Compound Identification
SMILES
CCN1C(=O)N(CCO[Si](C)(C)C(C)(C)C)C2=C(N(CC3=CC=CC=C3)C(NC3CCCCC3)=N2)C1=O
InChIKey
InChIKey=QNUKIARQBCDQDM-UHFFFAOYSA-N
Formula
C28H43N5O3Si
Mass
525.769
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 Xanthines
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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
Xanthines
Alternative Parents
6-oxopurines Alkaloids and derivatives Pyrimidones Aminoimidazoles Benzene and substituted derivatives N-substituted imidazoles Heteroaromatic compounds Vinylogous amides Trialkylheterosilanes Lactams Ureas Silyl ethers Organic metalloid salts Azacyclic compounds Organic oxides Amines Hydrocarbon derivatives Organooxygen compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Xanthine - 6-oxopurine - Purinone - Alkaloid or derivatives - Pyrimidone - Aminoimidazole - Monocyclic benzene moiety - N-substituted imidazole - Benzenoid - Pyrimidine - Trialkylheterosilane - Azole - Imidazole - Heteroaromatic compound - Vinylogous amide - Lactam - Silyl ether - Urea - Organic metalloid salt - Azacycle - Organoheterosilane - Organooxygen compound - Organonitrogen compound - Organic metalloid moeity - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Amine - Organosilicon compound - Organic oxygen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as xanthines. These are purine derivatives with a ketone group conjugated at carbons 2 and 6 of the purine moiety.
External Descriptors
Not available