SMB01030

Theviridoside

≥90% (LC/MS-ELSD)

• Synonym(s): Methyl (1S,4aR,7aR)-1-(β-D-glucopyranosyloxy)-1,4a,5,7a-tetrahydro-4a-hydroxy-7-(hydroxymethyl)cyclopenta[c]pyran-4-carboxylate (ACI), Theveridoside, Theveside methyl ester
• Empirical Formula (Hill Notation): C₁₇H₂₄O₁₁
• CAS Number: 23407-76-3
• Molecular Weight: 404.37
• MDL number: MFCD20260837
• UNSPSC Code: 12352205

Properties

• assay: ≥90% (LC/MS-ELSD)
• form: solid
• application(s): metabolomics; vitamins, nutraceuticals, and natural products
• storage temp.: −20°C
• InChI: 1S/C17H24O11/c1-25-14(23)8-6-26-15(10-7(4-18)2-3-17(8,10)24)28-16-13(22)12(21)11(20)9(5-19)27-16/h2,6,9-13,15-16,18-22,24H,3-5H2,1H3/t9-,10+,11-,12+,13-,15+,16+,17+/m1/s1
• InChI key: LDBMLOLBWUOZGG-DOFVRBEMSA-N

Description

General description

Theviridoside, an iridoid glycoside, is a natural product commonly found in plants of Cerbera odollam, Lippia javanica, Lippia turbinata and Thevetia neriifolia. In Cancer research, it exerts a significant effect on cell function and signal transduction, inducing cell cycle arrest and apoptosis in cancer cells while inhibiting the production of pro-inflammatory cytokines. This compound exhibits potent biological activity, including anti-cancer, antifungal, anti-inflammatory, and anti-viral activities.

Application

It is a natural product derived from plant source that finds application in compound screening libraries, metabolomics, phytochemical, and pharmaceutical research.

Biochem/physiol Actions

Theviridoside acts by inhibiting the Na+/K+-ATPase pump, leading to increased intracellular calcium levels and the activation of multiple signaling pathways.

Features and Benefits

• High quality compound suitable for multiple research applications
• Compatible with HPLC and mass spectrometry techniques

Other Notes

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Safety Information

• Storage Class: 11 - Combustible Solids
• wgk_germany: WGK 3
• flash_point_f: Not applicable
• flash_point_c: Not applicable