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 |
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5MG | 95 | Get Quote |
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10MG | 164 | Get Quote |
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25MG | 318 | Get Quote |
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50MG | 473 | Get Quote |
|
100MG | 673 | Get Quote |
|
200MG | Get Quote | Get Quote |
|
500MG | Get Quote | Get Quote |
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1G | Get Quote | Get Quote |
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Biological Information
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Product NameNaringenin chalcone (b)
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NoteResearch use only, not for human use.
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Brief DescriptionNaringenin chalcone is a product natural isolated from stems of Machaerium isadelphum (Fabaceae).
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DescriptionNaringenin chalcone is a product natural isolated from stems of Machaerium isadelphum (Fabaceae).
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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.
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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.
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Synonyms2',4,4',6'-TETRAHYDROXYCHALCONE | Chalconaringenin | Isosalipurpol | Chalcononaringenin
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PathwayOthers
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TargetOther Targets
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Recptor5-HT7
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Research Area——
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Indication——
Chemical Information
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CAS Number25515-46-2
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Formula Weight272.25
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Molecular FormulaC15H12O5
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Purity>98% (HPLC)
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Solubility——
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SMILES——
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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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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