Compound Identification
SMILES
CC(=O)O[C@@H]1CO[C@@H](NC(=S)NC2=CC=C(C=C2)N2C(C)=NC3=C(C=C(Br)C=C3)C2=O)[C@H](OC(C)=O)[C@H]1OC(C)=O
InChIKey
InChIKey=GOUFGVZHYVXCGB-ZFFYZDHPSA-N
Formula
C27H27BrN4O8S
Mass
647.5
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 Glycosylamines
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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
Glycosylamines
Alternative Parents
Quinazolines N-phenylthioureas Tricarboxylic acids and derivatives Pyrimidones Oxanes Aryl bromides Monosaccharides Heteroaromatic compounds Thioureas Carboxylic acid esters Lactams Oxacyclic compounds Azacyclic compounds Hydrocarbon derivatives Organonitrogen compounds Organopnictogen compounds Carbonyl compounds Organobromides Organic oxides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
N-glycosyl compound - Diazanaphthalene - N-phenylthiourea - Quinazoline - Tricarboxylic acid or derivatives - Pyrimidone - Aryl bromide - Aryl halide - Monocyclic benzene moiety - Monosaccharide - Oxane - Pyrimidine - Benzenoid - Heteroaromatic compound - Carboxylic acid ester - Thiourea - Lactam - Oxacycle - Carboxylic acid derivative - Azacycle - Organoheterocyclic compound - Organic oxide - Organopnictogen compound - Organic nitrogen compound - Hydrocarbon derivative - Organohalogen compound - Organobromide - Organonitrogen compound - Organosulfur compound - Carbonyl group - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as glycosylamines. These are compounds consisting of an amine with a beta-N-glycosidic bond to a carbohydrate, thus forming a cyclic hemiaminal ether bond (alpha-amino ether).
External Descriptors
Not available