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sirt 1 inhibitor  (MedChemExpress)


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    Structured Review

    MedChemExpress sirt 1 inhibitor
    Nob improved the antioxidant capacity of skeletal muscle in D‐gal‐induced aging mice. (A) ROS content, n = 3 mice/group; (B) SOD activity, n = 4 mice/group; (C) MDA content, n = 4 mice/group; (E–G) Western blot analysis of SIRT1, PGC‐1α, Nrf2, and GAPDH in D‐gal‐induced C2C12 cells treated with vehicle and Nob, n = 3. ** p < 0.01, *** p < 0.001, **** p < 0.0001.
    Sirt 1 Inhibitor, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 97/100, based on 347 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/sirt 1 inhibitor/product/MedChemExpress
    Average 97 stars, based on 347 article reviews
    sirt 1 inhibitor - by Bioz Stars, 2026-02
    97/100 stars

    Images

    1) Product Images from "Nobiletin Ameliorates Skeletal Muscle Performance in D‐Galactose‐Induced Aging Mice by Boosting Aerobic Metabolism"

    Article Title: Nobiletin Ameliorates Skeletal Muscle Performance in D‐Galactose‐Induced Aging Mice by Boosting Aerobic Metabolism

    Journal: Food Science & Nutrition

    doi: 10.1002/fsn3.71416

    Nob improved the antioxidant capacity of skeletal muscle in D‐gal‐induced aging mice. (A) ROS content, n = 3 mice/group; (B) SOD activity, n = 4 mice/group; (C) MDA content, n = 4 mice/group; (E–G) Western blot analysis of SIRT1, PGC‐1α, Nrf2, and GAPDH in D‐gal‐induced C2C12 cells treated with vehicle and Nob, n = 3. ** p < 0.01, *** p < 0.001, **** p < 0.0001.
    Figure Legend Snippet: Nob improved the antioxidant capacity of skeletal muscle in D‐gal‐induced aging mice. (A) ROS content, n = 3 mice/group; (B) SOD activity, n = 4 mice/group; (C) MDA content, n = 4 mice/group; (E–G) Western blot analysis of SIRT1, PGC‐1α, Nrf2, and GAPDH in D‐gal‐induced C2C12 cells treated with vehicle and Nob, n = 3. ** p < 0.01, *** p < 0.001, **** p < 0.0001.

    Techniques Used: Activity Assay, Western Blot



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    Image Search Results


    Perspective of the computational studies leading to the identification of selective and/or pan-Sirtuins modulators (shown in green). The chemical structure and the explored biological activity of the discovered hit compounds are reported. The applied virtual screening (VS) strategy is specified as structure-based (SBVS) or ligand-based (LBVS) methodology. The results are listed based on the sirtuin type (alternatively in gray and cyan), according to SBVS followed by LBVS and combined SB-LB approaches, as chronological order. Data about parasitic sirtuins (depicted in coral) are also detailed, referring to the Leishmania (Lm-Sirt), Trypanosoma cruzi (Tc-Sirt) and Schistosoma mansoni (Sm-Sirt) sirtuins.

    Journal: Molecules

    Article Title: Virtual Screening in the Identification of Sirtuins’ Activity Modulators

    doi: 10.3390/molecules27175641

    Figure Lengend Snippet: Perspective of the computational studies leading to the identification of selective and/or pan-Sirtuins modulators (shown in green). The chemical structure and the explored biological activity of the discovered hit compounds are reported. The applied virtual screening (VS) strategy is specified as structure-based (SBVS) or ligand-based (LBVS) methodology. The results are listed based on the sirtuin type (alternatively in gray and cyan), according to SBVS followed by LBVS and combined SB-LB approaches, as chronological order. Data about parasitic sirtuins (depicted in coral) are also detailed, referring to the Leishmania (Lm-Sirt), Trypanosoma cruzi (Tc-Sirt) and Schistosoma mansoni (Sm-Sirt) sirtuins.

    Article Snippet: 2021 , [ ] , Screening of SIRT-6 inhibitors and activators: A novel activator has an impact on breast cancer cells , 6 , LB-SB , LB: pharmacophore, similarity based , 1,2 , YES , ENAMINE (4 103 115), Chembridge (1 022 400), in house library of 1,4-dihydropyridine derivatives (∼100) , MOE (pharmacophore, similarity, docking), Glide/Maestro/ Schrodinger (docking) , 4H-chromen analogs (A), 1,4-dihydropyridine (I) , A, I , 80 μM (EC 50 , activator) 60% @200 μM (IC 50 , inhibitor).

    Techniques: Activity Assay, Biomarker Discovery, Software, Inhibition, In Silico, Functional Assay, In Vitro, Sequencing, Generated, Histone Deacetylase Assay, Binding Assay, Analogues, Drug discovery, Purification, Modification, Activation Assay, Derivative Assay

    Nob improved the antioxidant capacity of skeletal muscle in D‐gal‐induced aging mice. (A) ROS content, n = 3 mice/group; (B) SOD activity, n = 4 mice/group; (C) MDA content, n = 4 mice/group; (E–G) Western blot analysis of SIRT1, PGC‐1α, Nrf2, and GAPDH in D‐gal‐induced C2C12 cells treated with vehicle and Nob, n = 3. ** p < 0.01, *** p < 0.001, **** p < 0.0001.

    Journal: Food Science & Nutrition

    Article Title: Nobiletin Ameliorates Skeletal Muscle Performance in D‐Galactose‐Induced Aging Mice by Boosting Aerobic Metabolism

    doi: 10.1002/fsn3.71416

    Figure Lengend Snippet: Nob improved the antioxidant capacity of skeletal muscle in D‐gal‐induced aging mice. (A) ROS content, n = 3 mice/group; (B) SOD activity, n = 4 mice/group; (C) MDA content, n = 4 mice/group; (E–G) Western blot analysis of SIRT1, PGC‐1α, Nrf2, and GAPDH in D‐gal‐induced C2C12 cells treated with vehicle and Nob, n = 3. ** p < 0.01, *** p < 0.001, **** p < 0.0001.

    Article Snippet: SIRT‐1 inhibitor (EX‐527, HY‐15452) was obtained from MedChemExpress (Shanghai, China).

    Techniques: Activity Assay, Western Blot

    Acetylated StAR lysine residues (highlighted in red) under basal (DMSO, dimethyl sulfoxide) and Panobinostat (PANO)-,  SAHA-,  IV-, and  VII-treated  conditions in MCF7 cells.

    Journal: International Journal of Molecular Sciences

    Article Title: Acetylation of Steroidogenic Acute Regulatory Protein Sensitizes 17β-Estradiol Regulation in Hormone-Sensitive Breast Cancer Cells

    doi: 10.3390/ijms25168732

    Figure Lengend Snippet: Acetylated StAR lysine residues (highlighted in red) under basal (DMSO, dimethyl sulfoxide) and Panobinostat (PANO)-, SAHA-, IV-, and VII-treated conditions in MCF7 cells.

    Article Snippet: A number of key reagents were utilized in this study, as follows: Panobinostat (LBH589) was obtained from APExBIO (Houston, TX, USA); Vorinostat (SAHA) and SIRT 1 Inhibitors IV and VII were purchased from Millipore-Sigma (St. Louis, MO, USA); anti-StAR antibodies (Abs) (ab180804 or ab96637) were obtained from Abcam (Boston, MA, USA); and an ELISA kit for E2 was purchased from Cayman Chemical Co. (Ann Arbor, MI, USA) [ , ].

    Techniques: