Dicloxacillin Sodium
The sodium salt form of dicloxacillin, a beta-lactamase-stable penicillin antibiotic used for skin infections and other conditions caused by beta-lactamase-producing staphylococci. It is taken by mouth and well tolerated.
Berat Molekul
492,3000 g/mol
TPSA
141,00 Ų
Area Terapeutik
Mekanisme Kerja
Inhibits bacterial cell wall synthesis by binding to penicillin-binding proteins (PBPs), preventing transpeptidation and cross-linking of peptidoglycan chains. This weakens the bacterial cell wall, leading to osmotic lysis and cell death.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Inhibits bacterial cell wall synthesis by binding to penicillin-binding proteins (PBPs), preventing transpeptidation and cross-linking of peptidoglycan chains. This weakens the bacterial cell wall, leading to osmotic lysis and cell …
Struktur 2D
Cite this structure
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SMILES
Cc1onc(-c2c(Cl)cccc2Cl)c1C(=O)N[C@@H]1C(=O)N2[C@@H]1SC(C)(C)[C@@H]2C(=O)[O-].O.[Na+]
InChI
InChI=1S/C19H17Cl2N3O5S.Na.H2O/c1-7-10(12(23-29-7)11-8(20)5-4-6-9(11)21)15(25)22-13-16(26)24-14(18(27)28)19(2,3)30-17(13)24;;/h4-6,13-14,17H,1-3H3,(H,22,25)(H,27,28);;1H2/q;+1;/p-1/t13-,14+,17-;;/m1../s1
Molecular Formula
C19H16Cl2N3NaO5S
HBD / HBA
1 / 7
Ikatan yang Dapat Dirotasi
4
Atom Berat
31
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 dicloxacillin, a beta-lactamase-stable penicillin antibiotic used for skin infections and other conditions caused by beta-lactamase-producing staphylococci. It is taken by mouth and well tolerated.
Inhibits bacterial cell wall synthesis by binding to penicillin-binding proteins (PBPs), preventing transpeptidation and cross-linking of peptidoglycan chains. This weakens the bacterial cell wall, leading to osmotic lysis and cell death.
Yes, Dicloxacillin Sodium 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). CHEMBL1200701. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 23667628. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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