Structure Information
Structure

Compound Identification

SMILES

CCOP(=O)(OCC)[C@@H](NCC1=CC=C(OC)C=C1)[C@H]1O[C@H]([C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C)N1C=CC(=O)NC1=O

InChIKey

InChIKey=ARKLZMLCWPHQMO-ONBQWJCTSA-N

Formula

C33H58N3O9PSi2

Mass

727.983

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

5'-deoxyribonucleosides

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

5'-deoxyribonucleosides

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

5'-deoxyribonucleoside - Glycosyl compound - N-glycosyl compound - Phenoxy compound - Anisole - Methoxybenzene - Phenol ether - Alkyl aryl ether - Dialkyl alkylphosphonate - Pyrimidone - Phosphonic acid diester - Pyrimidine - Monocyclic benzene moiety - Hydropyrimidine - Phosphonic acid ester - Benzenoid - Trialkylheterosilane - Heteroaromatic compound - Organophosphonic acid derivative - Vinylogous amide - Oxolane - Silyl ether - Urea - Lactam - Organoheterosilane - Ether - Oxacycle - Azacycle - Organic metalloid salt - Organoheterocyclic compound - Secondary amine - Organic metalloid moeity - Organic oxygen compound - Hydrocarbon derivative - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Organophosphorus compound - Amine - Organosilicon compound - Organic oxide - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as 5'-deoxyribonucleosides. These are nucleosides in which the oxygen atom at the 5'position of the ribose moiety has been replaced by another atom. The nucleobases here are limited to purine, pyrimidine, and pyridine derivatives.

External Descriptors

Not available

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