Compound Identification
SMILES
NC1=NC2=C(N=CN2C[C@]2(COC(=O)C3=CC=CC=C3)C[C@H]2COC(=O)C2=CC=CC=C2)C(OCC2=CC=CC=C2)=N1
InChIKey
InChIKey=TVKSXDTWROKPIX-UKJJDJLKSA-N
Formula
C32H29N5O5
Mass
563.614
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Nucleosides, nucleotides, and analogues
-
Class
Nucleoside and nucleotide analogues
-
Subclass
Cyclopropyl nucleosides
- Level 5 Cyclopropyl purine nucleosides
-
Subclass
Cyclopropyl nucleosides
-
Class
Nucleoside and nucleotide analogues
-
Superclass
Nucleosides, nucleotides, and analogues
Kingdom
Organic compounds
Superclass
Nucleosides, nucleotides, and analogues
Class
Nucleoside and nucleotide analogues
Subclass
Cyclopropyl nucleosides
Intermediate Tree Nodes
Not available
Direct Parent
Cyclopropyl purine nucleosides
Alternative Parents
Hypoxanthines Benzoic acid esters Benzoyl derivatives Aminopyrimidines and derivatives Alkyl aryl ethers N-substituted imidazoles Heteroaromatic compounds Carboxylic acid esters Amino acids and derivatives Azacyclic compounds Primary amines Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Cyclopropyl purine nucleoside - Benzoate ester - Hypoxanthine - Benzoic acid or derivatives - Imidazopyrimidine - Purine - Benzoyl - Aminopyrimidine - Alkyl aryl ether - Benzenoid - Pyrimidine - Monocyclic benzene moiety - N-substituted imidazole - Heteroaromatic compound - Azole - Imidazole - Amino acid or derivatives - Carboxylic acid ester - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Ether - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Primary amine - Amine - Hydrocarbon derivative - Organic oxygen compound - Organic oxide - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as cyclopropyl purine nucleosides. These are nucleoside analogues with a structure that consists of a cyclopropane that is substituted a the 1-position with a hydroxyl group and at the 2- position with either a purine base.
External Descriptors
Not available