Compound Identification
SMILES
NC1=NC2=C(N)N(CN=C2N1[C@@H]1O[C@H](COP(O)(=O)OP(O)(O)=O)C=C1O)[C@@H]1O[C@H](CO)C(O)=C1O
InChIKey
InChIKey=WZEWLTIOWBOCDF-XWPVMSEFSA-N
Formula
C15H22N6O13P2
Mass
556.318
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Organic oxygen compounds
-
Class
Organic oxoanionic compounds
- Subclass Organic pyrophosphates
-
Class
Organic oxoanionic compounds
-
Superclass
Organic oxygen compounds
Kingdom
Organic compounds
Superclass
Organic oxygen compounds
Class
Organic oxoanionic compounds
Subclass
Organic pyrophosphates
Intermediate Tree Nodes
Not available
Direct Parent
Organic pyrophosphates
Alternative Parents
Purines and purine derivatives Monoalkyl phosphates Aminoimidazoles N-substituted imidazoles Monosaccharides Imidolactams Dihydrofurans Heteroaromatic compounds Enediols Azacyclic compounds Oxacyclic compounds Enols Primary amines Primary alcohols Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Organic pyrophosphate - Imidazopyrimidine - Purine - Monoalkyl phosphate - Aminoimidazole - Imidolactam - Alkyl phosphate - Monosaccharide - N-substituted imidazole - Phosphoric acid ester - Organic phosphoric acid derivative - Azole - Dihydrofuran - Heteroaromatic compound - Imidazole - Enediol - Oxacycle - Enol - Azacycle - Organoheterocyclic compound - Organic nitrogen compound - Amine - Alcohol - Hydrocarbon derivative - Organic oxide - Primary amine - Primary alcohol - Organooxygen compound - Organonitrogen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as organic pyrophosphates. These are organic compounds containing the pyrophosphate oxoanion, with the structure OP([O-])(=O)OP(O)([O-])=O.
External Descriptors
Not available