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Names | |
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IUPAC name
α-L-Rhamnopyranosyl-(1→2)-D-glucose
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Systematic IUPAC name
(2R,3S,4R,5R)-3,4,5,6-Tetrahydroxy-2-{[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}hexanal | |
Other names
2-O-alpha-L-Rhamnopyranosyl-D-glucopyranose
2-O-alpha-L-Rhamnosyl-D-glucose 2-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranose | |
Identifiers | |
3D model (JSmol)
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ChEBI | |
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.037.379 |
KEGG | |
PubChem CID
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CompTox Dashboard (EPA)
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Properties | |
C12H22O10 | |
Molar mass | 326.29 g/mol |
Density | 1.662 g/mL |
Related compounds | |
Related compounds
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Rhamnose Glucose |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Neohesperidose is the disaccharide which is present in some flavonoids. It can be found in species of Typha.[1] [2]
Neohesperidosides
[edit]- Cyanidin-3-neohesperidoside[2]
- Delphinidin-3-neohesperidoside[2]
- Rhoifolin or apigenin 7-O-neohesperidoside
- Myricetin-3-O-neohesperidoside found in Physalis angulata[3]
- Neohesperidin (hesperetin 7-O-neohesperidoside)
- Neoeriocitrin (eriodictyol 7-O-neohesperidoside)
See also
[edit]References
[edit]- ^ Flavonoids of citrus—VI *1: The structure of neohesperidose, R. M. Horowitz and Bruno Gentili, 1962[dead link]
- ^ a b c Delphinidin-3-neohesperidoside and cyanidin-3- neohesperidoside from receptacles of Podocarpus species, Oyvind M. Andersen, Phytochemistry, 1989, Volume 28, Issue 2, Pages 495–497, doi:10.1016/0031-9422(89)80039-1
- ^ A novel cytotoxic flavonoid glycoside from Physalis angulata. N. Ismail and M. Alam, Fitoterapia, Volume 72, Issue 6, August 2001, Pages 676-679, doi:10.1016/S0367-326X(01)00281-7