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Structure Information
Structure

Compound Identification

SMILES

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

InChIKey

InChIKey=CFMAWYXPTOOLPT-MPOLUYMFSA-N

Formula

C48H59N18O19P3S3

Mass

1381.21

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Nucleoside and nucleotide analogues

Subclass

Phosphorothioate oligonucleotides

Intermediate Tree Nodes

Not available

Direct Parent

Phosphorothioate oligonucleotides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Phosphorothioate oligonucleotide - 6-aminopurine - 6-oxopurine - Hypoxanthine - Imidazopyrimidine - Purine - Aminopyrimidine - Pyrimidone - Hydropyrimidine - N-substituted imidazole - Pyrimidine - Imidolactam - Azole - Imidazole - Heteroaromatic compound - Oxolane - Vinylogous amide - Urea - Secondary alcohol - Lactam - Azacycle - Sulfenyl compound - Organothiophosphorus compound - Organoheterocyclic compound - Oxacycle - Nitrile - Carbonitrile - Primary amine - Organonitrogen compound - Organooxygen compound - Alcohol - Organic oxygen compound - Hydrocarbon derivative - Organic oxide - Organic nitrogen compound - Organosulfur compound - Cyanide - Amine - Primary alcohol - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as phosphorothioate oligonucleotides. These are oligonucleotides in which one of the non-bridging oxygens in each phosphodiester linkage has been replaced by sulfur.

External Descriptors

Not available

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