Compound Identification
SMILES
CCC1=CN([C@H]2C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](CO[Si](C)(C)C(C)(C)C)[S@]2=O)C(=O)NC1=O
InChIKey
InChIKey=SZKHDFGCVITIPA-SBGPOEGFSA-N
Formula
C23H44N2O5SSi2
Mass
516.84
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Nucleosides, nucleotides, and analogues
-
Class
Nucleoside and nucleotide analogues
- Subclass Thionucleosides
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Class
Nucleoside and nucleotide analogues
-
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
Pyrimidones Hydropyrimidines Vinylogous amides Heteroaromatic compounds Trialkylheterosilanes Thiolanes Ureas Sulfoxides Lactams Silyl ethers Organic metalloid salts Sulfinyl compounds Azacyclic compounds Organic oxides Hydrocarbon derivatives Organonitrogen compounds Organooxygen compounds
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Pyrimidine thionucleoside - Pyrimidone - Hydropyrimidine - Pyrimidine - Trialkylheterosilane - Thiolane - Vinylogous amide - Heteroaromatic compound - Lactam - Silyl ether - Urea - Sulfoxide - Organic metalloid salt - Organoheterocyclic compound - Organoheterosilane - Azacycle - Sulfinyl compound - Organic oxide - Organic nitrogen compound - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Organosilicon compound - Organic metalloid moeity - Hydrocarbon derivative - Aromatic heteromonocyclic 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