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Hederacoside C

analytical standard

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About This Item

Formula empirica (notazione di Hill):
C59H96O26
Numero CAS:
Peso molecolare:
1221.38
Beilstein:
4229541
Numero CE:
Numero MDL:
Codice UNSPSC:
85151701
ID PubChem:
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

Punto di fusione

222 °C (dec.) (lit.)

applicazioni

food and beverages

Formato

neat

Temperatura di conservazione

2-8°C

Stringa SMILE

[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
RYHDIBJJJRNDSX-WBOYGZCJSA-N

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Descrizione generale

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.

Applicazioni

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

Confezionamento

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

Altre note

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

Pittogrammi

Exclamation mark

Avvertenze

Warning

Indicazioni di pericolo

Classi di pericolo

Acute Tox. 4 Oral

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

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves


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Certificati d'analisi (COA)

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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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