Structure Information
Structure

Compound Identification

SMILES

[B][B]C1CC(OP(O)(=O)OCC2OC([B])CC2OC)C(COP(O)(=O)OC2CC(OC2COP(O)(=O)OP(O)(=O)OCC2OC(C(O)C2C)N2C=NC3=C2N=CN=C3N)B([B])[B])O1

InChIKey

InChIKey=UYXCUSINEBXELH-UHFFFAOYSA-N

Formula

C27H42B6N5O21P4

Mass

961.4

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Purine nucleotides

Subclass

Purine nucleotide sugars

Intermediate Tree Nodes

Not available

Direct Parent

Purine nucleotide sugars

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine nucleotide sugar - Purine 3'-deoxyribonucleoside diphosphate - 6-aminopurine - Organic pyrophosphate - Imidazopyrimidine - Purine - Aminopyrimidine - Dialkyl phosphate - Monoalkyl phosphate - N-substituted imidazole - Organic phosphoric acid derivative - Phosphoric acid ester - Pyrimidine - Imidolactam - Alkyl phosphate - Heteroaromatic compound - Azole - Imidazole - Oxolane - Secondary alcohol - Boronic acid derivative - Organoheterocyclic compound - Organic metalloid salt - Dialkyl ether - Ether - Oxacycle - Azacycle - Monoalkylborane - Organic metalloid moeity - Organic oxygen compound - Organic nitrogen compound - Amine - Organonitrogen compound - Organooxygen compound - Organic oxide - Hydrocarbon derivative - Alkylborane - Alcohol - Primary amine - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine nucleotide sugars. These are purine nucleotides bound to a saccharide derivative through the terminal phosphate group.

External Descriptors

Not available

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