Active Ingredient History

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  • Now
Decitabine was first synthesized by Pliml and Sorm in the Institute of Organic Chemistry, Czechoslovak Academy of Sciences in 1964. Later, the drug was approved by FDA for the treatment of myelodysplastic syndromes in patients with cancer. Upon administration the decitabine is metabolized to the active phosphorylated metabolite which is incorporated into DNA and thus inhibits DNA methyltransferase (decitabine deplete DNMT1).   NCATS

  • SMILES: NC1=NC(=O)N(C=N1)[C@H]2C[C@H](O)[C@@H](CO)O2
  • InChIKey: XAUDJQYHKZQPEU-KVQBGUIXSA-N
  • Mol. Mass: 228.2053
  • ALogP: -2.14
  • ChEMBL Molecule:
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Drug Pricing (per unit)

United States

$1.4872 - $182.2100
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Note: This drug pricing data is preliminary, incomplete, and may contain errors.

Combination drugs

( decitabine (dacogen), cedazuridine (Inqovi) - other name: decitabine and cedazuridine )
2'-deoxy-5-azacytidine | 4-amino-1-(2-deoxy-beta-d-erythro-pentofuranosyl)-s-triazin-2(1h)-one | 5-aza-2'-deoxycytidine | 5-azadeoxycytidine | 5-aza-deoxycytidine | 5-deoxyazacytidine | azadc | azadc compound | dac | dacogen | decitabine | decitabine mesilate | decitabine mesylate | decitabine plus modified bucy | dezocitidine | jnj-30979754 | nsc 127716 | nsc-127716

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