S cells[1].

[1]. Punit Saraon, et al. A Drug Discovery Platform to Identify Compounds That Inhibit EGFR Triple Mutants.Nat Chem Biol. 2020 May;16(5):577-586.

مراجعات

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Average Rating: 5 ★★★★★ (Based on Reviews and 27 reference(s) in Google Scholar.)

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