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sirt2 inhibitor ak7  (MedChemExpress)


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    MedChemExpress sirt2 inhibitor ak7
    Expression of <t>SIRT2</t> and its prognostic impact after SAH in rats. A-B, Western blot and quantifications of SIRT2 level at different time courses. C-E, Representative images show in the temporal cortex stained with antibodies to SIRT2 and Iba1 (C), NeuN (D), or GFAP (E) at 24 h post-SAH. F, The mean fluorescence intensity (MFI) of SIRT2 immunoreactivity. G, Percentages of Iba1 + SIRT2 + , NeuN + SIRT2 + and GFAP + SIRT2 + in the temporal cortex of each group. H , Neurological score, I , brain water content ( J ) and Evan’s blue in different (Sham, SAH, Vehicle and <t>AK7)</t> groups at 24 h after SAH. K-L , FJC staining in the cortex with quantification. Scale bar: 50 μm. ** P < 0.01, *** P < 0.001, **** P < 0.0001
    Sirt2 Inhibitor Ak7, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 93/100, based on 8 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/sirt2 inhibitor ak7/product/MedChemExpress
    Average 93 stars, based on 8 article reviews
    sirt2 inhibitor ak7 - by Bioz Stars, 2026-03
    93/100 stars

    Images

    1) Product Images from "SIRT2 Inhibition promotes microglia LC3-associated phagocytosis via NRF2/CD36 after the experimental subarachnoid hemorrhage"

    Article Title: SIRT2 Inhibition promotes microglia LC3-associated phagocytosis via NRF2/CD36 after the experimental subarachnoid hemorrhage

    Journal: Journal of Neuroinflammation

    doi: 10.1186/s12974-025-03623-z

    Expression of SIRT2 and its prognostic impact after SAH in rats. A-B, Western blot and quantifications of SIRT2 level at different time courses. C-E, Representative images show in the temporal cortex stained with antibodies to SIRT2 and Iba1 (C), NeuN (D), or GFAP (E) at 24 h post-SAH. F, The mean fluorescence intensity (MFI) of SIRT2 immunoreactivity. G, Percentages of Iba1 + SIRT2 + , NeuN + SIRT2 + and GFAP + SIRT2 + in the temporal cortex of each group. H , Neurological score, I , brain water content ( J ) and Evan’s blue in different (Sham, SAH, Vehicle and AK7) groups at 24 h after SAH. K-L , FJC staining in the cortex with quantification. Scale bar: 50 μm. ** P < 0.01, *** P < 0.001, **** P < 0.0001
    Figure Legend Snippet: Expression of SIRT2 and its prognostic impact after SAH in rats. A-B, Western blot and quantifications of SIRT2 level at different time courses. C-E, Representative images show in the temporal cortex stained with antibodies to SIRT2 and Iba1 (C), NeuN (D), or GFAP (E) at 24 h post-SAH. F, The mean fluorescence intensity (MFI) of SIRT2 immunoreactivity. G, Percentages of Iba1 + SIRT2 + , NeuN + SIRT2 + and GFAP + SIRT2 + in the temporal cortex of each group. H , Neurological score, I , brain water content ( J ) and Evan’s blue in different (Sham, SAH, Vehicle and AK7) groups at 24 h after SAH. K-L , FJC staining in the cortex with quantification. Scale bar: 50 μm. ** P < 0.01, *** P < 0.001, **** P < 0.0001

    Techniques Used: Expressing, Western Blot, Staining, Fluorescence

    SIRT2 inhibition promotes microglia phagocytosis. A-B , Western blot and quantitative analysis of SIRT2 expressions in microglia (Con, OxyHb, DMSO and AK7) groups. C-D ,phagocytic index level and analysis by pHrodo. E-F ,Immunofluorescence staining and quantitative analysis of LC3 and Phrodo in microglia. Scale bar: 10 μm. G-K , Western blot and quantitative analysis of Rubicon, NOX2, Beclin1 and LC3 A/B expressions. * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001
    Figure Legend Snippet: SIRT2 inhibition promotes microglia phagocytosis. A-B , Western blot and quantitative analysis of SIRT2 expressions in microglia (Con, OxyHb, DMSO and AK7) groups. C-D ,phagocytic index level and analysis by pHrodo. E-F ,Immunofluorescence staining and quantitative analysis of LC3 and Phrodo in microglia. Scale bar: 10 μm. G-K , Western blot and quantitative analysis of Rubicon, NOX2, Beclin1 and LC3 A/B expressions. * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001

    Techniques Used: Inhibition, Western Blot, Immunofluorescence, Staining

    SIRT2 deacetylates NRF2 and promotes its nuclear translocation in microglia. A-C , Heatmap analyses and q-PCR detects different NRF2 target genes in microglia (SIRT2 and SIRT2 KD) groups. D , Molecular docking shown the obvious interaction force between SIRT2 and NRF2. E-G , Co-immunoprecipitation and quantitative analysis of acetylated NRF2 in SIRT2 WT and KD microglia. H , Western blot and quantitative analysis of SIRT2 in microglia (Con, OxyHb, DMSO and AK7) group with Cyto and nucleus. I-K , The co-localization of SIRT2 and nucleus with laser confocal and analysis in Con group and OxyHb group of microglia. Scale bar: 10 μm. * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001, n.s., no significant
    Figure Legend Snippet: SIRT2 deacetylates NRF2 and promotes its nuclear translocation in microglia. A-C , Heatmap analyses and q-PCR detects different NRF2 target genes in microglia (SIRT2 and SIRT2 KD) groups. D , Molecular docking shown the obvious interaction force between SIRT2 and NRF2. E-G , Co-immunoprecipitation and quantitative analysis of acetylated NRF2 in SIRT2 WT and KD microglia. H , Western blot and quantitative analysis of SIRT2 in microglia (Con, OxyHb, DMSO and AK7) group with Cyto and nucleus. I-K , The co-localization of SIRT2 and nucleus with laser confocal and analysis in Con group and OxyHb group of microglia. Scale bar: 10 μm. * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001, n.s., no significant

    Techniques Used: Translocation Assay, Immunoprecipitation, Western Blot

    SIRT2 through NRF2/CD36 regulates microglial phagocytosis. A , JASPAR predict NRF2 bind to the promoter region of CD36. B-C , phagocytic index level and analysis by pHrodo in microglia (Con, OxyHb, DMSO, AK7 and AK7+ML385) groups. D-E , Western blot and quantitative analysis of CD36 expression. F-H , ELISA quantitative analysis of pro-inflammatory cytokines (TNF-α, IL-1β and IL-6) level in different groups. * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001
    Figure Legend Snippet: SIRT2 through NRF2/CD36 regulates microglial phagocytosis. A , JASPAR predict NRF2 bind to the promoter region of CD36. B-C , phagocytic index level and analysis by pHrodo in microglia (Con, OxyHb, DMSO, AK7 and AK7+ML385) groups. D-E , Western blot and quantitative analysis of CD36 expression. F-H , ELISA quantitative analysis of pro-inflammatory cytokines (TNF-α, IL-1β and IL-6) level in different groups. * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001

    Techniques Used: Western Blot, Expressing, Enzyme-linked Immunosorbent Assay

    SIRT2 via LAP inhibits phagocytosis in microglia. A-F ,Western blot and quantitative analysis of Rubicon, ULK1, CD36, NOX2 and LC3 A/B expressions. G-H , The co-localization of LC3 and pHrodo with laser confocal and analysis indifferent groups of microglia. Scale bar: 10 μm. I-J , Representative TEM images of LAPosomes in microglia. (The black triangle refers to the single membrane structure characteristic of LAPosomes and star refers to the Rubicon particles). Scale bar: 3 μm (upper panels), 1 μm (lower panels). * P < 0.05 vs. Hb, # P < 0.05 vs. Hb+AK7, & P < 0.05 vs. Hb+shRNA, $ P < 0.05 vs. Hb+AK7+shRNA, ☆ P < 0.05 vs. Hb+AK7+ML385, *** P < 0.001, **** P < 0.0001
    Figure Legend Snippet: SIRT2 via LAP inhibits phagocytosis in microglia. A-F ,Western blot and quantitative analysis of Rubicon, ULK1, CD36, NOX2 and LC3 A/B expressions. G-H , The co-localization of LC3 and pHrodo with laser confocal and analysis indifferent groups of microglia. Scale bar: 10 μm. I-J , Representative TEM images of LAPosomes in microglia. (The black triangle refers to the single membrane structure characteristic of LAPosomes and star refers to the Rubicon particles). Scale bar: 3 μm (upper panels), 1 μm (lower panels). * P < 0.05 vs. Hb, # P < 0.05 vs. Hb+AK7, & P < 0.05 vs. Hb+shRNA, $ P < 0.05 vs. Hb+AK7+shRNA, ☆ P < 0.05 vs. Hb+AK7+ML385, *** P < 0.001, **** P < 0.0001

    Techniques Used: Western Blot, Membrane, shRNA

    Inhibition of SIRT2 improves long-term neurological function after SAH. A-B , The falling latency of rotarod test (5RPM and 10 RPM) at 1, 2, and 3 weeks after SAH in rats. C-E ,Escape latency and swimming distance of Morris water maze test on days 23 to 27 after SAH. F-G , Quantification of probe quadrant duration and swimming velocities. H-I , Representative images and neuronal quantifications of Nissl staining in CA1 hippocampal region. Scale bar: 200 μm (upper panels), 50 μm (lower panels). * P < 0.05, ** P< 0.01, *** P < 0.001, **** P < 0.0001, n.s., no significant
    Figure Legend Snippet: Inhibition of SIRT2 improves long-term neurological function after SAH. A-B , The falling latency of rotarod test (5RPM and 10 RPM) at 1, 2, and 3 weeks after SAH in rats. C-E ,Escape latency and swimming distance of Morris water maze test on days 23 to 27 after SAH. F-G , Quantification of probe quadrant duration and swimming velocities. H-I , Representative images and neuronal quantifications of Nissl staining in CA1 hippocampal region. Scale bar: 200 μm (upper panels), 50 μm (lower panels). * P < 0.05, ** P< 0.01, *** P < 0.001, **** P < 0.0001, n.s., no significant

    Techniques Used: Inhibition, Staining

    Schematic diagram of our study. SIRT2 modified NRF2 by deacetylation and inhibited its entry into the nucleus, affecting the transcription of downstream CD36, thereby reducing LAP in microglia
    Figure Legend Snippet: Schematic diagram of our study. SIRT2 modified NRF2 by deacetylation and inhibited its entry into the nucleus, affecting the transcription of downstream CD36, thereby reducing LAP in microglia

    Techniques Used: Modification



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    Image Search Results


    Expression of SIRT2 and its prognostic impact after SAH in rats. A-B, Western blot and quantifications of SIRT2 level at different time courses. C-E, Representative images show in the temporal cortex stained with antibodies to SIRT2 and Iba1 (C), NeuN (D), or GFAP (E) at 24 h post-SAH. F, The mean fluorescence intensity (MFI) of SIRT2 immunoreactivity. G, Percentages of Iba1 + SIRT2 + , NeuN + SIRT2 + and GFAP + SIRT2 + in the temporal cortex of each group. H , Neurological score, I , brain water content ( J ) and Evan’s blue in different (Sham, SAH, Vehicle and AK7) groups at 24 h after SAH. K-L , FJC staining in the cortex with quantification. Scale bar: 50 μm. ** P < 0.01, *** P < 0.001, **** P < 0.0001

    Journal: Journal of Neuroinflammation

    Article Title: SIRT2 Inhibition promotes microglia LC3-associated phagocytosis via NRF2/CD36 after the experimental subarachnoid hemorrhage

    doi: 10.1186/s12974-025-03623-z

    Figure Lengend Snippet: Expression of SIRT2 and its prognostic impact after SAH in rats. A-B, Western blot and quantifications of SIRT2 level at different time courses. C-E, Representative images show in the temporal cortex stained with antibodies to SIRT2 and Iba1 (C), NeuN (D), or GFAP (E) at 24 h post-SAH. F, The mean fluorescence intensity (MFI) of SIRT2 immunoreactivity. G, Percentages of Iba1 + SIRT2 + , NeuN + SIRT2 + and GFAP + SIRT2 + in the temporal cortex of each group. H , Neurological score, I , brain water content ( J ) and Evan’s blue in different (Sham, SAH, Vehicle and AK7) groups at 24 h after SAH. K-L , FJC staining in the cortex with quantification. Scale bar: 50 μm. ** P < 0.01, *** P < 0.001, **** P < 0.0001

    Article Snippet: SIRT2 inhibitor AK7 (MCE, USA) was dissolved in dimethyl sulfoxide (DMSO).

    Techniques: Expressing, Western Blot, Staining, Fluorescence

    SIRT2 inhibition promotes microglia phagocytosis. A-B , Western blot and quantitative analysis of SIRT2 expressions in microglia (Con, OxyHb, DMSO and AK7) groups. C-D ,phagocytic index level and analysis by pHrodo. E-F ,Immunofluorescence staining and quantitative analysis of LC3 and Phrodo in microglia. Scale bar: 10 μm. G-K , Western blot and quantitative analysis of Rubicon, NOX2, Beclin1 and LC3 A/B expressions. * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001

    Journal: Journal of Neuroinflammation

    Article Title: SIRT2 Inhibition promotes microglia LC3-associated phagocytosis via NRF2/CD36 after the experimental subarachnoid hemorrhage

    doi: 10.1186/s12974-025-03623-z

    Figure Lengend Snippet: SIRT2 inhibition promotes microglia phagocytosis. A-B , Western blot and quantitative analysis of SIRT2 expressions in microglia (Con, OxyHb, DMSO and AK7) groups. C-D ,phagocytic index level and analysis by pHrodo. E-F ,Immunofluorescence staining and quantitative analysis of LC3 and Phrodo in microglia. Scale bar: 10 μm. G-K , Western blot and quantitative analysis of Rubicon, NOX2, Beclin1 and LC3 A/B expressions. * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001

    Article Snippet: SIRT2 inhibitor AK7 (MCE, USA) was dissolved in dimethyl sulfoxide (DMSO).

    Techniques: Inhibition, Western Blot, Immunofluorescence, Staining

    SIRT2 deacetylates NRF2 and promotes its nuclear translocation in microglia. A-C , Heatmap analyses and q-PCR detects different NRF2 target genes in microglia (SIRT2 and SIRT2 KD) groups. D , Molecular docking shown the obvious interaction force between SIRT2 and NRF2. E-G , Co-immunoprecipitation and quantitative analysis of acetylated NRF2 in SIRT2 WT and KD microglia. H , Western blot and quantitative analysis of SIRT2 in microglia (Con, OxyHb, DMSO and AK7) group with Cyto and nucleus. I-K , The co-localization of SIRT2 and nucleus with laser confocal and analysis in Con group and OxyHb group of microglia. Scale bar: 10 μm. * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001, n.s., no significant

    Journal: Journal of Neuroinflammation

    Article Title: SIRT2 Inhibition promotes microglia LC3-associated phagocytosis via NRF2/CD36 after the experimental subarachnoid hemorrhage

    doi: 10.1186/s12974-025-03623-z

    Figure Lengend Snippet: SIRT2 deacetylates NRF2 and promotes its nuclear translocation in microglia. A-C , Heatmap analyses and q-PCR detects different NRF2 target genes in microglia (SIRT2 and SIRT2 KD) groups. D , Molecular docking shown the obvious interaction force between SIRT2 and NRF2. E-G , Co-immunoprecipitation and quantitative analysis of acetylated NRF2 in SIRT2 WT and KD microglia. H , Western blot and quantitative analysis of SIRT2 in microglia (Con, OxyHb, DMSO and AK7) group with Cyto and nucleus. I-K , The co-localization of SIRT2 and nucleus with laser confocal and analysis in Con group and OxyHb group of microglia. Scale bar: 10 μm. * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001, n.s., no significant

    Article Snippet: SIRT2 inhibitor AK7 (MCE, USA) was dissolved in dimethyl sulfoxide (DMSO).

    Techniques: Translocation Assay, Immunoprecipitation, Western Blot

    SIRT2 through NRF2/CD36 regulates microglial phagocytosis. A , JASPAR predict NRF2 bind to the promoter region of CD36. B-C , phagocytic index level and analysis by pHrodo in microglia (Con, OxyHb, DMSO, AK7 and AK7+ML385) groups. D-E , Western blot and quantitative analysis of CD36 expression. F-H , ELISA quantitative analysis of pro-inflammatory cytokines (TNF-α, IL-1β and IL-6) level in different groups. * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001

    Journal: Journal of Neuroinflammation

    Article Title: SIRT2 Inhibition promotes microglia LC3-associated phagocytosis via NRF2/CD36 after the experimental subarachnoid hemorrhage

    doi: 10.1186/s12974-025-03623-z

    Figure Lengend Snippet: SIRT2 through NRF2/CD36 regulates microglial phagocytosis. A , JASPAR predict NRF2 bind to the promoter region of CD36. B-C , phagocytic index level and analysis by pHrodo in microglia (Con, OxyHb, DMSO, AK7 and AK7+ML385) groups. D-E , Western blot and quantitative analysis of CD36 expression. F-H , ELISA quantitative analysis of pro-inflammatory cytokines (TNF-α, IL-1β and IL-6) level in different groups. * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001

    Article Snippet: SIRT2 inhibitor AK7 (MCE, USA) was dissolved in dimethyl sulfoxide (DMSO).

    Techniques: Western Blot, Expressing, Enzyme-linked Immunosorbent Assay

    SIRT2 via LAP inhibits phagocytosis in microglia. A-F ,Western blot and quantitative analysis of Rubicon, ULK1, CD36, NOX2 and LC3 A/B expressions. G-H , The co-localization of LC3 and pHrodo with laser confocal and analysis indifferent groups of microglia. Scale bar: 10 μm. I-J , Representative TEM images of LAPosomes in microglia. (The black triangle refers to the single membrane structure characteristic of LAPosomes and star refers to the Rubicon particles). Scale bar: 3 μm (upper panels), 1 μm (lower panels). * P < 0.05 vs. Hb, # P < 0.05 vs. Hb+AK7, & P < 0.05 vs. Hb+shRNA, $ P < 0.05 vs. Hb+AK7+shRNA, ☆ P < 0.05 vs. Hb+AK7+ML385, *** P < 0.001, **** P < 0.0001

    Journal: Journal of Neuroinflammation

    Article Title: SIRT2 Inhibition promotes microglia LC3-associated phagocytosis via NRF2/CD36 after the experimental subarachnoid hemorrhage

    doi: 10.1186/s12974-025-03623-z

    Figure Lengend Snippet: SIRT2 via LAP inhibits phagocytosis in microglia. A-F ,Western blot and quantitative analysis of Rubicon, ULK1, CD36, NOX2 and LC3 A/B expressions. G-H , The co-localization of LC3 and pHrodo with laser confocal and analysis indifferent groups of microglia. Scale bar: 10 μm. I-J , Representative TEM images of LAPosomes in microglia. (The black triangle refers to the single membrane structure characteristic of LAPosomes and star refers to the Rubicon particles). Scale bar: 3 μm (upper panels), 1 μm (lower panels). * P < 0.05 vs. Hb, # P < 0.05 vs. Hb+AK7, & P < 0.05 vs. Hb+shRNA, $ P < 0.05 vs. Hb+AK7+shRNA, ☆ P < 0.05 vs. Hb+AK7+ML385, *** P < 0.001, **** P < 0.0001

    Article Snippet: SIRT2 inhibitor AK7 (MCE, USA) was dissolved in dimethyl sulfoxide (DMSO).

    Techniques: Western Blot, Membrane, shRNA

    Inhibition of SIRT2 improves long-term neurological function after SAH. A-B , The falling latency of rotarod test (5RPM and 10 RPM) at 1, 2, and 3 weeks after SAH in rats. C-E ,Escape latency and swimming distance of Morris water maze test on days 23 to 27 after SAH. F-G , Quantification of probe quadrant duration and swimming velocities. H-I , Representative images and neuronal quantifications of Nissl staining in CA1 hippocampal region. Scale bar: 200 μm (upper panels), 50 μm (lower panels). * P < 0.05, ** P< 0.01, *** P < 0.001, **** P < 0.0001, n.s., no significant

    Journal: Journal of Neuroinflammation

    Article Title: SIRT2 Inhibition promotes microglia LC3-associated phagocytosis via NRF2/CD36 after the experimental subarachnoid hemorrhage

    doi: 10.1186/s12974-025-03623-z

    Figure Lengend Snippet: Inhibition of SIRT2 improves long-term neurological function after SAH. A-B , The falling latency of rotarod test (5RPM and 10 RPM) at 1, 2, and 3 weeks after SAH in rats. C-E ,Escape latency and swimming distance of Morris water maze test on days 23 to 27 after SAH. F-G , Quantification of probe quadrant duration and swimming velocities. H-I , Representative images and neuronal quantifications of Nissl staining in CA1 hippocampal region. Scale bar: 200 μm (upper panels), 50 μm (lower panels). * P < 0.05, ** P< 0.01, *** P < 0.001, **** P < 0.0001, n.s., no significant

    Article Snippet: SIRT2 inhibitor AK7 (MCE, USA) was dissolved in dimethyl sulfoxide (DMSO).

    Techniques: Inhibition, Staining

    Schematic diagram of our study. SIRT2 modified NRF2 by deacetylation and inhibited its entry into the nucleus, affecting the transcription of downstream CD36, thereby reducing LAP in microglia

    Journal: Journal of Neuroinflammation

    Article Title: SIRT2 Inhibition promotes microglia LC3-associated phagocytosis via NRF2/CD36 after the experimental subarachnoid hemorrhage

    doi: 10.1186/s12974-025-03623-z

    Figure Lengend Snippet: Schematic diagram of our study. SIRT2 modified NRF2 by deacetylation and inhibited its entry into the nucleus, affecting the transcription of downstream CD36, thereby reducing LAP in microglia

    Article Snippet: SIRT2 inhibitor AK7 (MCE, USA) was dissolved in dimethyl sulfoxide (DMSO).

    Techniques: Modification