Chidamide

CAS No. 743420-02-2

Chidamide( CS055 | CS-055 | CS 055 | HBI8000 | HBI 8000 | HBI-8000 | Chidamide | Tucidinostat )

Catalog No. M15838 CAS No. 743420-02-2

Chidamide(CS055; HBI-8000) is a class I HDAC inhibitor with IC50s of 95/160/67/733 nM for HDAC1/2/3/8; also inhibits HDAC10/11(IC50=78/432 nM).

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 113 In Stock
2MG 75 In Stock
5MG 132 In Stock
10MG 227 In Stock
25MG 453 In Stock
50MG 649 In Stock
100MG 923 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Chidamide
  • Note
    Research use only, not for human use.
  • Brief Description
    Chidamide(CS055; HBI-8000) is a class I HDAC inhibitor with IC50s of 95/160/67/733 nM for HDAC1/2/3/8; also inhibits HDAC10/11(IC50=78/432 nM).
  • Description
    Chidamide(CS055; HBI-8000) is a class I HDAC inhibitor with IC50s of 95/160/67/733 nM for HDAC1/2/3/8; also inhibits HDAC10/11(IC50=78/432 nM); no inhibition on HDAC4/5/7/9/6(IC50>30 uM).
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    CS055 | CS-055 | CS 055 | HBI8000 | HBI 8000 | HBI-8000 | Chidamide | Tucidinostat
  • Pathway
    Cell Cycle/DNA Damage
  • Target
    HDAC
  • Recptor
    HDAC1| HDAC2| HDAC3| HDAC8
  • Research Area
    Cancer
  • Indication
    ——

Chemical Information

  • CAS Number
    743420-02-2
  • Formula Weight
    390.41
  • Molecular Formula
    C22H19FN4O2
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO: 10 mM
  • SMILES
    O=C(NC1=CC(F)=CC=C1N)C2=CC=C(CNC(/C=C/C3=CC=CN=C3)=O)C=C2
  • Chemical Name
    (E)-N-(2-amino-5-fluorophenyl)-4-((3-(pyridin-3-yl)acrylamido)methyl)benzamide

Shipping & Storage Information

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

Reference

1. L, et al. Biochem Biophys Res Commun. 2010 Feb 5;392(2):190-5.
molnova catalog
related products
  • HDAC-IN-57

    HDAC-IN-57 is an orally active pan-inhibitor of histone deacetylase (HDAC), inhibiting HDAC1, HDAC2, HDAC6, and HDAC8 with IC50 values of 2.07 nM, 4.71 nM, 2.4 nM, and 107 nM, respectively.

  • Corin

    Corin is a dual action LSD1/HDAC inhibitor (IC50=0.33/0.20 uM) that potently targets the CoREST complex.

  • BRD 8184

    BRD 8184 is a potent, selective HDAC6 inhibitor with IC50 of 8 nM.