Compound Identification
SMILES
OC[C@H]1C[C@H](C[C@H]1O)N1C=C(\C=C\Br)C(=O)NC1=O
InChIKey
InChIKey=KAVDAMFOTJIBCK-YLTSPFDWSA-N
Formula
C12H15BrN2O4
Mass
331.166
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 Cyclopentanols Hydropyrimidines Vinylogous amides Heteroaromatic compounds Ureas Cyclic alcohols and derivatives Lactams Vinyl bromides Azacyclic compounds Bromoalkenes Hydrocarbon derivatives Organic oxides Organobromides Organonitrogen compounds Organopnictogen compounds Primary alcohols
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Cyclopentyl nucleoside - Pyrimidone - Cyclopentanol - Hydropyrimidine - Pyrimidine - Cyclic alcohol - Heteroaromatic compound - Vinylogous amide - Lactam - Secondary alcohol - Urea - Azacycle - Bromoalkene - Haloalkene - Vinyl bromide - Vinyl halide - Organoheterocyclic compound - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Organonitrogen compound - Organobromide - Organohalogen compound - Alcohol - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - 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