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Chemical Structure
Chemical Structure
Chemical Structure

5-Azacytidine [320-67-2]

Research Use Only
CDX-A0271
Chemodex
CAS Number320-67-2
Product group Chemicals
Estimated Purity>98%
Molecular Weight244.2
Price on request
Packing Size
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Overview

  • Supplier
    Chemodex
  • Product Name
    5-Azacytidine [320-67-2]
  • Delivery Days Customer
    10
  • CAS Number
    320-67-2
  • Certification
    Research Use Only
  • Estimated Purity
    >98%
  • Hazard Information
    Danger,Non-hazardous
  • Molecular Formula
    C8H12N4O5
  • Molecular Weight
    244.2
  • Scientific Description
    5-Azacytidine, a chemical analogue of the DNA and RNA nucleoside cytidine, is an cell permeable inhibitor of DNA methyltransferases, potentially serving to reverse epigenetic changes. It reduces hypermethylation associated with certain diseases, including myelodysplastic syndromes (IC50s = 2.4 and 2.6microM for in vitro anti-myeloma activity) and cancer (IC50s ~ 0.4microM for inhibiting proliferation of various cancer cell lines). It has a reported half-life of 17 hours and is considerably cytotoxic; it must be incorporated into DNA to covalently trap DNA methyltransferases. Induces demethylation and reactivation of silenced genes. Improves the efficiency of reprogramming of stem cells; induces differentiation of mesenchymal stem cells into cardiomyocytes. - Chemical. CAS: 320-67-2. Formula: C8H12N4O5. MW: 244.2. Synthetic. 5-Azacytidine, a chemical analogue of the DNA and RNA nucleoside cytidine, is an cell permeable inhibitor of DNA methyltransferases, potentially serving to reverse epigenetic changes. It reduces hypermethylation associated with certain diseases, including myelodysplastic syndromes (IC50s = 2.4 and 2.6microM for in vitro anti-myeloma activity) and cancer (IC50s ~ 0.4microM for inhibiting proliferation of various cancer cell lines). It has a reported half-life of 17 hours and is considerably cytotoxic; it must be incorporated into DNA to covalently trap DNA methyltransferases. Induces demethylation and reactivation of silenced genes. Improves the efficiency of reprogramming of stem cells; induces differentiation of mesenchymal stem cells into cardiomyocytes.
  • SMILES
    OC[C@@H]1[C@@H](O)[C@@H](O)[C@H](N2C=NC(N)=NC2=O)O1
  • Storage Instruction
    2°C to 8°C,-20°C
  • UNSPSC
    12352200