Chloramphenicol Sodium Succinate
The sodium succinate ester prodrug of chloramphenicol is hydrolyzed in the body to release active chloramphenicol, suitable for intravenous administration when oral or ophthalmic routes are not feasible. It is used for serious infections such as bacterial meningitis in settings where alternatives are unavailable. Hematological monitoring is essential due to the risk of bone marrow suppression.
Молекулярная масса
445,2000 g/mol
TPSA
162,00 Ų
Механизм действия
Administered as an inactive precursor that is metabolically converted to its active form in the body. This prodrug design improves bioavailability, absorption, or targeted delivery compared to the active compound.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Administered as an inactive precursor that is metabolically converted to its active form in the body. This prodrug design improves bioavailability, absorption, or targeted delivery compared to the active compound.
2D Структура
Cite this structure
Embed this structure
SMILES
O=C([O-])CCC(=O)OC[C@@H](NC(=O)C(Cl)Cl)[C@H](O)c1ccc([N+](=O)[O-])cc1.[Na+]
InChI
InChI=1S/C15H16Cl2N2O8.Na/c16-14(17)15(24)18-10(7-27-12(22)6-5-11(20)21)13(23)8-1-3-9(4-2-8)19(25)26;/h1-4,10,13-14,23H,5-7H2,(H,18,24)(H,20,21);/q;+1/p-1/t10-,13-;/m1./s1
Molecular Formula
C15H15Cl2N2NaO8
HBD / HBA
2 / 8
Вращаемые Связи
9
Тяжёлые Атомы
28
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.
Часто задаваемые вопросы
The sodium succinate ester prodrug of chloramphenicol is hydrolyzed in the body to release active chloramphenicol, suitable for intravenous administration when oral or ophthalmic routes are not feasible. It is used for serious infections such as bacterial meningitis in settings where alternatives are unavailable. Hematological monitoring is essential due to the risk of bone marrow suppression.
Administered as an inactive precursor that is metabolically converted to its active form in the body. This prodrug design improves bioavailability, absorption, or targeted delivery compared to the active compound.
Yes, Chloramphenicol Sodium Succinate 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). CHEMBL1200729. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 656833. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
Медицинский отказ от ответственности
This content is for educational and informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider before making medication decisions.
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