Compound Identification
SMILES
CSCCC1=C2N=CN([C@@H]3C[C@H](O)[C@@H](CO)O3)C2=NC(NC(=O)COC2=CC=CC=C2)=N1
InChIKey
InChIKey=YTVDVQOGJQEEBX-JZXOWHBKSA-N
Formula
C21H25N5O5S
Mass
459.52
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Nucleosides, nucleotides, and analogues
-
Class
Purine nucleosides
- Subclass Purine 2'-deoxyribonucleosides
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Class
Purine nucleosides
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Superclass
Nucleosides, nucleotides, and analogues
Kingdom
Organic compounds
Superclass
Nucleosides, nucleotides, and analogues
Class
Purine nucleosides
Subclass
Purine 2'-deoxyribonucleosides
Intermediate Tree Nodes
Not available
Direct Parent
Purine 2'-deoxyribonucleosides
Alternative Parents
Purines and purine derivatives Phenoxy compounds Phenol ethers N-arylamides Alkyl aryl ethers Pyrimidines and pyrimidine derivatives N-substituted imidazoles Heteroaromatic compounds Oxolanes Secondary carboxylic acid amides Secondary alcohols Sulfenyl compounds Azacyclic compounds Dialkylthioethers Oxacyclic compounds Primary alcohols Hydrocarbon derivatives Carbonyl compounds Organic oxides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine 2'-deoxyribonucleoside - Imidazopyrimidine - Purine - Phenoxy compound - Phenol ether - N-arylamide - Alkyl aryl ether - Monocyclic benzene moiety - N-substituted imidazole - Pyrimidine - Benzenoid - Azole - Imidazole - Oxolane - Heteroaromatic compound - Secondary alcohol - Secondary carboxylic acid amide - Carboxamide group - Organoheterocyclic compound - Azacycle - Oxacycle - Dialkylthioether - Sulfenyl compound - Thioether - Carboxylic acid derivative - Ether - Primary alcohol - Organic oxide - Organic nitrogen compound - Hydrocarbon derivative - Organonitrogen compound - Organooxygen compound - Carbonyl group - Organic oxygen compound - Organosulfur compound - Alcohol - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as purine 2'-deoxyribonucleosides. These are compounds consisting of a purine linked to a ribose which lacks a hydroxyl group at position 2.
External Descriptors
Not available