Compound Identification
SMILES
CC1=CC=C(C=C1)N=NC1=C(C)N(C2OC(CO)C(O)C(O)C2O)C(=S)C(C#N)=C1C
InChIKey
InChIKey=JYJLAZOWRAUFBK-UHFFFAOYSA-N
Formula
C21H24N4O5S
Mass
444.51
Taxonomic Classification
Taxonomy Tree
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Kingdom
Organic compounds
-
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
-
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
Hexoses 3-pyridinecarbonitriles Toluenes Methylpyridines Dihydropyridines Oxanes Thiolactams Heteroaromatic compounds Secondary alcohols Azo compounds Propargyl-type 1,3-dipolar organic compounds Polyols Oxacyclic compounds Azacyclic compounds Nitriles Hydrocarbon derivatives Organosulfur compounds Primary alcohols
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Hexose monosaccharide - N-glycosyl compound - 3-pyridinecarbonitrile - Dihydropyridine - Methylpyridine - Toluene - Monocyclic benzene moiety - Hydropyridine - Monosaccharide - Oxane - Pyridine - Benzenoid - Heteroaromatic compound - Thiolactam - Secondary alcohol - Azo compound - Azacycle - Oxacycle - Polyol - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Nitrile - Carbonitrile - Organic nitrogen compound - Hydrocarbon derivative - Cyanide - Organonitrogen compound - Organosulfur compound - Alcohol - Primary alcohol - Aromatic heteromonocyclic 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