Structure Information
Structure

Compound Identification

SMILES

CCCCCCCCCCCCSCC(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=FGKNTEQMFKAUQB-VETMKXQESA-N

Formula

C35H62ClFN5O7PS

Mass

782.39

Export to:

JSON SDF CSV

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

Previous Back Next