QUINOVOSE

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

InChIKey=PNNNRSAQSRJVSB-JGWLITMVSA-N

InChI=1S/C6H12O5/c1-3(8)5(10)6(11)4(9)2-7/h2-6,8-11H,1H3/t3-,4+,5-,6-/m1/s1

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	4 / 4
E/Z Centers	0
Optical Activity	UNSPECIFIED

PubMed

Title	Date	PubMed
Application of quantitative structure-toxicity relationships for acute NSAID cytotoxicity in rat hepatocytes.	2005 Feb 10	15733539
Functional differentiation of the glycosyltransferases that contribute to the chemical diversity of bioactive flavonol glycosides in grapevines (Vitis vinifera).	2010 Aug	20693356
The ascorbic acid content of tomato fruits is associated with the expression of genes involved in pectin degradation.	2010 Aug 6	20691085
Anti-angiogenic effects of resveratrol mediated by decreased VEGF and increased TSP1 expression in melanoma-endothelial cell co-culture.	2010 Dec	20927579

Substance Class	Chemical Created by `admin` on `Fri Dec 15 18:44:34 GMT 2023` Edited by `admin` on `Fri Dec 15 18:44:34 GMT 2023`
Record UNII	O654621E3T
Record Status	`Validated (UNII)`
Record Version

Name

Type

Language

QUINOVOSE

Common Name

English

QUINOVOSE [MI]

Common Name

English

CHINOVOSE

Common Name

English

D-EPIRHAMNOSE

Common Name

English

EPIFUCOSE

Common Name

English

D-ISORHAMNOSE

Common Name

English

ISORHODEOSE

Common Name

English

Code System Code Type Description

FDA UNII

O654621E3T