Structure Information
Structure

Compound Identification

SMILES

NC(=O)C1=CSC(=N1)C1OC(COP(O)(=O)OP(O)(=O)OCC2OC(C(O)C2F)N2C=NC3=C2N=CN=C3N)C(O)C1O

InChIKey

InChIKey=GKVVJZPLCCETPD-UHFFFAOYSA-N

Formula

C19H24FN7O13P2S

Mass

671.44

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Purine nucleotides

Subclass

Purine nucleotide sugars

Intermediate Tree Nodes

Not available

Direct Parent

Purine nucleotide sugars

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine nucleotide sugar - Purine 3'-deoxyribonucleoside diphosphate - Pentose phosphate - Pentose-5-phosphate - Glycosyl compound - C-glycosyl compound - Monosaccharide phosphate - Organic pyrophosphate - 6-aminopurine - Imidazopyrimidine - Purine - Thiazolecarboxylic acid or derivatives - Thiazolecarboxamide - 2-heteroaryl carboxamide - Monoalkyl phosphate - Aminopyrimidine - 2,4-disubstituted 1,3-thiazole - Alkyl phosphate - Imidolactam - Pyrimidine - Monosaccharide - N-substituted imidazole - Organic phosphoric acid derivative - Phosphoric acid ester - Thiazole - Azole - Imidazole - Heteroaromatic compound - Oxolane - 1,2-diol - Carboxamide group - Halohydrin - Primary carboxylic acid amide - Fluorohydrin - Secondary alcohol - Amino acid or derivatives - Oxacycle - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Dialkyl ether - Ether - Alcohol - Primary amine - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Amine - Alkyl fluoride - Alkyl halide - Organooxygen compound - Organonitrogen compound - Organofluoride - Organohalogen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine nucleotide sugars. These are purine nucleotides bound to a saccharide derivative through the terminal phosphate group.

External Descriptors

Not available

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