Structure Information
Structure

Compound Identification

SMILES

NC1=NC(=O)C2=C(N1)N(C=N2)[C@H]1C[C@H](OP(O)(=O)OC[C@H]2O[C@H](C[C@@H]2O)N2C=CC(N)=NC2=O)[C@@H](COP(O)(=O)O[C@H]2C[C@@H](O[C@@H]2COP(O)(=O)O[C@H]2C[C@@H](O[C@@H]2COP(O)(=O)O[C@H]2C[C@@H](O[C@@H]2CO)N2C=CC(N)=NC2=O)N2C=CC(N)=NC2=O)N2C=NC3=C2NC(N)=NC3=O)O1

InChIKey

InChIKey=PDXRJUGDJLLAIG-YNNXNZCNSA-N

Formula

C47H61N19O28P4

Mass

1464.005

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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 heteropolycyclic compounds

Substituents

(3'->5')-oligonucleotide - Purine deoxyribonucleoside 3',5'-bisphosphate - Purine deoxyribonucleoside bisphosphate - Pyrimidine deoxyribonucleoside 3',5'-bisphosphate - Pyrimidine deoxyribonucleoside bisphosphate - Pyrimidine 2'-deoxyribonucleoside monophosphate - Ribonucleoside 3'-phosphate - 6-oxopurine - Hypoxanthine - Imidazopyrimidine - Purine - Aminopyrimidine - Dialkyl phosphate - Pyrimidone - Hydropyrimidine - N-substituted imidazole - Organic phosphoric acid derivative - Phosphoric acid ester - Imidolactam - Pyrimidine - Alkyl phosphate - Heteroaromatic compound - Azole - Vinylogous amide - Oxolane - Imidazole - Secondary alcohol - Oxacycle - Organoheterocyclic compound - Azacycle - Primary amine - Alcohol - Hydrocarbon derivative - Amine - Organic oxide - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Primary alcohol - Organic nitrogen compound - Aromatic heteropolycyclic 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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