3-Phenyltoxoflavin

CAS No. 32502-63-9

3-Phenyltoxoflavin( ZINC267655 | Phenyltoxoflavin )

Catalog No. M28065 CAS No. 32502-63-9

3-Phenyltoxoflavin is an inhibitor of HSP90 (Kd = 585 nM) with anti-cancer activity.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 128 In Stock
5MG 117 In Stock
10MG 187 In Stock
25MG 337 In Stock
50MG 500 In Stock
100MG 737 In Stock
200MG 1014 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    3-Phenyltoxoflavin
  • Note
    Research use only, not for human use.
  • Brief Description
    3-Phenyltoxoflavin is an inhibitor of HSP90 (Kd = 585 nM) with anti-cancer activity.
  • Description
    3-Phenyltoxoflavin is an inhibitor of HSP90 (Kd = 585 nM) with anti-cancer activity.(In Vitro):3-Phenyltoxoflavin (0.56 nM-100 μM) dose-dependently competes with biotinylated Hsp90 peptide for binding to TPR2A. In BT474 cells, 3-Phenyltoxoflavin (1 nM-100 μM) dose-dependently inhibits cell proliferation with an IC50 of 690 nM.
  • In Vitro
    3-Phenyltoxoflavin (1 nM-100 μM; 4 d) inhibits BT474 cells proliferation in a concentration-dependent manner, with an IC50 of 690 nM.3-Phenyltoxoflavin (0.56 nM-100 μM; 2 h) competes with biotinylated Hsp90 peptide for its binding to TPR2A in a dose-dependent manner.
  • In Vivo
    ——
  • Synonyms
    ZINC267655 | Phenyltoxoflavin
  • Pathway
    Cytoskeleton/Cell Adhesion Molecules
  • Target
    HSP
  • Recptor
    ——
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    32502-63-9
  • Formula Weight
    269.26
  • Molecular Formula
    C13H11N5O2
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 7.14 mg/mL (26.52 mM)
  • SMILES
    O=C1N=C2C(=NC(=NN2C)C3=CC=CC=C3)C(=O)N1C
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Ajeet. QSAR Study of Methionine Aminopeptidase Inhibitors as Anti-cancer Agents Using MLR Approach[J]. american journal of pharmacological sciences. 2013;1(5):80-83, 4 pp.
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