Structure Information
Structure

Compound Identification

SMILES

CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1N1C=NC2=C1N=C(NC(=O)CC1=CC=CC=C1)N=C2SCCC#N

InChIKey

InChIKey=LWXMLXWJHBWFEX-PXOHRUDZSA-N

Formula

C27H36N6O5SSi

Mass

584.77

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Purine nucleosides

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Purine nucleosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine nucleoside - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - Phenylacetamide - 6-thiopurine - Imidazopyrimidine - Purine - Aryl thioether - N-arylamide - Alkylarylthioether - Monocyclic benzene moiety - Monosaccharide - N-substituted imidazole - Pyrimidine - Benzenoid - Heteroaromatic compound - Azole - Imidazole - Oxolane - Trialkylheterosilane - Silyl ether - Secondary carboxylic acid amide - Secondary alcohol - Carboxamide group - Oxacycle - Organoheterosilane - Azacycle - Thioether - Organoheterocyclic compound - Carboxylic acid derivative - Sulfenyl compound - Organic metalloid salt - Carbonitrile - Nitrile - Hydrocarbon derivative - Organic metalloid moeity - Organonitrogen compound - Cyanide - Organooxygen compound - Organic oxygen compound - Organic nitrogen compound - Organosulfur compound - Primary alcohol - Organic oxide - Carbonyl group - Alcohol - Organosilicon compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine nucleosides. These are compounds comprising a purine base attached to a ribosyl or deoxyribosyl moiety.

External Descriptors

Not available

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