Compound Identification
SMILES
CC(C)C(C)(C)[Si](C)(C)OC[C@@H]1C[C@@H](C=C1CO)N1C=C(F)C(=O)NC1=O
InChIKey
InChIKey=UTDQEENNAURHOD-LSDHHAIUSA-N
Formula
C19H31FN2O4Si
Mass
398.55
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 Halopyrimidines Aryl fluorides Hydropyrimidines Vinylogous amides Trialkylheterosilanes Heteroaromatic compounds Ureas Silyl ethers Lactams Azacyclic compounds Organic metalloid salts Hydrocarbon derivatives Organic oxides Organofluorides Organonitrogen compounds Primary alcohols
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Cyclopentyl nucleoside - Halopyrimidine - Pyrimidone - Aryl fluoride - Aryl halide - Hydropyrimidine - Pyrimidine - Trialkylheterosilane - Heteroaromatic compound - Vinylogous amide - Lactam - Urea - Silyl ether - Organoheterosilane - Azacycle - Organic metalloid salt - Organoheterocyclic compound - Primary alcohol - Organooxygen compound - Organonitrogen compound - Organofluoride - Organic metalloid moeity - Organohalogen compound - Hydrocarbon derivative - Organic oxide - Alcohol - Organic nitrogen compound - Organic oxygen compound - Organosilicon compound - 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