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α tocopherol  (MedChemExpress)


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    Structured Review

    MedChemExpress α tocopherol
    α Tocopherol, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 94/100, based on 10 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/α tocopherol/product/MedChemExpress
    Average 94 stars, based on 10 article reviews
    α tocopherol - by Bioz Stars, 2026-02
    94/100 stars

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    MedChemExpress α tocopherol α toc
    Inhibition of ferroptosis decreased the cytotoxicity of PAE in U118 and U251 cells. (A, B) The phenotypes and survival of U118 and U251 cells cotreatment with ferrostatin‐1 (Fer‐1, 1 μM) orα‐tocopherol <t>(α‐Toc,</t> 100 μM) were examined by fluorescence microscope (scale bar: 25 μm) and a live/dead assay (scale bar: 100 μm). (C, D) The LPO and ROS level of U118 and U251 cells cotreatment with Fer‐1and α‐Toc were examined by fluorescence microscope (scale bar: 25 μm). (E) The LD level of U118 and U2511 cells cotreatment with Fer‐1and α‐Toc were examined by fluorescence microscope (scale bar: 25 μm).
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    MedChemExpress α135 tocopherol phosphate
    Inhibition of ferroptosis decreased the cytotoxicity of PAE in U118 and U251 cells. (A, B) The phenotypes and survival of U118 and U251 cells cotreatment with ferrostatin‐1 (Fer‐1, 1 μM) orα‐tocopherol <t>(α‐Toc,</t> 100 μM) were examined by fluorescence microscope (scale bar: 25 μm) and a live/dead assay (scale bar: 100 μm). (C, D) The LPO and ROS level of U118 and U251 cells cotreatment with Fer‐1and α‐Toc were examined by fluorescence microscope (scale bar: 25 μm). (E) The LD level of U118 and U2511 cells cotreatment with Fer‐1and α‐Toc were examined by fluorescence microscope (scale bar: 25 μm).
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    MedChemExpress α tocopherol phosphate
    PS-T restrains BCSCs by inducing ferroptosis in TNBC. ( A - B ) Cell viability heatmap of the effects of different cell death inhibitors on PS-T–induced cell death. ALDH + MDA-MB-231 cells were treated with indicated concentration of PS-T with or without Z-VAD-FMK (30 µM), Necrostatin-1 (Necro-1, 20 µM), LDC7559 (5 <t>µM),</t> <t>α-tocopherol</t> (α-toc, 100 µM) or liproxstatin-1 (Lip-1, 200 nM) for 24 h ( n = 9). ( C ) GSEA result of MDA-MB-231 cells treated with or without PS-T using WP_FERROPTOSIS gene set. ( D - F ) The ROS fluorescence ( D ), C11 BODIPY fluorescence ( E ), and relative MDA concentration ( F ) of 0, 10, 20, and 50 µg/mL PS-T–treated ALDH + MDA-MB-231 cells ( n = 9). Scale bars = 20 μm. ( G - H ) The relative MDA concentration ( G ) and C11 BODIPY fluorescence ( H ) of breast cancer tissue of xenograft models treated with or without PS-T ( n = 9). ( D , G , H ) The Student’s t-test was employed. ( E , F ) One-way analysis of variance and post-hoc Bonferroni tests were utilized. Each experiment was repeated three times, and data was pooled. (mean ± standard deviation; *** P < 0.001)
    α Tocopherol Phosphate, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Inhibition of ferroptosis decreased the cytotoxicity of PAE in U118 and U251 cells. (A, B) The phenotypes and survival of U118 and U251 cells cotreatment with ferrostatin‐1 (Fer‐1, 1 μM) orα‐tocopherol (α‐Toc, 100 μM) were examined by fluorescence microscope (scale bar: 25 μm) and a live/dead assay (scale bar: 100 μm). (C, D) The LPO and ROS level of U118 and U251 cells cotreatment with Fer‐1and α‐Toc were examined by fluorescence microscope (scale bar: 25 μm). (E) The LD level of U118 and U2511 cells cotreatment with Fer‐1and α‐Toc were examined by fluorescence microscope (scale bar: 25 μm).

    Journal: Pharmacology Research & Perspectives

    Article Title: Paeonol Inhibits Cell Growth by Inducing Ferroptosis in Human Glioma Cells

    doi: 10.1002/prp2.70213

    Figure Lengend Snippet: Inhibition of ferroptosis decreased the cytotoxicity of PAE in U118 and U251 cells. (A, B) The phenotypes and survival of U118 and U251 cells cotreatment with ferrostatin‐1 (Fer‐1, 1 μM) orα‐tocopherol (α‐Toc, 100 μM) were examined by fluorescence microscope (scale bar: 25 μm) and a live/dead assay (scale bar: 100 μm). (C, D) The LPO and ROS level of U118 and U251 cells cotreatment with Fer‐1and α‐Toc were examined by fluorescence microscope (scale bar: 25 μm). (E) The LD level of U118 and U2511 cells cotreatment with Fer‐1and α‐Toc were examined by fluorescence microscope (scale bar: 25 μm).

    Article Snippet: Paeonol (PAE), α‐Tocopherol (α‐Toc), and Ferrostatin‐1 (Fer‐1) were obtained from Med Chem Express (NJ, USA).

    Techniques: Inhibition, Fluorescence, Microscopy, Live Dead Assay

    PS-T restrains BCSCs by inducing ferroptosis in TNBC. ( A - B ) Cell viability heatmap of the effects of different cell death inhibitors on PS-T–induced cell death. ALDH + MDA-MB-231 cells were treated with indicated concentration of PS-T with or without Z-VAD-FMK (30 µM), Necrostatin-1 (Necro-1, 20 µM), LDC7559 (5 µM), α-tocopherol (α-toc, 100 µM) or liproxstatin-1 (Lip-1, 200 nM) for 24 h ( n = 9). ( C ) GSEA result of MDA-MB-231 cells treated with or without PS-T using WP_FERROPTOSIS gene set. ( D - F ) The ROS fluorescence ( D ), C11 BODIPY fluorescence ( E ), and relative MDA concentration ( F ) of 0, 10, 20, and 50 µg/mL PS-T–treated ALDH + MDA-MB-231 cells ( n = 9). Scale bars = 20 μm. ( G - H ) The relative MDA concentration ( G ) and C11 BODIPY fluorescence ( H ) of breast cancer tissue of xenograft models treated with or without PS-T ( n = 9). ( D , G , H ) The Student’s t-test was employed. ( E , F ) One-way analysis of variance and post-hoc Bonferroni tests were utilized. Each experiment was repeated three times, and data was pooled. (mean ± standard deviation; *** P < 0.001)

    Journal: Cancer Cell International

    Article Title: Polysaccharides from Huaier induce autophagy-dependent ferroptosis to inhibit breast cancer stem cells in triple-negative breast cancer

    doi: 10.1186/s12935-025-04102-4

    Figure Lengend Snippet: PS-T restrains BCSCs by inducing ferroptosis in TNBC. ( A - B ) Cell viability heatmap of the effects of different cell death inhibitors on PS-T–induced cell death. ALDH + MDA-MB-231 cells were treated with indicated concentration of PS-T with or without Z-VAD-FMK (30 µM), Necrostatin-1 (Necro-1, 20 µM), LDC7559 (5 µM), α-tocopherol (α-toc, 100 µM) or liproxstatin-1 (Lip-1, 200 nM) for 24 h ( n = 9). ( C ) GSEA result of MDA-MB-231 cells treated with or without PS-T using WP_FERROPTOSIS gene set. ( D - F ) The ROS fluorescence ( D ), C11 BODIPY fluorescence ( E ), and relative MDA concentration ( F ) of 0, 10, 20, and 50 µg/mL PS-T–treated ALDH + MDA-MB-231 cells ( n = 9). Scale bars = 20 μm. ( G - H ) The relative MDA concentration ( G ) and C11 BODIPY fluorescence ( H ) of breast cancer tissue of xenograft models treated with or without PS-T ( n = 9). ( D , G , H ) The Student’s t-test was employed. ( E , F ) One-way analysis of variance and post-hoc Bonferroni tests were utilized. Each experiment was repeated three times, and data was pooled. (mean ± standard deviation; *** P < 0.001)

    Article Snippet: The total carbohydrate content is 96.5%, as measured by the phenol-sulfuric acid method. α-Tocopherol phosphate (HY-16686, 100 μM) and Erastin (HY-15763, 10 μM) were obtained from MedChemExpress (USA).

    Techniques: Concentration Assay, Fluorescence, Standard Deviation

    Ferroptosis inhibitors reverse the effect of PS-T on BCSCs. ( A - C ) The ROS fluorescence ( A ), C11 BODIPY fluorescence ( B ), and relative MDA concentration ( C ) in ALDH + MDA-MB-231 cells that were treated alone or in combination with PS-T (10 µg/mL) and ferroptosis inhibitors α-tocopherol (α-toc, 100 µM) or liproxstatin-1 (Lip-1, 200 nM) for 24 h ( n = 9). Scale bars = 20 μm. ( D - E ) The mRNA levels of POU5F1, SOX2, and NAONG in MDA-MB-231 cells that treated with PS-T combined with α-toc ( D ) or Lip-1 ( E ) ( n = 9). ( F - G ) The proportion of ALDH + ( up ) and CD44 high CD24 low cells ( down ) in PS-T–treated MDA-MB-231 cells that co-treated with or without α-toc ( F ) or Lip-1 ( G ) ( n = 9). ( H - I ) Colony formation ( H ) ( n = 3) and mammosphere assays ( I ) ( n = 9) of ALDH + MDA-MB-231 cells treated with PS-T, ferroptosis inhibitors, and a combination of both. Scale bars = 50 μm. ( A - I ) One-way analysis of variance and post-hoc Bonferroni tests were utilized. Each experiment was repeated three times, and data was pooled. (mean ± standard deviation; (A-I) One-way ANOVA with Bonferroni’s post-hoc test was used. ** P < 0.01; *** P < 0.001)

    Journal: Cancer Cell International

    Article Title: Polysaccharides from Huaier induce autophagy-dependent ferroptosis to inhibit breast cancer stem cells in triple-negative breast cancer

    doi: 10.1186/s12935-025-04102-4

    Figure Lengend Snippet: Ferroptosis inhibitors reverse the effect of PS-T on BCSCs. ( A - C ) The ROS fluorescence ( A ), C11 BODIPY fluorescence ( B ), and relative MDA concentration ( C ) in ALDH + MDA-MB-231 cells that were treated alone or in combination with PS-T (10 µg/mL) and ferroptosis inhibitors α-tocopherol (α-toc, 100 µM) or liproxstatin-1 (Lip-1, 200 nM) for 24 h ( n = 9). Scale bars = 20 μm. ( D - E ) The mRNA levels of POU5F1, SOX2, and NAONG in MDA-MB-231 cells that treated with PS-T combined with α-toc ( D ) or Lip-1 ( E ) ( n = 9). ( F - G ) The proportion of ALDH + ( up ) and CD44 high CD24 low cells ( down ) in PS-T–treated MDA-MB-231 cells that co-treated with or without α-toc ( F ) or Lip-1 ( G ) ( n = 9). ( H - I ) Colony formation ( H ) ( n = 3) and mammosphere assays ( I ) ( n = 9) of ALDH + MDA-MB-231 cells treated with PS-T, ferroptosis inhibitors, and a combination of both. Scale bars = 50 μm. ( A - I ) One-way analysis of variance and post-hoc Bonferroni tests were utilized. Each experiment was repeated three times, and data was pooled. (mean ± standard deviation; (A-I) One-way ANOVA with Bonferroni’s post-hoc test was used. ** P < 0.01; *** P < 0.001)

    Article Snippet: The total carbohydrate content is 96.5%, as measured by the phenol-sulfuric acid method. α-Tocopherol phosphate (HY-16686, 100 μM) and Erastin (HY-15763, 10 μM) were obtained from MedChemExpress (USA).

    Techniques: Fluorescence, Concentration Assay, Standard Deviation