Structure Information
Structure

Compound Identification

SMILES

CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H]([C@H](O[Si](C)(C)C(C)(C)C)C11OS(=O)(=O)C=C1N)N1C=C(CBr)N=N1

InChIKey

InChIKey=VKRQBWKDUSVRJY-SHCSQFHYSA-N

Formula

C22H41BrN4O6SSi2

Mass

625.73

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Triazole ribonucleosides and ribonucleotides

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Triazole ribonucleosides and ribonucleotides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

N-ribosyl-1,2,3-triazole - Glycosyl compound - N-glycosyl compound - Monosaccharide - Sulfonic acid ester - Organosulfonic acid ester - Trialkylheterosilane - Heteroaromatic compound - Azole - 1,2,3-triazole - Tetrahydrofuran - 1,2-oxathiole - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Silyl ether - Oxacycle - Azacycle - Organic metalloid salt - Organoheterocyclic compound - Organoheterosilane - Enamine - Hydrocarbon derivative - Alkyl halide - Primary amine - Amine - Organooxygen compound - Organonitrogen compound - Organobromide - Organohalogen compound - Alkyl bromide - Primary aliphatic amine - Organic oxygen compound - Organic nitrogen compound - Organosilicon compound - Organopnictogen compound - Organic oxide - Organic salt - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as triazole ribonucleosides and ribonucleotides. These are nucleoside derivatives containing a ribose (or deoxyribose) moiety which is N-glycosylated to a triazole. Nucleotides have a phosphate group linked to the C5 carbon of the ribose (or deoxyribose) moiety.

External Descriptors

Not available

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