:Neohesperidose
{{Chembox
| Verifiedfields = changed
| Watchedfields = changed
| verifiedrevid = 415344475
| Name = Neohesperidose
| ImageFile = Neohesperidose.svg
| ImageFile2 = Neohesperidose 3D BS.png
| IUPACName = α-L-Rhamnopyranosyl-(1→2)-D-glucose
| SystematicName = (2R,3S,4R,5R)-3,4,5,6-Tetrahydroxy-2-
| OtherNames = 2-O-alpha-L-Rhamnopyranosyl-D-glucopyranose
2-O-alpha-L-Rhamnosyl-D-glucose
2-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranose
|Section1={{Chembox Identifiers
| CASNo_Ref = {{cascite|correct|??}}
| CASNo = 17074-02-1
| PubChem = 441426
| EINECS =
| ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}}
| ChemSpiderID = 390159
| ChEBI_Ref = {{ebicite|changed|EBI}}
| ChEBI = 73992
| ChEMBL_Ref = {{ebicite|changed|EBI}}
| ChEMBL = 1651520
| KEGG_Ref = {{keggcite|changed|kegg}}
| KEGG = C08244
| 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
| 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
| InChIKey = VSRVRBXGIRFARR-OUEGHFHCBJ
| StdInChI_Ref = {{stdinchicite|changed|chemspider}}
| StdInChI = 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
| StdInChIKey_Ref = {{stdinchicite|changed|chemspider}}
| StdInChIKey = VSRVRBXGIRFARR-OUEGHFHCSA-N
}}
|Section2={{Chembox Properties
| Formula = C12H22O10
| MolarMass = 326.29 g/mol
| Appearance =
| Density = 1.662 g/mL
| MeltingPt =
| BoilingPt =
| Solubility =
}}
|Section3={{Chembox Hazards
| MainHazards =
| FlashPt =
| AutoignitionPt =
}}
| Section8 = {{Chembox Related
| OtherCompounds = Rhamnose
Glucose
}}
}}
Neohesperidose is the disaccharide which is present in some flavonoids. It can be found in species of Typha.{{cite journal | url=https://www.sciencedirect.com/science/article/abs/pii/S0040402001992117 | doi=10.1016/S0040-4020(01)99211-7 | title=Flavonoids of citrus—VI: The structure of neohesperidose | journal=Tetrahedron | date=January 1963 | volume=19 | issue=5 | pages=773–782 | last1=Horowitz | first1=R. M. | last2=Gentili | first2=Bruno | url-access=subscription }}{{Cite journal |doi=10.1016/0031-9422(89)80039-1 |title=Delphinidin-3-neohesperidoside and cyanidin-3- neohesperidoside from receptacles of Podocarpus species |date=1989 |last1=Andersen |first1=Oyvind M. |journal=Phytochemistry |volume=28 |issue=2 |pages=495–497 |bibcode=1989PChem..28..495A }}
Neohesperidosides
- Cyanidin-3-neohesperidoside
- Delphinidin-3-neohesperidoside
- Rhoifolin or apigenin 7-O-neohesperidoside
- Myricetin-3-O-neohesperidoside found in Physalis angulata{{Cite journal |doi=10.1016/S0367-326X(01)00281-7 |title=A novel cytotoxic flavonoid glycoside from Physalis angulata |date=2001 |last1=Ismail |first1=N. |last2=Alam |first2=M. |journal=Fitoterapia |volume=72 |issue=6 |pages=676–679 |pmid=11543968 }}
- Neohesperidin (hesperetin 7-O-neohesperidoside)
- Neoeriocitrin (eriodictyol 7-O-neohesperidoside)
See also
References
- [http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6THR-436X607-4&_user=10&_coverDate=12%2F31%2F1968&_alid=989895831&_rdoc=2&_fmt=high&_orig=search&_cdi=5289&_docanchor=&view=c&_ct=101&_acct=C000050221&_version=1&_urlVersion=0&_userid=10&md5=4c2b6cd1646e71ebf0b420f1abe696a6 Synthesis of neohesperidose, B. H. Koeppen, 1968]{{dead link|date=January 2025|bot=medic}}{{cbignore|bot=medic}}
{{Reflist}}
External links
- [http://www.rdchemicals.com/chemicals.php?mode=details&mol_id=8100 Neohesperidose on rdchemicals.com]
{{organic-compound-stub}}