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Structure Information
Structure

Compound Identification

SMILES

CCC(=O)OCSP(=O)(OC[C@H]1O[C@H](C[C@H]1OP(=O)(OC[C@H]1O[C@H](C[C@H]1OC(=O)CCC(C)=O)N1C=C(C)C(=O)NC1=O)SC1=CC=C(Cl)C=C1)N1C=C(C)C(=O)NC1=O)O[C@@H]1C[C@@H](O[C@@H]1CO)N1C=NC2=C1N=C(NC(=O)C(C)C)N=C2OC1=C(Cl)C=CC(Cl)=C1

InChIKey

InChIKey=WAAHMXSVKYZQOB-DJTXKFDJSA-N

Formula

C55H62Cl3N9O21P2S2

Mass

1417.56

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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 - Diaryl ether - Hypoxanthine - Imidazopyrimidine - Purine - Phenoxy compound - Gamma-keto acid - 1,4-dichlorobenzene - Phenol ether - N-arylamide - Halobenzene - Fatty acid ester - Pyrimidone - Chlorobenzene - Benzenoid - N-substituted imidazole - Aryl halide - Hydropyrimidine - Aryl chloride - Monocyclic benzene moiety - Dicarboxylic acid or derivatives - Fatty acyl - Pyrimidine - Keto acid - Vinylogous amide - Oxolane - Heteroaromatic compound - Imidazole - Azole - Lactam - Ketone - Carboxamide group - Carboxylic acid ester - Urea - Secondary carboxylic acid amide - Oxacycle - Carboxylic acid derivative - Azacycle - Organoheterocyclic compound - Sulfenyl compound - Organothiophosphorus compound - Ether - Primary alcohol - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Alcohol - Hydrocarbon derivative - Carbonyl group - 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 These are oligonucleotides in which one of the non-bridging oxygens in each phosphodiester linkage has been replaced by sulfur.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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