Compound Identification
SMILES
CC1=CN([C@H]2C[C@H](N=[N+]=[N-])[C@@H](CO[P+](=O)OC34CCC(CC3)C4)O2)C(=O)NC1=O
InChIKey
InChIKey=KBIWHRKMJPILGP-GBDWWVHMSA-O
Formula
C17H23N5O6P
Mass
424.373
Taxonomic Classification
Taxonomy Tree
- Kingdom Organic compounds
Kingdom
Organic compounds
Superclass
Nucleosides, nucleotides, and analogues
Class
Deoxyribo- and ribonucleoside phosphonates
Subclass
Purine ribonucleoside phosphonates
Intermediate Tree Nodes
Not available
Direct Parent
Purine ribonucleoside phosphonates
Alternative Parents
Pyrimidine 2',3'-dideoxyribonucleosides Aromatic monoterpenoids Bicyclic monoterpenoids Pyrimidones Hydropyrimidines Vinylogous amides Oxolanes Heteroaromatic compounds Ureas Azo compounds Azo imides Lactams Oxacyclic compounds Azacyclic compounds Organic oxides Organic salts Organooxygen compounds Hydrocarbon derivatives Organic cations
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine ribonucleoside phosphonate - Pyrimidine 2',3'-dideoxyribonucleoside - Pyrimidine nucleoside - Aromatic monoterpenoid - Bicyclic monoterpenoid - Monoterpenoid - Norbornane monoterpenoid - Pyrimidone - Hydropyrimidine - Pyrimidine - Oxolane - Heteroaromatic compound - Vinylogous amide - Urea - Lactam - Azo imide - Azo compound - Organoheterocyclic compound - Oxacycle - Azacycle - Organic nitrogen compound - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organic oxide - Organic oxygen compound - Organic salt - Organic cation - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as purine ribonucleoside phosphonates. These are n-glycosyl compound that possess both a purine nucleobase linked to either a ribose or deoxyribose, which in turn carries a phosphonate group at the 5'-position.
External Descriptors
Not available