Description
Mogroside IIIe is a minor sweet element of the traditional Chinese medicinal herb Siraitia grosvenori (Luohanguo).
| Product Unit Size | Cost | Quantity | Stock |
|---|
Mogroside IIIe is a minor sweet element of the traditional Chinese medicinal herb Siraitia grosvenori (Luohanguo).
| Cas No. | 88901-37-5 |
|---|---|
| Purity | ≥98% |
| Formula | C48H82O19 |
| Formula Wt. | 963.15 |
| IUPAC Name | (2R,3R,4S,5S,6R)-2-[[(3S,8S,9R,10R,11R,13R,14S,17R)-17-[(2R,5R)-5-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-hydroxy-6-methylheptan-2-yl]-11-hydroxy-4,4,9,13,14-pentamethyl-2,3,7,8,10,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol |
| Synonym | Mogroside III-E; Mogroside IIIe; Mogroside e; HY-N6928 |
| Store Temp | 4°C |
|---|---|
| Ship Temp | Ambient |
| MSDS | |
|---|---|
| Info Sheet |
Bhusari S, Rodriguez C, Tarka S, et al. Comparative in vitro metabolism of purified mogrosides derived from monk fruit extracts. Regul Toxicol Pharmacol. 2021 Mar;120:104856. PMID: 33387567.
Xue W, Mao J, Chen Q, et al. Mogroside IIIe alleviates high glucose-induced inflammation, oxidative stress and apoptosis of podocytes by the activation of AMPK/SIRT1 signaling pathway. Diabetes Metab Syndr Obes. 2020 Oct 20;13:3821-3830. PMID: 33116729.
Zou C, Zhang Q, Zhang S. Mogroside IIIe attenuates gestational diabetes mellitus through activating of AMPK signaling pathway in mice. J Pharmacol Sci. 2018 Nov;138(3):161-166. PMID: 30316692.
Tao L, Cao F, Xu G, et al. Mogroside IIIe attenuates LPS-induced acute lung injury in mice partly through regulation of the TLR4/MAPK/NP-kB axis via AMPK activation. Phytother Res. 2017 Jul;31(7):1097-1106. PMID: 28512854.
Tao L, Yang J, Cao F, et al. Mogroside IIIe, a novel anti-fibrotic compound, reduces pulmonary fibrosis throguh toll-like receptor 4 pathways. J Pharmacol Exp Ther. 2017 May;361(2):268-279. PMID: 28280123.
Reversible DNMT1-selective inhibitor
Specific inhibitor of histone methyltransferase...
PLK1 inhibitor.
α1-adrenergic antagonist.
Aminocyclitol; protein synthesis inhibitor.
Impurity of rapamycin
NSAID; COX-1/2 inhibitor.
Benzisoxazole phenylethanone; D2 and 5-HT2A ant...
Resveratrol prodrug; potential SIRT1 activator....
Synthetic compound related to sulforaphane.
α-glucosidase inhibitor, potential GLP-1 agoni...
Wee1 inhibitor.
Abl (T315I) inhibitor.
Neuroactive mycotoxin produced by Penicillum an...
Polyether ionophore, autophagy inhibitor.
EGFR inhibitor.
Phenylethanoid glycoside found in Echinacea.
Endogenous peptide hormone fragment, involved i...
Folic acid derivative
Intermediate in the synthesis of purine analogs...