Structure Information
Structure

Compound Identification

SMILES

CC1=CN([C@H]2C[C@@H](OP(O)(=O)OC[C@H]3O[C@H](C[C@H]3OP(O)(O)=O)N3C=NC4=C3N=CN=C4N)[C@@H](CO)O2)C(=O)NC1=O

InChIKey

InChIKey=MBGMMNDKSOTOAO-BXLXJSPXSA-N

Formula

C20H27N7O13P2

Mass

635.42

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

(3'->5')-dinucleotides and analogues

Subclass

(3'->5')-dinucleotides

Intermediate Tree Nodes

Not available

Direct Parent

(3'->5')-dinucleotides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

(3'->5')-dinucleotide - Purine deoxyribonucleoside 3',5'-bisphosphate - Purine deoxyribonucleoside bisphosphate - Ribonucleoside 3'-phosphate - 6-aminopurine - Imidazopyrimidine - Purine - Aminopyrimidine - Pyrimidone - Monoalkyl phosphate - Dialkyl phosphate - Hydropyrimidine - N-substituted imidazole - Organic phosphoric acid derivative - Phosphoric acid ester - Pyrimidine - Alkyl phosphate - Imidolactam - Heteroaromatic compound - Vinylogous amide - Azole - Oxolane - Imidazole - Urea - Lactam - Oxacycle - Organoheterocyclic compound - Azacycle - Organic nitrogen compound - Alcohol - Amine - Organic oxide - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Primary alcohol - Primary amine - Hydrocarbon derivative - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as (3'->5')-dinucleotides. These are dinucleotides where the two bases are connected via a (3'->5')-phosphodiester linkage.

External Descriptors

Not available

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