Tucidinostat

CAS No. 1616493-44-7

Tucidinostat( Chidamide | HBI-8000 | CS055 )

Catalog No. M12363 CAS No. 1616493-44-7

Tucidinostat (Chidamide, HBI-8000, CS055) is a novel histone deacetylase (HDAC) inhibitor.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 55 In Stock
5MG 55 In Stock
10MG 87 In Stock
25MG 162 In Stock
50MG 258 In Stock
100MG 412 In Stock
200MG 578 In Stock
500MG 860 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Tucidinostat
  • Note
    Research use only, not for human use.
  • Brief Description
    Tucidinostat (Chidamide, HBI-8000, CS055) is a novel histone deacetylase (HDAC) inhibitor.
  • Description
    Tucidinostat (Chidamide, HBI-8000, CS055) is a novel histone deacetylase (HDAC) inhibitor with IC50 of 95/160/67/733/78/432 nM for HDAC1/2/3/8/10/11, respectively; shows no activity against Class IIa HDAC4/4/7/9 and HDAC6; demonstrates significant and broad spectrum in vitro and in vivo antitumor activity, induces G1 arrest, ROS-dependent apoptosis and differentiation in human leukaemia cells.Blood Cancer Approved.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    Chidamide | HBI-8000 | CS055
  • Pathway
    Cell Cycle/DNA Damage
  • Target
    HDAC
  • Recptor
    HDAC1|HDAC2|HDAC3|HDAC10
  • Research Area
    Cancer
  • Indication
    Blood cancer

Chemical Information

  • CAS Number
    1616493-44-7
  • Formula Weight
    390.418
  • Molecular Formula
    C22H19FN4O2
  • Purity
    >98% (HPLC)
  • Solubility
    Ethanol: 1 mg/mL Water: InsolubleDMSO: 50 mg/mL ( < 1 mg/ml refers to the product slightly soluble or insoluble )
  • SMILES
    O=C(NC1=CC=C(F)C=C1N)C2=CC=C(CNC(/C=C/C3=CC=CN=C3)=O)C=C2
  • Chemical Name
    N-(2-amino-4-fluorophenyl)-4-[[[(E)-3-pyridin-3-ylprop-2-enoyl]amino]methyl]benzamide

Shipping & Storage Information

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

Reference

1. Ning ZQ, et al. Cancer Chemother Pharmacol. 2012 Apr;69(4):901-9. 2. Gong K, et al. Biochem J. 2012 May 1;443(3):735-46. 3. Dong M, et al. Cancer Chemother Pharmacol. 2012 Jun;69(6):1413-22. 4. Gao S, et al. Anticancer Agents Med Chem. 2017;17(6):802-812.
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