Compound Identification
SMILES
CC1=CN([C@@H]2O[C@H](COCC3=CC=CC=C3)[C@H](OCC3=CC=CC=C3)[C@H]2N=[N+]=[N-])C(=O)NC1=O
InChIKey
InChIKey=MXUPOTPTOMOUAW-CUDBPUKSSA-N
Formula
C24H25N5O5
Mass
463.494
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Nucleosides, nucleotides, and analogues
-
Class
Pyrimidine nucleosides
- Subclass Pyrimidine 2'-deoxyribonucleosides
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Class
Pyrimidine nucleosides
-
Superclass
Nucleosides, nucleotides, and analogues
Kingdom
Organic compounds
Superclass
Nucleosides, nucleotides, and analogues
Class
Pyrimidine nucleosides
Subclass
Pyrimidine 2'-deoxyribonucleosides
Intermediate Tree Nodes
Not available
Direct Parent
Pyrimidine 2'-deoxyribonucleosides
Alternative Parents
Glycosylamines Benzylethers Pyrimidones Hydropyrimidines Vinylogous amides Oxolanes Heteroaromatic compounds Ureas Azo compounds Azo imides Lactams Azacyclic compounds Oxacyclic compounds Dialkyl ethers Organic salts Organic zwitterions Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Pyrimidine 2'-deoxyribonucleoside - Glycosyl compound - N-glycosyl compound - Benzylether - Pyrimidone - Monocyclic benzene moiety - Hydropyrimidine - Pyrimidine - Benzenoid - Vinylogous amide - Oxolane - Heteroaromatic compound - Azo compound - Lactam - Azo imide - Urea - Azacycle - Oxacycle - Ether - Dialkyl ether - Organoheterocyclic compound - Organooxygen compound - Organonitrogen compound - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic zwitterion - Organic salt - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as pyrimidine 2'-deoxyribonucleosides. These are compounds consisting of a pyrimidine linked to a ribose which lacks a hydroxyl group at position 2.
External Descriptors
Not available