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  2. Anthracycline - Wikipedia

    en.wikipedia.org/wiki/Anthracycline

    Daunorubicin was adopted as the international name. [5] Initially it was seen to have activity against murine tumours and then in clinical trials it was found to be active against leukaemia and lymphomas. Doxorubicin was isolated from a mutated variant of S. peucetius (var. caesius). It differs from daunorubicin only by the addition of a ...

  3. Doxorubicin - Wikipedia

    en.wikipedia.org/wiki/Doxorubicin

    Doxorubicin showed better activity than daunorubicin against mouse tumors, and especially solid tumors. It also showed a higher therapeutic index, yet the cardiotoxicity remained. [50] Doxorubicin and daunorubicin together can be thought of as prototype compounds for the anthracyclines. Subsequent research has led to many other anthracycline ...

  4. Daunorubicin - Wikipedia

    en.wikipedia.org/wiki/Daunorubicin

    Daunorubicin, also known as daunomycin, is a chemotherapy medication used to treat cancer. [2] Specifically it is used for acute myeloid leukemia (AML), acute lymphoblastic leukemia (ALL), chronic myelogenous leukemia (CML), and Kaposi's sarcoma . [ 2 ]

  5. Biosynthesis of doxorubicin - Wikipedia

    en.wikipedia.org/wiki/Biosynthesis_of_doxorubicin

    In contrast, only one known non-wild type species, Streptomyces peucetius subspecies caesius ATCC 27952, was initially found to be capable of producing the more widely used doxorubicin. [1] This strain was created by Arcamone et al. in 1969 by mutating a strain producing daunorubicin, but not DXR, at least in detectable quantities. [2]

  6. Epirubicin - Wikipedia

    en.wikipedia.org/wiki/Epirubicin

    Epirubicin is a 4'-epi-isomer of doxorubicin and a derivative of daunorubicin. As an anthracycline antibiotic it belongs to several chemical classes such as: aminoglycosides , tetracene quinones , p-quinones, primary alpha-hydroxy ketone and tertiary alpha-hydroxy ketones.

  7. Topoisomerase inhibitor - Wikipedia

    en.wikipedia.org/wiki/Topoisomerase_inhibitor

    Idarubicin is able to pass through cell membranes easier than daunorubicin and doxorubicin because it possesses less polar subunits, making it more lipophilic. [ 17 ] [ 66 ] It is hypothesized that doxorubicin, which possesses a hydroxyl group and a methoxy group not present in idarubicin, can form hydrogen bonding aggregates with itself on the ...

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  9. Streptomyces isolates - Wikipedia

    en.wikipedia.org/wiki/Streptomyces_isolates

    Doxorubicin intercalating DNA. Streptomyces, yielded the medicines doxorubicin (Doxil), daunorubicin (DaunoXome), and streptozotocin (Zanosar). Doxorubicin is the precursor to valrubicin (Valstar), myocet, and pirarubicin. Daunorubicin is the precursor to idarubicin (Idamycin), epirubicin (Ellence), and zorubicin. [citation needed]

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