ZM 336372

CAS No. 208260-29-1

ZM 336372( ZM336372 | ZM-336372 )

Catalog No. M13244 CAS No. 208260-29-1

ZM 336372 is a potent, specific inhibitor of Raf isoforms in vitro (c-Raf IC50=70 nM).

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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2MG 31 In Stock
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10MG 79 In Stock
25MG 149 In Stock
50MG 272 In Stock
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Biological Information

  • Product Name
    ZM 336372
  • Note
    Research use only, not for human use.
  • Brief Description
    ZM 336372 is a potent, specific inhibitor of Raf isoforms in vitro (c-Raf IC50=70 nM).
  • Description
    ZM 336372 is a potent, specific inhibitor of Raf isoforms in vitro (c-Raf IC50=70 nM), paradoxically induces >100-fold activation of c-Raf (Raf-1 activator), but without triggering any activation of MKK1 or p42 MAPK/ERK2; suppresses growth and neuroendocrine hormone levels in carcinoid tumor cells, with marked induction of the cell cycle inhibitors p21 and p18; blocks cellular proliferation and suppresses NE vasoactive peptide production in pheochromocytoma cells.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    ZM336372 | ZM-336372
  • Pathway
    MAPK/ERK Signaling
  • Target
    Raf
  • Recptor
    C-Raf
  • Research Area
    Cancer
  • Indication
    ——

Chemical Information

  • CAS Number
    208260-29-1
  • Formula Weight
    389.4
  • Molecular Formula
    C23H23N3O3
  • Purity
    >98% (HPLC)
  • Solubility
    10 mM in DMSO
  • SMILES
    O=C(NC1=CC=C(C)C(NC(C2=CC=C(O)C=C2)=O)=C1)C3=CC=CC(N(C)C)=C3
  • Chemical Name
    Benzamide, 3-(dimethylamino)-N-[3-[(4-hydroxybenzoyl)amino]-4-methylphenyl]-

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1. Hall-Jackson CA, et al. Chem Biol. 1999 Aug;6(8):559-68. 2. Van Gompel JJ, et al. Mol Cancer Ther. 2005 Jun;4(6):910-7. 3. Kappes A, et al. J Surg Res. 2006 Jun 1;133(1):42-5. 4. Kunnimalaiyaan M, et al. Surgery. 2007 Dec;142(6):959-64; discussion 959-64.
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