Home - Products - Angiogenesis - c-Kit - N-Desethylsunitinib hydrochloride

N-Desethylsunitinib hydrochloride

CAS No. 1261432-05-6

N-Desethylsunitinib hydrochloride( —— )

Catalog No. M23434 CAS No. 1261432-05-6

N-Desethylsunitinib hydrochloride is a major and pharmacologically active metabolite of sunitinib, which is potent, ATP-competitive VEGFR, PDGFRβ, and KIT inhibitor.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 326 In Stock
5MG 287 In Stock
10MG 430 In Stock
25MG 710 In Stock
100MG Get Quote In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    N-Desethylsunitinib hydrochloride
  • Note
    Research use only, not for human use.
  • Brief Description
    N-Desethylsunitinib hydrochloride is a major and pharmacologically active metabolite of sunitinib, which is potent, ATP-competitive VEGFR, PDGFRβ, and KIT inhibitor.
  • Description
    N-Desethylsunitinib hydrochloride is a major and pharmacologically active metabolite of sunitinib, which is potent, ATP-competitive VEGFR, PDGFRβ, and KIT inhibitor.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Angiogenesis
  • Target
    c-Kit
  • Recptor
    KIT|PDGFRβ|VEGFR
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    1261432-05-6
  • Formula Weight
    406.88
  • Molecular Formula
    C20H24ClFN4O2
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO:10 mM
  • SMILES
    O=C1C(C2=CC(F)=CC=C2N1)=CC(NC(C)=C3C(NCCNCC)=O)=C3C.Cl
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Determination of Sunitinib and Its Active Metabolite N-Desethylsunitinib in Sweat of a Patient.[J]. Journal of Analytical Toxicology, 2011.
molnova catalog
related products
  • RGB-286638 free base

    RGB-286638 free base is a novel CDK inhibitor.

  • KI8751

    Ki8751 is a potent and selective inhibitor of VEGFR2 with IC50 of 0.9 nM.

  • AZD2932

    AZD2932 is a new series of quinazoline ether inhibitor which potently inhibits VEGFR-2 and PDGFR with IC50s of 4 nM/8 nM/ 7 nM for PDGFRβ/VEGFR-2/Flt-3.