Compound Identification
SMILES
COC1=CC2=C(C=C1)N=C1N(N=C(C)C1=C2Cl)[C@@H]1O[C@H](COC(=O)CC2=CC=CC=C2)[C@@H](OC(=O)CC2=CC=CC=C2)[C@H]1OC(=O)CC1=CC=CC=C1
InChIKey
InChIKey=LBLBBBQLEYADIB-WCCISFPSSA-N
Formula
C41H36ClN3O8
Mass
734.2
Taxonomic Classification
Taxonomy Tree
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Kingdom
Organic compounds
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Superclass
Organic oxygen compounds
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Class
Organooxygen compounds
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Subclass
Carbohydrates and carbohydrate conjugates
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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
Chloroquinolines Tricarboxylic acids and derivatives Pyrazolopyridines Anisoles Alkyl aryl ethers Pyridines and derivatives Aryl chlorides Benzene and substituted derivatives Monosaccharides Pyrazoles Oxolanes Heteroaromatic compounds Carboxylic acid esters Azacyclic compounds Oxacyclic compounds Organochlorides Carbonyl compounds Organonitrogen compounds Hydrocarbon derivatives Organic oxides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Haloquinoline - N-glycosyl compound - Chloroquinoline - Quinoline - Tricarboxylic acid or derivatives - Pyrazolopyridine - Anisole - Phenol ether - Alkyl aryl ether - Aryl chloride - Monosaccharide - Aryl halide - Monocyclic benzene moiety - Benzenoid - Pyridine - Heteroaromatic compound - Pyrazole - Oxolane - Azole - Carboxylic acid ester - Oxacycle - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Ether - Carbonyl group - Organic oxide - Hydrocarbon derivative - Organonitrogen compound - Organic nitrogen compound - Organochloride - Organohalogen compound - 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