Structure Information
Structure

Compound Identification

SMILES

CCCCCCCCCCCCSC(CCOP(O)(=O)OC[C@H]1O[C@H]([C@@H](O)[C@@H]1O)N1C=NC2=C1N=C(F)N=C2N)OCCCCCCCCCC

InChIKey

InChIKey=JAOIHOZXTNLYIJ-MBWHZDNJSA-N

Formula

C35H63FN5O8PS

Mass

763.95

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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 - Pentose monosaccharide - Monosaccharide phosphate - Imidazopyrimidine - Purine - 2-halopyrimidine - Aminopyrimidine - Halopyrimidine - Dialkyl phosphate - Pyrimidine - Alkyl phosphate - Imidolactam - Monosaccharide - Phosphoric acid ester - Aryl halide - Organic phosphoric acid derivative - Aryl fluoride - N-substituted imidazole - Monothioacetal - Heteroaromatic compound - Imidazole - Oxolane - Azole - 1,2-diol - Secondary alcohol - Oxacycle - Azacycle - Organoheterocyclic compound - Sulfenyl compound - Organosulfur compound - Primary amine - Amine - Alcohol - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Organonitrogen compound - Organofluoride - Organohalogen 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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