Compound Identification
SMILES
OC1=NC(=N)C=CN1C1CC2OP(O)(=S)OCC3OC(CC3OP(O)(=S)OCC2O1)N1C=CC(=N)N=C1O
InChIKey
InChIKey=PZIKOQPCCOWCSL-UHFFFAOYSA-N
Formula
C18H24N6O10P2S2
Mass
610.49
Taxonomic Classification
Taxonomy Tree
Kingdom
Organic compounds
Superclass
Nucleosides, nucleotides, and analogues
Class
(3'->5')-dinucleotides and analogues
Subclass
(3'->5')-cyclic dinucleotides and analogues
Intermediate Tree Nodes
Not available
Direct Parent
(3'->5')-cyclic dinucleotide bis(phosphoromonothioate) analogues
Alternative Parents
Thiophosphate diesters Hydroxypyrimidines Hydropyrimidines Tetrahydrofurans Heteroaromatic compounds Oxacyclic compounds Azacyclic compounds Organopnictogen compounds Organooxygen compounds Organonitrogen compounds Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
(3'->5')-cyclic dinucleotide bis(phosphoromonothioate) analogue - Hydroxypyrimidine - Thiophosphate diester - Hydropyrimidine - Thiophosphoric acid ester - Pyrimidine - Organic thiophosphoric acid or derivatives - Tetrahydrofuran - Heteroaromatic compound - Oxacycle - Organoheterocyclic compound - Azacycle - Organic nitrogen compound - Hydrocarbon derivative - Organopnictogen compound - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as (3'->5')-cyclic dinucleotide bis(phosphoromonothioate) analogues. These are cyclic compounds consisting of two ribose moieties connected two 5',3'-phosphomonothioic acid O,O'-diester bonds to form a cycle. Each ribose unit is N-linked to a nucleic base or an analogue thereof.
External Descriptors
Not available