NVP-ADW742 b

CAS No. 475488-23-4

NVP-ADW742 b( ADW | GSK 552602A | ADW742 )

Catalog No. M19445 CAS No. 475488-23-4

NVP-ADW742 is an IGF-1R inhibitor with IC50 of 0.17 μM >16-fold more potent against IGF-1R than InsR; little activity to HER2 PDGFR VEGFR-2 Bcr-Abl and c-Kit.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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Biological Information

  • Product Name
    NVP-ADW742 b
  • Note
    Research use only, not for human use.
  • Brief Description
    NVP-ADW742 is an IGF-1R inhibitor with IC50 of 0.17 μM >16-fold more potent against IGF-1R than InsR; little activity to HER2 PDGFR VEGFR-2 Bcr-Abl and c-Kit.
  • Description
    NVP-ADW742 is an IGF-1R inhibitor with IC50 of 0.17 μM >16-fold more potent against IGF-1R than InsR; little activity to HER2 PDGFR VEGFR-2 Bcr-Abl and c-Kit.
  • In Vitro
    NVP-ADW742 (ADW742; 0.1-10 μM; 72 hours) dose-dependently inhibits serum-induced cell growth in all cell lines. NVP-ADW742 (0.1-9 μM; 20 min) blocks IGF-1-induced phosphorylation of IGF-1R and its known downstream target Akt at submicromolar concentrations. NVP-ADW742 has much higher IC50 values for other kinases (IC50>10 μM for HER2, PDGFR, VEGFR-2, or Bcr-Abl p210; and IC50>5 μM for c-Kit). Cell Viability Assay Cell Line:A panel of cell lines from multiple myeloma (MM), other hematologic malignancies and solid tumors Concentration:0.1, 0.5, 1, 2, 5, 10 μM Incubation Time:72 hours Result:Dose-dependently inhibited serum-induced cell growth in all cell lines.Western Blot Analysis Cell Line:NWT-21 cells Concentration:0.1, 0.3, 1, 3, 9 μM Incubation Time:20 min Result:Blocked IGF-1-induced phosphorylation of IGF-1R and its known downstream target Akt at submicromolar concentrations.
  • In Vivo
    NVP-ADW742 (ADW742; 10 mg/kg for IP or 50 mg/kg for orally; twice daily for 19 days) significantly suppresses tumor growth and prolongs the survival of mice. Animal Model:6- to 8-week-old male SCID/NOD mice with diffuse skeletal lesions of luciferase-expressing MM cells Dosage:10 mg/kg (IP) or 50 mg/kg (orally) Administration:IP or orally; twice daily for 19 days Result:Significantly suppressed tumor growth and prolonged the survival of mice.
  • Synonyms
    ADW | GSK 552602A | ADW742
  • Pathway
    Angiogenesis
  • Target
    IGF-1R
  • Recptor
    IGF-1R
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    475488-23-4
  • Formula Weight
    453.58
  • Molecular Formula
    C28H31N5O
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO:10 mg/mL (22.04 mM) warmed;Ethanol:3 mg/mL (6.61 mM);Water:<1 mg/mL
  • SMILES
    C1CCN(C1)CC2CC(C2)N3C=C(C4=C3N=CN=C4N)C5=CC(=CC=C5)OCC6=CC=CC=C6
  • Chemical Name
    5-(3-(benzyloxy)phenyl)-7-((1r3r)-3-(pyrrolidin-1-ylmethyl)cyclobutyl)-7H-pyrrolo[23-d]pyrimidin-4-amine

Shipping & Storage Information

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

Reference

1.Mitsiades CS et al. Cancer Cell 2004 5(3) 221-230.
molnova catalog
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