Cytarabine, also called cytosine arabinoside or ara-C, is a chemotherapy medicine used to treat acute myeloid leukemia, acute lymphocytic leukemia, chronic myelogenous leukemia and non-Hodgkin lymphoma. It belongs to the antimetabolite and nucleoside analog families of drugs. After it is rapidly converted inside the body to cytarabine 5' triphosphate, it blocks DNA polymerase and interferes with DNA synthesis, damaging DNA while cells are dividing in the S phase of the cell cycle. It is given by injection into a vein, under the skin, or into the cerebrospinal fluid. The compound was patented in 1960 and received United States approval in June 1969, and it is sold under brand names including Cytosar-U and Depocyt.
Facts
Classification
Approval Status ATC ClassSourced to the subject's own accountL: Antineoplastic and Immunomodulating Agents 2 Route of Administration WHO Essential MedicineSourced to the subject's own account First Approved / Isolated Year Connections
Sources
1. Cytarabine (Wikipedia)
https://en.wikipedia.org/wiki/Cytarabine, lead section
(CML), and non-Hodgkin's lymphoma. It is given by injection into a vein, under the skin, or into the cerebrospinal fluid. There is a liposomal formulation for which there is tentative evidence of better outcomes in lymphoma involving the meninges.
- Regulatory approval status
View the Source2. Anatomical Therapeutic Chemical Classification System (Wikipedia)
WikipediaFirst-level anatomical group codes, Code LQuote, First-level anatomical group codes, Code L
Antineoplastic and immunomodulating agents
View the Source 3. Wikipedia
Wikipedia contributors, Wikimedia Foundation
4. WHO Model List of Essential Medicines (Wikipedia)
WikipediaWHO Model List of Essential Medicines, Cytotoxic medicines sectionQuote, WHO Model List of Essential Medicines, Cytotoxic medicines section
Cytarabine
View the Source 5. FDA: Cytosar-U (cytarabine) Label
Approval historyQuote, Approval history
Cytarabine (Cytosar-U) was approved by the FDA in June 1969
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