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Structure Information
Structure

Compound Identification

SMILES

CC1=CC=C(C=C1)S(=O)(=O)OC1C(CO)OC(C1O)N1C=C(C(N)=NC1=O)[N+]([O-])=O

InChIKey

InChIKey=XETACHZHDDTBET-UHFFFAOYSA-N

Formula

C16H18N4O9S

Mass

442.4

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Pyrimidine nucleosides

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Pyrimidine nucleosides

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Pyrimidine nucleoside - Glycosyl compound - Benzenesulfonate ester - N-glycosyl compound - P-methylbenzenesulfonate - Pentose monosaccharide - Benzenesulfonate - Tosyl compound - Arylsulfonic acid or derivatives - Benzenesulfonyl group - Nitroaromatic compound - Aminopyrimidine - Pyrimidone - Toluene - Monocyclic benzene moiety - Hydropyrimidine - Monosaccharide - Pyrimidine - Organosulfonic acid ester - Imidolactam - Benzenoid - Sulfonyl - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Heteroaromatic compound - Oxolane - Organic nitro compound - Secondary alcohol - C-nitro compound - Organoheterocyclic compound - Organic 1,3-dipolar compound - Azacycle - Propargyl-type 1,3-dipolar organic compound - Oxacycle - Allyl-type 1,3-dipolar organic compound - Organic oxoazanium - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Organosulfur compound - Primary alcohol - Organic nitrogen compound - Amine - Hydrocarbon derivative - Alcohol - Organic salt - Organic zwitterion - Organic oxide - Primary amine - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as pyrimidine nucleosides. These are compounds comprising a pyrimidine base attached to a ribosyl or deoxyribosyl moiety.

External Descriptors

Not available

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