staphylococcus aureus atcc 6538 p fda 209p sa (ATCC)

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ATCC staphylococcus aureus atcc 6538 p fda 209p sa
Bacterial resistance studies of compounds 8c , 12c–d , 13a – d , 14c , 15c , norfloxacin , amoxicillin against S. aureus ATCC <t>209P.</t>

Bacterial resistance studies of compounds 8c , 12c–d , 13a – d , 14c , 15c , norfloxacin , amoxicillin against S. aureus ATCC <t>209P.</t>

Staphylococcus Aureus Atcc 6538 P Fda 209p Sa, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 3513 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/staphylococcus+aureus+atcc+6538+p/Staphylococcus+aureus+subsp%2E+aureus+Rosenbach/pmc13207327-154-18-20
Average 99 stars, based on 3513 article reviews

staphylococcus aureus atcc 6538 p fda 209p sa - by Bioz Stars, 2026-10

99/100 stars

Images

1) Product Images from "Phosphonamidates Integrating Sterically Hindered Phenols with Membrane-Active Cations: A Redox-Activated Approach to Antimicrobial Agents"

Article Title: Phosphonamidates Integrating Sterically Hindered Phenols with Membrane-Active Cations: A Redox-Activated Approach to Antimicrobial Agents

Journal: International Journal of Molecular Sciences

doi: 10.3390/ijms27104524

Figure Legend Snippet: Bacterial resistance studies of compounds 8c , 12c–d , 13a – d , 14c , 15c , norfloxacin , amoxicillin against S. aureus ATCC 209P.

Techniques Used:

Selection:

Article Title: Synthesis, Antimicrobial Activity and Cytotoxicity of Novel (Piperidin-4-yl)adamantane-1-carboxylate N -Substituted Derivatives.
Article Snippet: .. The selection of test organisms included both Gram-positive and Gram-negative microorganisms: Staphylococcus aureus ATCC 6538-P, Escherichia coli ATCC 8739, as well as yeast-like fungi: Candida albicans ATCC 10231. .. The results of the antibacterial and fungicidal activity of the tested compounds (4a–f) against the susceptible microorganisms Staphylococcus aureus ATCC 6538-P, Escherichia coli ATCC 8739 and Candida albicans ATCC 10231 are presented in Tables 1–3, Figures 2 and 3.

Article Title: Synthesis, Antimicrobial Activity and Cytotoxicity of Novel (Piperidin-4-yl)adamantane-1-carboxylate N -Substituted Derivatives
Article Snippet: .. The selection of test organisms included both Gram-positive and Gram-negative microorganisms: Staphylococcus aureus ATCC 6538-P, Escherichia coli ATCC 8739, as well as yeast-like fungi: Candida albicans ATCC 10231. .. The results of the antibacterial and fungicidal activity of the tested compounds ( 4a – f ) against the susceptible microorganisms Staphylococcus aureus ATCC 6538-P, Escherichia coli ATCC 8739 and Candida albicans ATCC 10231 are presented in , and , and .

Bacteria:

Article Title: ZnO-Containing Ca-P Composite Coatings on Ti6Al4V with Dual Antibacterial and Bioactive Functions Prepared by Micro-Arc Oxidation and Hydrothermal Treatment
Article Snippet: Titanium alloys are widely used as bone implant materials due to their excellent mechanical properties.. However, their insufficient bioactivity and antibacterial capacity often lead to prolonged osseointegration and postoperative infection risks.. In this study, a dual-functional micro-arc oxidation (MAO) coating integrated with zinc oxide (ZnO) nanoparticles was developed on Ti6Al4V substrates, followed by hydrothermal treatment to enhance bioactivity.

Isolation:

Article Title: Multitarget bioactive benzo[f]quinoline heterocycles from a thiocarbohydrazone scaffold: synthesis, biological assays, and in silico mechanistic rationale.
Article Snippet: A series of benzo[f]quinoline–thiocarbohydrazone derivatives (3¡12) was synthesized from 3-chlorobenzo[f] quinoline-2-carbaldehyde and thiocarbohydrazide through controlled cyclization/acylation pathways, affording the target heterocycles in 73–91% yields.. Compound 7 was a potent antioxidant measured by DPPH (88.14 ± 1.19% scavenging) and ABTS (79.18 ± 1.60% scavenging) assays compared to ascorbic acid (96.64 ± 0.65% and 95.76 ± 0.83%, respectively).. Additionally, compound 7 had the highest inhibition of microbial growth against S. aureus, B. subtilis and E. coli (83.75 ± 3.75%, 83.65 ± 2.34%, and 84.48 +/− 0.91% respectively) at 50 μg/mL in antibacterial assays, whereas compound 10 exhibited the highest inhibition of P. aeruginosa (78.70 ± 1.79%).

Virus:

Article Title: Iodine-Based Coordination Compounds: A Strategy Toward Antibiotic Potentiation
Article Snippet: The bacterial and fungal test strains were obtained from the American Type Culture Collection (ATCC) through the official distributor for Central Asia LGC Standards (Poland). .. Both reference (museum) and clinical strains, including sensitive and multidrug-resistant variants, were employed as follows: Staphylococcus aureus ATCC 6538-P (museum, sensitive strain) Staphylococcus aureus ATCC 333591 (museum, multidrug-resistant strain) Escherichia coli ATCC 8739 (museum, sensitive strain) Escherichia coli ATCC BAA-2523 (museum, multidrug-resistant strain) Pseudomonas aeruginosa ATCC 9027 (museum, sensitive strain) Pseudomonas aeruginosa TA2 (clinical, multidrug-resistant strain) Klebsiella pneumoniae ATCC 10031 (museum, sensitive strain) Klebsiella pneumoniae ATCC 2524 (museum, multidrug-resistant strain) Salmonella enterica ATCC 14028 (museum, sensitive strain) Salmonella enterica ATCC 35988 (museum, multidrug-resistant strain) Enterococcus hirae ATCC 10541 (museum, sensitive strain) Enterococcus faecalis ATCC 51575 (museum, multidrug-resistant strain) Candida albicans ATCC 10231 (museum, sensitive strain) Candida albicans SCID PHRX 1-2019 (clinical, multidrug-resistant strain) Virus strains—Influenza A virus A/Swine/Iowa/15/30 (H1N1) and Herpes Simplex Virus type 1 (strain “Victory”), obtained from the Laboratory of Viral Ecology, Institute of Virology and Microbiology, Committee of Science, MES RK. ..

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