Structure Information
Structure

Compound Identification

SMILES

CCOP(=O)(OCC)[C@]1(C[C@@H](O[C@@H]1CO[Si](C1=CC=CC=C1)(C1=CC=CC=C1)C(C)(C)C)N1C=NC2=C1NC(NC(=O)C1=CC=CC=C1)=NC2=O)O[Si](C)(C)C

InChIKey

InChIKey=FGLXVSBUDUBZQE-WFXWLMSVSA-N

Formula

C40H52N5O8PSi2

Mass

818.027

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organoheterocyclic compounds

Class

Imidazopyrimidines

Subclass

Purines and purine derivatives

Intermediate Tree Nodes

Purinones

Direct Parent

Hypoxanthines

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

6-oxopurine - Hypoxanthine - Benzamide - Benzoic acid or derivatives - Benzoyl - Dialkyl alkylphosphonate - Pyrimidone - Alkylarylsilane - Phosphonic acid diester - Monocyclic benzene moiety - N-substituted imidazole - Phosphonic acid ester - Pyrimidine - Benzenoid - Vinylogous amide - Heteroaromatic compound - Trialkylheterosilane - Azole - Oxolane - Imidazole - Organophosphonic acid derivative - Silyl ether - Secondary carboxylic acid amide - Carboxamide group - Azacycle - Organic metalloid salt - Oxacycle - Organoheterosilane - Carboxylic acid derivative - Organic oxide - Organic nitrogen compound - Organic oxygen compound - Organosilicon compound - Hydrocarbon derivative - Organophosphorus compound - Organic metalloid moeity - Organooxygen compound - Organonitrogen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as hypoxanthines. These are compounds containing the purine derivative 1H-purin-6(9H)-one. Purine is a bicyclic aromatic compound made up of a pyrimidine ring fused to an imidazole ring.

External Descriptors

Not available

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