Structure Information
Structure

Compound Identification

SMILES

CC1=CN([C@H]2C[C@H](O)[C@@H](COP(O)(=O)O[C@H]3C4OCC[C@]3(COP(O)(=O)O[C@H]3C[C@@H](O[C@@H]3CO)N3C=C(C)C(=O)NC3=O)O[C@H]4N3C=C(C)C(=O)NC3=O)O2)C(=O)NC1=O

InChIKey

InChIKey=ZFJZSUNMDPJZFR-WWTBJQCWSA-N

Formula

C32H42N6O20P2

Mass

892.658

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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 - Pyrimidine 2'-deoxyribonucleoside monophosphate - Pentose-5-phosphate - Ribonucleoside 3'-phosphate - Pentose phosphate - Glycosyl compound - N-glycosyl compound - Monosaccharide phosphate - Dialkyl phosphate - Dioxepane - Pyrimidone - 1,4-dioxepane - Monosaccharide - Organic phosphoric acid derivative - Oxane - Alkyl phosphate - Phosphoric acid ester - Pyrimidine - Hydropyrimidine - Heteroaromatic compound - Vinylogous amide - Oxolane - Secondary alcohol - Urea - Lactam - Dialkyl ether - Ether - Organoheterocyclic compound - Azacycle - Oxacycle - Primary alcohol - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organonitrogen compound - Organic oxygen compound - Organooxygen compound - Alcohol - 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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