CHEBI:136943 - 6-sinapoylglucoraphenin

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ChEBI Name 6-sinapoylglucoraphenin
ChEBI ID CHEBI:136943
Definition A glucosinolic acid that is glucoraphenin in which the hydroxy hydrogen at position 6 on the glucose fragment has been replaced by a sinapoyl group.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information ChemicalBook:CB3167375, ChemicalBook:CB4183426, eMolecules:494487, ZINC000000899824
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Roles Classification
Biological Role(s): Arabidopsis thaliana metabolite
Any plant metabolite that is produced by Arabidopsis thaliana.
plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
(via glucosinolic acid )
Related Structures
6-sinapoylglucoraphenin is a Structural Derivative of
glucoraphenin
Mass : 419.495
Formula : C12H21NO9S3
79367
trans-sinapic acid
Mass : 224.21000
Formula : C11H12O5
15714
desulfoglucosinolic acid
Mass : 238.240
Formula : C7H12NO6SR
136442
1-thio-beta-D-glucopyranose
Mass : 196.22100
Formula : C6H12O5S
42896
glucose
Mass : 180.15588
Formula : C6H12O6
17234
carbohydrate
Definition : Any member of the class of organooxygen compounds that is a polyhydroxy-aldehyde or -ketone or a lactol resulting from their intramolecular condensation (monosaccharides); substances derived from these by reduction of the carbonyl group (alditols), by oxidation of one or more hydroxy groups to afford the corresponding aldehydes, ketones, or carboxylic acids, or by replacement of one or more hydroxy group(s) by a hydrogen atom; and polymeric products arising by intermolecular acetal formation between two or more such molecules (disaccharides, polysaccharides and oligosaccharides). Carbohydrates contain only carbon, hydrogen and oxygen atoms; prior to any oxidation or reduction, most have the empirical formula Cm(H2O)n. Compounds obtained from carbohydrates by substitution, etc., are known as carbohydrate derivatives and may contain other elements. Cyclitols are generally not regarded as carbohydrates.
sulfuric acid
Mass : 98.07948
Formula : H2O4S
26836
oxoacid
Definition : A compound which contains oxygen, at least one other element, and at least one hydrogen bound to oxygen, and which produces a conjugate base by loss of positive hydrogen ion(s) (hydrons).
cinnamic acids
Definition : Any alpha,beta-unsaturated monocarboxylic acid based on the cinnamic acid skeleton and its substituted derivatives.
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thioglucoside
sulfoxide
molecular entity
chemical entity
molecule
organic sulfate
oxygen molecular entity
phenylpropanoid
sulfates
sulfur molecular entity
oxoacid derivative
organosulfur compound
heteroorganic entity
pnictogen molecular entity
chalcogen molecular entity
carboxylic ester
sulfur oxoacid derivative
main group molecular entity
carbon group molecular entity
cyclic compound
aromatic compound
organic aromatic compound
p-block molecular entity
organic cyclic compound
S-glycosyl compound
organonitrogen compound
ester
cinnamate ester
polyatomic entity
carbonyl compound
organic oxo compound
organochalcogen compound
organooxygen compound
heteroatomic molecular entity
sulfuric acid derivative
organic molecular entity
nitrogen molecular entity
enoate ester
alpha,beta-unsaturated carboxylic ester
thioacetal
monothioacetal
glycosyl compound
carbohydrate derivative
organic molecule
thiosugar
carbohydrates and carbohydrate derivatives
olefinic compound
glycosinolic acid
glucosinolic acid
D-thioglucoside
beta-D-thioglucoside
6-sinapoylglucoraphenin
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