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Pinocembrin chalcone
CAS No. 4197-97-1
Pinocembrin chalcone( 2',4',6'-Trihydroxychalcone | Pinocembrinchalcone )
Catalog No. M29214 CAS No. 4197-97-1
Pinocembrin chalcone is an inhibitor of tyrosinase with antimutagenic effects. Pinocembrin chalcone can be used in studies about the prevention of gastric ulcers.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 264 | Get Quote |
|
| 10MG | 399 | Get Quote |
|
| 25MG | 659 | Get Quote |
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| 100MG | Get Quote | Get Quote |
|
| 200MG | Get Quote | Get Quote |
|
| 500MG | Get Quote | Get Quote |
|
| 1G | Get Quote | Get Quote |
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Biological Information
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Product NamePinocembrin chalcone
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NoteResearch use only, not for human use.
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Brief DescriptionPinocembrin chalcone is an inhibitor of tyrosinase with antimutagenic effects. Pinocembrin chalcone can be used in studies about the prevention of gastric ulcers.
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DescriptionPinocembrin chalcone is an inhibitor of tyrosinase with antimutagenic effects. Pinocembrin chalcone can be used in studies about the prevention of gastric ulcers.(In Vitro):Pinocembrin chalcone exhibits antibacterial activity against the antibiotic-susceptible NG strain WHO V and Candida albicans with a MIC of 100 μg/mL.
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In Vitro——
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In Vivo——
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Synonyms2',4',6'-Trihydroxychalcone | Pinocembrinchalcone
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PathwayGPCR/G Protein
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TargetCalcium Channel
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RecptorCalcium Channel
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Research Area——
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Indication——
Chemical Information
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CAS Number4197-97-1
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Formula Weight256.257
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Molecular FormulaC15H12O4
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Purity>98% (HPLC)
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Solubility——
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SMILESOc1cc(O)c(C(=O)C=Cc2ccccc2)c(O)c1
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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
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(±)-Liquiritigenin
(±)-Liquiritigenin ((±)-4',7-Dihydroxyflavanone), a flavonoid extracted from Angelica keiskei, inhibits the calcium-activated chloride channel TMEM16A.(±)-Liquiritigenin induces an increase in apoptosis and an enhancement of caspase3 activity.
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YM-244769
YM-244769 is an effective inhibitor of Na+/Ca2+ exchange 3 (NCX3) with an IC50 of 18 nM. YM-244769 has efficient protective effects on neurons and kidneys.
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MMK 1
Potent and selective human formyl peptide receptor FPR2 agonist (EC50 values are 1, 2 and > 10 000 nM at mFRP2, hFPR2 and hFPR1 respectively). Induces migration of human monocytes and neutrophils via a chemotactic mechanism and enhances production of proinflammatory cytokines IL-1β and IL-6. Also activates the neutrophil superoxide-generating NADPH-oxidase.
