Phenylethyl isothiocyanate

CAS No. 2257-09-2

Phenylethyl isothiocyanate( JC-5411,JC5411,JC 5411 )

Catalog No. M22864 CAS No. 2257-09-2

Phenylethyl isothiocyanate is an HDAC inhibitor. It potentially for the treatment of benign prostatic hypertrophy.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
500MG 38 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Phenylethyl isothiocyanate
  • Note
    Research use only, not for human use.
  • Brief Description
    Phenylethyl isothiocyanate is an HDAC inhibitor. It potentially for the treatment of benign prostatic hypertrophy.
  • Description
    Phenylethyl isothiocyanate is an HDAC inhibitor. It potentially for the treatment of benign prostatic hypertrophy.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    JC-5411,JC5411,JC 5411
  • Pathway
    Cell Cycle/DNA Damage
  • Target
    HDAC
  • Recptor
    HDAC
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    2257-09-2
  • Formula Weight
    163.23
  • Molecular Formula
    C9H9NS
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO:Soluble
  • SMILES
    C1=CC=C(C=C1)CCN=C=S
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Zhu Y , Liu S , Yan S , et al. Phenylethyl isothiocyanate induces oxidative damage of porcine kidney cells mediated by reactive oxygen species[J]. Journal of Biochemical and Molecular Toxicology, 2020, 34(2).
molnova catalog
related products
  • TYA-018

    TYA-018 is an orally available and selective HDAC6 inhibitor with cardioprotective properties for the study of dilated heart disease and heart failure.TYA-018 prevents sarcomere damage and decreases Nppb expression.

  • 4SC-202 free base

    4SC-202 is a selective class I HDAC inhibitor with IC50 of 1.20 μM, 1.12 μM, and 0.57 μM for HDAC1, HDAC2, and HDAC3, respectively.

  • SIS17

    SIS17 is a potent and selective HDAC 11 inhibitor with an IC50 value of 0.83 μM. SIS17 is active in cells and inhibited the demyristoylation of a known HDAC11 substrate serine hydroxymethyl transferase 2 without inhibiting other HDACs.