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Ara-C

M.D. Anderson Cancer Center · FDA-approved active Small molecule

Ara-C is a cytidine analog that inhibits DNA synthesis by being incorporated into DNA and blocking cell division, primarily affecting rapidly dividing cancer cells.

Ara-C is a cytidine analog that inhibits DNA synthesis by being incorporated into DNA and blocking cell division, primarily affecting rapidly dividing cancer cells. Used for Acute myeloid leukemia (AML), Acute lymphoblastic leukemia (ALL), Chronic myeloid leukemia (CML) in blast crisis.

At a glance

Generic nameAra-C
Also known asCytarabine, Cytosar-U®, DepoCyt, Cytosine arabinosine hydrochloride, Arabinosylcytosine
SponsorM.D. Anderson Cancer Center
Drug classNucleoside analog, antimetabolite
TargetDNA polymerase, ribonucleotide reductase
ModalitySmall molecule
Therapeutic areaOncology
PhaseFDA-approved

Mechanism of action

Ara-C (cytarabine) is a nucleoside analog that mimics cytidine and becomes incorporated into DNA during the S phase of the cell cycle. Once integrated, it inhibits DNA polymerase and prevents further DNA synthesis, leading to cell death. It is particularly effective against hematologic malignancies where rapidly dividing cells are most vulnerable to disruption of nucleotide metabolism.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results