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Documentos Principais

SMB01030

Sigma-Aldrich

Theviridoside

≥90% (LC/MS-ELSD)

Sinônimo(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

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About This Item

Fórmula empírica (Notação de Hill):
C17H24O11
Número CAS:
Peso molecular:
404.37
Número MDL:
Código UNSPSC:
12352205
NACRES:
NA.25

fonte biológica

plant

Ensaio

≥90% (LC/MS-ELSD)

Formulário

solid

peso molecular

404.37

solubilidade

water: soluble

aplicação(ões)

metabolomics
vitamins, nutraceuticals, and natural products

temperatura de armazenamento

−20°C

cadeia de caracteres SMILES

O1[C@H]([C@@H]([C@H]([C@@H]([C@H]1CO)O)O)O)O[C@@H]2OC=C([C@@]3([C@H]2C(=CC3)CO)O)C(=O)OC

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

chave InChI

LDBMLOLBWUOZGG-DOFVRBEMSA-N

Descrição geral

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.

Aplicação

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

Ações bioquímicas/fisiológicas

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

Características e benefícios

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

Outras notas

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Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable


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Frédéric Martin et al.
Phytochemistry, 68(9), 1307-1311 (2007-03-27)
Sixteen crude extracts from six Panamanian plants of the family Bignoniaceae were submitted to rapid TLC tests against DPPH and acetylcholinesterase. Pithecoctenium crucigerum (L.) A.H. Gentry, which showed interesting activity against DPPH, has been studied. The chemical investigation of the

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