Euxanthic acid
Euxanthic acid
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Names
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IUPAC name
(8-Hydroxy-9-oxo-9H-xanthen-2-yl) β-D-glucopyranosiduronic acid
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Systematic IUPAC name
(2S,3S,4S,5R,6S)-3,4,5-Trihydroxy-6-[(8-hydroxy-9-oxo-9H-xanthen-2-yl)oxy]oxane-2-carboxylic acid
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Identifiers
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ChemSpider
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UNII
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InChI=1S/C19H16O10/c20-9-2-1-3-11-12(9)13(21)8-6-7(4-5-10(8)28-11)27-19-16(24)14(22)15(23)17(29-19)18(25)26/h1-6,14-17,19-20,22-24H,(H,25,26)/t14-,15-,16+,17-,19+/m0/s1 YKey: JGIDSJGZGFYYNX-YUAHOQAQSA-N YInChI=1/C19H16O10/c20-9-2-1-3-11-12(9)13(21)8-6-7(4-5-10(8)28-11)27-19-16(24)14(22)15(23)17(29-19)18(25)26/h1-6,14-17,19-20,22-24H,(H,25,26)/t14-,15-,16+,17-,19+/m0/s1 Key: JGIDSJGZGFYYNX-YUAHOQAQBY
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OC(=O)[C@H]4O[C@@H](Oc1ccc2Oc3cccc(O)c3C(=O)c2c1)[C@H](O)[C@@H](O)[C@@H]4O
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Properties
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C19H16O10
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Molar mass
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404.327 g·mol−1
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Density
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1.737 g/ml
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Chemical compound
Euxanthic acid is a xanthonoid glycoside, a conjugate of the aglycone euxanthone with glucuronic acid. Its magnesium salt is the primary colourant of the pigment Indian Yellow.[1]
References
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Aglycones |
- Apetalinone A, B, C and D
- Bellidifolin
- Calozeyloxanthone
- Desoxygambogenin
- Desoxymorellin
- Euxanthone
- Forbesione
- Gambogellic acid
- Gambogenic acid
- Gambogenin
- Gambogenin dimethyl acetal
- Gambogic acid
- Gambogin
- Gaudichaudiic acid A, B, C, D and E
- Gaudichaudione A, B, C, D, E, F, G and H
- Hanburin
- Isogambogenin
- Isojacareubin
- Isomorellin
- Isomoreollin B
- Methylswertianin
- Morellic acid
- Morellin dimethyl acetal
- Moreollic acid
- Norathyriol
- Psorospermin
- 2,3′,4,6-tetrahydroxybenzophenone
- Tomentonone
- Zeyloxanthonone
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Glycosides | |
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Acetylated | |
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Misc. | |
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