To install click the Add extension button. That's it.

The source code for the WIKI 2 extension is being checked by specialists of the Mozilla Foundation, Google, and Apple. You could also do it yourself at any point in time.

4,5
Kelly Slayton
Congratulations on this excellent venture… what a great idea!
Alexander Grigorievskiy
I use WIKI 2 every day and almost forgot how the original Wikipedia looks like.
Live Statistics
English Articles
Improved in 24 Hours
Added in 24 Hours
What we do. Every page goes through several hundred of perfecting techniques; in live mode. Quite the same Wikipedia. Just better.
.
Leo
Newton
Brights
Milds

Neohesperidose

From Wikipedia, the free encyclopedia

Neohesperidose
Names
IUPAC name
α-L-Rhamnopyranosyl-(1→2)-D-glucose
Systematic IUPAC name
(2R,3S,4R,5R)-3,4,5,6-Tetrahydroxy-2-{[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}hexanal
Other names
2-O-alpha-L-Rhamnopyranosyl-D-glucopyranose
2-O-alpha-L-Rhamnosyl-D-glucose
2-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranose
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.037.379 Edit this at Wikidata
KEGG
  • InChI=1S/C12H22O10/c1-3-5(14)7(16)9(18)12(20-3)22-10-8(17)6(15)4(2-13)21-11(10)19/h3-19H,2H2,1H3/t3-,4+,5-,6+,7+,8-,9+,10+,11+,12-/m0/s1 ☒N
    Key: VSRVRBXGIRFARR-OUEGHFHCSA-N ☒N
  • InChI=1/C12H22O10/c1-3-5(14)7(16)9(18)12(20-3)22-10-8(17)6(15)4(2-13)21-11(10)19/h3-19H,2H2,1H3/t3-,4+,5-,6+,7+,8-,9+,10+,11+,12-/m0/s1
    Key: VSRVRBXGIRFARR-OUEGHFHCBJ
  • O([C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O)[C@@H]2O[C@H]([C@H](O)[C@@H](O)[C@H]2O)C
Properties
C12H22O10
Molar mass 326.29 g/mol
Density 1.662 g/mL
Related compounds
Related compounds
Rhamnose
Glucose
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

Neohesperidose is the disaccharide which is present in some flavonoids. It can be found in species of Typha.[1] [2]

Neohesperidosides

See also

References

  1. ^ Flavonoids of citrus—VI *1: The structure of neohesperidose, R. M. Horowitz and Bruno Gentili, 1962[dead link]
  2. ^ a b c Delphinidin-3-neohesperidoside and cyanidin-3- neohesperidoside from receptacles of Podocarpus species, Oyvind M. Andersen, Phytochemistry, 1989, Volume 28, Issue 2, Pages 495–497, doi:10.1016/0031-9422(89)80039-1
  3. ^ A novel cytotoxic flavonoid glycoside from Physalis angulata. N. Ismail and M. Alam, Fitoterapia, Volume 72, Issue 6, August 2001, Pages 676-679, doi:10.1016/S0367-326X(01)00281-7

External links

This page was last edited on 5 December 2023, at 03:14
Basis of this page is in Wikipedia. Text is available under the CC BY-SA 3.0 Unported License. Non-text media are available under their specified licenses. Wikipedia® is a registered trademark of the Wikimedia Foundation, Inc. WIKI 2 is an independent company and has no affiliation with Wikimedia Foundation.