Structure Information
Structure

Compound Identification

SMILES

CC1=CN([C@H]2C[C@H](OP(O)(=O)OC[C@H]3O[C@H]([C@H](O)[C@@H]3OP(O)(=O)OC[C@H]3O[C@H]([C@H](O)[C@@H]3OP(O)(=O)OC[C@H]3O[C@H]([C@H](O)[C@@H]3O)N3C=NC4=C3NC(N)=NC4=O)N3C=CC(N)=NC3=O)N3C=NC4=C3N=CN=C4N)[C@@H](COP(O)(O)=O)O2)C(=O)NC1=O

InChIKey

InChIKey=ZPCWHNDTDDLZFN-ABZQLSLFSA-N

Formula

C39H51N15O28P4

Mass

1301.809

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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 ribonucleoside bisphosphate - Purine ribonucleoside 3',5'-bisphosphate - Pyrimidine ribonucleoside bisphosphate - Pyrimidine ribonucleoside 3',5'-bisphosphate - Pyrimidine deoxyribonucleoside bisphosphate - Pyrimidine deoxyribonucleoside 3',5'-bisphosphate - Purine ribonucleoside monophosphate - Ribonucleoside 3'-phosphate - Pentose phosphate - Pentose-5-phosphate - Glycosyl compound - N-glycosyl compound - Hypoxanthine - 6-oxopurine - 6-aminopurine - Monosaccharide phosphate - Purine - Imidazopyrimidine - Aminopyrimidine - Dialkyl phosphate - Monoalkyl phosphate - Pyrimidone - Alkyl phosphate - Pyrimidine - Imidolactam - Phosphoric acid ester - Hydropyrimidine - Organic phosphoric acid derivative - N-substituted imidazole - Monosaccharide - Vinylogous amide - Azole - Oxolane - Heteroaromatic compound - Imidazole - Secondary alcohol - Urea - Lactam - Organoheterocyclic compound - Azacycle - Oxacycle - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Alcohol - Organic nitrogen compound - Primary amine - Organonitrogen compound - Amine - Organic oxygen 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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