Structure Information
Structure

Compound Identification

SMILES

[Na+].CC1=CN(C2CC(OP(O)(=O)OCC3OC(CC3OP([O-])(=O)OCC3OC(CC3O)N3C=CC(N)=NC3=O)N3C=C(C)C(=O)NC3=O)C(CO)O2)C(=O)NC1=O

InChIKey

InChIKey=FEGPOODZSAKRAM-UHFFFAOYSA-M

Formula

C29H38N7NaO18P2

Mass

857.591

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Nucleoside and nucleotide analogues

Subclass

Oligonucleotides

Intermediate Tree Nodes

Not available

Direct Parent

Oligonucleotides

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

(3'->5')-oligonucleotide - Pyrimidine deoxyribonucleoside bisphosphate - Pyrimidine deoxyribonucleoside 3',5'-bisphosphate - Pyrimidine 2'-deoxyribonucleoside monophosphate - Ribonucleoside 3'-phosphate - Aminopyrimidine - Dialkyl phosphate - Pyrimidone - Hydropyrimidine - Alkyl phosphate - Organic phosphoric acid derivative - Phosphoric acid ester - Pyrimidine - Imidolactam - Oxolane - Heteroaromatic compound - Vinylogous amide - Lactam - Secondary alcohol - Urea - Oxacycle - Organoheterocyclic compound - Azacycle - Organic alkali metal salt - Organic zwitterion - Organic sodium salt - Primary amine - Primary alcohol - Organic salt - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organic oxide - Alcohol - Organic oxygen compound - Amine - Organic nitrogen compound - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as oligonucleotides. These are organic polymers made up of a sequence of 3 to 12 purine or pyrimidine nucleotide residues linked to one another from the 5' -end to the 3'-end through a phosphate group.

External Descriptors

Not available

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