Tanshinone IIA
CAS No. 568-72-9
Tanshinone IIA( Dan Shen ketone )
Catalog No. M18827 CAS No. 568-72-9
Tanshinone IIA(Tanshinone B) is the diterpene quinone in Danshen, which is utilized in the treatment of cardiovascular and inflammatory.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 10MG | 61 | In Stock |
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| 25MG | 118 | In Stock |
|
| 50MG | 204 | In Stock |
|
| 100MG | Get Quote | In Stock |
|
| 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 NameTanshinone IIA
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NoteResearch use only, not for human use.
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Brief DescriptionTanshinone IIA(Tanshinone B) is the diterpene quinone in Danshen, which is utilized in the treatment of cardiovascular and inflammatory.
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DescriptionTanshinone IIA(Tanshinone B) is the diterpene quinone in Danshen, which is utilized in the treatment of cardiovascular and inflammatory.
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In Vitro——
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In VivoAnimal Model:Male ICR mice (25–30 g) Dosage:10 or 20 mg/kg Administration:P.o.Result:Significantly reversed scopolamine-induced cognitive impairments. Animal Model:STZ-treated rats Dosage:2, 4, 8 mg/kg Administration:I.p.Result:Decreased the expression levels of transforming growth factor-beta1, TSP-1, Grp78 and CHOP and attenuated the increase in the protein levels of p-PERK, p-elf2α and ATF-4 from the renal tissues of diabetic rats.Animal Model:Female Sprague-Dawley rats (180 -200g)Dosage:3 and 12 mg/kg Administration:I.p.Result:Significantly inhibited the growth of ectopic endometrium.
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SynonymsDan Shen ketone
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PathwayGPCR/G Protein
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TargetHistamine Receptor
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RecptorVEGFR2
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Research AreaCancer|Cardiovascular Disease
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Indication——
Chemical Information
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CAS Number568-72-9
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Formula Weight294.35
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Molecular FormulaC19H18O3
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Purity>98% (HPLC)
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SolubilityDMSO : 3.85 mg/mL 13.08 mM; H2O : < 0.1 mg/mL
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SMILESc12c(C(=O)C(=O)c3c1ccc1c3CCCC1(C)C)c(co2)C
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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. Fu J, et al. Eur J Pharmacol, 2007, 568(1-3), 213-221.
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