4SC-202 free base

CAS No. 910462-43-0

4SC-202 free base ( 4SC202; 4SC-202; 4SC 202; domatinostat )

Catalog No. M16538 CAS No. 910462-43-0

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.

Purity : >98%(HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 57 In Stock
5MG 91 In Stock
10MG 135 In Stock
25MG 258 In Stock
50MG 397 In Stock
100MG 584 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    4SC-202 free base
  • Note
    Research use only, not for human use.
  • Brief Description
    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.
  • Description
    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. Also displays inhibitory activity against Lysine specific demethylase 1 (LSD1). Phase 1.
  • Synonyms
    4SC202; 4SC-202; 4SC 202; domatinostat
  • Pathway
    Cell Cycle/DNA Damage
  • Target
    HDAC
  • Recptor
    HDAC3; HDAC2; HDAC1
  • Research Area
    Cancer
  • Indication
    ——

Chemical Information

  • CAS Number
    910462-43-0
  • Formula Weight
    447.51
  • Molecular Formula
    CHNOS
  • Purity
    >98%(HPLC)
  • Solubility
    DMSO:82 mg/mL (183.2 mM);Ethanol:<1 mg/mL;Water:<1 mg/mL
  • SMILES
    O=C(NC1=CC=CC=C1N)/C=C/C2=CN(S(=O)(C3=CC=C(C4=CN(C)N=C4)C=C3)=O)C=C2.O=S(C5=CC=C(C)C=C5)(O)=O
  • Chemical Name
    (E)-N-(2-aminophenyl)-3-(1-((4-(1-methyl-1H-pyrazol-4-yl)phenyl)sulfonyl)-1H-pyrrol-3-yl)acrylamide.

Shipping & Storage Information

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

Reference

1.Henning SW, et al. 22nd EORTC-NCI-AACR symposium. 2010. Abstract # 178.
molnova catalog
related products
  • Vorinostat

    A potent HDAC inhibitor, inhibits the activities of HDAC1 and HDAC3 with IC50 of 10 nM and 20 nM, respectively.

  • ACY-775

    ACY-775 (ACY775) is a potent and specific HDAC6 inhibitor (IC50=7.5 nM) with improved brain bioavailability.

  • RGFP966

    RGFP966 is an HDAC3 inhibitor with IC50 of 0.08 μM in cell-free assay.