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]1COP(=O)(O[C@H]1C[C@@H](O[C@@H]1CO)N1C=C(C)C(=O)NC1=O)SC1=CC=C(Cl)C=C1)N1C=NC2=C1NC(N)=NC2=O)SC1=CC=C(Cl)C=C1)N1C=NC2=C1N=CN=C2N)SC1=CC=C(Cl)C=C1)N1C=CC(N)=NC1=O

InChIKey

InChIKey=ISYJKBQGCLQGBC-QSGKPSBQSA-N

Formula

C62H65Cl3N15O21P3S3

Mass

1651.74

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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 - Pyrimidine 2'-deoxyribonucleoside - Pyrimidine nucleoside - 6-aminopurine - 6-oxopurine - Hypoxanthine - Imidazopyrimidine - Purine - Gamma-keto acid - Aminopyrimidine - Halobenzene - Fatty acid ester - Chlorobenzene - Pyrimidone - Keto acid - N-substituted imidazole - Hydropyrimidine - Aryl chloride - Aryl halide - Fatty acyl - Imidolactam - Benzenoid - Pyrimidine - Monocyclic benzene moiety - Imidazole - Oxolane - Azole - Vinylogous amide - Heteroaromatic compound - Carboxylic acid ester - Lactam - Amino acid or derivatives - Ketone - Urea - Oxacycle - Azacycle - Organoheterocyclic compound - Sulfenyl compound - Carboxylic acid derivative - Organothiophosphorus compound - Monocarboxylic acid or derivatives - Primary alcohol - Primary amine - Organic oxide - Carbonyl group - Amine - Alcohol - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organochloride - Organohalogen compound - 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 These are oligonucleotides in which one of the non-bridging oxygens in each phosphodiester linkage has been replaced by sulfur.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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