Naringenin chalcone (b)

CAS No. 25515-46-2

Naringenin chalcone (b)( 2',4,4',6'-TETRAHYDROXYCHALCONE | Chalconaringenin | Isosalipurpol | Chalcononaringenin )

Catalog No. M28570 CAS No. 25515-46-2

Naringenin chalcone is a product natural isolated from stems of Machaerium isadelphum (Fabaceae).

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 61 Get Quote
5MG 95 Get Quote
10MG 164 Get Quote
25MG 318 Get Quote
50MG 473 Get Quote
100MG 673 Get Quote
200MG Get Quote Get Quote
500MG Get Quote Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    Naringenin chalcone (b)
  • Note
    Research use only, not for human use.
  • Brief Description
    Naringenin chalcone is a product natural isolated from stems of Machaerium isadelphum (Fabaceae).
  • Description
    Naringenin chalcone is a product natural isolated from stems of Machaerium isadelphum (Fabaceae).
  • In Vitro
    (E)-Naringenin chalcone (25-125 μg/mL, 10 min) inhibits histamine release from rat peritoneal mast cells, with an IC50 value of 68 μg/mL.(E)-Naringenin chalcone (25-50 μM, 8 days) improves adipocyte (3T3-L1) functions by enhancing adiponectin production.(E)-Naringenin chalcone (25-100 μM, 24 h) stimulates the activity of PPARγ in NIH-3T3 cells.(E)-Naringenin chalcone (0-200 μM 24 h) inhibits the production of TNF-alpha, MCP-1, and nitric oxide (NO) by LPS-stimulated RAW 264 macrophages. RT-PCR Cell Line:3T3-L1 adipocytes Concentration:25-100 μM Incubation Time:8 days Result:Increased adiponectin mRNA levels up to 8.0-fold in a dose-dependent manner. Western Blot Analysis Cell Line:RAW 264 macrophages Concentration:0,25, 50, 100, 200 μM Incubation Time:24 h Result:Suppressed the degradation of IκB-α.
  • In Vivo
    (E)-Naringenin chalcone (0.8 mg/kg, oral administration) shows anti-allergic effect in type I allergic mice.(E)-Naringenin chalcone (0.8 mg/kg, oral administration) suppresses allergic asthma by inhibiting the type-2 function of CD4 T cells in allergic airway inflammatory mice. Animal Model:Mouse type I allergic modelDosage:0.8 mg/kg Administration:Oral administration Result:Inhibited the ear-swelling response, with the inhibitory ratio of 46.7%.Animal Model:Allergic airway inflammation induced in miceDosage:0.8 mg/kg Administration:Oral administration, dailyResult:Decreased cell numbers of the infiltrating leukocyte and eosinophils.
  • Synonyms
    2',4,4',6'-TETRAHYDROXYCHALCONE | Chalconaringenin | Isosalipurpol | Chalcononaringenin
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    5-HT7
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    25515-46-2
  • Formula Weight
    272.25
  • Molecular Formula
    C15H12O5
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    ——
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Pascual-ramon, et al. 5HT7 RECEPTOR LIGANDS AND COMPOSITIONS COMPRISING THE SAME. 20110183991 A1.
molnova catalog
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