Neohesperidose

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
CAS Number	17074-02-1 ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:73992 ;
ChEMBL	ChEMBL1651520 ;
ChemSpider	390159 ;
ECHA InfoCard	100.037.379
KEGG	C08244 ;
PubChem CID	441426;
CompTox Dashboard (EPA)	DTXSID20937829 ;
	InChI 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 Key: VSRVRBXGIRFARR-OUEGHFHCSA-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;
	SMILES 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
Chemical formula	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). verify (what is ?) Infobox references

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

Neohesperidosides

^ Horowitz, R. M.; Gentili, Bruno (January 1963). "Flavonoids of citrus—VI: The structure of neohesperidose". Tetrahedron. 19 (5): 773–782. doi:10.1016/S0040-4020(01)99211-7.773-782&rft.date=1963-01&rft_id=info:doi/10.1016/S0040-4020(01)99211-7&rft.aulast=Horowitz&rft.aufirst=R. M.&rft.au=Gentili, Bruno&rft_id=https://www.sciencedirect.com/science/article/abs/pii/S0040402001992117&rfr_id=info:sid/en.wikipedia.org:Neohesperidose" class="Z3988">
^ ^a ^b ^c Andersen, Oyvind M. (1989). "Delphinidin-3-neohesperidoside and cyanidin-3- neohesperidoside from receptacles of Podocarpus species". Phytochemistry. 28 (2): 495–497. Bibcode:1989PChem..28..495A. doi:10.1016/0031-9422(89)80039-1.495-497&rft.date=1989&rft_id=info:doi/10.1016/0031-9422(89)80039-1&rft_id=info:bibcode/1989PChem..28..495A&rft.aulast=Andersen&rft.aufirst=Oyvind M.&rfr_id=info:sid/en.wikipedia.org:Neohesperidose" class="Z3988">
^ Ismail, N.; Alam, M. (2001). "A novel cytotoxic flavonoid glycoside from Physalis angulata". Fitoterapia. 72 (6): 676–679. doi:10.1016/S0367-326X(01)00281-7.676-679&rft.date=2001&rft_id=info:doi/10.1016/S0367-326X(01)00281-7&rft.aulast=Ismail&rft.aufirst=N.&rft.au=Alam, M.&rfr_id=info:sid/en.wikipedia.org:Neohesperidose" class="Z3988">

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