PD158780

CAS No. 171179-06-9

PD158780 ( —— )

Catalog No. M20133 CAS No. 171179-06-9

PD 158780 reversibly inhibits auto and transphosphorylation of all four members of the ErbB receptor superfamily: EGFR ErbB2 ErbB3 and ErbB4 (IC50s: 8μM 49 nM 52 nM and 52 nM in cell assay).

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 69 In Stock
10MG 110 In Stock
25MG 205 In Stock
50MG 357 In Stock
100MG 524 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    PD158780
  • Note
    Research use only not for human use.
  • Brief Description
    PD 158780 reversibly inhibits auto and transphosphorylation of all four members of the ErbB receptor superfamily: EGFR ErbB2 ErbB3 and ErbB4 (IC50s: 8μM 49 nM 52 nM and 52 nM in cell assay).
  • Description
    PD 158780 reversibly inhibits auto and transphosphorylation of all four members of the ErbB receptor superfamily: EGFR ErbB2 ErbB3 and ErbB4 (IC50s: 8μM 49 nM 52 nM and 52 nM in cell assay).
  • Synonyms
    ——
  • Pathway
    Angiogenesis
  • Target
    EGFR
  • Recptor
    EGFR; ErbB2; ErbB3; ErbB4
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    171179-06-9
  • Formula Weight
    330.19
  • Molecular Formula
    C14H12BrN5
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO: 30 mg/mL (90.86 mM);Ethanol: 8 mg/mL (24.23 mM)
  • SMILES
    CNc1cc2c(Nc3cccc(Br)c3)ncnc2cn1
  • Chemical Name
    4-N-(3-bromophenyl)-6-N-methylpyrido[34-d]pyrimidine-46-diamine

Shipping & Storage Information

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

Reference

1.Fry DW et al. Biochemical and antiproliferative properties of 4-[ar(alk)ylamino]pyridopyrimidines a new chemical class of potent and specific epidermal growth factor receptor tyrosine kinase inhibitor. Biochem Pharmacol. 1997 Oct 15;54(8):877-87.
molnova catalog
related products
  • O-Desmethyl gefitini...

    O-Desmethyl gefitinib inhibits EGFR (IC50: 36 nM in subcellular assays). In human plasma, O-Desmethyl gefitinib is an active metabolite of Gefitinib.

  • RO 46-8443

    RO 46-8443 is the first non-peptide endothelin ETB receptor selective antagonist. RO 46-8443 displays up to 2000-fold selectivity for ETB receptors both in terms of binding inhibitory potency and functional inhibition.

  • EGFR Inhibitor

    EGFR inhibitor is a cell permeable and selective inhibitor of EGFR kinase (IC50: 21 nM) and blocks receptor autophosphorylation in cells.