Structure Information
Structure

Compound Identification

SMILES

CCCCCCCCCCCCSC(CCCCCC)C(C)OOP(O)(=O)OP(=O)(OCCC)OC[C@H]1O[C@H]([C@H](O)[C@@H]1F)N1C=NC2=C1N=CN=C2N

InChIKey

InChIKey=IMTKLEOSYWUEHC-YPVARKLSSA-N

Formula

C34H62FN5O10P2S

Mass

813.9

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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 diphosphates

Direct Parent

Purine 3'-deoxyribonucleoside diphosphates

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine 3'-deoxyribonucleoside diphosphate - 6-aminopurine - Organic pyrophosphate - Imidazopyrimidine - Purine - Aminopyrimidine - Dialkyl phosphate - N-substituted imidazole - Organic phosphoric acid derivative - Phosphoric acid ester - Imidolactam - Alkyl phosphate - Pyrimidine - Azole - Imidazole - Heteroaromatic compound - Oxolane - Secondary alcohol - Fluorohydrin - Halohydrin - Organoheterocyclic compound - Thioether - Azacycle - Sulfenyl compound - Dialkylthioether - Oxacycle - Primary amine - Alkyl fluoride - Organohalogen compound - Hydrocarbon derivative - Organic oxide - Alcohol - Organofluoride - Organonitrogen compound - Organic nitrogen compound - Organic oxygen compound - Amine - Organooxygen compound - Organosulfur compound - Alkyl halide - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine 3'-deoxyribonucleoside diphosphates. These are purine nucleotides with diphosphate group linked to the ribose moiety lacking a hydroxyl group at position 3.

External Descriptors

Not available

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