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
An iridoid glucoside dimer and a non-glycosidic iridoid from the leaves of Lasianthus wallichii.	2002 Oct	12372873
Differential apoptosis-inducing effect of quercetin and its glycosides in human promyeloleukemic HL-60 cells by alternative activation of the caspase 3 cascade.	2003 Aug 1	12874837
Anti-Sindbis activity of flavanones hesperetin and naringenin.	2003 Jan	12520185
Purification and characterization of a flavonol 3-O-beta-heterodisaccharidase from the dried herb of Fagopyrum esculentum Moench.	2003 Sep	12943757
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
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 Apr 20	15826066
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
Silver complexation and tandem mass spectrometry for differentiation of isomeric flavonoid diglycosides.	2005 Mar 15	15762583
Potential antitumor agents: flavones and their derivatives from Linaria reflexa Desf.	2005 Nov 1	16125932
Fate of anthocyanins and antioxidant capacity in contents of the gastrointestinal tract of weanling pigs following black raspberry consumption.	2006 Jan 25	16417325
In vitro biological evaluation of novel 7-O-dialkylaminoalkyl cytotoxic pectolinarigenin derivatives against a panel of human cancer cell lines.	2008 Oct 15	18818071
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
Preparative separation of phenolic compounds from Halimodendron halodendron by high-speed counter-current chromatography.	2010 Aug 31	20877205
Two novel disaccharides, rutinose and methylrutinose, are involved in carbon metabolism in Datisca glomerata.	2010 Feb	19915863
Bioglycans and natural glycosides as a promising research topic in bioorganic chemistriy.	2010 Jul	22649639
Extracellular monoenzyme deglycosylation system of 7-O-linked flavonoid beta-rutinosides and its disaccharide transglycosylation activity from Stilbella fimetaria.	2010 May	20358178
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