• Compound libraries

    Arrow active
  • Products

    Arrow active
  • EBC main page

  • Search

  • Dyes

  • Impurities

  • Chemical probes

  • Contacts us

  • Pfizer reference compounds

  • Services

  • EBC Libraries
    Icon image 1Signaling Pathways and Protein Classes Related Libraries
    • Angiogenesis Related Ligands
    • Apoptosis Related Ligands
    • Cancer Immunology Related Ligands
    • Cell Cycle Related Ligands
    • Epigenetics Related Ligands
    • GPCR-binding Ligands
    • Growth Factors and Cytokines Ligands
    • Hippo signaling pathway ligands
    • Ion Channel Ligands
    • JAK-STAT Signaling Ligands
    • Kinase Inhibitors
    • Membrane Receptor Ligands
    • Neuronal Signaling Related Ligands
    • Nuclear Hormone Receptor Ligands
    • Protease Inhibitors
    • RNA-Binders
    • RNA-Binding Protein Ligands
    • Signal Transduction Related Ligands
    • Transporter Ligands
    Icon image 2Bioactive Screening Compound Libraries
    • Bioactive Compounds I
    • Bioactive Compounds II
    • Bioactive Compounds III
    • Bioactive Compounds Max
    • Flavour and Fragrance Compounds
    • High-Potency Chemical Probes
    • Natural Product Derivatives
    • Natural Products
    • QED Bioactive Compounds
    • Traditional Chinese Medicine Active Compounds
    Icon image 4Disease Related Compound Libraries
    • Anticancer Compounds
    • Antiviral Compounds
    • Cardiotoxic Compounds
    • Most-DILI-Concern Drugs
    • Neurodegenerative Disease Related Compounds
    • Psychoactive Drugs
    Icon image 3Drug Repurposing and Related Libraries
    • Approved Drugs
    • FDA Approved and Potential Drugs
    • FDA Approved Drugs
    • Impurity Reference Standards
    • Investigational Drugs
  • Products
    Libraries
    Signaling Pathways and Protein Classes Related LibrariesDisease Related Compound LibrariesBioactive Screening Compound LibrariesDrug Repurposing and Related Libraries
    Categorized products
    AgonistsInhibitors
    Reagents for Chemical Biology
    Bioorthogonal ReagentsPhotoaffinity Labeling (PAL)
    Bioorthogonal ReagentsPhotoaffinity Labeling (PAL)Drugs & Investigational CompoundsExploratory Compounds & Research ToolsMarine ProductsPesticides and pollutantsPfizer Reference CompoundsAntiviral Compounds
    Drugs and impuritiesChemical probes
    Dyes
  • Drugs & Impurities
  • Chemical probes
  • Services
  • Dyes
  • Search
  • Pfizer reference compounds
LogoEnamine store logo
Logo
  • Terms of Service
  • Privacy Policy
  • Publications
  • Contact us
  • About us
Enamine store logo

© 2026 Copyright Enamine

Back

Product details:

Aztreonam

Molecule product

ID

EBC-27089

|

PF-02537520

CAS

78110-38-0

Purity

95%

Aztreonam is a synthetic monocyclic beta-lactam antibiotic, which has a very high affinity for penicillin-binding protein 3. It is used to treat Gram-negative aerobic bacteria infection.

Properties

cLogP:0.337
MW:435.052
Pharmacopoeia:FDA

Name

Aztreonam

Smiles

C[C@H]1[C@H](NC(=O)/C(=N\OC(C)(C)C(=O)O)/C2=CSC(N)=N2)C(=O)N1S(=O)(=O)O

Targets

Please log in to see this information

Licensing Information

Sold for research purposes under agreement from Pfizer Inc.

About Aztreonam (CAS 78110-38-0)

Aztreonam is a synthetic monobactam antibiotic widely used in antibacterial research focused on Gram-negative aerobic pathogens. In scientific catalogs and procurement systems, it is commonly identified by CAS 78110-38-0 and 78110-38-0. Researchers also search aztreonam, aztreonam structure, aztreonam chemical structure, Pfizer aztreonam, and aztreonam Pfizer when aligning internal compound records with published data and supplier documentation. According to technical supplier information, Aztreonam molecular formula is C13H17N5O8S2 and its molecular weight is 435.43, making structural verification especially important for teams comparing analytical data, reference materials, and product specifications.

Application of Aztreonam

In research settings, aztreonam is applied in microbiology, anti-infective screening, beta-lactam resistance studies, and host-pathogen interaction models. Its relevance comes from a well-established activity profile against Gram-negative aerobic bacteria and from its value as a reference molecule in studies of antibiotic stability and susceptibility. Because it is a recognized antibacterial tool compound, aztreonam is useful in workflows that examine monotherapy effects, combination responses, and the relationship between bacterial burden and cellular protection in infection-related systems. This makes it suitable for discovery teams that need a defined and traceable compound for mechanism-oriented antibacterial research.

Biological Activity

Supplier reference pages describe aztreonam as active against Gram-negative aerobic bacterial infection models and note its use as a bacterial chemical in research. Mechanistic summaries further report that the compound can reduce colony-forming units in selected strains and, in some cystic fibrosis airway cell models, lower biofilm burden while helping preserve monolayer integrity. These details matter for product-oriented content because researchers reviewing aztreonam structure and aztreonam chemical structure are often also checking whether the biological profile matches infection, resistance, or biofilm-related applications relevant to their assay design.

Biochemical and Physiological Actions

At the biochemical level, aztreonam belongs to the beta-lactam class and is notable for its interactions with beta-lactamases. Selleck’s technical summary states that aztreonam is hydrolyzed at measurable rates by selected class A beta-lactamases, while remaining highly stable to the common class C cephalosporinase produced by Citrobacter freundii and by acting as both a competitive and time-dependent inhibitor of that enzyme. The same source also notes synergistic effects when combined with clindamycin in certain bacterial settings. Together, these properties make aztreonam relevant for studies of enzyme stability, resistance mechanisms, and antibacterial combination strategies.

Features and Benefits of Aztreonam

  • Clearly defined identifiers, including CAS 78110-38-0, Aztreonam molecular formula, and documented structural data
  • Recognized activity in Gram-negative antibacterial research and beta-lactamase-focused studies
  • Useful for screening, reference comparison, biofilm-related work, and combination-response experiments

For EBC-27089, aztreonam offers a strong combination of technical clarity and research relevance. Its established antibacterial profile, documented enzyme-related behavior, and searchable identity across supplier systems support confident selection for microbiology and anti-infective discovery workflows.

Synonyms

ATM | Aztreonam | azthreonam

Transportation & Handlings
Storage temperature:RT
Transport temperature:Standard
Dangerous goods:Yes
Solubility

No data available

Purity & Quality Control

The compound has purity validated by NMR and/or LCMS methods.

Prices

1 mg

$37

2 mg

$39

5 mg

$41

10 mg

$43

15 mg

$45

20 mg

$48

25 mg

$53

30 mg

$55

35 mg

$58

40 mg

$60

45 mg

$63

50 mg

$65

75 mg

$68

100 mg

$POA

Quantity

-

1

+

Total amount

$ 41

Your current project

This compound is considered a Dangerous good for shipping. Our team will contact you with details on lead time and costs

In Stock

Synonyms

ATM | Aztreonam | azthreonam

Transportation & Handlings
Storage temperature:RT
Transport temperature:Standard
Dangerous goods:Yes
Solubility

No data available

Purity & Quality Control

The compound has purity validated by NMR and/or LCMS methods.

Target activity features

It should be emphasized that the product may be active against a larger number of targets than shown on the card. The information represented here refers to the targets with the largest value of pX or the targets with ΔpX less than 1.5 from the largest pX value.