Durlobactam Sodium
A sodium salt form of durlobactam used in combination therapy to treat multidrug-resistant bacterial infections. Like the parent compound, it inhibits bacterial enzymes that would otherwise inactivate the accompanying antibiotic.
분자량
299.2400 g/mol
TPSA
141.00 Ų
작용 기전
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 …
2D 구조
Cite this structure
Embed this structure
SMILES
CC1=C[C@@H]2CN(C(=O)N2OS(=O)(=O)[O-])[C@@H]1C(N)=O.[Na+]
InChI
InChI=1S/C8H11N3O6S.Na/c1-4-2-5-3-10(6(4)7(9)12)8(13)11(5)17-18(14,15)16;/h2,5-6H,3H2,1H3,(H2,9,12)(H,14,15,16);/q;+1/p-1/t5-,6+;/m1./s1
Molecular Formula
C8H10N3NaO6S
HBD / HBA
1 / 6
회전 가능 결합
3
무거운 원자
19
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.
자주 묻는 질문
A sodium salt form of durlobactam used in combination therapy to treat multidrug-resistant bacterial infections. Like the parent compound, it inhibits bacterial enzymes that would otherwise inactivate the accompanying antibiotic.
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, Durlobactam 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). CHEMBL4297378. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 89851851. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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