Structure Information
Structure

Compound Identification

SMILES

NC1=NC=NC2=C1C(=NN2[C@H]1O[C@H](CO)[C@@H](O)[C@H]1O)C#CCNC(=O)CCCCCNC(=O)CCCCC1SC[C@@H]2NC(=O)N[C@H]12

InChIKey

InChIKey=JTYOPXAEILBDQY-ANPUSPMCSA-N

Formula

C29H41N9O7S

Mass

659.76

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Pyrazolo[3,4-d]pyrimidine glycosides

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Pyrazolo[3,4-d]pyrimidine glycosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Pyrazolo[3,4-d]pyrimidine glycoside - Biotin_derivative - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - Pyrazolo[3,4-d]pyrimidine - Pyrazolopyrimidine - Thienoimidazolidine - Aminopyrimidine - Fatty amide - Imidazolidinone - Monosaccharide - N-acyl-amine - Pyrimidine - Fatty acyl - Imidolactam - Imidazolidine - Thiolane - Thiophene - Oxolane - Heteroaromatic compound - Azole - Pyrazole - Amino acid or derivatives - Carboxamide group - Urea - 1,2-diol - Secondary alcohol - Secondary carboxylic acid amide - Dialkylthioether - Carboxylic acid derivative - Oxacycle - Organoheterocyclic compound - Azacycle - Thioether - Organic nitrogen compound - Organic oxide - Hydrocarbon derivative - Alcohol - Carbonyl group - Organic oxygen compound - Amine - Organonitrogen compound - Organooxygen compound - Primary alcohol - Primary amine - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as pyrazolo[3,4-d]pyrimidine glycosides. These are nucleosides or derivatives thereof that consist of a pyazolo[3,2-d]pyrimidine ring system that is N-glycosidically linked to a ribose or deoxyribose. They bear the sugar moiety on the pyrimidine part of the molecule.

External Descriptors

Not available

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