Compound Identification
SMILES
COC1OC(CO)C(OCC2=CC=CC=C2)C(OCC2=CC=CC=C2)C1OCCCC1(O)OC(C(CC2=CC=CC=C2)C(=O)N2C(COC2=O)C(C)C)C(=O)C=C1Br
InChIKey
InChIKey=LBHOVLCAMIXQMH-UHFFFAOYSA-N
Formula
C44H52BrNO12
Mass
866.799
Taxonomic Classification
Taxonomy Tree
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Kingdom
Organic compounds
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Superclass
Organic oxygen compounds
-
Class
Organooxygen compounds
-
Subclass
Carbohydrates and carbohydrate conjugates
-
Level 5
Glycosyl compounds
- Level 6 O-glycosyl compounds
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Level 5
Glycosyl compounds
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Subclass
Carbohydrates and carbohydrate conjugates
-
Class
Organooxygen compounds
-
Superclass
Organic oxygen compounds
Kingdom
Organic compounds
Superclass
Organic oxygen compounds
Class
Organooxygen compounds
Subclass
Carbohydrates and carbohydrate conjugates
Intermediate Tree Nodes
Glycosyl compounds
Direct Parent
O-glycosyl compounds
Alternative Parents
Benzylethers Dihydropyranones Oxazolidinones Oxanes Monosaccharides Vinylogous halides Carbamate esters Dicarboximides Bromohydrins Cyclic ketones Hemiacetals Acetals Azacyclic compounds Vinyl bromides Bromoalkenes Oxacyclic compounds Dialkyl ethers Aldehydes Organopnictogen compounds Primary alcohols Organonitrogen compounds Organobromides Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
O-glycosyl compound - Benzylether - Dihydropyranone - Monocyclic benzene moiety - Monosaccharide - Oxane - Oxazolidinone - Pyran - Benzenoid - Dicarboximide - Oxazolidine - Carbamic acid ester - Vinylogous halide - Cyclic ketone - Bromohydrin - Halohydrin - Hemiacetal - Ketone - Organoheterocyclic compound - Vinyl bromide - Vinyl halide - Carboxylic acid derivative - Dialkyl ether - Acetal - Ether - Haloalkene - Bromoalkene - Oxacycle - Azacycle - Organic oxide - Aldehyde - Carbonyl group - Primary alcohol - Hydrocarbon derivative - Organic nitrogen compound - Organohalogen compound - Organobromide - Organonitrogen compound - Organopnictogen compound - Alcohol - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond.
External Descriptors
Not available