Structure Information
Structure

Compound Identification

SMILES

COC1=CC=C(C=C1)[S@](=O)C(Cl)(Cl)[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC2=C1N=CN=C2N

InChIKey

InChIKey=ZBNWHYPZKXTBJC-AQMHXLDDSA-N

Formula

C17H17Cl2N5O5S

Mass

474.31

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

5'-deoxyribonucleosides

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

5'-deoxyribonucleosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

5'-deoxyribonucleoside - N-glycosyl compound - Glycosyl compound - 6-aminopurine - Imidazopyrimidine - Phenyl sulfoxide - Purine - Phenoxy compound - Phenol ether - Anisole - Methoxybenzene - Alkyl aryl ether - Aminopyrimidine - Benzenoid - Pyrimidine - N-substituted imidazole - Imidolactam - Monocyclic benzene moiety - Azole - Heteroaromatic compound - Oxolane - Imidazole - Sulfoxide - Secondary alcohol - 1,2-diol - Oxacycle - Azacycle - Organoheterocyclic compound - Ether - Sulfinyl compound - Primary amine - Alkyl chloride - Organic oxide - Alcohol - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Amine - Alkyl halide - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organohalogen compound - Organochloride - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as 5'-deoxyribonucleosides. These are nucleosides in which the oxygen atom at the 5'position of the ribose moiety has been replaced by another atom. The nucleobases here are limited to purine, pyrimidine, and pyridine derivatives.

External Descriptors

Not available

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