Cytarabine, known as cytosine arabinoside, is a chemotherapy medication used to treat acute myeloid leukemia, acute lymphocytic leukemia, chronic myelogenous leukemia, and non-Hodgkin's lymphoma.
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Cytarabine, known as cytosine arabinoside, is a chemotherapy medication used to treat acute myeloid leukemia, acute lymphocytic leukemia, chronic myelogenous leukemia, and non-Hodgkin's lymphoma.
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Cytarabine is in the antimetabolite and nucleoside analog families of medication.
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Cytarabine was patented in 1960 and approved for medical use in 1969.
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Cytarabine is mainly used in the treatment of acute myeloid leukaemia, acute lymphocytic leukaemia and in lymphomas, where it is the backbone of induction chemotherapy.
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Cytarabine possesses antiviral activity, and it has been used for the treatment of generalised herpesvirus infection.
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Cytarabine is used in the study of the nervous system to control the proliferation of glial cells in cultures, the amount of glial cells having an important impact on neurons.
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Cytarabine is the first of a series of cancer drugs that altered the sugar component of nucleosides.
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Cytarabine is often given by continuous intravenous infusion, which follows a biphasic elimination – initial fast clearance rate followed by a slower rate of the analog.
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Cytarabine is rapidly deaminated by cytidine deaminase in the serum into the inactive uracil derivative.
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Cytarabine-5´-monophosphate is deaminated by deoxycytidylate deaminase, leading to the inactive uridine-5´-monophosphate analog.
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Cytarabine is able to inhibit herpesvirus and vaccinia virus replication in cells during tissue culture.
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Cytarabine was first synthesized in 1959 by Richard Walwick, Walden Roberts, and Charles Dekker at the University of California, Berkeley.
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