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Structure Information
Structure

Compound Identification

SMILES

CC(=O)CCC(=O)O[C@H]1C[C@@H](O[C@@H]1COP(=O)(O[C@H]1C[C@@H](O[C@@H]1COP(=O)(O[C@H]1C[C@@H](O[C@@H]1CO)N1C=C(C)C(=O)NC1=O)SCCC#N)N1C=NC2=C1NC(N)=NC2=O)SCCC#N)N1C=NC2=C1N=CN=C2N

InChIKey

InChIKey=QOICCRMNKSHHLV-KKPAIZBHSA-N

Formula

C41H50N14O16P2S2

Mass

1121.0

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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 - Gamma-keto acid - Aminopyrimidine - Fatty acid ester - Pyrimidone - Fatty acyl - Imidolactam - Hydropyrimidine - Pyrimidine - Keto acid - N-substituted imidazole - Azole - Vinylogous amide - Heteroaromatic compound - Imidazole - Oxolane - Amino acid or derivatives - Carboxylic acid ester - Urea - Ketone - Lactam - Organothiophosphorus compound - Nitrile - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Sulfenyl compound - Oxacycle - Monocarboxylic acid or derivatives - Carbonitrile - Alcohol - Organic nitrogen compound - Organooxygen compound - Organic oxygen compound - Organosulfur compound - Cyanide - Hydrocarbon derivative - Organic oxide - Primary amine - Amine - Organonitrogen compound - Primary alcohol - Carbonyl group - 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 These are oligonucleotides in which one of the non-bridging oxygens in each phosphodiester linkage has been replaced by sulfur.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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