Compound Identification
SMILES
NC1=NC=NC2=C1C1=C(NC(=S)NC1=O)N2C1OC(CO)C(O)C1O
InChIKey
InChIKey=RQLJWVFGMWLLHU-UHFFFAOYSA-N
Formula
C13H14N6O5S
Mass
366.35
Taxonomic Classification
Taxonomy Tree
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Kingdom
Organic compounds
-
Superclass
Organic oxygen compounds
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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
Pentoses Pyrrolo[2,3-d]pyrimidines Aminopyrimidines and derivatives 2-Thiopyrimidines Pyrimidones Pyrimidinethiones Substituted pyrroles Imidolactams Heteroaromatic compounds Oxolanes Vinylogous amides Lactams Thioureas Secondary alcohols Oxacyclic compounds Azacyclic compounds Organic oxides Primary amines Hydrocarbon derivatives Primary alcohols
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
N-glycosyl compound - Pentose monosaccharide - Pyrrolo[2,3-d]pyrimidine - Pyrrolopyrimidine - Thiopyrimidine - Aminopyrimidine - 2-thiopyrimidine - Pyrimidinethione - Pyrimidone - Monosaccharide - Pyrimidine - Imidolactam - Substituted pyrrole - Heteroaromatic compound - Oxolane - Pyrrole - Vinylogous amide - Lactam - Secondary alcohol - Thiourea - Oxacycle - Azacycle - Organoheterocyclic compound - Amine - Organosulfur compound - Organonitrogen compound - Alcohol - Hydrocarbon derivative - Organic oxide - Organic nitrogen compound - Primary alcohol - Primary amine - 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