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Results for "

Baicalein

" in MedChemExpress (MCE) Product Catalog:

10

Inhibitors & Agonists

8

Natural
Products

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-N0196
    Baicalein
    15+ Cited Publications

    5,6,7-Trihydroxyflavone

    Xanthine Oxidase Influenza Virus Ferroptosis Cancer
    Baicalein (5,6,7-Trihydroxyflavone) is a xanthine oxidase inhibitor with an IC50 value of 3.12 μM.
    <em>Baicalein</em>
  • HY-N0197
    Baicalin
    Maximum Cited Publications
    19 Publications Verification

    Baicalein 7-O-β-D-glucuronide

    NF-κB Autophagy HIV Inflammation/Immunology Cancer
    Baicalin, as a flavonoid glycoside, is an allosteric carnitine palmityl transferase 1 (CPT1) activator. Baicalin reduces the expression of NF-κB .
    Baicalin
  • HY-N8352

    Xanthine Oxidase Cancer
    Baicalein 6-O-glucoside is a glucuronidation metabolite of Baicalein .
    <em>Baicalein</em> 6-O-glucoside
  • HY-N8788

    Others Inflammation/Immunology Cancer
    Baicalein 7-O-β-D-ethylglucuronide is a natural flavone glycoside that can be extracted from Scutellaria baicalensis Georgi. Baicalein 7-O-β-D-ethylglucuronide has antioxidant activity. Baicalein 7-O-β-D-ethylglucuronide inhibits FeSO4-Cys-induced lipid peroxidation of liver homogenate. Baicalein 7-O-β-D-ethylglucuronide also shows strong cytoprotective effect on H2O2-induced oxidative damage of human umbilical vein endothelial cells .
    <em>Baicalein</em> 7-O-β-D-ethylglucuronide
  • HY-N0196A

    5,6,7-Trihydroxyflavone hydrate

    Influenza Virus Ferroptosis Xanthine Oxidase Cancer
    Baicalein hydrate (ALA; C18:3 (9Z,12Z,15Z); C18:3 n-3) is a xanthine oxidase inhibitor with an IC50 value of 3.12 μM.
    <em>Baicalein</em> hydrate
  • HY-110398

    Baicalein trimethyl ether

    p38 MAPK Inflammation/Immunology Cancer
    5,6,7-Trimethoxyflavone is a novel p38-α MAPK inhibitor with an anti-inflammatory effect. 5,6,7-Trimethoxyflavone is isolated from several plants including Zeyhera tuberculosa, Callicarpa japonica, and Kickxia lanigera .
    5,6,7-Trimethoxyflavone
  • HY-N0560
    Oroxylin A
    5+ Cited Publications

    Baicalein 6-methyl ether; 6-MethoxyBaicalein

    HIF/HIF Prolyl-Hydroxylase Autophagy Virus Protease Cancer
    Oroxylin A is an active flavonoid compound with strong anti-cancer effects. Oroxylin A inhibits the IL-6/STAT3 pathway and NF-κB signaling, inhibits cell proliferation and induces apoptosis. Oroxylin A inhibits colitis-related carcinogenesis .
    Oroxylin A
  • HY-N11886

    Drug Metabolite Others
    5-NH2-Baicalein is an aminated metabolite of Baicalein (HY-N0196). 5-NH2-Baicalein can be used for research of ammonia and ammonia-associated chronic diseases .
    5-NH2-<em>Baicalein</em>
  • HY-116282
    Dextran sulfate sodium salt (MW 5000)
    1 Publications Verification

    DSS (MW 5000); DXS (MW 5000)

    HIV Apoptosis Infection Inflammation/Immunology
    Dextran sulfate sodium salt (MW 5000) is a polymer of anhydroglucose with a molecular weight of 5000. Dextran sulfate sodium salt (MW 5000) can be used to induce acute colitis and cause apoptosis of colonic epithelial cells in mice. The concentration dose used in the study was 5% (in feed, w/w). The sulfated polysaccharide dextran sulfate is also an effective inhibitor of HIV. Dextran sulfate sodium salt (MW 5000) can significantly inhibit HIV-1 replication at a concentration that does not significantly inhibit the blood coagulation process. Dextran sulfate sodium salt (MW 5000) protects MT-4 cells from HIV-1-induced cellular pathogenicity. Dextran sulfate-induced colitis can be inhibited by Puerarin (HY-N0145), Baicalein (HY-N0196), β-Caryophyllene (HY-N1415).
    Dextran sulfate sodium salt (MW 5000)
  • HY-116282A

    DSS (MW 4500-5500); DXS (MW 4500-5500)

    HIV Apoptosis Infection Inflammation/Immunology
    Dextran sulfate sodium salt (MW 4500-5500) is a polymer of anhydroglucose with a molecular weight of 4500-5500. Dextran sulfate sodium salt (MW 4500-5500) can be used to induce acute colitis and cause apoptosis of colonic epithelial cells in mice. The recommended molecular weight in the study is 5000 (HY-116282) and the use concentration is 5% (in feed, W/W). The sulfated polysaccharide dextran sulfate is also an effective inhibitor of HIV. Dextran sulfate sodium salt (MW 4500-5500) can significantly inhibit HIV-1 replication at concentrations that do not significantly inhibit the blood coagulation process. Dextran sulfate sodium salt (MW 4500-5500) protects MT-4 cells from HIV-1-induced cellular pathogenicity. Dextran sulfate-induced colitis can be inhibited by Puerarin (HY-N0145), Baicalein (HY-N0196), β-Caryophyllene (HY-N1415).
    Dextran sulfate sodium salt (MW 4500-5500)

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