Berberine hydrogen sulphate

CAS No. 633-66-9

Berberine hydrogen sulphate( —— )

Catalog No. M18934 CAS No. 633-66-9

Berberine sulfate, an alkaloid extracted from several plants, possesses antimicrobial activity against a wide variety of microorganisms including Gram-positive and Gram-negative bacteria, fungi, and protozoa.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
25MG 76 In Stock
100MG Get Quote In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Berberine hydrogen sulphate
  • Note
    Research use only, not for human use.
  • Brief Description
    Berberine sulfate, an alkaloid extracted from several plants, possesses antimicrobial activity against a wide variety of microorganisms including Gram-positive and Gram-negative bacteria, fungi, and protozoa.
  • Description
    Berberine sulfate, an alkaloid extracted from several plants, possesses antimicrobial activity against a wide variety of microorganisms including Gram-positive and Gram-negative bacteria, fungi, and protozoa.
  • In Vitro
    Cell Proliferation Assay Cell Line:Four colorectal carcinoma cell lines LoVo, HCT116, SW480, and HT-29 Concentration:1.25, 2.5, 5, 10, 20, 40, 80, and 160 μM Incubation Time:72 hours Result:Inhibited the proliferation of four cell lines. The IC50 ranged from 40.8±4.1 μM (LoVo) to 98.6±2.9 μM (HCT116).Cell Proliferation AssayCell Line:Colorectal carcinoma cell lines LoVo Concentration:1.25, 2.5, 5, 10, 20, 40, 80, and 160 μM Incubation Time:24, 48, 72 hours Result:Induced a time- and dose-dependent inhibition of cell growth. By 72 h, 160.0 μM induced 71.1±1.9 % growth inhibitions in LoVo cells.Cell Cycle Analysis Cell Line:LoVo cells Concentration:0, 10, 20, 40, or 80 μM Incubation Time:24 hours Result:Exposure to 40.0 μM induced G2/M-phase cell cycle arrest, an increase in the G2/M-phase population and a progressive decline in the G1 population.Western Blot Analysis Cell Line:LoVo cells Concentration:10, 20, 40, or 80 μM Incubation Time:24 hours Result:Suppressed cyclin B1, cdc2 and cdc25c protein expression.
  • In Vivo
    Animal Model:5-week-old BALB/c nu/nu mice with human colorectal adenocarcinoma LoVo xenograftsDosage:10, 30, or 50 mg/kg/day Administration:Gastrointestinal gavage; for 10 consecutive days Result:Showed inhibitory rates of 33.1% and 45.3% at doses of 30 and 50 mg/kg/day.
  • Synonyms
    ——
  • Pathway
    GPCR/G Protein
  • Target
    Antibacterial
  • Recptor
    Antibacterial
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    633-66-9
  • Formula Weight
    433.43
  • Molecular Formula
    C20H19NO8S
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?H2O : 50 mg/mL (115.36 mM)
  • SMILES
    COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC5=C(C=C4CC3)OCO5)OC.OS(=O)(=O)[O-]
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

molnova catalog
related products
  • (Rac)-AMXT-1501 4HCl

    (Rac)-AMXT-1501 4HCl is a polyamine transport inhibitor that inhibits polyamine transport and acts synergistically with cisplatin in HNSCC.

  • Relebactam

    Relebactam (MK-7655)?is a novel β-lactamase inhibitor that inhibited both class A and C β-lactamases in vitro.

  • Glycol chitosan

    Glycol chitosan is a chitosan derivative with hydrophilic ethylene glycol branches.