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compounds 3a 3i  (Shimadzu Corporation)


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    Structured Review

    Shimadzu Corporation compounds 3a 3i
    Compounds 3a 3i, supplied by Shimadzu Corporation, used in various techniques. Bioz Stars score: 99/100, based on 5718 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/compounds+3a+3i/UV-1900i/10__1016_slash_j__rechem__2023__101119-159-7-12
    Average 99 stars, based on 5718 article reviews
    compounds 3a 3i - by Bioz Stars, 2026-09
    99/100 stars

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    Related Articles

    Concentration Assay:

    Article Title: Design and synthesis of chalcone mediated novel pyrazoline scaffolds: Discovery of benzothiophene comprising antimicrobial inhibitors
    Article Snippet: .. Working solution with 5 μM concentration of compounds (3a-3i) for UV–Vis absorption (Shimadzu UV-1900i spectrophotometer) and fluorescence emission (Shimadzu RF-6000 fluorescence spectrometer) investigations were made by serial dilution. ..

    Spectrophotometry:

    Article Title: Design and synthesis of chalcone mediated novel pyrazoline scaffolds: Discovery of benzothiophene comprising antimicrobial inhibitors
    Article Snippet: .. Working solution with 5 μM concentration of compounds (3a-3i) for UV–Vis absorption (Shimadzu UV-1900i spectrophotometer) and fluorescence emission (Shimadzu RF-6000 fluorescence spectrometer) investigations were made by serial dilution. ..

    Fluorescence:

    Article Title: Design and synthesis of chalcone mediated novel pyrazoline scaffolds: Discovery of benzothiophene comprising antimicrobial inhibitors
    Article Snippet: .. Working solution with 5 μM concentration of compounds (3a-3i) for UV–Vis absorption (Shimadzu UV-1900i spectrophotometer) and fluorescence emission (Shimadzu RF-6000 fluorescence spectrometer) investigations were made by serial dilution. ..

    Serial Dilution:

    Article Title: Design and synthesis of chalcone mediated novel pyrazoline scaffolds: Discovery of benzothiophene comprising antimicrobial inhibitors
    Article Snippet: .. Working solution with 5 μM concentration of compounds (3a-3i) for UV–Vis absorption (Shimadzu UV-1900i spectrophotometer) and fluorescence emission (Shimadzu RF-6000 fluorescence spectrometer) investigations were made by serial dilution. ..



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    Image Search Results


    The overall correlation coefficients matrix between the MIC values of the compounds 3a–3i and their computational scores for each of the selected target enzymes.

    Journal: Journal of Enzyme Inhibition and Medicinal Chemistry

    Article Title: In vitro anti-TB properties, in silico target validation, molecular docking and dynamics studies of substituted 1,2,4-oxadiazole analogues against Mycobacterium tuberculosis

    doi: 10.1080/14756366.2021.1900162

    Figure Lengend Snippet: The overall correlation coefficients matrix between the MIC values of the compounds 3a–3i and their computational scores for each of the selected target enzymes.

    Article Snippet: The in vitro inhibitory activity of the designed compounds against H37Rv, MDR and XDR strains of MTB was performed as described in the methodology section. presents the anti-TB results of the compounds 3a–3i tested against H37Rv (ATCC: 25177), MDR and XDR strains of M. tuberculosis .

    Techniques:

    The top ranked docking scores of the tested compounds ( 3a–3i ) into MD-based Pks13-TE conformer, along with the relative docking (RD) score of the most active compounds ( 3a and 3d ).

    Journal: Journal of Enzyme Inhibition and Medicinal Chemistry

    Article Title: In vitro anti-TB properties, in silico target validation, molecular docking and dynamics studies of substituted 1,2,4-oxadiazole analogues against Mycobacterium tuberculosis

    doi: 10.1080/14756366.2021.1900162

    Figure Lengend Snippet: The top ranked docking scores of the tested compounds ( 3a–3i ) into MD-based Pks13-TE conformer, along with the relative docking (RD) score of the most active compounds ( 3a and 3d ).

    Article Snippet: The in vitro inhibitory activity of the designed compounds against H37Rv, MDR and XDR strains of MTB was performed as described in the methodology section. presents the anti-TB results of the compounds 3a–3i tested against H37Rv (ATCC: 25177), MDR and XDR strains of M. tuberculosis .

    Techniques:

    Calculated ADMET descriptors and toxicity parameters of compounds ( 3a–3i ).

    Journal: Journal of Enzyme Inhibition and Medicinal Chemistry

    Article Title: In vitro anti-TB properties, in silico target validation, molecular docking and dynamics studies of substituted 1,2,4-oxadiazole analogues against Mycobacterium tuberculosis

    doi: 10.1080/14756366.2021.1900162

    Figure Lengend Snippet: Calculated ADMET descriptors and toxicity parameters of compounds ( 3a–3i ).

    Article Snippet: The in vitro inhibitory activity of the designed compounds against H37Rv, MDR and XDR strains of MTB was performed as described in the methodology section. presents the anti-TB results of the compounds 3a–3i tested against H37Rv (ATCC: 25177), MDR and XDR strains of M. tuberculosis .

    Techniques: Inhibition, Activity Assay