Structure Information
Structure

Compound Identification

SMILES

CC1=CN([C@H]2C[C@H](N=[N+]=[N-])[C@@H](COP(=O)(OCCC#N)OC[C@@H]3CC[C@@H](O3)N3C=NC4=C3N=CN=C4N)O2)C(=O)NC1=O

InChIKey

InChIKey=ZZOQOCAXOCFBLH-GTTJKFTRSA-N

Formula

C23H28N11O8P

Mass

617.52

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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 2',3'-dideoxyribonucleoside monophosphate - Purine 2',3'-dideoxyribonucleoside - Purine nucleoside - 6-aminopurine - Purine - Imidazopyrimidine - Trialkyl phosphate - Aminopyrimidine - Pyrimidone - Hydropyrimidine - Pyrimidine - N-substituted imidazole - Organic phosphoric acid derivative - Alkyl phosphate - Imidolactam - Phosphoric acid ester - Azole - Vinylogous amide - Imidazole - Oxolane - Heteroaromatic compound - Azo compound - Azo imide - Lactam - Urea - Oxacycle - Azacycle - Organoheterocyclic compound - Nitrile - Carbonitrile - Primary amine - Organonitrogen compound - Organic oxygen compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Cyanide - Amine - Organic nitrogen compound - Organic salt - Organic zwitterion - 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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