Cedazuridine
A cytidine deaminase inhibitor that is co-administered with the chemotherapy agent decitabine to block its degradation in the gut and increase oral bioavailability. This combination allows for oral administration of decitabine, which previously required intravenous infusion. It is used in adults with myelodysplastic syndromes and chronic myelomonocytic leukemia.
Berat Molekul
268,2100 g/mol
LogP
-1,10
TPSA
102,00 Ų
Lipinski RO5
Lulus
Area Terapeutik
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Struktur 2D
Cite this structure
Embed this structure
SMILES
O=C1N[C@H](O)CCN1[C@@H]1O[C@H](CO)[C@@H](O)C1(F)F
InChI
InChI=1S/C9H14F2N2O5/c10-9(11)6(16)4(3-14)18-7(9)13-2-1-5(15)12-8(13)17/h4-7,14-16H,1-3H2,(H,12,17)/t4-,5-,6-,7-/m1/s1
Molecular Formula
C9H14F2N2O5
HBD / HBA
4 / 7
Ikatan yang Dapat Dirotasi
2
Atom Berat
18
No targets recorded
Target interaction data is not yet available for this drug.
No interactions recorded
Drug interaction data is not yet available for this compound.
No side effects recorded
Side effect data is not yet available for this drug.
Pertanyaan yang Sering Diajukan
A cytidine deaminase inhibitor that is co-administered with the chemotherapy agent decitabine to block its degradation in the gut and increase oral bioavailability. This combination allows for oral administration of decitabine, which previously required intravenous infusion. It is used in adults with myelodysplastic syndromes and chronic myelomonocytic leukemia.
Yes, Cedazuridine is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL3237547. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 25267009. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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