Ceftazidime Sodium

CHEMBL1200768 Phase 4 Disetujui Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
568.6 g/mol
LogP
Phase
4

The sodium salt form of ceftazidime, prepared for intravenous or intramuscular injection to treat serious gram-negative infections. It shares the anti-Pseudomonal coverage of the parent drug and is commonly used in intensive care settings. When used in combination with avibactam, it extends coverage to carbapenem-resistant Enterobacteriaceae.

Berat Molekul

568,6000 g/mol

TPSA

248,00 Ų

Area Terapeutik

Mekanisme Kerja

Selectively blocks angiotensin II type 1 (AT1) receptors, preventing the vasoconstrictive and aldosterone-secreting effects of angiotensin II. This results in vasodilation, reduced sodium retention, and decreased blood pressure.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mekanisme

Selectively blocks angiotensin II type 1 (AT1) receptors, preventing the vasoconstrictive and aldosterone-secreting effects of angiotensin II. This results in vasodilation, reduced sodium retention, and decreased blood pressure.

Struktur 2D

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SMILES

CC(C)(O/N=C(\C(=O)N[C@@H]1C(=O)N2C(C(=O)[O-])=C(C[n+]3ccccc3)CS[C@H]12)c1csc(N)n1)C(=O)[O-].[Na+]

InChI

InChI=1S/C22H22N6O7S2.Na/c1-22(2,20(33)34)35-26-13(12-10-37-21(23)24-12)16(29)25-14-17(30)28-15(19(31)32)11(9-36-18(14)28)8-27-6-4-3-5-7-27;/h3-7,10,14,18H,8-9H2,1-2H3,(H4-,23,24,25,29,31,32,33,34);/q;+1/p-1/b26-13-;/t14-,18-;/m1./s1

Molecular Formula

C22H21N6NaO7S2

HBD / HBA

2 / 12

Ikatan yang Dapat Dirotasi

7

Atom Berat

38

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

The sodium salt form of ceftazidime, prepared for intravenous or intramuscular injection to treat serious gram-negative infections. It shares the anti-Pseudomonal coverage of the parent drug and is commonly used in intensive care settings. When used in combination with avibactam, it extends coverage to carbapenem-resistant Enterobacteriaceae.

Selectively blocks angiotensin II type 1 (AT1) receptors, preventing the vasoconstrictive and aldosterone-secreting effects of angiotensin II. This results in vasodilation, reduced sodium retention, and decreased blood pressure.

Yes, Ceftazidime Sodium is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.

{# References & Data Sources section for drug detail pages. Renders standard pharmacological database links plus the drug's data_sources field. #}

References & Data Sources

  • ChEMBL — European Bioinformatics Institute (EBI). CHEMBL1200768. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 5488543. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.

Penyangkalan Medis

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.

Data sources: ChEMBL, PubChem, DailyMed.