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Diffutin

From Wikipedia - Reading time: 5 min
Diffutin
Chemical structure of diffutin
Names
IUPAC name
(2S)-2-(3,4-Dimethoxyphenyl)-7-hydroxy-3,4-dihydro-2H-1-benzopyran-5-yl β-D-glucopyranoside
Systematic IUPAC name
(2S,3R,4S,5S,6R)-2-{[(2S)-2-(3,4-Dimethoxyphenyl)-7-hydroxy-3,4-dihydro-2H-1-benzopyran-5-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
  • InChI=1S/C23H28O10/c1-29-15-5-3-11(7-18(15)30-2)14-6-4-13-16(31-14)8-12(25)9-17(13)32-23-22(28)21(27)20(26)19(10-24)33-23/h3,5,7-9,14,19-28H,4,6,10H2,1-2H3/t14-,19+,20+,21-,22+,23+/m0/s1 checkY
    Key: ZNWIOJJMPZWSQO-YRDUZITASA-N checkY
  • c(c4)(c(OC)cc(c4)[C@@H](O3)CCc(c31)c(O[C@@H]([C@@H](O)2)OC(CO)[C@@H]([C@@H]2O)O)cc(O)c1)OC
Properties
C23H28O10
Molar mass 464.467 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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Diffutin is a flavan, a type of flavonoid. It can be found in Canscora diffusa[1] and in Hoppea dichotoma.[2]

Metabolism

[edit]

Diffutin is a glucoside of diffutidin.[1]

References

[edit]
  1. ^ a b Shibnath Ghosal, Saini K. S. and Sinha B. N. (1983). "Diffutin, a new adaptogenic glucosyloxyflavan from Canscora diffusa". Journal of Chemical Research, Synopses (12).
  2. ^ Ghosal, Shibnath; k. Jaiswal, Dinesh; k. Singh, Sushil; s. Srivastava, Radhey (1985). "Dichotosin and dichotosinin, two adaptogenic glucosyloxy flavans from Hoppea dichotoma". Phytochemistry. 24 (4): 831–833. doi:10.1016/S0031-9422(00)84903-1.
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