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
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
| 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
| Title | Date | PubMed |
|---|---|---|
| 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
Edited
Mon Mar 31 22:29:22 GMT 2025
by
admin
on
Mon Mar 31 22:29:22 GMT 2025
|
| Record UNII |
0C4U3505G3
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Common Name | English | ||
|
Preferred Name | English | ||
|
Common Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
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 | |||
|
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 | |||
|
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 | |||
|
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 | |||
|
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 | ||
|
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 | |||
|
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 | |||
|
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 | |||
|
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 |