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Structure Information
Structure

Compound Identification

SMILES

CC(=O)N[C@H]1[C@H](O)[C@H](O)[C@H](CO)OC1OP(O)(=O)OP(O)(=O)OC[C@H]1OC([C@H](O)[C@@H]1O)N1C=CC(=O)NC1=O

InChIKey

InChIKey=LFTYTUAZOPRMMI-XHTWMWBESA-N

Formula

C17H27N3O17P2

Mass

607.355

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Pyrimidine nucleotides

Subclass

Pyrimidine nucleotide sugars

Intermediate Tree Nodes

Not available

Direct Parent

Pyrimidine nucleotide sugars

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Pyrimidine nucleotide sugar - Pyrimidine ribonucleoside diphosphate - Pentose phosphate - Pentose-5-phosphate - N-acyl-alpha-hexosamine - Glycosyl compound - N-glycosyl compound - Monosaccharide phosphate - Organic pyrophosphate - Pyrimidone - Monoalkyl phosphate - Alkyl phosphate - Organic phosphoric acid derivative - Oxane - Hydropyrimidine - Monosaccharide - Pyrimidine - Phosphoric acid ester - Heteroaromatic compound - Oxolane - Vinylogous amide - Acetamide - Secondary alcohol - Urea - 1,2-diol - Lactam - Carboxamide group - Secondary carboxylic acid amide - Carboxylic acid derivative - Oxacycle - Azacycle - Organoheterocyclic compound - Primary alcohol - Organic oxide - Hydrocarbon derivative - Organic oxygen compound - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Carbonyl group - Alcohol - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as pyrimidine nucleotide sugars. These are pyrimidine nucleotides bound to a saccharide derivative through the terminal phosphate group.

External Descriptors

Not available

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