Compound Identification
SMILES
CCOP(=O)(CCOCC1=CC=CC(CN2C=NC3=C2N=C(N)N=C3Cl)=C1)OCC
InChIKey
InChIKey=MRQNUPNIBGAYEQ-UHFFFAOYSA-N
Formula
C19H25ClN5O4P
Mass
453.86
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Organoheterocyclic compounds
-
Class
Imidazopyrimidines
- Subclass Purines and purine derivatives
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Class
Imidazopyrimidines
-
Superclass
Organoheterocyclic compounds
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Imidazopyrimidines
Subclass
Purines and purine derivatives
Intermediate Tree Nodes
Not available
Direct Parent
Purines and purine derivatives
Alternative Parents
Benzylethers Halopyrimidines Dialkyl alkylphosphonates Aminopyrimidines and derivatives Phosphonic acid esters N-substituted imidazoles Aryl chlorides Heteroaromatic compounds Dialkyl ethers Azacyclic compounds Primary amines Organophosphorus compounds Organochlorides Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Benzylether - Purine - Aminopyrimidine - Halopyrimidine - Dialkyl alkylphosphonate - Phosphonic acid diester - N-substituted imidazole - Aryl chloride - Phosphonic acid ester - Aryl halide - Monocyclic benzene moiety - Benzenoid - Pyrimidine - Imidazole - Organophosphonic acid derivative - Heteroaromatic compound - Azole - Azacycle - Dialkyl ether - Ether - Organooxygen compound - Organophosphorus compound - Organic nitrogen compound - Primary amine - Amine - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organonitrogen compound - Organohalogen compound - Organochloride - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as purines and purine derivatives. These are aromatic heterocyclic compounds containing a purine moiety, which is formed a pyrimidine-ring ring fused to an imidazole ring.
External Descriptors
Not available