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Hederacoside C

analytical standard

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About This Item

Formule empirique (notation de Hill):
C59H96O26
Numéro CAS:
Poids moléculaire :
1221.38
Numéro Beilstein :
4229541
Numéro CE :
Numéro MDL:
Code UNSPSC :
85151701
ID de substance PubChem :
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

Durée de conservation

limited shelf life, expiry date on the label

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Pf

222 °C (dec.) (lit.)

Application(s)

food and beverages

Format

neat

Température de stockage

2-8°C

Chaîne SMILES 

[H][C@]12CC=C3C4CC(C)(C)CC[C@@]4(CC[C@@]3(C)[C@]1(C)CCC5[C@](C)(CO)[C@H](CC[C@]25C)O[C@@H]6OC[C@H](O)[C@H](O)[C@H]6O[C@@H]7O[C@@H](C)[C@H](O)[C@@H](O)[C@H]7O)C(=O)O[C@@H]8O[C@H](CO[C@@H]9O[C@H](CO)[C@@H](O[C@@H]%10O[C@@H](C)[C@H](O)[C@@H](O)[C@H]%10O)[C@H](O)[C@H]9O)[C@@H](O)[C@H](O)[C@H]8O

InChI

1S/C59H96O26/c1-24-34(63)38(67)42(71)49(78-24)83-46-29(20-60)80-48(45(74)41(46)70)77-22-30-37(66)40(69)44(73)51(81-30)85-53(75)59-17-15-54(3,4)19-27(59)26-9-10-32-55(5)13-12-33(56(6,23-61)31(55)11-14-58(32,8)57(26,7)16-18-59)82-52-47(36(65)28(62)21-76-52)84-50-43(72)39(68)35(64)25(2)79-50/h9,24-25,27-52,60-74H,10-23H2,1-8H3/t24-,25-,27?,28-,29+,30+,31?,32+,33-,34-,35-,36-,37+,38+,39+,40-,41+,42+,43+,44+,45+,46+,47+,48+,49-,50-,51-,52-,55-,56-,57+,58+,59-/m0/s1

Clé InChI

RYHDIBJJJRNDSX-WBOYGZCJSA-N

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Description générale

Hederacoside C is a natural triterpenoid saponin. It is the primary bioactive ingredient of traditional Chinese herbal medicines, isolated from Hedera helix, also known as common ivy or English ivy. It is known for its expectorant, bronchodilator, antibacterial, and bronchospasmolytic properties in the treatment of respiratory disorders.

Application

This analytical standard can also be used as follows:
  • Development of a bioanalytical method to measure hederacoside c in rat plasma samples by ultra high-performance liquid chromatographic-tandem mass spectrometric (UPLC-MS/MS) method
  • Simultaneous analysis of six natural compounds isolated from ivy leaf extract samples by UHPLC coupled with electrospray ionization-triple quadrupole mass spectrometeric (ESI-MS/MS) detection
  • Ultra-high-performance liquid chromatography-quadrupole time-of-flight mass spectrometry (UHPLC‐Q‐TOF‐MS/MS) based phytochemical profiling of Hedera helix for pharmaceutical applications

Conditionnement

Bottomless glass bottle. The content inside is inserted in a fused cone.

Autres remarques

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Pictogrammes

Exclamation mark

Mention d'avertissement

Warning

Mentions de danger

Classification des risques

Acute Tox. 4 Oral

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Gloves


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Certificats d'analyse (COA)

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Les clients ont également consulté

A validated RP HPLC-PAD method for the determination of hederacoside C in Ivy-Thyme cough syrup
Khdair A, et al.
International Journal of Analytical Chemistry (2010)
Determination of saponins and flavonoids in ivy leaf extracts using HPLC-DA
Yu M, et al.
Journal of Chromatographic Science, 53(4), 478-483 (2014)
S H Cho et al.
Archives of pharmacal research, 14(1), 19-24 (1991-03-01)
One new triterpenoidal saponin, saponin F(2) has been isolated from the bark of Kalopanax pictum Nakai var. typicum (Araliaceae), together with one known saponin, kizuta saponin K12 (1). On the basis of chemico-spectral evidences, the structure of 2 has been
Eun-Ha Joh et al.
Phytotherapy research : PTR, 26(4), 546-551 (2011-09-20)
The stem-bark of Kalopanax pictus (KP, family Araliaceae), which contains triterpenoid saponins, has been shown to exhibit anticarcinogenic, antiinflammatory, antirheumatoid and antidiabetic activities. In a preliminary study, a KP methanol extract demonstrated acetylcholinesterase activity in vitro and memory enhancement in
D H Kim et al.
Biological & pharmaceutical bulletin, 21(4), 360-365 (1998-05-20)
To investigate the relationship between the intestinal bacterial metabolism of kalopanaxsaponin B and H from Kalopanax pictus (Araliaceae), and their antidiabetic effect, kalopanaxsaponin B and H were metabolized by human intestinal microflora and the antidiabetic activity of their metabolites was

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