Structure Information
Structure

Compound Identification

SMILES

NC1=C(Br)C2=C(N=CN2[C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)C(=O)N1

InChIKey

InChIKey=HPMGEMAYEPQLSB-ZUHFKWOFSA-N

Formula

C11H13BrN4O5

Mass

361.152

Export to:

JSON SDF CSV

Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Imidazole[4,5-c]pyridine ribonucleosides and ribonucleotides

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Imidazole[4,5-c]pyridine ribonucleosides and ribonucleotides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Imidazole[4,5-c]pyridine ribonucleoside,ribonucleotide or analogue - Glycosyl compound - N-glycosyl compound - Imidazopyridinone - Pentose monosaccharide - Imidazopyridine - Imidazo-[4,5-c]pyridine - Aminopyridine - Pyridinone - Aryl bromide - Aryl halide - Monosaccharide - N-substituted imidazole - Pyridine - Azole - Imidazole - Heteroaromatic compound - Vinylogous amide - Tetrahydrofuran - Secondary alcohol - Lactam - Oxacycle - Azacycle - Organoheterocyclic compound - Organooxygen compound - Organohalogen compound - Organobromide - Organonitrogen compound - Organic nitrogen compound - Amine - Hydrocarbon derivative - Organic oxide - Alcohol - Organopnictogen compound - Primary alcohol - Primary amine - Organic oxygen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as imidazole[4,5-c]pyridine ribonucleosides and ribonucleotides. These are organic compounds in which the C-1 of a ribosyl moiety is N-linked to an imidazole[4,5-c]pyridine ring system. Nucleotides have a phosphate group linked to the C5 carbon of the ribose (or deoxyribose) moiety.

External Descriptors

Not available

Previous Back Next