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Chemical Structure
Chemical Structure
Chemical Structure

Berberine chloride [633-65-8]

Research Use Only
CDX-B0212
Chemodex
CAS Number633-65-8
Product group Chemicals
Estimated Purity>98%
Molecular Weight335.3 . 36.5
Price on request
Packing Size
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Overview

  • Supplier
    Chemodex
  • Product Name
    Berberine chloride [633-65-8]
  • Delivery Days Customer
    10
  • CAS Number
    633-65-8
  • Certification
    Research Use Only
  • Estimated Purity
    >98%
  • Hazard Information
    Non-hazardous
  • Molecular Formula
    C20H17NO4 . HCl
  • Molecular Weight
    335.3 . 36.5
  • Scientific Description
    Chemical. CAS: 633-65-8. Formula: C20H17NO4 . HCl. MW: 335.3 . 36.5. Synthetic Natural fluorescent dye, used in histology for staining heparin in mast cells. An isoquinoline alkaloid, which shows antibacterial, antifungal, anti-inflammatory, anti-oxidant, antidiabetic, antiviral and anticancer activity. It inhibits cell growth and induces apoptosis in a variety of cancer cell lines. Broad spectrum enzyme inhibitor, affects N-acetyltransferase, cyclooxygenase-2, and topoisomerase activities and gene/protein expression. Increases adiponectin expression, upregulates LDLR and insulin receptor. Anti-hyperglycemic, by inhibition of aldose reductase, inducing glycolysis, preventing insulin resistance through increasing insulin receptor expression and acting like incretins. Activates AMPK and ERK. Potent, uncompetitive, reversible IDO 1 inhibitor with IC50 values of 7 microM (cell-based assay) and 9.3 microM (enzymatic assay), and Ki value 8microM. - Natural fluorescent dye, used in histology for staining heparin in mast cells. An isoquinoline alkaloid, which shows antibacterial, antifungal, anti-inflammatory, anti-oxidant, antidiabetic, antiviral and anticancer activity. It inhibits cell growth and induces apoptosis in a variety of cancer cell lines. Broad spectrum enzyme inhibitor, affects N-acetyltransferase, cyclooxygenase-2, and topoisomerase activities and gene/protein expression. Increases adiponectin expression, upregulates LDLR and insulin receptor. Anti-hyperglycemic, by inhibition of aldose reductase, inducing glycolysis, preventing insulin resistance through increasing insulin receptor expression and acting like incretins. Activates AMPK and ERK. Potent, uncompetitive, reversible IDO1 inhibitor with IC50 values of 7 microM (cell-based assay) and 9.3 microM (enzymatic assay), and Ki value 8microM. Inhibits BAFF production in H. pylori-induced chronic gastritis.
  • SMILES
    [Cl-].COC1=C(OC)C2=C[N+]3=C(C=C2C=C1)C1=CC2=C(OCO2)C=C1CC3
  • Storage Instruction
    2°C to 8°C
  • UNSPSC
    12352200