Compound Identification
SMILES
[H]C1(COP(O)(O)=O)OC([H])(C=C1O)N1C(N=[N+]=[N-])=NC2=C1N=CN=C2O
InChIKey
InChIKey=GAIDUVZRUCJAOG-UHFFFAOYSA-N
Formula
C10H10N7O7P
Mass
371.206
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
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Superclass
Organoheterocyclic compounds
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Class
Imidazopyrimidines
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Subclass
Purines and purine derivatives
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Level 5
Purinones
- Level 6 Hypoxanthines
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Level 5
Purinones
-
Subclass
Purines and purine derivatives
-
Class
Imidazopyrimidines
-
Superclass
Organoheterocyclic compounds
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Imidazopyrimidines
Subclass
Purines and purine derivatives
Intermediate Tree Nodes
Purinones
Direct Parent
Hypoxanthines
Alternative Parents
Monoalkyl phosphates Hydroxypyrimidines N-substituted imidazoles Heteroaromatic compounds Dihydrofurans Azo imides Azo compounds Oxacyclic compounds Enols Azacyclic compounds Organic zwitterions Organic salts Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Hypoxanthine - Monoalkyl phosphate - Hydroxypyrimidine - N-substituted imidazole - Organic phosphoric acid derivative - Phosphoric acid ester - Pyrimidine - Alkyl phosphate - Heteroaromatic compound - Imidazole - Azole - Dihydrofuran - Azo compound - Azo imide - Enol - Azacycle - Oxacycle - Organooxygen compound - Organonitrogen compound - Organic oxide - Organic zwitterion - Organic nitrogen compound - Organic salt - Hydrocarbon derivative - Organic oxygen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as hypoxanthines. These are compounds containing the purine derivative 1H-purin-6(9H)-one. Purine is a bicyclic aromatic compound made up of a pyrimidine ring fused to an imidazole ring.
External Descriptors
Not available