Structure Information
Structure

Compound Identification

SMILES

[H]C1(O)C([H])(O)C([H])(OC1([H])COP(O)(O)=O)N1CNC([H])(C(O)=N)C1=O

InChIKey

InChIKey=RKYRRKLLBTVGFL-UHFFFAOYSA-N

Formula

C9H16N3O9P

Mass

341.213

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Glycinamide ribonucleotides

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Glycinamide ribonucleotides

Alternative Parents

Molecular Framework

Aliphatic heteromonocyclic compounds

Substituents

Glycinamide-ribonucleotide - Pentose phosphate - Pentose-5-phosphate - Glycosyl compound - N-glycosyl compound - Alpha-amino acid or derivatives - Monosaccharide phosphate - Pentose monosaccharide - Monoalkyl phosphate - Imidazolidinone - Monosaccharide - Alkyl phosphate - Organic phosphoric acid derivative - Phosphoric acid ester - Imidazolidine - Tertiary carboxylic acid amide - Oxolane - Secondary alcohol - Lactam - 1,2-diol - Carboxamide group - Carboximidic acid - Organoheterocyclic compound - Azacycle - Oxacycle - Carboximidic acid derivative - Carboxylic acid derivative - Organonitrogen compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Alcohol - Carbonyl group - Amine - Organic nitrogen compound - Organooxygen compound - Aliphatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as glycinamide ribonucleotides. These are compounds in which the amide N atom of glycineamide is linked to the C-1 of a ribosyl (or deoxyribosyl) moiety. Nucleotides have a phosphate group linked to the C5 carbon of the ribose (or deoxyribose) moiety.

External Descriptors

Not available

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