Misplaced Pages

Diffutin

Article snapshot taken from Wikipedia with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.
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-{oxy}-6-(hydroxymethyl)oxane-3,4,5-triol
Identifiers
CAS Number
3D model (JSmol)
ChEBI
ChemSpider
PubChem CID
CompTox Dashboard (EPA)
InChI
  • 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/s1Key: ZNWIOJJMPZWSQO-YRDUZITASA-N
SMILES
  • c(c4)(c(OC)cc(c4)(O3)CCc(c31)c(O((O)2)OC(CO)(2O)O)cc(O)c1)OC
Properties
Chemical formula C23H28O10
Molar mass 464.467 g·mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). ☒N verify (what is  ?) Infobox references
Chemical compound

Diffutin is a flavan, a type of flavonoid. It can be found in Canscora diffusa and in Hoppea dichotoma.

Metabolism

Diffutin is a glucoside of diffutidin.

References

  1. ^ 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. Bibcode:1985PChem..24..831G. doi:10.1016/S0031-9422(00)84903-1.
Flavans and their glycosides
Flavans
Glycosides
acetylated
Glucosyloxyflavans
Stub icon

This article about an aromatic compound is a stub. You can help Misplaced Pages by expanding it.

Categories: