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Hederacoside C

Hederacoside C structure

CAS No:
14216-03-6
Formula:
C59H96O26
Chemical Name:
Hederacoside C
Synonyms:
Olean-12-en-28-oic acid,3-[[2-O-(6-deoxy-α-L-mannopyranosyl)-α-L-arabinopyranosyl]oxy]-23-hydroxy-,O-6-deoxy-α-L-mannopyranosyl-(1→4)-O-β-D-glucopyranosyl-(1→6)-β-D-glucopyranosyl ester,(3β,4α)-;Glucopyranose,O-6-deoxy-α-L-mannopyranosyl-(1→4)-O-β-D-glucopyranosyl-(1→6)-,1-ester with 3β-[[2-O-(6-deoxy-α-L-mannopyranosyl)-α-L-arabinopyranosyl]oxy]-23-hydroxyolean-12-en-28-oic acid,β-D-;Akebia saponin PK;Kizuta saponin K12;Hederacoside C;Kalopanaxsaponin B;Pulsatilla saponin F;Saponin K12;Hederoside H1;Koronaroside B;Tauroside St-H2;Akeboside Sth;Glycoside L-H2;Tauroside H2;Saponin PK;Pericarsaponin Pk;Hederasaponin C;Hederagenin 3-O-α-L-rhamnopyranosyl(1→2)-α-L-arabinopyranosyl-28-O-α-L-rhamnopyranosyl(1→4)-β-D-glucopyranosyl(1→6)-β-D-glucopyranoside;23-Hydroxy-3β-[(O-α-L-rhamnopyranosyl-(1→2)-α-L-arabinopyranosyl)oxy]olean-12-en-28-oic acid O-α-L-rhamnopyranosyl-(1→4)-O-β-D-glucopyranosyl-(1→6)-β-D-glucopyranosyl ester;3-O-α-L-Rhamnopyranosyl-(1→2)-α-L-arabinopyranosylhederagenin 28-O-α-L-rhamnopyranosyl-(1→4)-β-D-glucopyranosyl-(1→6)-β-D-glucopyranoside;Pulchinenoside B5;Clematangoside A;27013-76-9;52038-14-9;52229-78-4;56292-18-3;94021-48-4;103470-80-0;104748-89-2;1002105-94-3;1407838-40-7
Categories:
Biochemical Engineering > Plant Extracts

Description

Hederacoside C is a principal bioactive pharmaceutical ingredient of Hedera helix leaf that can treat respiratory disorders, because of its expectorant, bronchodilator, antibacterial, and bronchospasmolytic effects.

Hederacoside C Basic Attributes

Molecular Weight：

1221.38000

Exact Mass：

1221.38

EC Number：

238-072-2

Characteristics

PSA：

412.82000

XLogP3：

-2.54440

Density：

1.48g/cm3

Melting Point：

225-228 °C

Refractive Index：

1.637

Safety Information

Transport codes：

UN 2811 6.1/PG 3

wgk germany：

hazard class code：

R22

safety instructions：

S22; S24/25

Marks：

Hazard Statements：

H302

Hederacoside C Use and Manufacturing

Methods of Manufacturing

General procedure: Each compound (10mg) was refluxed with 5N NH4OH in 50% EtOH (10mL) for 15h. After cooling, the reaction mixture was neutralized with 2N HCl and extracted with n-BuOH. The n-BuOH layer was evaporated to dryness to give a residue, which was purified by semipreparative HPLC eluted with MeOH-H2O to yield the prosapogenins (5.5mg for 3a, 4.8mg for 4a and 5.2mg for 5a). Their structures were determined by NMR experiments and ESIMS analyses, and the identification date see Supplementary data.

Uses

Solubilizer, bio-availability enhancer in oral suspensions, capsules

Recommended Suppliers of Hederacoside C

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Hederacoside C

Unit Price: $4000-4200 /G EXW

CAS No.: 14216-03-6

Grade: Industrial Grade

Content: 98%

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Guide of Hederacoside C

Description
Basic Attributes
Characteristics
Safety Information
Use and Manufacturing
Recommended Suppliers
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Hederacoside C

SDS

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