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Structure Information
Structure

Compound Identification

SMILES

COc1cc2n[n+]([nH]c2cc1C(O)=NCC1CCCN1CC=C)C1OC(C(O)C(O)C1O)C(O)=O

InChIKey

InChIKey=QVFXMOQFKLNQFA-UHFFFAOYSA-O

Formula

C22H30N5O8

Mass

492.508

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Nucleoside and nucleotide analogues

Subclass

2-pyranosylbenzotriazoles

Intermediate Tree Nodes

Not available

Direct Parent

2-pyranosylbenzotriazoles

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

2-pyranosylbenzotriazole - Glucuronic acid or derivatives - Benzotriazole - Anisole - Alkyl aryl ether - Beta-hydroxy acid - N-alkylpyrrolidine - Oxane - Benzenoid - Hydroxy acid - Pyran - Pyrrolidine - Azole - 1,2,3-triazole - Triazole - Heteroaromatic compound - Secondary alcohol - Amino acid - Tertiary amine - Amino acid or derivatives - Tertiary aliphatic amine - Oxacycle - Carboximidic acid - Carboximidic acid derivative - Carboxylic acid derivative - Carboxylic acid - Ether - Azacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Polyol - Amine - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Alcohol - Organonitrogen compound - Organooxygen compound - Carbonyl group - Organic cation - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as 2-pyranosylbenzotriazoles. These are nucleoside and nucleotide analogs with a structure that consists of a benzotriazole base which is N-substituted at the 2-position with a pyranose moiety. Nucleotide analogues contain a phosphate group linked to the C5 carbon atom of the pyranose.

External Descriptors

Not available

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