Structure Information
Structure

Compound Identification

SMILES

N[C@H](CN[C@@H]([C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=C(CO)C(=O)NC1=O)C(O)=O)[C@H](O)[C@@H](O)COC(N)=O

InChIKey

InChIKey=BIQUIDGHLKTCEM-NWMPZBAOSA-N

Formula

C17H27N5O12

Mass

493.426

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

5'-deoxyribonucleosides

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

5'-deoxyribonucleosides

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

5'-deoxyribonucleoside - N-glycosyl compound - Glycosyl compound - L-alpha-amino acid - Alpha-amino acid or derivatives - Alpha-amino acid - Pyrimidone - Pyrimidine - Hydropyrimidine - Heteroaromatic compound - 1,3-aminoalcohol - Vinylogous amide - Carbamic acid ester - Oxolane - Amino acid or derivatives - 1,2-aminoalcohol - Lactam - Urea - Amino acid - Secondary alcohol - Carboxylic acid derivative - Carboxylic acid - Secondary aliphatic amine - Oxacycle - Azacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Secondary amine - Amine - Organic oxide - Organopnictogen compound - Alcohol - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Aromatic alcohol - Primary aliphatic amine - Hydrocarbon derivative - Organonitrogen compound - Organooxygen compound - Primary alcohol - Primary amine - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as 5'-deoxyribonucleosides. These are nucleosides in which the oxygen atom at the 5'position of the ribose moiety has been replaced by another atom. The nucleobases here are limited to purine, pyrimidine, and pyridine derivatives.

External Descriptors

Not available

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