Structure Information
Structure

Compound Identification

SMILES

C\C(=N/C1=C(N=CN1[C@@H]1O[C@H](CO)[C@H]2OC(C)(C)O[C@@H]12)C#N)N(CCC1=CC=C(Br)C=C1)CC1=CC=CC=C1

InChIKey

InChIKey=BEIGYTIYRMADAE-WWHHJLRSSA-N

Formula

C29H32BrN5O4

Mass

594.51

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Imidazole ribonucleosides and ribonucleotides

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Imidazole ribonucleosides and ribonucleotides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Imidazole ribonucleoside - Ketal - Bromobenzene - Halobenzene - Aryl bromide - Aryl halide - Monocyclic benzene moiety - Monosaccharide - Benzenoid - N-substituted imidazole - Meta-dioxolane - Azole - Heteroaromatic compound - Imidazole - Oxolane - Acetal - Amidine - Oxacycle - Carboxylic acid amidine - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carbonitrile - Nitrile - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Cyanide - Primary alcohol - Hydrocarbon derivative - Alcohol - Organohalogen compound - Organobromide - Organonitrogen compound - Organooxygen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as imidazole ribonucleosides and ribonucleotides. These are organic compounds in which the C-1 of a ribosyl moiety is N-linked to an imidazole ring. Nucleotides have a phosphate group linked to the C5 carbon of the ribose (or deoxyribose) moiety. This class does not contain benzimidazole nucleosides and nucleotides.

External Descriptors

Not available

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