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Aztreonam

Synonyms: SQ 26776

Aztreonam (SQ 26776) is a synthetic monocyclic beta-lactam antibiotic, used to treat Gram-negative aerobic bacteria infection.

Aztreonam Chemical Structure

Aztreonam Chemical Structure

CAS: 78110-38-0

Selleck's Aztreonam has been cited by 3 publications

Purity & Quality Control

Batch: Purity: 99.97%
99.97

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Biological Activity

Description Aztreonam (SQ 26776) is a synthetic monocyclic beta-lactam antibiotic, used to treat Gram-negative aerobic bacteria infection.
In vitro
In vitro Aztreonam causes significant suppression of human colony forming unit-erythroid (cfu-e), burst forming unit-erythroid (bfu-e) and colony forming unit-granulocyte macrophage (cfu-gm) at both peak and trough serum concentrations in human bone marrow cells. [1] Aztreonam is hydrolyzed at measurable rates by class A beta-lactamases, a TEM-2 type penicillinase and the Proteus vulgaris cephalosporinase with a broad substraterange. Aztreonam is extremely stable as to the typical class C cephalosporinase of Citrobacter freundii, and acts as a competitive and progressive inhibitor for the beta-lactamase. [2] Aztreonam (AZT) combined with clindamycin (CLDM) has synergistic effects on Staphylococcus aureus, Staphylococcus epidermidis, Streptococcus pneumoniae, and Haemophilus influenzae, which are sensitive or quasi-sensitive to CLDM, in the presence of CLDM at MIC or sub-MIC. [3] Aztreonam reduces the cfu of some strains by 1 log unit without preserving the integrity of cystic fibrosis airway cell monolayers, while decreasing the biofilms of other clinical isolates by 4 log units and protecting the monolayers from being compromised. [4]
In Vivo
In vivo Aztreonam (300 mg/kg) results in a significant decrease in the content of hepatic microsomal P450, while no significant change is observed in hepatic cytochrome b5 content and NADPH-cytochrome c (P450) reductase activity. [5]
NCT Number Recruitment Conditions Sponsor/Collaborators Start Date Phases
NCT04973826 Completed Healthy Pfizer August 20 2021 Phase 1
NCT04775238 Unknown status Nosocomial Infections Sohag University February 27 2021 Not Applicable
NCT04486625 Completed Renal Insufficiency Pfizer August 10 2020 Phase 1
NCT03696290 Recruiting Bronchiectasis Adult University of Dundee|Gilead Sciences October 19 2019 Phase 2
NCT03867734 Completed Gonorrhea of Pharynx|Gonorrhea University of Washington April 5 2019 Phase 2|Phase 3

Chemical lnformation & Solubility

Molecular Weight 435.43 Formula

C13H17N5O8S2
CAS No. 78110-38-0 SDF Download Aztreonam SDF
Smiles CC1C(C(=O)N1S(=O)(=O)O)NC(=O)C(=NOC(C)(C)C(=O)O)C2=CSC(=N2)N
Storage (From the date of receipt)

In vitro
Batch:

DMSO : 87 mg/mL ( (199.8 mM)； Moisture-absorbing DMSO reduces solubility. Please use fresh DMSO.)

Water : Insoluble

Ethanol : Insoluble


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In vivo
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Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

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Tech Support

Answers to questions you may have can be found in the inhibitor handling instructions. Topics include how to prepare stock solutions, how to store inhibitors, and issues that need special attention for cell-based assays and animal experiments.

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