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Details

Stereochemistry ABSOLUTE
Molecular Formula C12H22O10
Molecular Weight 326.2971
Optical Activity UNSPECIFIED
Defined Stereocenters 9 / 9
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of RUTINOSE

SMILES

C[C@@H]1O[C@@H](OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O)[C@H](O)[C@H](O)[C@H]1O

InChI

InChIKey=CPYCUQCIDSHOHI-IFLAJBTPSA-N
InChI=1S/C12H22O10/c1-4-7(16)10(19)11(20)12(22-4)21-3-6(15)9(18)8(17)5(14)2-13/h2,4-12,14-20H,3H2,1H3/t4-,5-,6+,7-,8+,9+,10+,11+,12+/m0/s1

HIDE SMILES / InChI

Molecular Formula C12H22O10
Molecular Weight 326.2971
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 9 / 9
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
An essential difference between the flavonoids monoHER and quercetin in their interplay with the endogenous antioxidant network.
2010-11-08
Preparative separation of phenolic compounds from Halimodendron halodendron by high-speed counter-current chromatography.
2010-08-31
Bioglycans and natural glycosides as a promising research topic in bioorganic chemistriy.
2010-07
Extracellular monoenzyme deglycosylation system of 7-O-linked flavonoid beta-rutinosides and its disaccharide transglycosylation activity from Stilbella fimetaria.
2010-05
Two novel disaccharides, rutinose and methylrutinose, are involved in carbon metabolism in Datisca glomerata.
2010-02
Immobilization of flavonol 3-O-beta-heterodisaccharidase on porous glass and production of rutinose from rutin.
2009-10
Quasi-MSn identification of flavanone 7-glycoside isomers in Da Chengqi Tang by high performance liquid chromatography-tandem mass spectrometry.
2009-07-24
Degradation of rutin by Thermoactinomyces vulgaris and other thermophilic compost isolates.
2009-06-10
Substrate specificities of glycosidases from Aspergillus species pectinase preparations on elderberry anthocyanins.
2009-02-11
Syntheses of R-beta-rutinosides by rutin-degrading reaction.
2009
In vitro biological evaluation of novel 7-O-dialkylaminoalkyl cytotoxic pectolinarigenin derivatives against a panel of human cancer cell lines.
2008-10-15
Metabolite annotations based on the integration of mass spectral information.
2008-06
Characteristic fragmentation patterns of the trimethylsilyl and trimethylsilyl-oxime derivatives of various saccharides as obtained by gas chromatography coupled to ion-trap mass spectrometry.
2008-01-04
Characterization and identification of isomeric flavonoid O-diglycosides from genus Citrus in negative electrospray ionization by ion trap mass spectrometry and time-of-flight mass spectrometry.
2007-08-13
Fate of anthocyanins and antioxidant capacity in contents of the gastrointestinal tract of weanling pigs following black raspberry consumption.
2006-01-25
Potential antitumor agents: flavones and their derivatives from Linaria reflexa Desf.
2005-11-01
Identification and characterization of anthocyanins by high-performance liquid chromatography-electrospray ionization-tandem mass spectrometry in common foods in the United States: vegetables, nuts, and grains.
2005-04-20
Silver complexation and tandem mass spectrometry for differentiation of isomeric flavonoid diglycosides.
2005-03-15
Threshold dissociation and molecular modeling of transition metal complexes of flavonoids.
2005-02
Anti-inflammatory effect of heme oxygenase 1: glycosylation and nitric oxide inhibition in macrophages.
2005-02
Protein-lipid interactions during liposome oxidation with added anthocyanin and other phenolic compounds.
2004-03-10
Structure-activity relationship (SAR) between some natural flavonoids and ocular blood flow in the rabbit.
2004-02
[HPLC investigation of antioxidant components in Solidago herba].
2004
Purification and characterization of a flavonol 3-O-beta-heterodisaccharidase from the dried herb of Fagopyrum esculentum Moench.
2003-09
Differential apoptosis-inducing effect of quercetin and its glycosides in human promyeloleukemic HL-60 cells by alternative activation of the caspase 3 cascade.
2003-08-01
t-BOOH-induced oxidative damage in sickle red blood cells and the role of flavonoids.
2003-06-24
Anti-Sindbis activity of flavanones hesperetin and naringenin.
2003-01
An iridoid glucoside dimer and a non-glycosidic iridoid from the leaves of Lasianthus wallichii.
2002-10
Structural characterization of flavonoid glycosides by collisionally activated dissociation of metal complexes.
2001-05
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:29:22 GMT 2025
Edited
by admin
on Mon Mar 31 22:29:22 GMT 2025
Record UNII
0C4U3505G3
Record Status Validated (UNII)
Record Version
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Name Type Language
RUTINOSE
MI  
Common Name English
D-GLUCOSE, 6-O-(6-DEOXY-.ALPHA.-L-MANNOPYRANOSYL)-
Preferred Name English
RUTINOSE [MI]
Common Name English
Code System Code Type Description
PUBCHEM
5460038
Created by admin on Mon Mar 31 22:29:22 GMT 2025 , Edited by admin on Mon Mar 31 22:29:22 GMT 2025
PRIMARY
CHEBI
27522
Created by admin on Mon Mar 31 22:29:22 GMT 2025 , Edited by admin on Mon Mar 31 22:29:22 GMT 2025
PRIMARY
CHEBI
61606
Created by admin on Mon Mar 31 22:29:22 GMT 2025 , Edited by admin on Mon Mar 31 22:29:22 GMT 2025
PRIMARY
WIKIPEDIA
Rutinose
Created by admin on Mon Mar 31 22:29:22 GMT 2025 , Edited by admin on Mon Mar 31 22:29:22 GMT 2025
PRIMARY
MERCK INDEX
m9709
Created by admin on Mon Mar 31 22:29:22 GMT 2025 , Edited by admin on Mon Mar 31 22:29:22 GMT 2025
PRIMARY Merck Index
EPA CompTox
DTXSID70896972
Created by admin on Mon Mar 31 22:29:22 GMT 2025 , Edited by admin on Mon Mar 31 22:29:22 GMT 2025
PRIMARY
ECHA (EC/EINECS)
202-014-4
Created by admin on Mon Mar 31 22:29:22 GMT 2025 , Edited by admin on Mon Mar 31 22:29:22 GMT 2025
PRIMARY
CAS
90-74-4
Created by admin on Mon Mar 31 22:29:22 GMT 2025 , Edited by admin on Mon Mar 31 22:29:22 GMT 2025
PRIMARY
FDA UNII
0C4U3505G3
Created by admin on Mon Mar 31 22:29:22 GMT 2025 , Edited by admin on Mon Mar 31 22:29:22 GMT 2025
PRIMARY