Compound Identification
SMILES
COP(=O)(OC)OC[C@H]1O[C@H]([C@@H]2OC(C)(C)O[C@H]12)N1C=NC2=C1N=CN=C2N
InChIKey
InChIKey=XJFSEQIXIIIYIX-IDTAVKCVSA-N
Formula
C15H22N5O7P
Mass
415.343
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Nucleosides, nucleotides, and analogues
-
Class
Purine nucleotides
- Subclass Purine ribonucleotides
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Class
Purine nucleotides
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Superclass
Nucleosides, nucleotides, and analogues
Kingdom
Organic compounds
Superclass
Nucleosides, nucleotides, and analogues
Class
Purine nucleotides
Subclass
Purine ribonucleotides
Intermediate Tree Nodes
Not available
Direct Parent
Purine ribonucleoside monophosphates
Alternative Parents
Pentose phosphates 6-aminopurines Monosaccharide phosphates Trialkyl phosphates Aminopyrimidines and derivatives Ketals Primary aromatic amines Imidolactams N-substituted imidazoles 1,3-dioxolanes Oxolanes Heteroaromatic compounds Oxacyclic compounds Azacyclic compounds Hydrocarbon derivatives Organopnictogen compounds Organic oxides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine ribonucleoside monophosphate - Pentose phosphate - Pentose-5-phosphate - 6-aminopurine - Monosaccharide phosphate - Imidazopyrimidine - Purine - Trialkyl phosphate - Aminopyrimidine - Ketal - Monosaccharide - N-substituted imidazole - Organic phosphoric acid derivative - Phosphoric acid ester - Primary aromatic amine - Pyrimidine - Alkyl phosphate - Imidolactam - Imidazole - Heteroaromatic compound - Oxolane - Azole - Meta-dioxolane - Organoheterocyclic compound - Azacycle - Acetal - Oxacycle - Amine - Organic oxide - Organopnictogen compound - Primary amine - Organic oxygen compound - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as purine ribonucleoside monophosphates. These are nucleotides consisting of a purine base linked to a ribose to which one monophosphate group is attached.
External Descriptors
Not available