Compound Identification
SMILES
CCN1C2=N[C@@H]3CCC[C@@H]3N2C2=C(N(CC3=CC=C(O)C=C3)C(=N2)C(F)(F)F)C1=O
InChIKey
InChIKey=IUAZGTKFBKCTGL-KGLIPLIRSA-N
Formula
C20H20F3N5O2
Mass
419.408
Taxonomic Classification
Taxonomy Tree
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Kingdom
Organic compounds
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Superclass
Organoheterocyclic compounds
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Class
Imidazopyrimidines
- 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
Purines and purine derivatives
Alternative Parents
1-hydroxy-2-unsubstituted benzenoids Benzene and substituted derivatives Imidolactams N-substituted imidazoles Vinylogous amides Heteroaromatic compounds Imidazolines Amino acids and derivatives Guanidines Tertiary amines Propargyl-type 1,3-dipolar organic compounds Carboximidamides Azacyclic compounds Hydrocarbon derivatives Alkyl fluorides Organooxygen compounds Organic oxides Organofluorides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Monocyclic benzene moiety - N-substituted imidazole - Benzenoid - Imidolactam - Azole - Imidazole - 2-imidazoline - Heteroaromatic compound - Vinylogous amide - Tertiary amine - Amino acid or derivatives - Guanidine - Carboximidamide - Azacycle - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carboxylic acid derivative - Hydrocarbon derivative - Organic oxygen compound - Amine - Alkyl halide - Organohalogen compound - Organofluoride - Organic nitrogen compound - Alkyl fluoride - Organonitrogen compound - Organooxygen compound - Organic oxide - 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