Compound Identification
SMILES
OC[C@H]1C[C@H](O)[C@H](C1)N1C=C(Br)C(=O)NC1=O
InChIKey
InChIKey=VUXYQPXAGVWPHV-DTLFHODZSA-N
Formula
C10H13BrN2O4
Mass
305.128
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Nucleosides, nucleotides, and analogues
-
Class
Nucleoside and nucleotide analogues
- Subclass Cyclopentyl 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
Cyclopentyl nucleosides
Intermediate Tree Nodes
Not available
Direct Parent
Cyclopentyl nucleosides
Alternative Parents
Pyrimidones Halopyrimidines Aryl bromides Cyclopentanols Hydropyrimidines Vinylogous amides Heteroaromatic compounds Ureas Cyclic alcohols and derivatives Lactams Azacyclic compounds Hydrocarbon derivatives Organonitrogen compounds Organopnictogen compounds Primary alcohols Organobromides Organic oxides
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Cyclopentyl nucleoside - Halopyrimidine - Pyrimidone - Aryl bromide - Aryl halide - Cyclopentanol - Hydropyrimidine - Pyrimidine - Vinylogous amide - Heteroaromatic compound - Cyclic alcohol - Urea - Secondary alcohol - Lactam - Azacycle - Organoheterocyclic compound - Organic oxide - Organonitrogen compound - Organobromide - Organohalogen compound - Organooxygen compound - Organic nitrogen compound - Alcohol - Primary alcohol - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - 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