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Merck
CN

07538

Echinacoside

analytical standard

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About This Item

Empirical Formula (Hill Notation):
C35H46O20
CAS Number:
Molecular Weight:
786.73
UNSPSC Code:
85151701
NACRES:
NA.24
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
4778612
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grade

analytical standard

Quality Segment

assay

≥98% (HPLC)

shelf life

limited shelf life, expiry date on the label

application(s)

food and beverages

format

neat

storage temp.

2-8°C

SMILES string

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

InChI key

FSBUXLDOLNLABB-ISAKITKMSA-N

General description

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.

Biochem/physiol Actions

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

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.


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Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable



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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



Global Trade Item Number

SKUGTIN
T5130-10KG04061837347054
T5130-100G04061837347047
T5130-50KG04061832552514
V900367-500G04061833494950
T9659-10KG04061833690918
108320025004022536102443
T5130-5KG04061837347085
T5130-25G04061837347078
T5316-25G04061833613900
T5130-250G04061832552491
T5316-500G04061833624821
T5316-100G04061833436028
T5316-1KG04061826759141
T9659-1KG04061837381928
T9659-250G04061833614242
T9659-100G04061833614235
V900367-100G04061833469736
108320002504022536102436
394675-1KG07790788049867
T5130-1KG04061826187685
07538-10MG04061838648204