RUTINOSE

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 Search

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

Title	Date	PubMed
Structural characterization of flavonoid glycosides by collisionally activated dissociation of metal complexes.	2001 May	11349951
An iridoid glucoside dimer and a non-glycosidic iridoid from the leaves of Lasianthus wallichii.	2002 Oct	12372873
Anti-Sindbis activity of flavanones hesperetin and naringenin.	2003 Jan	12520185
t-BOOH-induced oxidative damage in sickle red blood cells and the role of flavonoids.	2003 May-Jun	12818473
Purification and characterization of a flavonol 3-O-beta-heterodisaccharidase from the dried herb of Fagopyrum esculentum Moench.	2003 Sep	12943757
[HPLC investigation of antioxidant components in Solidago herba].	2004	16316050
Structure-activity relationship (SAR) between some natural flavonoids and ocular blood flow in the rabbit.	2004 Feb	15006157
Protein-lipid interactions during liposome oxidation with added anthocyanin and other phenolic compounds.	2004 Mar 10	14995106
Threshold dissociation and molecular modeling of transition metal complexes of flavonoids.	2005 Feb	15694764
Anti-inflammatory effect of heme oxygenase 1: glycosylation and nitric oxide inhibition in macrophages.	2005 Feb	15316927
Fate of anthocyanins and antioxidant capacity in contents of the gastrointestinal tract of weanling pigs following black raspberry consumption.	2006 Jan 25	16417325
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 Aug 13	17693314
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 Jan 4	18061601
Substrate specificities of glycosidases from Aspergillus species pectinase preparations on elderberry anthocyanins.	2009 Feb 11	19191672
Degradation of rutin by Thermoactinomyces vulgaris and other thermophilic compost isolates.	2009 Jun 10	19489631
Immobilization of flavonol 3-O-beta-heterodisaccharidase on porous glass and production of rutinose from rutin.	2009 Oct	19452439
Bioglycans and natural glycosides as a promising research topic in bioorganic chemistriy.	2010 Jul	22649639
An essential difference between the flavonoids monoHER and quercetin in their interplay with the endogenous antioxidant network.	2010 Nov 8	21079733

Patents

Substance Class	Chemical Created by `admin` on `Sat Dec 16 09:05:40 GMT 2023` Edited by `admin` on `Sat Dec 16 09:05:40 GMT 2023`
Record UNII	0C4U3505G3
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

RUTINOSE

Common Name

English

RUTINOSE [MI]

Common Name

English

D-GLUCOSE, 6-O-(6-DEOXY-.ALPHA.-L-MANNOPYRANOSYL)-

Common Name

English

Code System Code Type Description

PUBCHEM

5460038