Compound Identification
SMILES
CC(C)(C)[Si](OC[C@H]1S[C@H]([C@@H](F)[C@@H]1OCC1=CC=CC=C1)N1C=NC2=C1N=C(N)N=C2N)(C1=CC=CC=C1)C1=CC=CC=C1
InChIKey
InChIKey=RFKYJLZCZAPOCQ-IWQUTFRXSA-N
Formula
C33H37FN6O2SSi
Mass
628.84
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Nucleosides, nucleotides, and analogues
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Class
Nucleoside and nucleotide analogues
- Subclass Thionucleosides
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Class
Nucleoside and nucleotide analogues
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Superclass
Nucleosides, nucleotides, and analogues
Kingdom
Organic compounds
Superclass
Nucleosides, nucleotides, and analogues
Class
Nucleoside and nucleotide analogues
Subclass
Thionucleosides
Intermediate Tree Nodes
Not available
Direct Parent
Thionucleosides
Alternative Parents
6-aminopurines Benzylethers Alkylarylsilanes Aminopyrimidines and derivatives N-substituted imidazoles Imidolactams Thiolanes Heteroaromatic compounds Silyl ethers Organoheterosilanes Organic metalloid salts Dialkylthioethers Dialkyl ethers Azacyclic compounds Hydrocarbon derivatives Organofluorides Alkyl fluorides Primary amines
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine thionucleoside - 6-aminopurine - Benzylether - Purine - Imidazopyrimidine - Aminopyrimidine - Alkylarylsilane - Pyrimidine - Monocyclic benzene moiety - Imidolactam - N-substituted imidazole - Benzenoid - Azole - Imidazole - Heteroaromatic compound - Thiolane - Silyl ether - Organoheterosilane - Azacycle - Dialkyl ether - Ether - Organic metalloid salt - Organoheterocyclic compound - Dialkylthioether - Thioether - Organic nitrogen compound - Organic oxygen compound - Amine - Alkyl halide - Alkyl fluoride - Organohalogen compound - Organic metalloid moeity - Organofluoride - Organonitrogen compound - Organooxygen compound - Primary amine - Organosilicon compound - Hydrocarbon derivative - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as thionucleosides. These are nucleoside analogues that contain a thiolane or a thietane that is 1,3-disubstituted with a hydroxyl group and pyrimidine or purine base, at the 1- and 3-position, respectively.
External Descriptors
Not available