Compound Identification
SMILES
CS(=O)(=O)OC[C@@H]1[C@H](COCC2=CC=CC=C2)[C@H](OCC2=CC=CC=C2)[C@H]1N1C=NC2=C1N=CN=C2N
InChIKey
InChIKey=NTUPBDROZWMILN-KJBBBAAKSA-N
Formula
C26H29N5O5S
Mass
523.61
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Nucleosides, nucleotides, and analogues
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Class
Nucleoside and nucleotide analogues
- Subclass Cyclobutyl nucleosides
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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
Cyclobutyl nucleosides
Intermediate Tree Nodes
Not available
Direct Parent
Cyclobutyl nucleosides
Alternative Parents
6-aminopurines Benzylethers Aminopyrimidines and derivatives Sulfonic acid esters Organosulfonic acid esters N-substituted imidazoles Imidolactams Sulfonyls Methanesulfonates Heteroaromatic compounds Dialkyl ethers Azacyclic compounds Primary amines Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Cyclobutyl purine nucleoside - Cyclobutyl nucleoside - 6-aminopurine - Benzylether - Imidazopyrimidine - Purine - Aminopyrimidine - Imidolactam - Monocyclic benzene moiety - Benzenoid - Organosulfonic acid ester - Sulfonic acid ester - Pyrimidine - N-substituted imidazole - Heteroaromatic compound - Azole - Sulfonyl - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Imidazole - Methanesulfonate - Organoheterocyclic compound - Azacycle - Dialkyl ether - Ether - Primary amine - Hydrocarbon derivative - Organic nitrogen compound - Organic oxygen compound - Organic oxide - Amine - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as cyclobutyl nucleosides. These are nucleoside analogues with a structure that consists of a cyclobutane that is substituted a the 1-position with a hydroxyl group and at the 3- position with either a purine or pyrimidine base.
External Descriptors
Not available