An antioxidant and free radical scavenger
Technical Support & Resources

Information provided in the product description is from published literature. Due to the nature of scientific experimentation, your results (e.g., selectivity and effective concentrations) or specific application for this product may differ. If you have questions about how this product fits your application, please contact our technical support staff.

Visit our FAQ

Contact Us

Toll Free Phone (USA and Canada Only): (888) 526-5351
Direct Phone: (734) 975-3888

Request Technical Support

Technical Support Request

To streamline the process attach the appropriate questionnaire to your inquiry.

Download IHC QuestionnaireDownload WB Questionnaire

View Our Privacy Statement for details on how we use and protect your data. In addition, this site is protected by hCaptcha and its Privacy Policy and Terms of Service apply.

Salvianolic Acid B

Item No. 9001577

Technical Information
Formal Name
4-[(1E)-3-[(1R)-1-carboxy-2-(3,4-dihydroxyphenyl)ethoxy]-3-oxo-1-propen-1-yl]-2-(3,4-dihydroxyphenyl)-2,3-dihydro-7-hydroxy-3-benzofurancarboxylic acid (2S,3S)-3-[(1R)-1-carboxy-2-(3,4-dihydroxyphenyl)ethyl] ester
CAS Number
121521-90-2
Synonyms
  • Lithospermate B
Molecular Formula
C36H30O16
Formula Weight
Purity
≥95%
A crystalline solid
DMF: 20 mg/mlDMSO: 20 mg/mlEthanol: 10 mg/mlPBS (pH 7.2): 1 mg/ml
SMILES
OC1=CC=C(C[C@H](C(O)=O)OC(/C=C/C2=CC=C(O)C3=C2[C@H](C(O[C@@H](C(O)=O)CC4=CC(O)=C(O)C=C4)=O)[C@@H](C5=CC(O)=C(O)C=C5)O3)=O)C=C1O
InChi Code
InChI=1S/C36H30O16/c37-20-6-1-16(11-24(20)41)13-27(34(45)46)50-29(44)10-5-18-3-9-23(40)33-30(18)31(32(52-33)19-4-8-22(39)26(43)15-19)36(49)51-28(35(47)48)14-17-2-7-21(38)25(42)12-17/h1-12,15,27-28,31-32,37-43H,13-14H2,(H,45,46)(H,47,48)/b10-5+/t27-,2
InChi Key
SNKFFCBZYFGCQN-VWUOOIFGSA-N
Origin
Plant/Salviae Miltiorrhizae Radix et Rhizoma
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
Certificates of Analysis & Batch Specific Data

Provide batch numbers separated by commas to download or request available product inserts, QC sheets, certificates of analysis, data packs, and GC-MS data.

    Add

    Add

    Add

    Add

    Cayman Chemical
    Neutrophil Biology Wall Poster

    Explore how neutrophils shape the immune response in health and disease. This poster highlights neutrophil pathogen defense mechanisms, including phagocytosis, degranulation, and NETosis, as well as neutrophil roles in inflammation and NET-associated pathologies.

    DOWNLOAD NOW
    Product Description

    Salvianolic acid B is an antioxidant and free radical scavenging compound extracted from S. miltiorrhiza that has been investigated for its cardioprotective and chemopreventative properties.1,2 It has been reported to reduce leukocyte-endothelial adherence, inhibit inflammation and metalloproteinase expression from aortic smooth muscle cells, and regulate immune function and certain intracellular kinase associated signaling pathways by competitively inhibiting the protein-protein interactions mediated by key binding domains.1,3

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Ho, J.H.C., and Hong, C.Y. Salvianolic acids: Small compounds with multiple mechanisms for cardiovascular protection. J. Biomed. Sci. 18(1), 30 (2011).

    2. Liu, G.T., Zhang, T.M., Wang, B.e., et alProtective action of seven natural phenolic compounds against peroxidative damage to biomembranes. Biochem. Pharmacol. 43(2), 147-152 (1992).

    3. Zhao, Y., Guo, Y., and Gu, X. Salvianolic Acid B, a potential chemopreventive agent, for head and neck squamous cell cancer. J. Oncol. 534548 (2011).