OSI-420

CAS No. 183320-51-6

OSI-420( OSI420 | CP 473420 | Desmethyl Erlotinib )

Catalog No. M17392 CAS No. 183320-51-6

OSI-420 (Desmethyl Erlotinib, CP-473420) is an active metabolite of erlotinib which is an orally active EGFR tyrosin kinase inhibitor with IC50 of 2 and 20 nM for human EGFR and EGFR autophosphorylation in tumor cells.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 123 In Stock
2MG 72 In Stock
5MG 111 In Stock
10MG 188 In Stock
25MG 335 In Stock
50MG 495 In Stock
100MG 705 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    OSI-420
  • Note
    Research use only, not for human use.
  • Brief Description
    OSI-420 (Desmethyl Erlotinib, CP-473420) is an active metabolite of erlotinib which is an orally active EGFR tyrosin kinase inhibitor with IC50 of 2 and 20 nM for human EGFR and EGFR autophosphorylation in tumor cells.
  • Description
    OSI-420 (CP-473420) is an active metabolite of erlotinib which is an orally active EGFR tyrosin kinase inhibitor with IC50 of 2 and 20 nM for the inhibition of human EGFR and EGFR autophosphorylation in tumor cells.
  • In Vitro
    ——
  • In Vivo
    Desmethyl Erlotinib exhibits t1/2 of 11.96±2.01 h in a pharmacokinetic study in Wistar rats.
  • Synonyms
    OSI420 | CP 473420 | Desmethyl Erlotinib
  • Pathway
    Neuroscience
  • Target
    GluR
  • Recptor
    EGFR
  • Research Area
    Cancer
  • Indication
    ——

Chemical Information

  • CAS Number
    183320-51-6
  • Formula Weight
    415.87
  • Molecular Formula
    C21H21N3O4·HCl
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO : ≥ 4.2 mg/mL; 10.10 mM
  • SMILES
    Cl.COCCOC1=CC2=C(C=C1OCCO)C(NC1=CC=CC(=C1)C#C)=NC=N2
  • Chemical Name
    2-[[4-[(3-Ethynylphenyl)amino]-7-(2-methoxyethoxy)-6-quinazolinyl]oxy]ethanol

Shipping & Storage Information

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

Reference

1. Svedberg A,et al. J Pharm Biomed Anal. 2015 Mar 25;107:186-95.
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