An HDAC inhibitor
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Information provided in the product description is from published literature. Due to the nature of scientific experimentation, your results (e.g., selectivity and effective concentrations) or specific application for this product may differ. If you have questions about how this product fits your application, please contact our technical support staff.

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CAY10398

Item No. 89740

Technical Information
Formal Name
4-(dimethylamino)-N-[6-(hydroxyamino)-6-oxohexyl]-benzamide
CAS Number
193551-00-7
Synonyms
  • MD 85
  • PX 089274
Molecular Formula
C15H23N3O3
Formula Weight
Purity
≥98%
A crystalline solid
DMF: 20 mg/mlDMF:PBS (pH 7.2) (1:5): 300 µg/mlDMSO: 14 mg/mlEthanol: 1 mg/ml
λmax
301 nm
SMILES
ONC(=O)CCCCCNC(=O)c1ccc(cc1)N(C)C
InChi Code
InChI=1S/C15H23N3O3/c1-18(2)13-9-7-12(8-10-13)15(20)16-11-5-3-4-6-14(19)17-21/h7-10,21H,3-6,11H2,1-2H3,(H,16,20)(H,17,19)
InChi Key
RGWSSTALGUXZMU-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    CAY10398 is a histone deacetylase (HDAC) inhibitor (IC50 = 0.244 µM in H1299 cell lysates).1 It inhibits HDAC1, HDAC3, and HDAC6 (IC50s = 0.39, 0.39, and 0.33 µM, respectively) and inhibits the proliferation of K562 leukemia cells (IC50 = 2.2 µM).2 CAY10398 is also active against drug-sensitive and -resistant strains of P. falciparum (IC50s = 0.2723-0.726 µM).3

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Remiszewski, S.W., Sambucetti, L.C., Atadja, P., et alInhibitors of human histone deacetylase: Synthesis and enzyme and cellular activity of straight chain hydroxamates. J. Med. Chem. 45(4), 753-757 (2002).

    2. Wittich, S., Scherf, H., Xie, C., et alEffect of inhibitors of histone deacetylase on the induction of cell differentiation in murine and human erythroleukemia cell lines. Anticancer Drugs 16(6), 635-643 (2005).

    3. Coetzee, N., von Grüning, H., Opperman, D., et alEpigenetic inhibitors target multiple stages of Plasmodium falciparum parasites. Sci. Rep. 10(1), (2020).