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Salvianolic Acid C
58 CAD – 1,904 CADPrice range: 58 CAD through 1,904 CAD
For Research Use Only (RUO). This product is sold strictly for laboratory research use. Not for human or veterinary consumption, therapeutic, or diagnostic use.For sale to research organizations and laboratories only; not for patients or for personal use.
Products Details
Product Description
– Salvianolic Acid C is extracted from the root of Salvia miltiorrhiza, a perennial plant in the genus Salvia.
For Research Use Only (RUO). This product is sold strictly for laboratory research use only. Not for human or veterinary consumption, therapeutic, or diagnostic use. Any pharmacological, therapeutic, cosmetic, or biological effects described above are provided as research context only and do not represent intended or approved uses of this product.
Web ID
– T3149
Storage Temperature
– -20℃
Shipping
– Blue Ice
Molecular Formula
– C26H20O10
Citations
– 1. Chan Yang, Xiaoyan Pan, Xinfeng Xu, Chen Cheng, Yuan Huang, Lin Li, Shibo Jiang, Wei Xu, Gengfu Xiao Salvianolic acid C potently inhibits SARS-CoV-2 infection by blocking the formation of six-helix bundle core of spike protein. Signal Transduction and Targeted Therapy. 2020 Oct 6;5(1):220
2. Zhang H, Liang B, Sang X, et al.Discovery of Potential Inhibitors of SARS-CoV-2 Main Protease by a Transfer Learning Method.Viruses.2023, 15(4): 891.
3. Wu M, Lin J, Huang D, et al.Salvianolic Acid C Inhibits the Epithelial-Mesenchymal Transition and Ameliorates Renal Tubulointerstitial Fibrosis.Frontiers in Bioscience-Landmark.2023, 28(6): 121.
4. Xing Y, Huang D, Lin P, et al.Salvianolic acid C promotes renal gluconeogenesis in fibrotic kidneys through PGC1α.Biochemical and Biophysical Research Communications.2024: 151174.
References
– Duan Y, et al. Salvianolic Acid C Attenuates LPS-Induced Inflammation and Apoptosis in Human Periodontal Ligament Stem Cells via Toll-Like Receptors 4 (TLR4)/Nuclear Factor kappa B (NF-κB) Pathway. Med Sci Monit. 2019 Dec 13;25:9499-9508.
CAS Number
– 115841-09-3
Molecular Weight
– C26H20O10
Compound Purity
– 0.996
SMILES
– OC(=O)[C@@H](Cc1ccc(O)c(O)c1)OC(=O)C=Cc1ccc(O)c2oc(cc12)-c1ccc(O)c(O)c1
Pathway
– Metabolism
Product type
– Natural Product
Disclaimer: All products are for Research use only unless clearly stated otherwise on the product datasheet. Datasheets provided on the website are drafts for reference purpose only and you are requested to always refer to the hard copy included in the kit for your experimentation. Agdia Products are available for delivery only in Canada.
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