Geniposide
| Names | |
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| IUPAC name
Methyl (1S,4aS,7aS)-1-(β-D-glucopyranosyloxy)-7-(hydroxymethyl)-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carboxylate
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| Systematic IUPAC name
Methyl (1S,4aS,7aS)-7-(hydroxymethyl)-1-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carboxylate | |
| Other names
Jasminoidin; methyl 1-(hexopyranosyloxy)-7-(hydroxymethyl)-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carboxylate
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| Identifiers | |
3D model (JSmol)
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| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.208.687 |
| EC Number |
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| KEGG | |
| MeSH | geniposide |
PubChem CID
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| UNII | |
CompTox Dashboard (EPA)
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| Properties | |
| C17H24O10 | |
| Molar mass | 388.369 g·mol−1 |
| Melting point | 245.23 °C (473.41 °F; 518.38 K) |
| Boiling point | 641.4±55.0 °C at 760 mmHg |
| log P | −1.854 |
| Acidity (pKa) | 12.80±0.70 |
| Hazards | |
| GHS labelling: | |
| Danger | |
| H301 | |
| P264, P270, P301+P310, P321, P330, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
(what is ?)
Infobox references
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Geniposide, the glycoside form of genipin, is a bioactive iridoid glycoside that is found in a wide variety of medicinal herbs, such as Genipa americana y Gardenia jasminoides (fruits) . Geniposide shows several pharmacological effects (in vitro and in vivo) including neuroprotective, antidiabetic, hepatoprotective, anti-inflammatory, analgesic, antidepressant-like, cardioprotective, antioxidant, immune-regulatory, antithrombotic and antitumoral activity. These pharmacology benefits arise through the modulating action of geniposide on several proteins and genes that are associated with inflammatory and oxidative stress processes.