Structure Information
Structure

Compound Identification

SMILES

COC1=CC=C(C=C1)N1C(CN2N=NC(=N2)C2=CN=CC=C2)=NN(C2OC(COC(=O)C3=CC=CC=C3)C(OC(=O)C3=CC=CC=C3)C2OC(=O)C2=CC=CC=C2)C1=S

InChIKey

InChIKey=UEIPEKPIGSRPKA-UHFFFAOYSA-N

Formula

C42H34N8O8S

Mass

810.84

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Triazole ribonucleosides and ribonucleotides

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Triazole ribonucleosides and ribonucleotides

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

N-ribosyl-1,2,4-triazole - Phenyltriazole - Phenyl-1,2,4-triazole - N-glycosyl compound - Glycosyl compound - Benzoate ester - Benzoic acid or derivatives - Methoxyaniline - Tricarboxylic acid or derivatives - Benzoyl - Methoxybenzene - Anisole - Phenoxy compound - Phenol ether - Alkyl aryl ether - Monocyclic benzene moiety - Monosaccharide - Benzenoid - Pyridine - Azole - Heteroaromatic compound - 1,2,4-triazole - Triazole - Tetrahydrofuran - Tetrazole - Carboxylic acid ester - Organoheterocyclic compound - Azacycle - Oxacycle - Ether - Carboxylic acid derivative - Organonitrogen compound - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Organosulfur compound - Organic nitrogen compound - Organopnictogen compound - Organic oxide - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as triazole ribonucleosides and ribonucleotides. These are nucleoside derivatives containing a ribose (or deoxyribose) moiety which is N-glycosylated to a triazole. Nucleotides have a phosphate group linked to the C5 carbon of the ribose (or deoxyribose) moiety.

External Descriptors

Not available

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