Weight | 533.961 g/mol |
---|---|
Formula | C26H28ClNO9 |
Hydrogen Acceptors | 10 |
Hydrogen Donors | 5 |
Aromatic Rings | 2 |
Rotatable Bonds | 3 |
idarubicin hydrochloride (57852-57-0)
Idarubicin · IMI30 · 4-Demethoxydaunorubicin
Score:
#1483 in Biochemistry
,
#3484 in Biology
,
#4360 in Chemistry
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- Molecular Remission in PML/RAR-Positive Acute Promyelocytic Leukemia by Combined All-trans Retinoic Acid and Idarubicin (AIDA) Therapy (Blood, 1997)
- Cytarabine Plus Idarubicin or Daunorubicin as Induction and Consolidation Therapy for Previously Untreated Adult Patients With Acute Myeloid Leukemia (Blood, 1992)
- Results of a randomized trial comparing idarubicin and cytosine arabinoside with daunorubicin and cytosine arabinoside in adult patients with newly diagnosed acute myelogenous leukemia (Blood, 1991)
- A phase III trial comparing idarubicin and daunorubicin in combination with cytarabine in acute myelogenous leukemia: a Southeastern Cancer Study Group Study. (Journal of Clinical Oncology, 1992)
- Phase I/II Study of Combination Therapy With Sorafenib, Idarubicin, and Cytarabine in Younger Patients With Acute Myeloid Leukemia (Journal of Clinical Oncology, 2010)
- Randomized Phase II Study of Fludarabine + Cytosine Arabinoside + Idarubicin All-Trans Retinoic Acid Granulocyte Colony-Stimulating Factor in Poor Prognosis Newly Diagnosed Acute Myeloid Leukemia and Myelodysplastic Syndrome (Blood, 1999)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Idarubicin
- IMI30
- 4-Demethoxydaunorubicin
- IMI 30
- 4-Desmethoxydaunorubicin
- 4 Desmethoxydaunorubicin
- NSC256439
- NSC 256439
- 4 Demethoxydaunorubicin
- IMI-30
- NSC-256439
-
SMILESCC1C(C(CC(O1)OC2CC(CC3=C(C4=C(C(=C23)O)C(=O)C5=CC=CC=C5C4=O)O)(C(=O)C)O)N)O.Cl
-
InChIKeyJVHPTYWUBOQMBP-UHFFFAOYSA-N
- Pubchem - idarubicin hydrochloride
- Wikipedia - idarubicin hydrochloride
Idarubicin or 4-demethoxydaunorubicin is an anthracycline antileukemic drug. It inserts 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.
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