Cedazuridine hydrochloride
Based on 1 publication(s) in Google Scholar
Cedazuridine (E7727) (Compound 7a) hydrochloride is an orally active cytidine deaminase (CDA) inhibitor with an IC50 value of 0.4 μM. Cedazuridine hydrochloride can be used for cancer research.
For research use only. We do not sell to patients.
- Formula: C9H15ClF2N2O5
- Molecular Weight:304.68
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Publications Citing Use of MedChemExpress (MCE) Cedazuridine hydrochloride
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Biological Activity
IC50: 0.4 μM (CDA)[1]
Cedazuridine (Compound 7a) exhibits superior acid stability[1].
Cedazuridine (0-10 μM; 72 h) does not enhance effects of AZA (5-Azacytidine, HY-10586) in growth inhibition of AML cell lines[2].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:Female NSGS mice, 6–8 weeks old, human cell line-derived (CDX) and primary patient-derived xenograft (PDX) models[2]
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Dosage:3 mg/kg
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Administration:Oral administration, in combination with 2.5 mg/kg AZA, daily for 7 days
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Result:Led to reduction of leukemic expansion in combination with AZA in a cell line-derived xenograft transplantation, and exhibited preliminary safety and efcacy in a primary AML PDX model.
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Animal Model:NSGS male mice[2]
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Dosage:1, 3, 10 and 30 mg/kg
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Administration:Oral, in combination with 2.5 mg/kg AZA (Pharmacokinetic Studies)
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Result:Dose-dependently increased the AUC of oral AZA and in comparison to dosing of standard i.p. AZA.
| NCT Number | Sponsor | Condition | Start Date |
Phase
|
|---|---|---|---|---|
| NCT01329991 | Plexxikon| | 2011-05 | PHASE1 |
Chemical Information
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Molecular Weight 304.68
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Formula C9H15ClF2N2O5
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SMILES
[H]Cl.FC1([C@H](N(CC[C@@H](O)N2)C2=O)O[C@H](CO)[C@H]1O)F
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Synonyms
E7727 hydrochloride
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Publications (1)
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Journal Impact Factor
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Most Recent
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Cancer Res Commun
Mechanisms Underlying Cedazuridine-Mediated Enhancement of Oral Decitabine Bioavailability. [Abstract]2026 Mar 2. PMID: 41770597
Purity & Documentation
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)