MC-1575

CAS No.

MC-1575 ( MC1575 )

Catalog No. M17051 CAS No.

MC-1575 is a potent and selective class IIa HDAC inhibitor with IC50 of 440 nM for maize HD1-A.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
100MG Get Quote Get Quote
200MG Get Quote Get Quote
500MG Get Quote Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    MC-1575
  • Note
    Research use only, not for human use.
  • Brief Description
    MC-1575 is a potent and selective class IIa HDAC inhibitor with IC50 of 440 nM for maize HD1-A.
  • Description
    MC-1575 is a potent and selective class IIa HDAC inhibitor with IC50 of 440 nM for maize HD1-A, displays >70-fold selectivity over HD1-B; exhibits a dose-dependent antiproliferative effect and induces cell cycle arrest although this blockade occurred at a different level than TSA; increases p21(waf1/CIP1) mRNA levels and induces ERbeta gene expression; also suppress IL-8 expression in human melanoma cells.
  • Synonyms
    MC1575
  • Pathway
    Cell Cycle/DNA Damage
  • Target
    HDAC
  • Recptor
    HDAC
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    --
  • Formula Weight
    329.78
  • Molecular Formula
    C18H16ClNO3
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    ——
  • Chemical Name
    (E)-3-(3-((E)-3-(3-chlorophenyl)-3-oxoprop-1-en-1-yl)-5-methylcyclopenta-1,3-dien-1-yl)-N-hydroxyacrylamide

Shipping & Storage Information

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

Reference

1. Mai A, et al. J Med Chem. 2005 May 5;48(9):3344-53.
2. Duong V, et al. Mol Cancer Res. 2008 Dec;6(12):1908-19.
3. Venza I, et al. Pigment Cell Melanoma Res. 2013 Mar;26(2):193-204.
molnova catalog
related products
  • Cedryl acetate

    The fungal transformation of cedryl acetate was investigated for the first time by using Cunninghamella elegans.

  • ITSA-1

    A small molecule suppressor that counteracts trichostatin A (TSA)-induced cell cycle arrest.

  • Pracinostat

    Pracinostat (SB939) is a potent, orally active HDAC inhibitor that potently inhibits class I, II, and IV HDACsw with Ki of 15-100 nM, inhibits HDAC1 with IC50 of 77 nM.