Structure Information
Structure

Compound Identification

SMILES

CC1=C(CCC(=O)NC[C@H]2O[C@H](C[C@@H]2O)N2C=C(C)C(=O)NC2=O)C(=O)C2=C(N1)C(C)=C1C(NC3=C1C=C(Cl)C=C3)=C2C

InChIKey

InChIKey=WTLFDCRXMMKKFG-WMTXJRDZSA-N

Formula

C31H32ClN5O6

Mass

606.08

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

2',5'-dideoxyribonucleosides

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

2',5'-dideoxyribonucleosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

2',5'-dideoxyribonucleoside - Carbazole - Pyrroloquinoline - Dihydroquinolone - Dihydroquinoline - Pyridopyrimidine - Quinoline - Indole - Indole or derivatives - Methylpyridine - Pyrimidone - Fatty acyl - Aryl halide - Benzenoid - Fatty amide - Hydropyrimidine - Aryl chloride - Pyrimidine - Pyridine - Heteroaromatic compound - Vinylogous amide - Pyrrole - Oxolane - Carboxamide group - Urea - Secondary carboxylic acid amide - Secondary alcohol - Lactam - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Oxacycle - Organic nitrogen compound - Organic oxide - Organic oxygen compound - Alcohol - Hydrocarbon derivative - Carbonyl group - Organohalogen compound - Organochloride - Organonitrogen compound - Organooxygen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as 2',5'-dideoxyribonucleosides. These are nucleosides characterized by a purine or pyrimidine base, which is N-linked to a 2',5'-dideoxyribose moiety.

External Descriptors

Not available

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