Structure Information
Structure

Compound Identification

SMILES

CCCCCCCCCCCCS(=O)CC(COP(O)(=O)OC[C@H]1O[C@H]([C@@H](F)[C@@H]1O)N1C=NC2=C1N=C(Cl)N=C2N)OCCCCCCCCCC

InChIKey

InChIKey=AMSAIPNFCCQJHS-FTHYUBEESA-N

Formula

C35H62ClFN5O8PS

Mass

798.39

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Purine nucleotides

Subclass

Purine deoxyribonucleotides

Intermediate Tree Nodes

Purine deoxyribonucleoside monophosphates

Direct Parent

Purine 2'-deoxyribonucleoside monophosphates

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine 2'-deoxyribonucleoside monophosphate - 6-aminopurine - Imidazopyrimidine - Purine - Aminopyrimidine - 2-halopyrimidine - Halopyrimidine - Dialkyl phosphate - Organic phosphoric acid derivative - N-substituted imidazole - Aryl chloride - Phosphoric acid ester - Aryl halide - Pyrimidine - Alkyl phosphate - Imidolactam - Imidazole - Azole - Oxolane - Heteroaromatic compound - Secondary alcohol - Sulfoxide - Fluorohydrin - Halohydrin - Oxacycle - Dialkyl ether - Ether - Azacycle - Organoheterocyclic compound - Sulfinyl compound - Primary amine - Organic oxygen compound - Amine - Alkyl halide - Alkyl fluoride - Alcohol - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organosulfur compound - Organooxygen compound - Organohalogen compound - Organonitrogen compound - Organochloride - Organofluoride - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine 2'-deoxyribonucleoside monophosphates. These are purine nucleotides with monophosphate group linked to the ribose moiety lacking a hydroxyl group at position 2.

External Descriptors

Not available

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