Compound Identification
SMILES
OC[C@H]1C[C@H](CC1N=[N+]=[N-])N1C=C(\C=C\Br)C(=O)NC1=O
InChIKey
InChIKey=QVNGHENVGKCFHP-CXXRZQJKSA-N
Formula
C12H14BrN5O3
Mass
356.18
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 Hydropyrimidines Vinylogous amides Heteroaromatic compounds Ureas Azo compounds Azo imides Lactams Vinyl bromides Azacyclic compounds Bromoalkenes Hydrocarbon derivatives Organic oxides Organic salts Organic zwitterions Organobromides Primary alcohols
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Cyclopentyl nucleoside - Pyrimidone - Hydropyrimidine - Pyrimidine - Heteroaromatic compound - Vinylogous amide - Azo compound - Azo imide - Lactam - Urea - Azacycle - Bromoalkene - Haloalkene - Vinyl bromide - Vinyl halide - Organoheterocyclic compound - Alcohol - Primary alcohol - Organooxygen compound - Organonitrogen compound - Organobromide - Organohalogen compound - Organic nitrogen compound - Organic oxygen compound - Organic oxide - Organic zwitterion - Hydrocarbon derivative - Organic salt - 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