Compound Identification
SMILES
CC(C)OP(=O)(C\C=C\C1=CC(CN2C=NC3=C2N=C(N)N=C3Cl)=CC=C1)OC(C)C
InChIKey
InChIKey=UGIMWXBIAFBFMT-RMKNXTFCSA-N
Formula
C21H27ClN5O3P
Mass
463.9
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
Styrenes Halopyrimidines Dialkyl alkylphosphonates Aminopyrimidines and derivatives Phosphonic acid esters N-substituted imidazoles Aryl chlorides Heteroaromatic compounds Azacyclic compounds Primary amines Organophosphorus compounds Organooxygen compounds Organochlorides Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine - Styrene - Aminopyrimidine - Halopyrimidine - Phosphonic acid diester - Dialkyl alkylphosphonate - Aryl chloride - Benzenoid - Pyrimidine - Aryl halide - Phosphonic acid ester - Monocyclic benzene moiety - N-substituted imidazole - Heteroaromatic compound - Azole - Imidazole - Organophosphonic acid derivative - Azacycle - Organic oxide - Organochloride - Organohalogen compound - Organonitrogen compound - Organooxygen compound - Amine - Organophosphorus compound - Primary amine - Organic nitrogen compound - Organic oxygen compound - Hydrocarbon derivative - 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