Compound Identification
SMILES
NC1=NC2C(N=C(Cl)N2[C@H]2O[C@@H]3COP(O)(=S)O[C@H]3[C@H]2O)C(=O)N1
InChIKey
InChIKey=TYJBHDGBDWOLCD-RMOYWJHGSA-N
Formula
C10H13ClN5O6PS
Mass
397.73
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
6-oxopurines Alpha amino acids and derivatives Thiophosphate diesters Hydropyrimidines Monosaccharides Oxolanes Imidazolines Secondary alcohols Guanidines Propargyl-type 1,3-dipolar organic compounds Oxacyclic compounds Azacyclic compounds Carboximidamides Carbonyl compounds Amines Organochlorides Hydrocarbon derivatives Organic oxides
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
N-glycosyl compound - 6-oxopurine - Alpha-amino acid or derivatives - Purinone - Imidazopyrimidine - Purine - Thiophosphate diester - Hydropyrimidine - 1,4,5,6-tetrahydropyrimidine - Monosaccharide - Organic thiophosphoric acid or derivatives - Thiophosphoric acid ester - 2-imidazoline - Oxolane - Guanidine - Secondary alcohol - Carboxylic acid derivative - Carboximidamide - Oxacycle - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Organoheterocyclic compound - Azacycle - Alcohol - Organohalogen compound - Organic nitrogen compound - Hydrocarbon derivative - Organochloride - Carbonyl group - Amine - Organic oxide - Organonitrogen compound - Aliphatic 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