Poncirin
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This article relies largely or entirely on a single source. (October 2014) |
Names | |
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IUPAC name
(2S)-5-Hydroxy-4′-methoxy-7-[α-L-rhamnopyranosyl-(1→2)-β-D-glucopyranosyloxy]flavan-4-one
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Systematic IUPAC name
(2S)-7-{[(2S,3R,4S,5S,6R)-4,5-Dihydroxy-6-(hydroxymethyl)-3-{[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-2-yl]oxy}-5-hydroxy-2-(4-methoxyphenyl)-2,3-dihydro-4H-1-benzopyran-4-one | |
Other names
Isosakuranetin-7-neohesperidoside
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Identifiers | |
3D model (JSmol)
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ChEBI | |
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.035.458 |
PubChem CID
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UNII | |
CompTox Dashboard (EPA)
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Properties | |
C28H34O14 | |
Molar mass | 594.566 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Poncirin is the 7-O-neohesperidoside of isosakuranetin. Poncirin can be extracted from trifoliate orange (Poncirus trifoliata).[1]
References
- ^ Kim, Dong-Hyun; Bae, Eun-Ah; Han, Myung Joo (1999). "Anti-Helicobacter pylori Activity of the Metabolites of Poncirin from Poncirus trifoliata by Human Intestinal Bacteria". Biological and Pharmaceutical Bulletin. 22 (4): 422–424. doi:10.1248/bpb.22.422. PMID 10328566.
External links
- Media related to Poncirin at Wikimedia Commons
Categories:
- Articles needing additional references from October 2014
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- Articles without KEGG source
- Articles with changed EBI identifier
- Articles with changed ChemSpider identifier
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- O-methylated flavanones
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