Compound Identification
SMILES
CC(C)(C)OC(=O)N[C@@]1(CO)C[C@H]1CN1C=NC2=C1N=CN=C2N1C=CC=C1
InChIKey
InChIKey=QRYKQELKRFWYEO-ORAYPTAESA-N
Formula
C19H24N6O3
Mass
384.44
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
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Superclass
Nucleosides, nucleotides, and analogues
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Class
Nucleoside and nucleotide analogues
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Subclass
Cyclopropyl nucleosides
- Level 5 Cyclopropyl purine nucleosides
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Subclass
Cyclopropyl nucleosides
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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
Cyclopropyl nucleosides
Intermediate Tree Nodes
Not available
Direct Parent
Cyclopropyl purine nucleosides
Alternative Parents
Purines and purine derivatives Substituted pyrroles Pyrimidines and pyrimidine derivatives N-substituted imidazoles Heteroaromatic compounds Carbamate esters Azacyclic compounds Primary alcohols Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Cyclopropyl purine nucleoside - Imidazopyrimidine - Purine - N-substituted imidazole - Pyrimidine - Substituted pyrrole - Heteroaromatic compound - Imidazole - Pyrrole - Azole - Carbamic acid ester - Azacycle - Organoheterocyclic compound - Organic oxygen compound - Primary alcohol - Organooxygen compound - Organonitrogen compound - Alcohol - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - 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