Compound Identification
SMILES
CC1OC(C(O)C1O)N1C=C(C(N)=O)C2=C1N=CN=C2N
InChIKey
InChIKey=HXTSROMHHXTVDO-UHFFFAOYSA-N
Formula
C12H15N5O4
Mass
293.283
Taxonomic Classification
Taxonomy Tree
-
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
Pyrrolo[2,3-d]pyrimidines Pyrimidinecarboxamides Pyrrole carboxamides Aminopyrimidines and derivatives Substituted pyrroles Imidolactams Vinylogous amides Heteroaromatic compounds Oxolanes Secondary alcohols Amino acids and derivatives 1,2-diols Primary carboxylic acid amides Oxacyclic compounds Azacyclic compounds Organic oxides Hydrocarbon derivatives Primary amines
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
N-glycosyl compound - Pyrrolo[2,3-d]pyrimidine - Pyrimidinecarboxamide - Pyrrolopyrimidine - Pyrrole-3-carboxamide - Pyrrole-3-carboxylic acid or derivatives - Aminopyrimidine - Pyrimidine - Substituted pyrrole - Imidolactam - Oxolane - Heteroaromatic compound - Pyrrole - Vinylogous amide - Amino acid or derivatives - Secondary alcohol - Primary carboxylic acid amide - 1,2-diol - Carboxamide group - Azacycle - Oxacycle - Organoheterocyclic compound - Carboxylic acid derivative - Alcohol - Organic oxide - Organonitrogen compound - Organic nitrogen compound - Amine - Primary amine - Hydrocarbon derivative - 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