Compound Identification
SMILES
CC1=CN([C@H]2C[C@H](N=[N+]=[N-])[C@@H](CO[P+](=O)OCC(C)(C)C)O2)C(=O)NC1=O
InChIKey
InChIKey=ZLAQAPANTPZNOY-QJPTWQEYSA-O
Formula
C15H23N5O6P
Mass
400.351
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 Pyrimidones Hydropyrimidines Vinylogous amides Oxolanes Heteroaromatic compounds Ureas Azo compounds Azo imides Lactams Oxacyclic compounds Azacyclic compounds Organopnictogen compounds Hydrocarbon derivatives Organic oxides Organic salts Organooxygen compounds Organic cations
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Purine ribonucleoside phosphonate - Pyrimidine 2',3'-dideoxyribonucleoside - Pyrimidine nucleoside - Pyrimidone - Hydropyrimidine - Pyrimidine - Oxolane - Heteroaromatic compound - Vinylogous amide - Azo compound - Azo imide - Lactam - Urea - Oxacycle - Azacycle - Organoheterocyclic compound - Organic nitrogen compound - Organic oxygen compound - Organic salt - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organic oxide - Organopnictogen compound - Organic cation - Aromatic heteromonocyclic 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