Compound Identification
SMILES
COP(O)(=O)OC[C@H]1O[C@H](C[C@@H]1S)N1C=C(C)C(=O)NC1=O
InChIKey
InChIKey=JAYIXUVQIPUIMQ-HRDYMLBCSA-N
Formula
C11H17N2O7PS
Mass
352.3
Taxonomic Classification
Taxonomy Tree
- Kingdom Organic compounds
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
2',3'-dideoxy-3'-thionucleosides Dialkyl phosphates Pyrimidones Hydropyrimidines Vinylogous amides Heteroaromatic compounds Oxolanes Lactams Ureas Azacyclic compounds Alkylthiols Oxacyclic compounds Organic oxides Hydrocarbon derivatives Organonitrogen compounds Organooxygen compounds
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
2',3'-dideoxy-3'-thionucleoside monophosphate - 2',3'-dideoxy-3'-thionucleoside - Pyrimidone - Dialkyl phosphate - Hydropyrimidine - Organic phosphoric acid derivative - Phosphoric acid ester - Pyrimidine - Alkyl phosphate - Oxolane - Heteroaromatic compound - Vinylogous amide - Urea - Lactam - Oxacycle - Alkylthiol - Azacycle - Organoheterocyclic compound - Hydrocarbon derivative - Organic oxide - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Organic nitrogen compound - 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