Compound Identification
SMILES
CCCC[Sn](CCCC)(CCCC)C1=CN([C@H]2C[C@H](O)[C@@H](CO)S2)C(=O)NC1=O
InChIKey
InChIKey=WKDIEGOUCDCHNI-OIXZBRQUSA-N
Formula
C21H38N2O4SSn
Mass
533.32
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
-
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 Metal aryls Heteroaromatic compounds Vinylogous amides Thiolanes Ureas Lactams Trialkyltins Secondary alcohols Dialkylthioethers Azacyclic compounds Primary alcohols Organonitrogen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Pyrimidine thionucleoside - Pyrimidone - Hydropyrimidine - Metal aryl - Pyrimidine - Heteroaromatic compound - Thiolane - Vinylogous amide - Lactam - Secondary alcohol - Trialkyltin - Urea - Azacycle - Thioether - Organoheterocyclic compound - Dialkylthioether - Alcohol - Hydrocarbon derivative - Organic oxide - Primary alcohol - Organooxygen compound - Organonitrogen compound - Organometallic compound - Organic post-transition metal moeity - Organic nitrogen compound - Organic oxygen compound - Organotin compound - 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