Poncirin
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Names | |
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IUPAC name (2S)-5-Hydroxy-4′-methoxy-7-[α-L-rhamnopyranosyl-(1→2)-β-D-glucopyranosyloxy]flavan-4-one | |
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 | |
Identifiers | |
CAS Number |
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3D model (JSmol) |
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ChEMBL |
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ECHA InfoCard | 100.035.458 ![]() |
PubChem CID |
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CompTox Dashboard (EPA) |
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InChI
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Properties | |
Chemical formula | 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). ![]() ![]() ![]() Infobox references |
Chemical compound
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
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Flavanones and their glycosides
- Butin
- Eriodictyol
- Naringenin
- Pinocembrin
- Alpinetin
- Hesperetin
- Homoeriodictyol
- Isosakuranetin
- Pinostrobin (Pinocembrin-7-methylether)
- Sakuranetin
- Sterubin
- Eriocitrin
- Neoeriocitrin
- Hesperidin
- Liquiritin
- Naringin (Narigenin 7-O-neohesperidoside)
- Narirutin (Naringenin 7-O-rutinoside)
- Poncirin
- Prunin (Naringenin-7-O-glucoside)
- Sakuranin
- Nirurin
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