MDVN-1003

CAS No. 2058116-54-2

MDVN-1003( MDVN1003 | MDVN 1003 )

Catalog No. M13199 CAS No. 2058116-54-2

A first-in-class, selective, orally bioavailable, dual inhibitor of BTK and PI3Kδ kinases with IC50 of 32.3 nM and 16.9 nM, respectively.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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Biological Information

  • Product Name
    MDVN-1003
  • Note
    Research use only, not for human use.
  • Brief Description
    A first-in-class, selective, orally bioavailable, dual inhibitor of BTK and PI3Kδ kinases with IC50 of 32.3 nM and 16.9 nM, respectively.
  • Description
    A first-in-class, selective, orally bioavailable, dual inhibitor of BTK and PI3Kδ kinases with IC50 of 32.3 nM and 16.9 nM, respectively; inhibits B cell activation upon BCR cross-linking ex vivo and in vivo, induces apoptosis and decreases viability of DOHH-2 cells; shows significant anti-tumor effects in an NHL xenograft model in mice.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    MDVN1003 | MDVN 1003
  • Pathway
    Tyrosine Kinase
  • Target
    BTK
  • Recptor
    BTK
  • Research Area
    Cancer
  • Indication
    ——

Chemical Information

  • CAS Number
    2058116-54-2
  • Formula Weight
    417.45
  • Molecular Formula
    C22H20FN7O
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    C1COC2=C(N1)C=C(C=C2F)C3=NN(C4=NC=NC(=C34)N)C5CC6=C(C5)C=C(C=C6)N
  • Chemical Name
    1-(5-amino-2,3-dihydro-1H-inden-2-yl)-3-(8-fluoro-3,4-dihydro-2H-benzo[b][1,4]oxazin-6-yl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine

Shipping & Storage Information

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

Reference

1. Alfaro J, et al. J Pharmacol Exp Ther. 2017 May;361(2):312-321.
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