Idarubicin

Anthracycline antileukemic drug
  • L01DB06 (WHO)
Legal statusLegal status
  • US: ℞-only
Pharmacokinetic dataProtein binding97%Elimination half-life22 hoursIdentifiers
  • (1S,3S)-3-acetyl-3,5,12-trihydroxy-6,11-dioxo-1,2,3,4,6,11-hexahydrotetracen-1-yl 3-amino-2,3,6-trideoxo-α-L-lyxo-hexopyranoside
CAS Number
  • 58957-92-9 checkY
PubChem CID
  • 42890
IUPHAR/BPS
  • 7083
DrugBank
  • DB01177 checkY
ChemSpider
  • 39117 checkY
UNII
  • ZRP63D75JW
KEGG
  • D08062 checkY
ChEBI
  • CHEBI:42068 checkY
ChEMBL
  • ChEMBL1117 checkY
CompTox Dashboard (EPA)
  • DTXSID7023142 Edit this at Wikidata
Chemical and physical dataFormulaC26H27NO9Molar mass497.500 g·mol−13D model (JSmol)
  • Interactive image
  • O=C2c1c(O)c5c(c(O)c1C(=O)c3ccccc23)C[C@@](O)(C(=O)C)C[C@@H]5O[C@@H]4O[C@H]([C@@H](O)[C@@H](N)C4)C
  • InChI=1S/C26H27NO9/c1-10-21(29)15(27)7-17(35-10)36-16-9-26(34,11(2)28)8-14-18(16)25(33)20-19(24(14)32)22(30)12-5-3-4-6-13(12)23(20)31/h3-6,10,15-17,21,29,32-34H,7-9,27H2,1-2H3/t10-,15-,16-,17-,21+,26-/m0/s1 checkY
  • Key:XDXDZDZNSLXDNA-TZNDIEGXSA-N checkY
  (verify)

Idarubicin /ˌdəˈrbɪsɪn/ or 4-demethoxydaunorubicin is an anthracycline antileukemic drug. It inserts[1] itself into DNA and prevents DNA unwinding by interfering with the enzyme topoisomerase II. It is an analog of daunorubicin, but the absence of a methoxy group increases its fat solubility and cellular uptake.[2] Similar to other anthracyclines, it also induces histone eviction from chromatin.[3]

It belongs to the family of drugs called antitumor antibiotics.

It is currently combined with cytosine arabinoside as a first line treatment of acute myeloid leukemia.[4]

It is used for treatment of acute lymphoblastic leukemia and chronic myelogenous leukemia in blast crisis.[5]

It is distributed under the trade names Zavedos (UK) and Idamycin (USA).

Side effects

Diarrhea, stomach cramps, nausea and vomiting are common among patients treated with idarubicin.[6]

References

  1. ^ Miller JP, Stoodley RJ (2013). "Studies directed towards anthracyclinone syntheses: The use of d-glucose as a chiral auxiliary in asymmetric Diels–Alder reactions". J. Saudi Chem. Soc. 17: 29–42. doi:10.1016/j.jscs.2011.02.019.
  2. ^ "Idamycin Package insert" (PDF). Pfizer. January 2006.
  3. ^ Pang B, Qiao X, Janssen L, Velds A, Groothuis T, Kerkhoven R, et al. (2013). "Drug-induced histone eviction from open chromatin contributes to the chemotherapeutic effects of doxorubicin". Nature Communications. 4: 1908. Bibcode:2013NatCo...4.1908P. doi:10.1038/ncomms2921. PMC 3674280. PMID 23715267.
  4. ^ Arwanih EY, Louisa M, Rinaldi I, Wanandi SI (December 2022). "Resistance Mechanism of Acute Myeloid Leukemia Cells Against Daunorubicin and Cytarabine: A Literature Review". Cureus. 14 (12): e33165. doi:10.7759/cureus.33165. PMC 9885730. PMID 36726936.
  5. ^ Katzung BG (2017-11-30). Basic & clinical pharmacology. McGraw-Hill Education. ISBN 9781259641152. OCLC 1009849139.
  6. ^ "Idarubicin Side Effects: Common, Severe, Long Term". Drugs.com. Retrieved 2019-06-21.

External links

  • Idarubicin bound to proteins in the PDB
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SPs/MIs
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Block microtubule assembly
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DNA replication
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antimetabolites
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Folic acid
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Topoisomerase inhibitors
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