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| | Gypenoside LI Basic information |
| Product Name: | Gypenoside LI | | Synonyms: | Gypenoside LI;β-D-Glucopyranoside, (2α,3β,12β,20R)-2,12,20-trihydroxydammar-24-en-3-yl 2-O-β-D-glucopyranosyl-;Gypenoside LI (Standard) | | CAS: | 94987-10-7 | | MF: | C42H72O14 | | MW: | 801.02 | | EINECS: | | | Product Categories: | | | Mol File: | 94987-10-7.mol |  |
| | Gypenoside LI Chemical Properties |
| Boiling point | 912.3±65.0 °C(Predicted) | | density | 1.33±0.1 g/cm3(Predicted) | | storage temp. | 4°C, away from moisture and light | | pka | 12.85±0.70(Predicted) | | form | Solid | | color | White to off-white |
| | Gypenoside LI Usage And Synthesis |
| Uses | Gypenoside LI, a gypenoside monomer, possesses anti-tumor activity. Gypenoside LI induces cell apoptosis, cell cycle and migration[1][2]. | | References | [1] Shao-Fang Xing, et al. The inhibitory effect of gypenoside stereoisomers, gypenoside L and gypenoside LI, isolated from Gynostemma pentaphyllum on the growth of human lung cancer A549 cells. J Ethnopharmacol. 2018 Jun 12;219:161-172. DOI:10.1016/j.jep.2018.03.012
[2] Ma-Li Zu, et al. Monomer gypenoside LI from Gynostemma pentaphyllum inhibits cell proliferation and upregulates expression of miR-128-3p in melanoma cells. J Biochem Mol Toxicol. 2020 May;34(5):e22460. DOI:10.1002/jbt.22460 |
| | Gypenoside LI Preparation Products And Raw materials |
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