Compound Identification
SMILES
OC[C@H]1OC([C@H](O)[C@@H]1O)N1C=C(C(O)CI)C(=O)NC1=O
InChIKey
InChIKey=QRHWSWOLWKGFDK-UHSHOCGUSA-N
Formula
C11H15IN2O7
Mass
414.152
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Nucleosides, nucleotides, and analogues
- Class Pyrimidine nucleosides
-
Superclass
Nucleosides, nucleotides, and analogues
Kingdom
Organic compounds
Superclass
Nucleosides, nucleotides, and analogues
Class
Pyrimidine nucleosides
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Pyrimidine nucleosides
Alternative Parents
Glycosylamines Pentoses Pyrimidones Hydropyrimidines Vinylogous amides Tetrahydrofurans Heteroaromatic compounds Ureas Secondary alcohols Iodohydrins Lactams Azacyclic compounds Oxacyclic compounds Organic oxides Organoiodides Hydrocarbon derivatives Organonitrogen compounds Organopnictogen compounds Primary alcohols Aromatic alcohols Alkyl iodides
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Pyrimidine nucleoside - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - Pyrimidone - Hydropyrimidine - Monosaccharide - Pyrimidine - Heteroaromatic compound - Vinylogous amide - Tetrahydrofuran - Halohydrin - Iodohydrin - Lactam - Secondary alcohol - Urea - Oxacycle - Organoheterocyclic compound - Azacycle - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Organoiodide - Organohalogen compound - Organic oxide - Alkyl iodide - Alkyl halide - Organopnictogen compound - Alcohol - Organic oxygen compound - Hydrocarbon derivative - Primary alcohol - Aromatic alcohol - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as pyrimidine nucleosides. These are compounds comprising a pyrimidine base attached to a ribosyl or deoxyribosyl moiety.
External Descriptors
Not available