Structure Information
Structure

Compound Identification

SMILES

CCC(=C)C(=O)C1=C(Cl)C(Cl)=C(OCC(=O)NC[C@H]2O[C@H]([C@H](O)[C@@H]2O)N2C=CC(=O)NC2=O)C=C1

InChIKey

InChIKey=MGIMCXWIKKFMOQ-PJBPFLDMSA-N

Formula

C22H23Cl2N3O8

Mass

528.34

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

5'-deoxyribonucleosides

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

5'-deoxyribonucleosides

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

5'-deoxyribonucleoside - Butyrophenone - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - Phenoxy compound - Benzoyl - 1,2-dichlorobenzene - Phenol ether - Aryl ketone - Alkyl aryl ether - Chlorobenzene - Halobenzene - Pyrimidone - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Hydropyrimidine - Monosaccharide - Pyrimidine - Alpha-branched alpha,beta-unsaturated-ketone - Benzenoid - Alpha,beta-unsaturated ketone - Acryloyl-group - Vinylogous halide - Heteroaromatic compound - Enone - Oxolane - Vinylogous amide - Lactam - Ketone - 1,2-diol - Urea - Carboxamide group - Secondary carboxylic acid amide - Secondary alcohol - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Oxacycle - Ether - Carbonyl group - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Organohalogen compound - Alcohol - Organooxygen compound - Hydrocarbon derivative - Organonitrogen compound - Organochloride - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as 5'-deoxyribonucleosides. These are nucleosides in which the oxygen atom at the 5'position of the ribose moiety has been replaced by another atom. The nucleobases here are limited to purine, pyrimidine, and pyridine derivatives.

External Descriptors

Not available

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