Structure Information
Structure

Compound Identification

SMILES

CC(C)(C)[Si](C)(C)OC[C@@H]1[C@@H](CO[Si](C)(C)C(C)(C)C)C1CN1C=NC2=C1N=C(N)N=C2OCC1=CC=CC=C1

InChIKey

InChIKey=FUPJRRWTXRMBIL-ZEQRLZLVSA-N

Formula

C30H49N5O3Si2

Mass

583.924

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Nucleoside and nucleotide analogues

Subclass

Cyclopropyl nucleosides

Intermediate Tree Nodes

Not available

Direct Parent

Cyclopropyl purine nucleosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Cyclopropyl purine nucleoside - Hypoxanthine - Imidazopyrimidine - Purine - Aminopyrimidine - Alkyl aryl ether - Monocyclic benzene moiety - Benzenoid - Pyrimidine - N-substituted imidazole - Trialkylheterosilane - Heteroaromatic compound - Azole - Imidazole - Silyl ether - Organoheterosilane - Azacycle - Organic metalloid salt - Organoheterocyclic compound - Ether - Organosilicon compound - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Amine - Organic metalloid moeity - Organonitrogen compound - Organooxygen compound - Primary amine - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as cyclopropyl purine nucleosides. These are nucleoside analogues with a structure that consists of a cyclopropane that is substituted a the 1-position with a hydroxyl group and at the 2- position with either a purine base.

External Descriptors

Not available

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