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07538

Supelco

Echinacoside

analytical standard

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About This Item

Formula empirica (notazione di Hill):
C35H46O20
Numero CAS:
Peso molecolare:
786.73
Beilstein:
4778612
Numero MDL:
Codice UNSPSC:
85151701
ID PubChem:
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

Saggio

≥98% (HPLC)

Durata

limited shelf life, expiry date on the label

applicazioni

food and beverages

Formato

neat

Temperatura di conservazione

2-8°C

Stringa SMILE

C[C@@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OCCc3ccc(O)c(O)c3)O[C@H](CO[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@H]2OC(=O)\C=C\c5ccc(O)c(O)c5)[C@H](O)[C@H](O)[C@H]1O

InChI

1S/C35H46O20/c1-14-24(42)26(44)29(47)35(51-14)55-32-30(48)34(49-9-8-16-3-6-18(38)20(40)11-16)53-22(13-50-33-28(46)27(45)25(43)21(12-36)52-33)31(32)54-23(41)7-4-15-2-5-17(37)19(39)10-15/h2-7,10-11,14,21-22,24-40,42-48H,8-9,12-13H2,1H3/b7-4+/t14-,21+,22+,24-,25+,26+,27-,28+,29+,30+,31+,32+,33+,34+,35-/m0/s1
FSBUXLDOLNLABB-ISAKITKMSA-N

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Descrizione generale

Echinacoside (ECH) is a typical phenylethanoid glycoside. It is known to contain multiple unstable chemical bonds and high reactive functional groups which aids to pathways involving degradation and metabolism. It is isolated from the stems of Cistanches salsa. It is a crude drug mostly used as antisenium and antifatigue agents.

Azioni biochim/fisiol

Caffeic acid glycoside found in herbal medicine. Potential therapeutic for Parkinson′s disease.

Confezionamento

Bottomless glass bottle. Contents are inside inserted fused cone.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable


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Sigma-Aldrich

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Wen-Jun He et al.
Planta medica, 75(13), 1400-1404 (2009-05-27)
The aim of this study was to identify and elucidate the vasorelaxant activity of echinacoside, a phenylethanoid glycoside isolated from the medicinal herb Cistanche tubulosa, and its possible underlying mechanism on isolated rat thoracic aortic rings pre-contracted with phenylephrine (PE
Min Zhu et al.
Journal of neurochemistry, 124(4), 571-580 (2012-11-30)
Neurotrophins exert their physiological functions mainly through Trk receptors, and the neurotrophic signaling network is critical to the survival of neurons. However, therapeutic use of neurotrophins in treating neurodegenerative diseases is hampered by a number of pharmacological challenges, and the
Pavel Mučaji et al.
Molecules (Basel, Switzerland), 16(10), 8198-8208 (2011-10-01)
The aim of the study was a HPLC evaluation of the lipoxygenase activity inhibiting activity of a water infusion of Ligustrum vulgare L. leaves and selected isolates from it. The antiradical activity of the water infusion was determined using DPPH
Yuxin Wang et al.
Talanta, 80(2), 572-580 (2009-10-20)
Metabolite identification for the compounds that undergo multiple and sequential metabolism is still a great challenge. Echinacoside (ECH), a typical phenylethanoid glycoside, contains multiple unstable chemical bonds and high reactive functional groups which are susceptible to multiple pathways of degradation
Rong Kuang et al.
Planta medica, 75(14), 1499-1504 (2009-06-24)
We have investigated the protective effects of echinacoside (ECH), one of the phenylethanoid glycosides, on H(2)O(2)-induced cytotoxicity in the rat pheochromocytoma cell line (PC12 cells). Our data show that application of ECH to H(2)O(2)-injured PC12 cells (HIPCs) increased cell viability

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