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dichlorophene  (Millipore)


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    Structured Review

    Millipore dichlorophene
    Dichlorophene, supplied by Millipore, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/dichlorophene/dichlorophene/pmc06693830-520-15-16
    Average 90 stars, based on 1 article reviews
    dichlorophene - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    other:

    Article Title: Niclosamide repurposed for the treatment of inflammatory airway disease
    Article Snippet: All compounds used were of highest available grade of purity: niclosamide, Eact, OVA, MCh, NFA, dichlorophene, (MilliporeSigma).

    Article Title: Genotoxicity of an organochlorine pesticide dichlorophene by micronucleus and chromosomal aberration assays using bone marrow cells ofRattus norvegicus
    Article Snippet: Taylor & Francis makes every effort to ensure the accuracy of all the information (the “Content”) contained in the publications on our platform.. However, Taylor & Francis, our agents, and our licensors make no representations or warranties whatsoever as to the accuracy, completeness, or suitability for any purpose of the Content.. Any opinions and views expressed in this publication are the opinions and views of the authors, and are not the views of or endorsed by Taylor & Francis.

    Article Title: Novel phototoxicity assay using human embryonic stem cell-derived retinal pigment epithelial cells.
    Article Snippet: Some chemicals are harmful in to light-exposed tissues such as skin and eyes.. The 3T3 Neutral Red Uptake Phototoxicity Test has been validated and adopted by the Organization of Economic and Community Development (OECD) as a method of evaluating chemical phototoxicity using mouse 3T3 fibroblasts.. However, the high rate of false positive results associated with this test eventually led to increased laboratory animal usage.



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    Image Search Results


    Drug screening against A. calcoaceticus . Zones of inhibition of A. calcoaceticus growth by 1 μL of 3.3 mM Miconazole, Dichlorophen, Doxycycline (positive control, halo circled with the dotted line for reference), and DMSO (negative control) on lawns of 75 μL of A. calcoaceticus culture incubated overnight at 37 °C. Normalized fold changes of the halos are shown at the bottom right corner of the images.

    Journal: ACS Omega

    Article Title: Identification of Bithionol, Dichlorophen, and Miconazole as Antibacterial Agents against Acinetobacter calcoaceticus

    doi: 10.1021/acsomega.0c03211

    Figure Lengend Snippet: Drug screening against A. calcoaceticus . Zones of inhibition of A. calcoaceticus growth by 1 μL of 3.3 mM Miconazole, Dichlorophen, Doxycycline (positive control, halo circled with the dotted line for reference), and DMSO (negative control) on lawns of 75 μL of A. calcoaceticus culture incubated overnight at 37 °C. Normalized fold changes of the halos are shown at the bottom right corner of the images.

    Article Snippet: Dichlorophen structural analogues, Bithionol and Triclosan, were obtained from Fluka Analytical and Alfa Aesar, respectively.

    Techniques: Drug discovery, Inhibition, Positive Control, Negative Control, Incubation

    Diffusion susceptibility test on A. calcoaceticus . Representative zones of inhibition of A. calcoaceticus growth by 1 μL of MIC and sub-MIC of Miconazole, Dichlorophen, Bithionol, and Triclosan. DMSO serves as the negative control. MIC and sub-MIC values are indicated above corresponding halo images. Normalized fold changes of the halos are shown at the bottom right corner of the images.

    Journal: ACS Omega

    Article Title: Identification of Bithionol, Dichlorophen, and Miconazole as Antibacterial Agents against Acinetobacter calcoaceticus

    doi: 10.1021/acsomega.0c03211

    Figure Lengend Snippet: Diffusion susceptibility test on A. calcoaceticus . Representative zones of inhibition of A. calcoaceticus growth by 1 μL of MIC and sub-MIC of Miconazole, Dichlorophen, Bithionol, and Triclosan. DMSO serves as the negative control. MIC and sub-MIC values are indicated above corresponding halo images. Normalized fold changes of the halos are shown at the bottom right corner of the images.

    Article Snippet: Dichlorophen structural analogues, Bithionol and Triclosan, were obtained from Fluka Analytical and Alfa Aesar, respectively.

    Techniques: Diffusion-based Assay, Inhibition, Negative Control

    Kinetic growth of A. calcoaceticus with varying concentrations of hits. Antimicrobial activity of Miconazole, Dichlorophen, Bithionol, and Triclosan at concentrations ranging from 32 to 1 μM on A. calcoaceticus growth.

    Journal: ACS Omega

    Article Title: Identification of Bithionol, Dichlorophen, and Miconazole as Antibacterial Agents against Acinetobacter calcoaceticus

    doi: 10.1021/acsomega.0c03211

    Figure Lengend Snippet: Kinetic growth of A. calcoaceticus with varying concentrations of hits. Antimicrobial activity of Miconazole, Dichlorophen, Bithionol, and Triclosan at concentrations ranging from 32 to 1 μM on A. calcoaceticus growth.

    Article Snippet: Dichlorophen structural analogues, Bithionol and Triclosan, were obtained from Fluka Analytical and Alfa Aesar, respectively.

    Techniques: Activity Assay

    Broad-spectrum antibacterial activity of hits. Zones of inhibition by our hits on SMR A. calcoaceticus , E. coli , C. freundii , E. aerogenes , B. cereus , and B. subtilis . Normalized fold changes are indicated at the bottom right corner of images. E. aerogenes was insensitive to Miconazole, Dichlorophen, and Bithionol.

    Journal: ACS Omega

    Article Title: Identification of Bithionol, Dichlorophen, and Miconazole as Antibacterial Agents against Acinetobacter calcoaceticus

    doi: 10.1021/acsomega.0c03211

    Figure Lengend Snippet: Broad-spectrum antibacterial activity of hits. Zones of inhibition by our hits on SMR A. calcoaceticus , E. coli , C. freundii , E. aerogenes , B. cereus , and B. subtilis . Normalized fold changes are indicated at the bottom right corner of images. E. aerogenes was insensitive to Miconazole, Dichlorophen, and Bithionol.

    Article Snippet: Dichlorophen structural analogues, Bithionol and Triclosan, were obtained from Fluka Analytical and Alfa Aesar, respectively.

    Techniques: Activity Assay, Inhibition

    Broad-spectrum antibacterial activity of hits. Minimum inhibitory concentrations (MICs) and standard deviations of Miconazole, Dichlorophen, Bithionol, and Triclosan versus select bacterial strains on solid growth medium.

    Journal: ACS Omega

    Article Title: Identification of Bithionol, Dichlorophen, and Miconazole as Antibacterial Agents against Acinetobacter calcoaceticus

    doi: 10.1021/acsomega.0c03211

    Figure Lengend Snippet: Broad-spectrum antibacterial activity of hits. Minimum inhibitory concentrations (MICs) and standard deviations of Miconazole, Dichlorophen, Bithionol, and Triclosan versus select bacterial strains on solid growth medium.

    Article Snippet: Dichlorophen structural analogues, Bithionol and Triclosan, were obtained from Fluka Analytical and Alfa Aesar, respectively.

    Techniques: Activity Assay

    Broad-spectrum antibacterial activity of combinations of hits. Images depict zones of inhibition of B. subtilis , E. coli , C. freundii , B. cereus , A. calcoaceticus , and SMR A. calcoaceticus treated with Miconazole, Dichlorophen, Bithionol, and Triclosan combinations at concentrations shown in Table . DMSO serves as the negative control. Normalized fold changes are shown on the bottom right corner of each image.

    Journal: ACS Omega

    Article Title: Identification of Bithionol, Dichlorophen, and Miconazole as Antibacterial Agents against Acinetobacter calcoaceticus

    doi: 10.1021/acsomega.0c03211

    Figure Lengend Snippet: Broad-spectrum antibacterial activity of combinations of hits. Images depict zones of inhibition of B. subtilis , E. coli , C. freundii , B. cereus , A. calcoaceticus , and SMR A. calcoaceticus treated with Miconazole, Dichlorophen, Bithionol, and Triclosan combinations at concentrations shown in Table . DMSO serves as the negative control. Normalized fold changes are shown on the bottom right corner of each image.

    Article Snippet: Dichlorophen structural analogues, Bithionol and Triclosan, were obtained from Fluka Analytical and Alfa Aesar, respectively.

    Techniques: Activity Assay, Inhibition, Negative Control

    Broad-Spectrum Antimicrobial Activity of Hits and Analogues as Assessed by MIC on Solid Growth Medium

    Journal: ACS Omega

    Article Title: Identification of Bithionol, Dichlorophen, and Miconazole as Antibacterial Agents against Acinetobacter calcoaceticus

    doi: 10.1021/acsomega.0c03211

    Figure Lengend Snippet: Broad-Spectrum Antimicrobial Activity of Hits and Analogues as Assessed by MIC on Solid Growth Medium

    Article Snippet: Dichlorophen structural analogues, Bithionol and Triclosan, were obtained from Fluka Analytical and Alfa Aesar, respectively.

    Techniques: Activity Assay, Analogues, Bacteria, Standard Deviation

    Concentrations of Drugs Used in Broad-Spectrum Analysis of Hit Combination of Hits <xref ref-type= a " width="100%" height="100%">

    Journal: ACS Omega

    Article Title: Identification of Bithionol, Dichlorophen, and Miconazole as Antibacterial Agents against Acinetobacter calcoaceticus

    doi: 10.1021/acsomega.0c03211

    Figure Lengend Snippet: Concentrations of Drugs Used in Broad-Spectrum Analysis of Hit Combination of Hits a

    Article Snippet: Dichlorophen structural analogues, Bithionol and Triclosan, were obtained from Fluka Analytical and Alfa Aesar, respectively.

    Techniques: Bacteria