Structure Information
Structure

Compound Identification

SMILES

[H]C1(S)CC([H])(OC1([H])COP(O)(=O)OP(O)(=O)OP(O)(O)=O)N1C=NC2=C1NC(=N)N=C2O

InChIKey

InChIKey=ANPKDAOHZSAQQR-UHFFFAOYSA-N

Formula

C10H16N5O12P3S

Mass

523.24

Export to:

JSON SDF CSV

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 - Imidazopyrimidine - Purine - Hydroxypyrimidine - Monoalkyl phosphate - N-substituted imidazole - Organic phosphoric acid derivative - Phosphoric acid ester - Pyrimidine - Alkyl phosphate - Azole - Imidazole - Oxolane - Heteroaromatic compound - Alkylthiol - Oxacycle - Azacycle - Organoheterocyclic compound - Hydrocarbon derivative - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organic oxide - Organic oxygen compound - Organic nitrogen compound - 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

Previous Back Next