Oltipraz

CAS No. 64224-21-1

Oltipraz( RP 35972 | NSC 347901 )

Catalog No. M15443 CAS No. 64224-21-1

Oltipraz (RP 35972, NSC 347901) is a cancer chemopreventive agent with inhibitory effect on angiogenesis and tumor growth.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 28 In Stock
10MG 45 In Stock
25MG 64 In Stock
50MG 80 In Stock
100MG 113 In Stock
200MG 145 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Oltipraz
  • Note
    Research use only, not for human use.
  • Brief Description
    Oltipraz (RP 35972, NSC 347901) is a cancer chemopreventive agent with inhibitory effect on angiogenesis and tumor growth.
  • Description
    Oltipraz (RP 35972, NSC 347901) is a cancer chemopreventive agent with inhibitory effect on angiogenesis and tumor growth, inhibits insulin- or hypoxia-induced HIF-1α expression through an increase in ubiquitination; abrogates insulin-induced H(2)O(2) production, thereby preventing H(2)O(2)-enhanced HIF-1alpha expression and promoting its ubiquitination and degradation; inhibits HIF-1α activity and HIF-1α-dependent tumor growth both in vitro and in vivo.Steatohepatitis Phase 3 Clinical.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    RP 35972 | NSC 347901
  • Pathway
    Angiogenesis
  • Target
    HIF/HIF Prolyl-hydroxylase
  • Recptor
    ReverseTranscriptase
  • Research Area
    Other Indications
  • Indication
    Steatohepatitis

Chemical Information

  • CAS Number
    64224-21-1
  • Formula Weight
    226.3416
  • Molecular Formula
    C8H6N2S3
  • Purity
    >98% (HPLC)
  • Solubility
    10 mM in DMSO
  • SMILES
    S=C1SSC(C2=NC=CN=C2)=C1C
  • Chemical Name
    3H-1,2-Dithiole-3-thione, 4-methyl-5-(2-pyrazinyl)-

Shipping & Storage Information

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

Reference

1. Lee WH, et al. Mol Cancer Ther. 2009 Oct;8(10):2791-802. 2. Kang SG, et al. Carcinogenesis. 2012 Mar;33(3):661-9. 3. Lee YH, et al. Bioorg Med Chem. 2016 Jun 15;24(12):2843-51.
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