Structure Information
Structure

Compound Identification

SMILES

CC(C)(C)C(=O)OCN1C(=O)N(C=C(CO[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C1=O)[C@H]1C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](CO[Si](C)(C)C(C)(C)C)O1

InChIKey

InChIKey=BGZMUNBAZRWCEJ-QTLJGGJLSA-N

Formula

C34H62N2O13Si2

Mass

763.041

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Pyrimidine nucleosides

Subclass

Pyrimidine 2'-deoxyribonucleosides

Intermediate Tree Nodes

Not available

Direct Parent

Pyrimidine 2'-deoxyribonucleosides

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Pyrimidine 2'-deoxyribonucleoside - Glycosyl compound - O-glycosyl compound - Pyrimidone - Hydropyrimidine - Pyrimidine - Monosaccharide - Oxane - Vinylogous amide - Trialkylheterosilane - Oxolane - Heteroaromatic compound - Secondary alcohol - Urea - Lactam - Carboxylic acid ester - Silyl ether - Acetal - Carboxylic acid derivative - Organoheterosilane - Monocarboxylic acid or derivatives - Oxacycle - Azacycle - Polyol - Organic metalloid salt - Organoheterocyclic compound - Organic metalloid moeity - Hydrocarbon derivative - Organic oxide - Carbonyl group - Organonitrogen compound - Organooxygen compound - Alcohol - Organic nitrogen compound - Organic oxygen compound - Primary alcohol - Organopnictogen compound - Organosilicon compound - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as pyrimidine 2'-deoxyribonucleosides. These are compounds consisting of a pyrimidine linked to a ribose which lacks a hydroxyl group at position 2.

External Descriptors

Not available

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