
Rhamnetin
CAS No. 90-19-7
Rhamnetin( beta-Rhamnocitrin )
Catalog No. M29098 CAS No. 90-19-7
Rhamnetin, a quercetin derivative found in Coriandrum sativum, has antioxidant and anti-inflammatory activities. Rhamnetin inhibits secretory phospholipase A2.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
5MG | 250 | In Stock |
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10MG | 376 | In Stock |
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25MG | 614 | In Stock |
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50MG | 853 | In Stock |
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100MG | Get Quote | In Stock |
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200MG | Get Quote | In Stock |
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500MG | Get Quote | In Stock |
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1G | Get Quote | In Stock |
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Biological Information
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Product NameRhamnetin
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NoteResearch use only, not for human use.
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Brief DescriptionRhamnetin, a quercetin derivative found in Coriandrum sativum, has antioxidant and anti-inflammatory activities. Rhamnetin inhibits secretory phospholipase A2.
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DescriptionRhamnetin, a quercetin derivative found in Coriandrum sativum, has antioxidant and anti-inflammatory activities. Rhamnetin inhibits secretory phospholipase A2.
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In Vitro——
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In Vivo——
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Synonymsbeta-Rhamnocitrin
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PathwayOthers
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TargetOther Targets
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Recptor——
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Research Area——
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Indication——
Chemical Information
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CAS Number90-19-7
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Formula Weight316.265
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Molecular FormulaC16H12O7
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Purity>98% (HPLC)
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Solubility——
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SMILESCOc1cc(O)c2c(c1)oc(-c1ccc(O)c(O)c1)c(O)c2=O
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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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26Rfa, Hypothalamic ...
This human neuropeptide of the RFamide peptide family with orexigenic activity may be also involved in the control of feeding behavior. The 26RFa gene is exclusively expressed in the ventromedial hypothalamic nucleus and in the lateral hypothalamic area. The primary structures of human, rat, and frog 26RFa exhibit ≈80% identity. Other data suggest also the potential role of the 26RFa peptide in the control of the gonadotropic axis.
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Geniposide
Geniposide is an iridoid glycoside with a variety of biological activities including neuroprotective,anti-diabetic,antiproliferative,and antioxidative activity.
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MDH1-IN-1
MDH1-IN-1 (5i) is a potent MDH1 inhibitor with an IC50 of 6.79 μM for MDH1 and >40 μM for MDH2.