Compound Identification
SMILES
CC1=CN([C@H]2C[C@@H](CO)[C@H](O)[C@@H]2O)C(=O)N=C1N
InChIKey
InChIKey=ZMQRVVLKVUNUAE-XSPKLOCKSA-N
Formula
C11H17N3O4
Mass
255.274
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Nucleosides, nucleotides, and analogues
-
Class
Nucleoside and nucleotide analogues
- Subclass Cyclopentyl 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
Cyclopentyl nucleosides
Intermediate Tree Nodes
Not available
Direct Parent
Cyclopentyl nucleosides
Alternative Parents
Pyrimidones Imidolactams Hydropyrimidines Cyclopentanols Heteroaromatic compounds Organic carbonic acids and derivatives Cyclic alcohols and derivatives Propargyl-type 1,3-dipolar organic compounds Carboximidamides Azacyclic compounds Primary amines Organopnictogen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Cyclopentyl nucleoside - Pyrimidone - Imidolactam - Pyrimidine - 1,2-dihydropyrimidine - Hydropyrimidine - Cyclopentanol - Heteroaromatic compound - Cyclic alcohol - Secondary alcohol - Carbonic acid derivative - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carboximidamide - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Primary amine - Organooxygen compound - Organonitrogen compound - Amine - Alcohol - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as cyclopentyl 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 2- or the 3- position with either a purine or pyrimidine base.
External Descriptors
Not available