Structure Information
Structure

Compound Identification

SMILES

OC[C@H]1O[C@H](OP(O)(=O)OP(O)(=O)OP(O)(=O)OP(O)(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)N2C=CC(NOCC3=CC=CC=C3)=NC2=O)[C@H](O)[C@@H](F)[C@@H]1O

InChIKey

InChIKey=VNAVHLYUKQZQDG-PUTNOJKFSA-N

Formula

C22H32FN3O22P4

Mass

833.39

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Pyrimidine nucleotides

Subclass

Pyrimidine ribonucleotides

Intermediate Tree Nodes

Not available

Direct Parent

Pyrimidine ribonucleoside polyphosphates

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Pyrimidine ribonucleoside polyphosphate - Pyrimidine nucleotide sugar - Pentose phosphate - Pentose-5-phosphate - Glycosyl compound - N-glycosyl compound - Monosaccharide phosphate - Pyrimidone - Monoalkyl phosphate - Monocyclic benzene moiety - Hydropyrimidine - Monosaccharide - Organic phosphoric acid derivative - Oxane - Phosphoric acid ester - Pyrimidine - Alkyl phosphate - Benzenoid - Imidolactam - Oxolane - Heteroaromatic compound - Fluorohydrin - Halohydrin - Secondary alcohol - Organoheterocyclic compound - Azacycle - N-organohydroxylamine - Oxacycle - Alkyl fluoride - Organohalogen compound - Alkyl halide - Alcohol - Primary alcohol - Organofluoride - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as pyrimidine ribonucleoside polyphosphates. These are pyrimidine ribobucleotides with polyphosphate (with 4 or more phosphate) group linked to the ribose moiety.

External Descriptors

Not available

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