Drug pipeline
Full profile accessExplore the programs pursuing this target and their development progress.
- Drug candidates
- Developers
- Development stage
Target intelligence / Profile preview
This entry encompasses both cytidine deaminase (CDA) and DNA polymerase alpha (POLA) as the key targets relevant to the mechanism of action and metabolism of cytarabine. CDA is an enzyme responsible for inactivating cytarabine by deamination. DNA polymerase alpha is inhibited by the active triphosphate form of cytarabine, which gets incorporated into DNA, disrupting DNA synthesis and leading to cell death. This dual mechanism is crucial for cytarabine's antileukemic effects. Genetic variations in CDA can influence the drug's efficacy and toxicity.
Cytidine deaminase metabolizes/inactivates cytarabine; DNA polymerase alpha is inhibited by cytarabine triphosphate incorporation into DNA during replication, leading to chain termination or faulty elongation.
5 more in the full profile.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Explore the programs pursuing this target and their development progress.
Follow the clinical studies evaluating therapies directed at this target.
Compare approaches across drug candidates, modalities, and indications.
Investigate the research and source evidence behind target biology and development.
Explore patent activity around therapies and technologies addressing this target.
Connect target biology, drug development, and emerging evidence in your research.
See how Gosset can support your research on Cytidine Deaminase and DNA Polymerase Alpha (Cytarabine Targets) (CDA & POLA).