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sunitinib su11248  (MedChemExpress)


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    Structured Review

    MedChemExpress sunitinib su11248
    Sunitinib Su11248, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 95/100, based on 117 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/su11248/pm41922884-52-0-10?v=MedChemExpress
    Average 95 stars, based on 117 article reviews
    sunitinib su11248 - by Bioz Stars, 2026-07
    95/100 stars

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    95
    MedChemExpress sunitinib su11248
    Sunitinib Su11248, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/su11248/pm41922884-52-0-10?v=MedChemExpress
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    95
    MedChemExpress su11248
    A Western blot analyses of PDGF-B in BMDM or RAW264.7 treated with rTGFBI (ng/mL) with the indicated concentrations ( n = 3 independent experiments). B RT-qPCR analyses of PDGF-B in BMDM or RAW264.7 treated with rTGFBI (ng/mL) with the indicated concentrations ( n = 3 independent experiments). C Western blot analysis of the indicated proteins in BMDM or RAW264.7 treated with or without rTGFBI (200 ng/mL) for 6 h. D RT-qPCR analysis of Pdgfb in BMDM or RAW264.7 treated with rTGFBI (200 ng/mL) alone or in combination with integrin αvβ3 or αvβ5 neutralizing antibody ( n = 3 independent experiments). E Flow cytometry analysis and statistical analysis of the percentage of Trem2 + CD9 + subpopulation in BMDM or RAW264.7 transfected with the indicated siRNAs for 24 h and treated with or without rTGFBI (200 ng/mL) for 24 h ( n = 3 independent experiments). F RT-qPCR and Western blot analysis of α-SMA in HSCs cocultured with BMDMs transfected the indicated siRNAs for 24 h and treated with or without rTGFBI (200 ng/mL) for 24 h ( n = 3 independent experiments). G RT-qPCR and Western blot analyses of α-SMA in HSCs treated with rTGFBI or in combination with <t>SU11248</t> ( n = 3 independent experiments). Mice samples ( n = 4–6 per group). Data were presented as the mean ± SDs; scale bars, 50 µm; * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001; ns not significant (Student’s t test).
    Su11248, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Pfizer Inc sutent su11248
    A Western blot analyses of PDGF-B in BMDM or RAW264.7 treated with rTGFBI (ng/mL) with the indicated concentrations ( n = 3 independent experiments). B RT-qPCR analyses of PDGF-B in BMDM or RAW264.7 treated with rTGFBI (ng/mL) with the indicated concentrations ( n = 3 independent experiments). C Western blot analysis of the indicated proteins in BMDM or RAW264.7 treated with or without rTGFBI (200 ng/mL) for 6 h. D RT-qPCR analysis of Pdgfb in BMDM or RAW264.7 treated with rTGFBI (200 ng/mL) alone or in combination with integrin αvβ3 or αvβ5 neutralizing antibody ( n = 3 independent experiments). E Flow cytometry analysis and statistical analysis of the percentage of Trem2 + CD9 + subpopulation in BMDM or RAW264.7 transfected with the indicated siRNAs for 24 h and treated with or without rTGFBI (200 ng/mL) for 24 h ( n = 3 independent experiments). F RT-qPCR and Western blot analysis of α-SMA in HSCs cocultured with BMDMs transfected the indicated siRNAs for 24 h and treated with or without rTGFBI (200 ng/mL) for 24 h ( n = 3 independent experiments). G RT-qPCR and Western blot analyses of α-SMA in HSCs treated with rTGFBI or in combination with <t>SU11248</t> ( n = 3 independent experiments). Mice samples ( n = 4–6 per group). Data were presented as the mean ± SDs; scale bars, 50 µm; * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001; ns not significant (Student’s t test).
    Sutent Su11248, supplied by Pfizer Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Pfizer Inc sunitinib sutent® or su11248
    A Western blot analyses of PDGF-B in BMDM or RAW264.7 treated with rTGFBI (ng/mL) with the indicated concentrations ( n = 3 independent experiments). B RT-qPCR analyses of PDGF-B in BMDM or RAW264.7 treated with rTGFBI (ng/mL) with the indicated concentrations ( n = 3 independent experiments). C Western blot analysis of the indicated proteins in BMDM or RAW264.7 treated with or without rTGFBI (200 ng/mL) for 6 h. D RT-qPCR analysis of Pdgfb in BMDM or RAW264.7 treated with rTGFBI (200 ng/mL) alone or in combination with integrin αvβ3 or αvβ5 neutralizing antibody ( n = 3 independent experiments). E Flow cytometry analysis and statistical analysis of the percentage of Trem2 + CD9 + subpopulation in BMDM or RAW264.7 transfected with the indicated siRNAs for 24 h and treated with or without rTGFBI (200 ng/mL) for 24 h ( n = 3 independent experiments). F RT-qPCR and Western blot analysis of α-SMA in HSCs cocultured with BMDMs transfected the indicated siRNAs for 24 h and treated with or without rTGFBI (200 ng/mL) for 24 h ( n = 3 independent experiments). G RT-qPCR and Western blot analyses of α-SMA in HSCs treated with rTGFBI or in combination with <t>SU11248</t> ( n = 3 independent experiments). Mice samples ( n = 4–6 per group). Data were presented as the mean ± SDs; scale bars, 50 µm; * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001; ns not significant (Student’s t test).
    Sunitinib Sutent® Or Su11248, supplied by Pfizer Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Targeted inhibition pathways of VEGFR, PDGFR, FGFR, cMET and TIE-2 receptors by multi-kinase inhibitors. The blockade of VEGFR, PDGFR, FGFR, cMET and TIE-2 receptors and their signaling pathways by multi-kinase inhibitors leads to inhibition of glioma vascular permeability, migration, proliferation and survival within angiogenesis. The main FDA-approved multi-target angiogenesis drugs are axitinib, sorafenib, lenvatinib, pazopanib, <t>sunitinib,</t> cabozantinib, nintedanib, regorafenib, aflibercept and ramucirumab. Sharp arrows (→) illustrate stimulation while blunt arrows (┴) indicate inhibition.
    Sunitinib Sutent ® Or Su11248, supplied by Pfizer Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Pfizer Inc sunitinib su11248 sutenttm
    Targeted inhibition pathways of VEGFR, PDGFR, FGFR, cMET and TIE-2 receptors by multi-kinase inhibitors. The blockade of VEGFR, PDGFR, FGFR, cMET and TIE-2 receptors and their signaling pathways by multi-kinase inhibitors leads to inhibition of glioma vascular permeability, migration, proliferation and survival within angiogenesis. The main FDA-approved multi-target angiogenesis drugs are axitinib, sorafenib, lenvatinib, pazopanib, <t>sunitinib,</t> cabozantinib, nintedanib, regorafenib, aflibercept and ramucirumab. Sharp arrows (→) illustrate stimulation while blunt arrows (┴) indicate inhibition.
    Sunitinib Su11248 Sutenttm, supplied by Pfizer Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Targeted inhibition pathways of VEGFR, PDGFR, FGFR, cMET and TIE-2 receptors by multi-kinase inhibitors. The blockade of VEGFR, PDGFR, FGFR, cMET and TIE-2 receptors and their signaling pathways by multi-kinase inhibitors leads to inhibition of glioma vascular permeability, migration, proliferation and survival within angiogenesis. The main FDA-approved multi-target angiogenesis drugs are axitinib, sorafenib, lenvatinib, pazopanib, <t>sunitinib,</t> cabozantinib, nintedanib, regorafenib, aflibercept and ramucirumab. Sharp arrows (→) illustrate stimulation while blunt arrows (┴) indicate inhibition.
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    Image Search Results


    A Western blot analyses of PDGF-B in BMDM or RAW264.7 treated with rTGFBI (ng/mL) with the indicated concentrations ( n = 3 independent experiments). B RT-qPCR analyses of PDGF-B in BMDM or RAW264.7 treated with rTGFBI (ng/mL) with the indicated concentrations ( n = 3 independent experiments). C Western blot analysis of the indicated proteins in BMDM or RAW264.7 treated with or without rTGFBI (200 ng/mL) for 6 h. D RT-qPCR analysis of Pdgfb in BMDM or RAW264.7 treated with rTGFBI (200 ng/mL) alone or in combination with integrin αvβ3 or αvβ5 neutralizing antibody ( n = 3 independent experiments). E Flow cytometry analysis and statistical analysis of the percentage of Trem2 + CD9 + subpopulation in BMDM or RAW264.7 transfected with the indicated siRNAs for 24 h and treated with or without rTGFBI (200 ng/mL) for 24 h ( n = 3 independent experiments). F RT-qPCR and Western blot analysis of α-SMA in HSCs cocultured with BMDMs transfected the indicated siRNAs for 24 h and treated with or without rTGFBI (200 ng/mL) for 24 h ( n = 3 independent experiments). G RT-qPCR and Western blot analyses of α-SMA in HSCs treated with rTGFBI or in combination with SU11248 ( n = 3 independent experiments). Mice samples ( n = 4–6 per group). Data were presented as the mean ± SDs; scale bars, 50 µm; * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001; ns not significant (Student’s t test).

    Journal: Communications Biology

    Article Title: TGFBI promotes liver fibrosis through remodeling the profibrotic microenvironment by a positive feedback regulatory loop

    doi: 10.1038/s42003-026-09601-2

    Figure Lengend Snippet: A Western blot analyses of PDGF-B in BMDM or RAW264.7 treated with rTGFBI (ng/mL) with the indicated concentrations ( n = 3 independent experiments). B RT-qPCR analyses of PDGF-B in BMDM or RAW264.7 treated with rTGFBI (ng/mL) with the indicated concentrations ( n = 3 independent experiments). C Western blot analysis of the indicated proteins in BMDM or RAW264.7 treated with or without rTGFBI (200 ng/mL) for 6 h. D RT-qPCR analysis of Pdgfb in BMDM or RAW264.7 treated with rTGFBI (200 ng/mL) alone or in combination with integrin αvβ3 or αvβ5 neutralizing antibody ( n = 3 independent experiments). E Flow cytometry analysis and statistical analysis of the percentage of Trem2 + CD9 + subpopulation in BMDM or RAW264.7 transfected with the indicated siRNAs for 24 h and treated with or without rTGFBI (200 ng/mL) for 24 h ( n = 3 independent experiments). F RT-qPCR and Western blot analysis of α-SMA in HSCs cocultured with BMDMs transfected the indicated siRNAs for 24 h and treated with or without rTGFBI (200 ng/mL) for 24 h ( n = 3 independent experiments). G RT-qPCR and Western blot analyses of α-SMA in HSCs treated with rTGFBI or in combination with SU11248 ( n = 3 independent experiments). Mice samples ( n = 4–6 per group). Data were presented as the mean ± SDs; scale bars, 50 µm; * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001; ns not significant (Student’s t test).

    Article Snippet: SU11248 (PDGFR inhibitor, sunitinib, #HY-10255A, MedChemExpress) and Imatinib Mesylate (PDGFR inhibitor, #HY-50946, MedChemExpress) .

    Techniques: Western Blot, Quantitative RT-PCR, Flow Cytometry, Transfection

    Targeted inhibition pathways of VEGFR, PDGFR, FGFR, cMET and TIE-2 receptors by multi-kinase inhibitors. The blockade of VEGFR, PDGFR, FGFR, cMET and TIE-2 receptors and their signaling pathways by multi-kinase inhibitors leads to inhibition of glioma vascular permeability, migration, proliferation and survival within angiogenesis. The main FDA-approved multi-target angiogenesis drugs are axitinib, sorafenib, lenvatinib, pazopanib, sunitinib, cabozantinib, nintedanib, regorafenib, aflibercept and ramucirumab. Sharp arrows (→) illustrate stimulation while blunt arrows (┴) indicate inhibition.

    Journal: International Journal of Molecular Sciences

    Article Title: A Review of FDA-Approved Multi-Target Angiogenesis Drugs for Brain Tumor Therapy

    doi: 10.3390/ijms26052192

    Figure Lengend Snippet: Targeted inhibition pathways of VEGFR, PDGFR, FGFR, cMET and TIE-2 receptors by multi-kinase inhibitors. The blockade of VEGFR, PDGFR, FGFR, cMET and TIE-2 receptors and their signaling pathways by multi-kinase inhibitors leads to inhibition of glioma vascular permeability, migration, proliferation and survival within angiogenesis. The main FDA-approved multi-target angiogenesis drugs are axitinib, sorafenib, lenvatinib, pazopanib, sunitinib, cabozantinib, nintedanib, regorafenib, aflibercept and ramucirumab. Sharp arrows (→) illustrate stimulation while blunt arrows (┴) indicate inhibition.

    Article Snippet: Sunitinib (Sutent ® or SU11248, Pfizer Inc, New York, NY, USA) is also known as INN-sunitinib malate.

    Techniques: Inhibition, Protein-Protein interactions, Permeability, Migration

    Main in vitro and in vivo studies that demonstrate the efficacy of anti-angiogenic multi-target therapies on brain tumors.

    Journal: International Journal of Molecular Sciences

    Article Title: A Review of FDA-Approved Multi-Target Angiogenesis Drugs for Brain Tumor Therapy

    doi: 10.3390/ijms26052192

    Figure Lengend Snippet: Main in vitro and in vivo studies that demonstrate the efficacy of anti-angiogenic multi-target therapies on brain tumors.

    Article Snippet: Sunitinib (Sutent ® or SU11248, Pfizer Inc, New York, NY, USA) is also known as INN-sunitinib malate.

    Techniques: In Vitro, In Vivo, Activity Assay, Phospho-proteomics, Activation Assay, Irradiation, Inhibition, Migration

    Sunitinib chemical structure. The design was created with ACD/ChemSketch 2.0 (Freeware).

    Journal: International Journal of Molecular Sciences

    Article Title: A Review of FDA-Approved Multi-Target Angiogenesis Drugs for Brain Tumor Therapy

    doi: 10.3390/ijms26052192

    Figure Lengend Snippet: Sunitinib chemical structure. The design was created with ACD/ChemSketch 2.0 (Freeware).

    Article Snippet: Sunitinib (Sutent ® or SU11248, Pfizer Inc, New York, NY, USA) is also known as INN-sunitinib malate.

    Techniques:

    Main clinical studies that used anti-angiogenic multi-targeted therapy for glioma treatment.

    Journal: International Journal of Molecular Sciences

    Article Title: A Review of FDA-Approved Multi-Target Angiogenesis Drugs for Brain Tumor Therapy

    doi: 10.3390/ijms26052192

    Figure Lengend Snippet: Main clinical studies that used anti-angiogenic multi-targeted therapy for glioma treatment.

    Article Snippet: Sunitinib (Sutent ® or SU11248, Pfizer Inc, New York, NY, USA) is also known as INN-sunitinib malate.

    Techniques: Protein-Protein interactions, Drug discovery, Infection, Control, Concentration Assay, Clinical Proteomics, Reflux, Adjuvant