Decitabine

CAT:
804-HY-A0004-01
Size:
100 mg

For Laboratory Research Only. Not for Clinical or Personal Use.

  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
Decitabine - image 1

Decitabine

  • Description:

    Decitabine (NSC 127716) is an orally active deoxycytidine analogue antimetabolite and a DNA methyltransferase inhibitor. Decitabine incorporates into DNA in place of cytosine can covalently trap DNA methyltransferase to DNA causing irreversible inhibition of the enzyme. Decitabine induces cell G2/M arrest and cell apoptosis. Decitabine has potent anticancer activity[1][2].
  • Product Name Alternative:

    5-Aza-2'-deoxycytidine; 5-AZA-CdR; NSC 127716
  • UNSPSC:

    12352005
  • Hazard Statement:

    H302, H315, H319, H335, H341, H360
  • Target:

    Apoptosis; DNA Methyltransferase; Nucleoside Antimetabolite/Analog
  • Type:

    Reference compound
  • Related Pathways:

    Apoptosis; Cell Cycle/DNA Damage; Epigenetics
  • Applications:

    Cancer-programmed cell death
  • Field of Research:

    Cancer
  • Assay Protocol:

    https://www.medchemexpress.com/Decitabine.html
  • Concentration:

    10mM
  • Purity:

    99.97
  • Solubility:

    DMSO : ≥ 50 mg/mL|H2O : 20 mg/mL (ultrasonic)
  • Smiles:

    O[C@H]1C[C@H](N2C(N=C(N)N=C2)=O)O[C@@H]1CO
  • Molecular Formula:

    C8H12N4O4
  • Molecular Weight:

    228.21
  • Precautions:

    H302, H315, H319, H335, H341, H360
  • References & Citations:

    [1]Nakamura M, et al. Decitabine inhibits tumor cell proliferation and up-regulates E-cadherin expression in Epstein-Barr virus-associated gastric cancer. J Med Virol. 2016 Jul 19.|[2]Hagemann S, et al. Azacytidine and decitabine induce gene-specific and non-random DNA demethylation in human cancer cell lines. PLoS One. 2011 Mar 7;6 (3) :e17388.|[3]Requena CE, et al. The nucleotidohydrolases DCTPP1 and dUTPase are involved in the cellular response to decitabine. Biochem J. 2016 Jun 20.|[4]Terse P, et al. Subchronic oral toxicity study of decitabine in combination with tetrahydrouridine in CD-1 mice. Int J Toxicol. 2014 Mar-Apr;33 (2) :75-85.|[5]Yu J, et al. DNA methyltransferase expression in triple-negative breast cancer predicts sensitivity to decitabine. J Clin Invest. 2018 Jun 1;128 (6) :2376-2388.|[6]Wang LX, et al. Low dose decitabine treatment induces CD80 expression in cancer cells and stimulates tumorspecific cytotoxic T lymphocyte responses. PLoS One. 2013 May 9;8 (5) :e62924.|[7]Parker WB. Enzymology of purine and pyrimidine antimetabolites used in the treatment of cancer. Chem Rev. 2009 Jul;109 (7) :2880-93.
  • Shipping Conditions:

    Room Temperature
  • Storage Conditions:

    4°C (Powder, protect from light)
  • Scientific Category:

    Reference compound1
  • Clinical Information:

    Launched
  • Isoform:

    DNMT1; DNMT3
  • CAS Number:

    [2353-33-5]