الصفحة الرئيسية>>Signaling Pathways>> MAPK Signaling>> ERK>>ERK-IN-1

ERK-IN-1

رقم الكتالوجGC33206

ERK-IN-1 (المركب B) هو مثبط ERK1 و ERK2 متاح عن طريق الفم في علاج مرض تكاثر يتميز بتنشيط الطفرات في مسار MAPK. يرتبط النشاط بشكل خاص بعلاج KRAS-mutant NSCLC ، و BRAF-mutant NSCLC ، وسرطان البنكرياس المتحولة KRAS ، وسرطان القولون والمستقيم المتحولة KRAS (CRC) وسرطان المبيض المتحور KRAS. يمكن أن يمنع هيدروكلوريد ERK-IN-1 أيضًا RAF.

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ERK-IN-1 التركيب الكيميائي

Cas No.: 1715025-32-3

الحجم السعر المخزون الكميّة
5mg
225٫00
متوفر
10mM (in 1mL DMSO)
248٫00
متوفر
10mg
405٫00
متوفر
25mg
855٫00
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 Related Products

ERK-IN-1 (compound B) is a RAF and ERK1/2 inhibitor in the treatment of a proliferative disease characterized by activating mutations in the MAPK pathway. The activity is particularly related to the treatment of KRAS-mutant NSCLC (non-small celllung cancer), BRAF-mutant NSCLC, KRAS-mutant pancreatic cancer, KRAS-mutant colorectal cancer (CRC) and KRAS-mutant ovanan cancer[1].

ERK-IN-1 (compound B) (50, 75 mg/kg, p.o., qd/q2d, 27 days) treatment significantly reduces the tumor volume in the Calu-6 human NSCLC subcutaneous tumor xenograft model in mice[1].|| Animal Model:|Calu-6 NSCLC xenograft tumor models in mice[1].|Dosage:|50, 75 mg/kg.|Administration:|Orally either daily (qd) or every other day (q2d) for 27 days.|Result:|Significantly reduced the tumor volume.

[1]. WO2018051306A1.

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