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macrolides  (Pfizer Inc)

 
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    Pfizer Inc macrolides
    Macrolides, supplied by Pfizer Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/macrolides/product/Pfizer Inc
    Average 86 stars, based on 1 article reviews
    macrolides - by Bioz Stars, 2026-05
    86/100 stars

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    A The temporal degradation curves of the five macrolide antibiotics were OCA_1, reflecting the difference in the strength and weakness of esterases in the degradation of different types of antibiotics. The highest degradation rate was observed for tylosin, followed by tilmicosin. Data are given as mean ± SD, n = 3. B . Analysis of the plate inhibition zones of five macrolide antibiotics against Staphylococcus aureus <t>ATCC</t> <t>25923</t> following hydrolysis by OCA-1.
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    <t>Macrolide</t> susceptibility of B. pertussis isolates in Shanghai, 2018–2024. Stacked bars indicate the annual percentage of macrolide-sensitive B. pertussis (MSBP) and macrolide-resistant B. pertussis (MRBP) isolates, with the leftmost bar showing the overall (“Total”) distribution. Blue segments denote MSBP (ERY/AZM/CLR <t>MIC</t> ≤1 mg/L) and orange segments denote MRBP (ERY/AZM/CLR MIC ≥256 mg/L); the number within each segment indicates the count of isolates. The y-axis shows percentage of isolates, and the x-axis shows year of collection.
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    <t>Macrolide</t> susceptibility of B. pertussis isolates in Shanghai, 2018–2024. Stacked bars indicate the annual percentage of macrolide-sensitive B. pertussis (MSBP) and macrolide-resistant B. pertussis (MRBP) isolates, with the leftmost bar showing the overall (“Total”) distribution. Blue segments denote MSBP (ERY/AZM/CLR <t>MIC</t> ≤1 mg/L) and orange segments denote MRBP (ERY/AZM/CLR MIC ≥256 mg/L); the number within each segment indicates the count of isolates. The y-axis shows percentage of isolates, and the x-axis shows year of collection.
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    <t>Macrolide</t> susceptibility of B. pertussis isolates in Shanghai, 2018–2024. Stacked bars indicate the annual percentage of macrolide-sensitive B. pertussis (MSBP) and macrolide-resistant B. pertussis (MRBP) isolates, with the leftmost bar showing the overall (“Total”) distribution. Blue segments denote MSBP (ERY/AZM/CLR <t>MIC</t> ≤1 mg/L) and orange segments denote MRBP (ERY/AZM/CLR MIC ≥256 mg/L); the number within each segment indicates the count of isolates. The y-axis shows percentage of isolates, and the x-axis shows year of collection.
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    Image Search Results


    A The temporal degradation curves of the five macrolide antibiotics were OCA_1, reflecting the difference in the strength and weakness of esterases in the degradation of different types of antibiotics. The highest degradation rate was observed for tylosin, followed by tilmicosin. Data are given as mean ± SD, n = 3. B . Analysis of the plate inhibition zones of five macrolide antibiotics against Staphylococcus aureus ATCC 25923 following hydrolysis by OCA-1.

    Journal: npj Antimicrobials and Resistance

    Article Title: Functional characterization of macrolide esterase from cyanobacteria and their potential dissemination risk

    doi: 10.1038/s44259-026-00182-y

    Figure Lengend Snippet: A The temporal degradation curves of the five macrolide antibiotics were OCA_1, reflecting the difference in the strength and weakness of esterases in the degradation of different types of antibiotics. The highest degradation rate was observed for tylosin, followed by tilmicosin. Data are given as mean ± SD, n = 3. B . Analysis of the plate inhibition zones of five macrolide antibiotics against Staphylococcus aureus ATCC 25923 following hydrolysis by OCA-1.

    Article Snippet: Analysis of the plate inhibition zones of five macrolide antibiotics against Staphylococcus aureus ATCC 25923 following hydrolysis by OCA-1.

    Techniques: Inhibition

    Macrolide susceptibility of B. pertussis isolates in Shanghai, 2018–2024. Stacked bars indicate the annual percentage of macrolide-sensitive B. pertussis (MSBP) and macrolide-resistant B. pertussis (MRBP) isolates, with the leftmost bar showing the overall (“Total”) distribution. Blue segments denote MSBP (ERY/AZM/CLR MIC ≤1 mg/L) and orange segments denote MRBP (ERY/AZM/CLR MIC ≥256 mg/L); the number within each segment indicates the count of isolates. The y-axis shows percentage of isolates, and the x-axis shows year of collection.

    Journal: Journal of Clinical Microbiology

    Article Title: Genomic surveillance reveals global spread of macrolide-resistant Bordetella pertussis linked to vaccine changes

    doi: 10.1128/jcm.01064-25

    Figure Lengend Snippet: Macrolide susceptibility of B. pertussis isolates in Shanghai, 2018–2024. Stacked bars indicate the annual percentage of macrolide-sensitive B. pertussis (MSBP) and macrolide-resistant B. pertussis (MRBP) isolates, with the leftmost bar showing the overall (“Total”) distribution. Blue segments denote MSBP (ERY/AZM/CLR MIC ≤1 mg/L) and orange segments denote MRBP (ERY/AZM/CLR MIC ≥256 mg/L); the number within each segment indicates the count of isolates. The y-axis shows percentage of isolates, and the x-axis shows year of collection.

    Article Snippet: Quality control for macrolide MIC testing was performed with Streptococcus pneumoniae ATCC 49619 in accordance with CLSI recommendations ( , ).

    Techniques:

    Maximum-likelihood phylogeny of 178 B. pertussis isolates from Shanghai (2018–2024). Branches are colored by ptxP allele clade: ptxP1 (magenta) and macrolide-resistant ptxP3 (green).

    Journal: Journal of Clinical Microbiology

    Article Title: Genomic surveillance reveals global spread of macrolide-resistant Bordetella pertussis linked to vaccine changes

    doi: 10.1128/jcm.01064-25

    Figure Lengend Snippet: Maximum-likelihood phylogeny of 178 B. pertussis isolates from Shanghai (2018–2024). Branches are colored by ptxP allele clade: ptxP1 (magenta) and macrolide-resistant ptxP3 (green).

    Article Snippet: Quality control for macrolide MIC testing was performed with Streptococcus pneumoniae ATCC 49619 in accordance with CLSI recommendations ( , ).

    Techniques: