PHL89800
Stevioside
phyproof® Reference Substance
Synonym(s):
(4α)-13-[(2-O-β-D-Glucopyranosyl-β-D-glucopyranosyl)oxy]kaur-16-en-18-oic acid β-D-glucopyranosyl ester, Steviosin
About This Item
grade
primary reference standard
product line
phyproof® Reference Substance
Assay
≥95.0% (HPLC)
form
powder
manufacturer/tradename
PhytoLab
SMILES string
C[C@@]12CCC[C@](C)([C@H]1CC[C@]34CC(=C)[C@](CC[C@@H]23)(C4)O[C@@H]5O[C@H](CO)[C@@H](O)[C@H](O)[C@H]5O[C@@H]6O[C@H](CO)[C@@H](O)[C@H](O)[C@H]6O)C(=O)O[C@@H]7O[C@H](CO)[C@@H](O)[C@H](O)[C@H]7O
InChI
1S/C38H60O18/c1-16-11-37-9-5-20-35(2,7-4-8-36(20,3)34(50)55-32-29(49)26(46)23(43)18(13-40)52-32)21(37)6-10-38(16,15-37)56-33-30(27(47)24(44)19(14-41)53-33)54-31-28(48)25(45)22(42)17(12-39)51-31/h17-33,39-49H,1,4-15H2,2-3H3/t17-,18-,19-,20+,21+,22-,23-,24-,25+,26+,27+,28-,29-,30-,31+,32+,33+,35-,36-,37-,38+/m1/s1
InChI key
UEDUENGHJMELGK-HYDKPPNVSA-N
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General description
Component of stevia.
Application
- Stevioside reagent grade for biochemistry: Research has focused on the efficient conversion of stevioside to rebaudioside M in Saccharomyces cerevisiae, utilizing engineered hydrolase systems. This study highlights stevioside′s role in biochemical research, particularly in glycoside metabolism and its applications in the development of natural sweeteners for pharmaceutical formulations (Li et al., 2024).
- High-purity stevioside for metabolic syndrome studies: Stevioside has been investigated for its potential to ameliorate palmitic acid-induced abnormal glucose uptake in muscle cells. This research underscores stevioside′s pharmacological properties, particularly in addressing metabolic disorders, demonstrating its significant role in medical biochemistry and metabolic syndrome studies (Zhang et al., 2024).
Legal Information
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
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