SB-429201

CAS No. 1027971-34-1

SB-429201( SB 429201 | SB429201 )

Catalog No. M10136 CAS No. 1027971-34-1

A potent, selective HDAC1 inhibitor with IC50 of 1.5 uM.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 314 Get Quote
50MG 1602 Get Quote
100MG 2250 Get Quote
200MG Get Quote Get Quote
500MG Get Quote Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    SB-429201
  • Note
    Research use only, not for human use.
  • Brief Description
    A potent, selective HDAC1 inhibitor with IC50 of 1.5 uM.
  • Description
    A potent, selective HDAC1 inhibitor with IC50 of 1.5 uM; increases histone acetylation in SW620 cells.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    SB 429201 | SB429201
  • Pathway
    Cell Cycle/DNA Damage
  • Target
    HDAC
  • Recptor
    HDAC
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    1027971-34-1
  • Formula Weight
    436.511
  • Molecular Formula
    C28H24N2O3
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 100 mg/mL (229.10 mM)
  • SMILES
    O=C(NC1=CC=C(OC2=CC=CC=C2)C=C1)C3=CC=C(NC(CCC4=CC=CC=C4)=O)C=C3
  • Chemical Name
    N-(4-phenoxyphenyl)-4-(3-phenylpropanamido)benzamide

Shipping & Storage Information

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

Reference

1. Hu E, et al. J Pharmacol Exp Ther. 2003 Nov;307(2):720-8.
molnova catalog
related products
  • BML-210

    A novel histone deacetylase (HDAC) inhibitor that induces Ac-histone in A549 cells with EC50 of 181 uM.

  • Romidepsin

    Romidepsin (FK228, depsipeptide) is a potent HDAC1 and HDAC2 inhibitor with IC50 of 36 nM and 47 nM, respectively.

  • HDAC6-AR-IN-10

    HDAC6-AR-IN-10 is a potent dual HDAC6/AR inhibitor with IC50 of 35.6 nM/<30 nM.