Structure Information
Structure

Compound Identification

SMILES

CC1=C(OP(O)(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)N2C=NC3=C2NC(N)=NC3=O)C(C)=C(CC(O)=O)NC1=O

InChIKey

InChIKey=GTHOTKPHMGEHFD-ACDAHVMNSA-N

Formula

C19H23N6O11P

Mass

542.398

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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-5-phosphate - Pentose phosphate - Glycosyl compound - N-glycosyl compound - 6-oxopurine - Pentose monosaccharide - Monosaccharide phosphate - Hypoxanthine - Purine - Imidazopyrimidine - Dihydropyridine - Aminopyrimidine - Monoalkyl phosphate - Pyrimidone - Pyridinone - Methylpyridine - Hydropyridine - Monosaccharide - N-substituted imidazole - Organic phosphoric acid derivative - Alkyl phosphate - Phosphoric acid ester - Pyrimidine - Pyridine - Oxolane - Azole - Vinylogous amide - Heteroaromatic compound - Imidazole - Secondary alcohol - Amino acid or derivatives - Amino acid - 1,2-diol - Lactam - Organoheterocyclic compound - Carboxylic acid derivative - Carboxylic acid - Azacycle - Monocarboxylic acid or derivatives - Oxacycle - Organonitrogen compound - Carbonyl group - Organooxygen compound - Alcohol - Organic oxide - Organic nitrogen compound - Hydrocarbon derivative - Primary amine - Organic oxygen compound - Amine - 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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