Drug

D0067 | Idarubicin

Molecular Formula C26H27NO9
Molecular Weight 497.5
Structure
State solid
Route of elimination The drug is eliminated predominately by biliary and to a lesser extent by renal excretion, mostly in the form of idarubicinol.
Protein binding 0.97
Half life 22 hours

L

L01DB06 Idarubicin


[L01DB] Anthracyclines and related substances


[L01D] CYTOTOXIC ANTIBIOTICS AND RELATED SUBSTANCES


[L01] ANTINEOPLASTIC AGENTS


[L] Antineoplastic and immunomodulating agents


Toxicity Dose Time Species Model Method Action Positive criterion Reference
GLUCOSE GALACTOSE IC50 RATIO 7.9 ± 3.3 , 4.2 ± 2.0, 1.9, 11.5 ± 5.7 ,6.2 ± 4.0, 1.9 4hr H9c2 cells high-glucose–galactose cell viability assay with JC-1 mitochondrial membrane potential and ATP-depletion assays (CellTiter-Glo reagent ). glucose/galactose IC50 ratio (JC-1 IC50 in glucose, JC-1 IC50 in galactose, JC-1 glu/gla, ATP IC50 in glucose, ATP IC50 in galactose, ATP glu/gla ) 50

Organism Test type Route Dose (normalized dose) Effect Source
mouse LD50 unreported 4900ug/kg (4.9mg/kg) Biochemical Pharmacology. Vol. 38, Pg. 167, 1989.
mouse LD50 oral 16mg/kg (16mg/kg) Cancer Treatment Reports. Vol. 61, Pg. 893, 1977.
mouse LD50 intraperitoneal 3mg/kg (3mg/kg) Cancer Research. Vol. 48, Pg. 926, 1988.
mouse LD50 intravenous 4mg/kg (4mg/kg) Cancer Treatment Reports. Vol. 61, Pg. 893, 1977.

  • Acute coronary syndrome

  • Acute lymphocytic leukaemia

  • Acute myeloid leukaemia

  • Arrhythmia

  • Cardiac disorder

  • Cardiac failure congestive

  • Chest pain

  • Chronic myeloid leukaemia

  • Gastrointestinal disorder

  • Myocardial infarction

  • Non-Hodgkin's lymphoma

  • Abdominal pain

  • Alopecia

  • Body temperature increased

  • Convulsion

  • Diarrhoea

  • Haemoglobin

  • Haemorrhage

  • Headache

  • Hypersensitivity

  • Infection

  • Mucosal inflammation

  • Nausea

  • Vomiting

  • (1S,3S)-3-acetyl-3,5,12-trihydroxy-6,11-dioxo-1,2,3,4,6,11-hexahydronaphthacen-1-yl 3-amino-2,3,6-trideoxy-alpha-L-lyxo-hexopyranoside (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-trideoxy-alpha-L-lyxo-hexopyranoside (7S,9S)-7-[(2R,4S,5S,6S)-4-azanyl-6-methyl-5-oxidanyl-oxan-2-yl]oxy-9-ethanoyl-6,9,11-tris(oxidanyl)-8,10-dihydro-7H-tetracene-5,12-dione
    (7S,9S)-7-[(2R,4S,5S,6S)-4-azanyl-6-methyl-5-oxidanyl-oxan-2-yl]oxy-9-ethanoyl-6,9,11-tris(oxidanyl)-8,10-dihydro-7H-tetracene-5,12-dione;hydrochloride (7S,9S)-9-acetyl-7-((2R,4S,5S,6S)-4-amino-5-hydroxy-6-methyltetrahydro-2H-pyran-2-yloxy)-6,9,11-trihydroxy-7,8,9,10-tetrahydrotetracene-5,12-dione (7S,9S)-9-acetyl-7-[(2R,4S,5S,6S)-4-amino-5-hydroxy-6-methyl-tetrahydropyran-2-yl]oxy-6,9,11-trihydroxy-8,10-dihydro-7H-tetracene-5,12-dione
    (7S,9S)-9-acetyl-7-[(2R,4S,5S,6S)-4-amino-5-hydroxy-6-methyl-tetrahydropyran-2-yl]oxy-6,9,11-trihydroxy-8,10-dihydro-7H-tetracene-5,12-quinone;hydrochloride (7S,9S)-9-acetyl-7-[(2R,4S,5S,6S)-4-amino-5-hydroxy-6-methyloxan-2-yl]oxy-6,9,11-trihydroxy-8,10-dihydro-7H-tetracene-5,12-dione;hydrochloride (7S,9S)-9-acetyl-7-[[(2R,4S,5S,6S)-4-amino-5-hydroxy-6-methyl-2-oxanyl]oxy]-6,9,11-trihydroxy-8,10-dihydro-7H-tetracene-5,12-dione
    (7S,9S)-9-acetyl-7-[[(2R,4S,5S,6S)-4-amino-5-hydroxy-6-methyl-2-oxanyl]oxy]-6,9,11-trihydroxy-8,10-dihydro-7H-tetracene-5,12-dione;hydrochloride (7S,9S)-9-acetyl-7-{[(2R,4S,5S,6S)-4-amino-5-hydroxy-6-methyloxan-2-yl]oxy}-6,9,11-trihydroxy-5,7,8,9,10,12-hexahydrotetracene-5,12-dione 15158-EP2270008A1
    15158-EP2272827A1 15158-EP2275420A1 15158-EP2277879A1
    15158-EP2280012A2 15158-EP2281815A1 15158-EP2289892A1
    15158-EP2292615A1 15158-EP2292617A1 15158-EP2295055A2
    15158-EP2295416A2 15158-EP2295426A1 15158-EP2295427A1
    15158-EP2298748A2 15158-EP2298764A1 15158-EP2298765A1
    15158-EP2301928A1 15158-EP2301933A1 15158-EP2305640A2
    15158-EP2305642A2 15158-EP2305671A1 15158-EP2308833A2
    15158-EP2308855A1 15158-EP2311453A1 15158-EP2311808A1
    15158-EP2311825A1 15158-EP2311827A1 15158-EP2311829A1
    15158-EP2311842A2 15158-EP2316832A1 15158-EP2316833A1
    4-DEMETHOXY-DAUNORUBICIN 4-DMD 4-Demethoxydaunomycin
    4-Demethoxydaunorubicin 4-Demethoxydaunorubicin|||IMI-30|||NSC-256439|||(7S,9S)-9-Acetyl-7-[(2R,4S,5S,6S)-4-amino-5-hydroxy-6-methyloxan-2-yl]oxy-6,9,11-trihydroxy-8,10-dihydro-7H-tetracene-5,12-dione 4-Desmethoxydaunorubicin
    5,12-Naphthacenedione, 7,8,9,10-tetrahydro-9-acetyl-7-((3-amino-2,3,6-trideoxy-.alpha.-L-lyxo-hexopyranosyl)oxy)-6,9,11-trihydroxy-, (7S-cis)- 5,12-Naphthacenedione, 7,8,9,10-tetrahydro-9-acetyl-7-((3-amino-2,3,6-trideoxy-alpha-L-lyxo-hexopyranosyl)oxy)-6,9,11-trihydroxy-, (7S-cis)- 5,12-Naphthacenedione, 9-acetyl-7-((3-amino-2,3,6-trideoxy-alpha-L-lyxo-hexopyranosyl)oxy)-7,8,9,10-tetrahydro-6,9,11-trihydroxy-, (7S-cis)-
    58957-92-9 957I929 A832088
    AB00698511-06 AB00698511-08 AB00698511-09
    AB00698511-10 AB00698511_11 AC-9384
    AKOS015895563 API0002970 BCP9000773
    BCPP000207 BDBM58490 BRD-K69650333-001-01-1
    BRD-K69650333-001-02-9 BRD-K69650333-003-14-0 C-22925
    C26H27NO9 CC-29462 CCG-204689
    CCRIS 5083 CHEBI:42068 CHEMBL1117
    D08062 DB01177 DM5
    DTXSID7023142 Daunomycin, 4-demethoxy- EU-0100600
    FT-0621481 GTPL7083 HMS2089D05
    HMS3261H22 I 1656 IDARUBICIN
    IDARUBICIN(Hydrochloride form) IMI 30 IMI-30
    Idamycin Idarubicin (INN) Idarubicin Hcl
    Idarubicin [INN:BAN] Idarubicin hydrochloride, solid Idarubicin, United States Pharmacopeia (USP) Reference Standard
    Idarubicina Idarubicina [INN-Spanish] Idarubicine
    Idarubicine [INN-French] Idarubicinum Idarubicinum [INN-Latin]
    KBioSS_002388 LP00600 LS-94015
    Lopac0_000600 MLS001401448 NCGC00093976-01
    NCGC00093976-02 NCGC00093976-03 NCGC00093976-04
    NCGC00093976-05 NCGC00261285-01 NSC 256439
    NSC-256439 Q1063862 SC-17016
    SCHEMBL3750 SMR000466355 SR-01000075934
    SR-01000075934-1 Tox21_500600 UNII-ZRP63D75JW
    XDXDZDZNSLXDNA-TZNDIEGXSA-N Z-3092 ZINC3920266
    ZRP63D75JW Zavedos (TN) cid_636362

    DrugBank Name Idarubicin
    DrugBank DB01177
    CAS Number 57852-57-0, 58957-92-9
    PubChem Compound 42890
    KEGG Drug D08062
    PubChem.Substance 46506973
    ChEBI 42068
    PharmGKB PA449961
    ChemSpider 39117
    BindingDB 58490.0
    TTD DAP000050
    Wikipedia Idarubicin
    HET DM5
    DPD 1745

    1. Dykens et al. (2007)