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Quercetagitrin
CAS No. 548-75-4
Quercetagitrin( Quercetagetin-7-O-glucoside )
Catalog No. M21517 CAS No. 548-75-4
Quercetagitrin isolated from the African Marigold (Tagetes erecta) has anti-inflammatory activity.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 111 | In Stock |
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| 5MG | 101 | In Stock |
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| 10MG | 150 | In Stock |
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| 25MG | 282 | In Stock |
|
| 50MG | 423 | In Stock |
|
| 100MG | 641 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameQuercetagitrin
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NoteResearch use only, not for human use.
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Brief DescriptionQuercetagitrin isolated from the African Marigold (Tagetes erecta) has anti-inflammatory activity.
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DescriptionQuercetagitrin isolated from the African Marigold (Tagetes erecta) has anti-inflammatory activity.
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In Vitro——
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In Vivo——
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SynonymsQuercetagetin-7-O-glucoside
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PathwayOthers
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TargetOther Targets
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RecptorOthers
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Research Area——
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Indication——
Chemical Information
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CAS Number548-75-4
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Formula Weight480.38
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Molecular FormulaC21H20O13
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Purity>98% (HPLC)
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SolubilityDMSO:25 mg/mL (52.42 mM)
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SMILESOC[C@H]([C@H]([C@@H]([C@H]1O)O)O)O[C@H]1Oc(cc(c(C1=O)c2O)OC(c(cc3)cc(O)c3O)=C1O)c2O
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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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Skullcapflavone II
Skullcapflavone II is a flavonoid derived from Scutellaria baicalensis, a widely used herbal medicine in anti-inflammatory and anticancer therapy.?
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YK-2-69
YK-2-69 is a highly selective DYRK2 inhibitor with anti-prostate cancer effects.
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γ-2-MSH (41-58), ami...
Melanocortin (MC) 3-MSH (Melanocyte-Stimulating Hormone) is believed to signal through the MC 3 receptor. It induces a sustained increase in intracellular free calcium levels ([Ca2+]i) in a subpopulation of pituitary cells. Most of the cells responding to 3-MSH express more than one pituitary hormone mRNA. The effect of 3-MSH is blocked by SHU9119, a MC3R and MC4R antagonist, in only 50% of the responsive cells, suggesting that in half of these cells the mediating receptor is not the MC3R. Low picomolar doses of 3-MSH increase [Ca2+]i in the growth hormone (GH)- and prolactin (PRL)-secreting GH3 cell line.
