Danshensu
CAS No. 76822-21-4
Danshensu( Dan shen suan A | Salvianic acid A )
Catalog No. M19093 CAS No. 76822-21-4
Danshensu is an active ingredient of Salvia miltiorrhiza with wide cardiovascular benefit.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 29 | In Stock |
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| 10MG | 48 | In Stock |
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| 25MG | 75 | In Stock |
|
| 50MG | 100 | In Stock |
|
| 100MG | 151 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | 352 | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameDanshensu
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NoteResearch use only, not for human use.
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Brief DescriptionDanshensu is an active ingredient of Salvia miltiorrhiza with wide cardiovascular benefit.
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DescriptionDanshensu is an active ingredient of Salvia miltiorrhiza with wide cardiovascular benefit.
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In VitroCell Migration Assay Cell Line:FaDu and Ca9-22 cells Concentration:25, 50, and 100 μM Incubation Time:24 h Result:At higher concentrations (50 and 100 μM) caused significant reduction in migration and invasion of both FaDu and Ca9-22 cells.Western Blot Analysis Cell Line:FaDu and Ca9-22 cells Concentration:25, 50, and 100 μM Incubation Time:24 h Result:Phosphorylation of ERK reduced dose-dependently after 24 h in FaDu cell. Caused significant reduction in p38 phosphorylation.
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In VivoAnimal Model:Adult BALB/c mice (male, 6-8 weeks, 20±2?g)Dosage:25, 50, 100?mg/kg Administration:Oral administration (daily for 7 continuous days) or i.v. (once) Result:Could prevent SARS-CoV-2 S protein-induced acute lung inflammation. Ameliorated inflammatory cytokines in serum and lung tissue.
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SynonymsDan shen suan A | Salvianic acid A
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PathwayApoptosis
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TargetTNF
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RecptorOthers
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Research AreaCardiovascular Disease
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Indication——
Chemical Information
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CAS Number76822-21-4
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Formula Weight198.17
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Molecular FormulaC9H10O5
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Purity>98% (HPLC)
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SolubilityH2O : 6.2 mg/mL 31.29 mM
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SMILESc1cc(c(cc1C[C@H](C(=O)O)O)O)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
1. YG Cao, et al.Br J Pharmacol. 2009 Jun; 157(3): 482–490.
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