Structure Information
Structure

Compound Identification

SMILES

NC1=NC=NC2=C1N=CN2C1CC(S)C(COP(O)(=O)OP(O)(=O)OP(O)(O)=O)O1

InChIKey

InChIKey=IUZAADPBJTZICC-UHFFFAOYSA-N

Formula

C10H16N5O11P3S

Mass

507.24

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

2',3'-dideoxy-3'-thionucleoside triphosphates

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

2',3'-dideoxy-3'-thionucleoside triphosphates

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

2',3'-dideoxy-3'-thionucleoside triphosphate - Purine 2',3'-dideoxyribonucleoside - Purine nucleoside - 2',3'-dideoxy-3'-thionucleoside - 6-aminopurine - Imidazopyrimidine - Purine - Aminopyrimidine - Monoalkyl phosphate - N-substituted imidazole - Organic phosphoric acid derivative - Phosphoric acid ester - Pyrimidine - Alkyl phosphate - Imidolactam - Heteroaromatic compound - Azole - Imidazole - Oxolane - Organoheterocyclic compound - Azacycle - Oxacycle - Alkylthiol - Organic nitrogen compound - Organic oxide - Primary amine - Hydrocarbon derivative - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Amine - Aromatic heteropolycyclic compound

Description

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

External Descriptors

Not available

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