Pular para o conteúdo
Merck
Todas as fotos(1)

Key Documents

G1296

Sigma-Aldrich

Glycitin

≥98% (HPLC)

Sinônimo(s):

4′,7-Dihydroxy 6-methoxyisoflavone 7-O-glucoside, 4H-1-Benzopyran-4-one, 7-(β-D-glucopyranosyloxy)-3-(4-hydroxyphenyl)-6-methoxy-, Glycitein 7-O-β-glucoside

Faça loginpara ver os preços organizacionais e de contrato


About This Item

Fórmula empírica (Notação de Hill):
C22H22O10
Número CAS:
Peso molecular:
446.40
Número MDL:
Código UNSPSC:
12352201
NACRES:
NA.25

fonte biológica

plant (Pueraria thunbergianaI)

Nível de qualidade

Ensaio

≥98% (HPLC)

forma

powder

técnica(s)

HPLC: suitable

cor

white to faint beige

pf

203 - 204  °C ((397 - 399 °F ))

solubilidade

10 mg, clear, colorless to faintly yellow

temperatura de armazenamento

room temp

cadeia de caracteres SMILES

O=C1C2=CC(OC)=C(O[C@H]3[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O3)C=C2OC=C1C4=CC=C(O)C=C4

InChI

1S/C22H22O10/c1-29-15-6-12-14(30-9-13(18(12)25)10-2-4-11(24)5-3-10)7-16(15)31-22-21(28)20(27)19(26)17(8-23)32-22/h2-7,9,17,19-24,26-28H,8H2,1H3/t17-,19-,20+,21-,22-/m1/s1

chave InChI

OZBAVEKZGSOMOJ-MIUGBVLSSA-N

Procurando produtos similares? Visita Guia de comparação de produtos

Descrição geral

Glycitin is an isoflavonoid recently found in flowers of Pueraria thunbergianaI. Glycitin can be modified into the metabolite glycitein which has anti-inflammatory properties.

Aplicação


  • The antioxidant Glycitin protects against intervertebral disc degeneration through antagonizing inflammation and oxidative stress in nucleus pulposus cells.: This study highlights Glycitin′s therapeutic potential in mitigating intervertebral disc degeneration by counteracting inflammatory and oxidative processes, demonstrating its viability as a bioactive compound for degenerative diseases (Zhao W et al., 2023).

  • Spectrum-effect relationship study to reveal the pharmacodynamic substances in Flos Puerariae-Semen Hoveniae medicine pair for the treatment of alcohol-induced liver damage.: Analyzes the pharmacological effects of herbal components, including Glycitin, targeting liver damage recovery, illustrating the compound′s therapeutic relevance in traditional and modern medical applications (Zhang H et al., 2023).


Ações bioquímicas/fisiológicas

Glycitin is a soy isoflavone in the glucoside form. A rat model study demonstrated glycitin to be effective in preventing bone loss and reversing the unfavorable changes of lipid metabolism in this model.

Embalagem

Bottomless glass bottle. Contents are inside inserted fused cone.

Outras notas

To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.

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


Certificados de análise (COA)

Busque Certificados de análise (COA) digitando o Número do Lote do produto. Os números de lote e remessa podem ser encontrados no rótulo de um produto após a palavra “Lot” ou “Batch”.

Já possui este produto?

Encontre a documentação dos produtos que você adquiriu recentemente na biblioteca de documentos.

Visite a Biblioteca de Documentos

Os clientes também visualizaram

Slide 1 of 5

1 of 5

Genistein synthetic, ≥98% (HPLC), powder

Sigma-Aldrich

G6649

Genistein

Genistein from Glycine max (soybean), ~98% (HPLC)

Sigma-Aldrich

G6776

Genistein

Daidzein Pharmaceutical Secondary Standard; Certified Reference Material

Supelco

PHR1858

Daidzein

Formononetin ≥99.0% (TLC)

Sigma-Aldrich

47752

Formononetin

Kouya Yamaki et al.
Planta medica, 68(2), 97-100 (2002-02-23)
Previously, we reported that the isoflavones tectorigenin and tectoridin, a glycosylated tectorigenin, isolated from the rhizomes of Belamcanda chinensis have an activity to inhibit prostaglandin (PG) E2 production in 12-O-tetradecanoylphorbol 13-acetate (TPA)-stimulated rat peritoneal macrophages. The inhibitory effect of tectorigenin
Isoflavone glycosides from the flowers of Pueraria thunbergiana.
Park HJ
Phytochemistry, 51, 147-151 (1999)

Nossa equipe de cientistas tem experiência em todas as áreas de pesquisa, incluindo Life Sciences, ciência de materiais, síntese química, cromatografia, química analítica e muitas outras.

Entre em contato com a assistência técnica