Structure Information
Structure

Compound Identification

SMILES

NC1=NC=NC2=C1N=CN2[C@@H]1O[C@H](COP(O)(=O)OP(O)(O)=S)[C@@H](OC2=CC=CO2)[C@H]1O

InChIKey

InChIKey=PMMQRULHKWPREV-FRJWGUMJSA-N

Formula

C14H17N5O10P2S

Mass

509.32

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Taxonomic Classification

Taxonomy Tree

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

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine ribonucleoside monophosphate - Pentose phosphate - Pentose-5-phosphate - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Monosaccharide phosphate - Pentose monosaccharide - Imidazopyrimidine - Purine - Alkyl aryl ether - Aminopyrimidine - Monoalkyl phosphate - Imidolactam - Monosaccharide - N-substituted imidazole - Organic phosphoric acid derivative - Organic thiophosphoric acid or derivatives - Phosphoric acid ester - Primary aromatic amine - Alkyl phosphate - Pyrimidine - Oxolane - Furan - Azole - Heteroaromatic compound - Imidazole - Secondary alcohol - Ether - Oxacycle - Azacycle - Organoheterocyclic compound - Organic nitrogen compound - Alcohol - Organic oxide - Organic oxygen compound - Hydrocarbon derivative - Primary amine - Amine - Organopnictogen compound - Organonitrogen compound - Organooxygen compound - 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

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