Structure Information
Structure

Compound Identification

SMILES

CN(C)\C=N\C1=NC(=O)C2=C(N1)N(C=N2)[C@@H]1O[C@H](CO)[C@@H](O)C1NC(=O)N(CCCl)N=O

InChIKey

InChIKey=XLFYVDZNZRHNGP-XQFMNDDHSA-N

Formula

C16H22ClN9O6

Mass

471.86

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Purine nucleosides

Subclass

Purine 2'-deoxyribonucleosides

Intermediate Tree Nodes

Not available

Direct Parent

Purine 2'-deoxyribonucleosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine 2'-deoxyribonucleoside - Glycosyl compound - N-glycosyl compound - 6-oxopurine - Hypoxanthine - Imidazopyrimidine - Purine - Pyrimidone - N-substituted imidazole - Nitrosourea - Pyrimidine - Azole - Imidazole - Heteroaromatic compound - Nitrosamide - Vinylogous amide - Oxolane - Semicarbazide - Organic n-nitroso compound - Secondary alcohol - Formamidine - Amidine - Carboxylic acid amidine - Organic nitroso compound - Oxacycle - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Organic oxygen compound - Hydrocarbon derivative - Alcohol - Alkyl halide - Organic oxide - Organopnictogen compound - Organohalogen compound - Organochloride - Organonitrogen compound - Organooxygen compound - Carbonyl group - Primary alcohol - Organic nitrogen compound - Alkyl chloride - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine 2'-deoxyribonucleosides. These are compounds consisting of a purine linked to a ribose which lacks a hydroxyl group at position 2.

External Descriptors

Not available

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