Structure Information
Structure

Compound Identification

SMILES

COC(=O)N[C@@H]([C@H](O)CC1=C(C)N=C2N1C(=O)C1=C(N(C=N1)[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O)N2C)C(O)=O

InChIKey

InChIKey=SCPHBBZWZRZNKJ-WKUWILHWSA-N

Formula

C20H26N6O10

Mass

510.46

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Nucleoside and nucleotide analogues

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Nucleoside and nucleotide analogues

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Glycosyl compound - N-glycosyl compound - 6-oxopurine - Alpha-amino acid or derivatives - Pentose monosaccharide - Hypoxanthine - Imidazopyrimidine - Imidazo[1,2-a]pyrimidine - Purine - Beta-hydroxy acid - Pyrimidone - Monosaccharide - Pyrimidine - N-substituted imidazole - Hydroxy acid - Carbamic acid ester - Heteroaromatic compound - Azole - Oxolane - Imidazole - Methylcarbamate - Vinylogous amide - Secondary alcohol - Lactam - Carboxylic acid derivative - Carboxylic acid - Oxacycle - Azacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Organic oxygen compound - Alcohol - Organic nitrogen compound - Carbonyl group - Organic oxide - Primary alcohol - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as nucleoside and nucleotide analogues. These are analogues of nucleosides and nucleotides. These include phosphonated nucleosides, C-glycosylated nucleoside bases, analogues where the sugar unit is a pyranose, and carbocyclic nucleosides, among others.

External Descriptors

Not available

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