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Structure Information
Structure

Compound Identification

SMILES

CC1=CN([C@H]2C[C@H](SCC(=O)C3=CC=C(O)C=C3)[C@@H](COP(O)(O)=O)O2)C(=O)NC1=O

InChIKey

InChIKey=ZPUIOXGYMCCARA-OWCLPIDISA-N

Formula

C18H21N2O9PS

Mass

472.4

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

2',3'-dideoxy-3'-thionucleoside monophosphates

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

2',3'-dideoxy-3'-thionucleoside monophosphates

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

2',3'-dideoxy-3'-thionucleoside monophosphate - 2',3'-dideoxy-3'-thionucleoside - Alkyl-phenylketone - Phenylketone - Aryl ketone - Benzoyl - Aryl alkyl ketone - 1-hydroxy-2-unsubstituted benzenoid - Monoalkyl phosphate - Phenol - Pyrimidone - Pyrimidine - Phosphoric acid ester - Alkyl phosphate - Organic phosphoric acid derivative - Hydropyrimidine - Monocyclic benzene moiety - Benzenoid - Oxolane - Heteroaromatic compound - Vinylogous amide - Urea - Ketone - Lactam - Dialkylthioether - Sulfenyl compound - Thioether - Organoheterocyclic compound - Oxacycle - Azacycle - Organonitrogen compound - Hydrocarbon derivative - Organooxygen compound - Organosulfur compound - Organic nitrogen compound - Organic oxygen compound - Organic oxide - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as 2',3'-dideoxy-3'-thionucleoside monophosphates. These are 2',3'-deoxyribonucleoside derivatives, where the ribose unit is thio-substituted at the 3'-position, and at the 5'-position by a monophosphate group. The nucleobases here are limited to purine, pyrimidine, and pyridine derivatives.

External Descriptors

Not available

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