Compound Identification
SMILES
CC(C)[C@H](CO)NC1=NC2=C(N=CN2C(C)C)C(NC2=CC(Cl)=C(N)C=C2)=N1
InChIKey
InChIKey=AIKLCVAETRXWOB-HNNXBMFYSA-N
Formula
C19H26ClN7O
Mass
403.92
Taxonomic Classification
Taxonomy Tree
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Kingdom
Organic compounds
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Superclass
Organoheterocyclic compounds
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Class
Imidazopyrimidines
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Subclass
Purines and purine derivatives
- Level 5 6-aminopurines
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Subclass
Purines and purine derivatives
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Class
Imidazopyrimidines
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Superclass
Organoheterocyclic compounds
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Imidazopyrimidines
Subclass
Purines and purine derivatives
Intermediate Tree Nodes
Not available
Direct Parent
6-aminopurines
Alternative Parents
Aniline and substituted anilines Secondary alkylarylamines Chlorobenzenes Aminopyrimidines and derivatives N-substituted imidazoles Imidolactams Aryl chlorides Heteroaromatic compounds Azacyclic compounds Primary amines Primary alcohols Organochlorides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
6-aminopurine - Aniline or substituted anilines - Aminopyrimidine - Chlorobenzene - Secondary aliphatic/aromatic amine - Halobenzene - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Imidolactam - Benzenoid - Pyrimidine - N-substituted imidazole - Heteroaromatic compound - Azole - Imidazole - Secondary amine - Azacycle - Organohalogen compound - Primary alcohol - Amine - Primary amine - Alcohol - Organic nitrogen compound - Hydrocarbon derivative - Organic oxygen compound - Organochloride - Organonitrogen compound - Organooxygen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as 6-aminopurines. These are purines that carry an amino group at position 6. Purine is a bicyclic aromatic compound made up of a pyrimidine ring fused to an imidazole ring.
External Descriptors
Not available