Structure Information
Structure

Compound Identification

SMILES

CCCCCCCCCCCCCCCC(=O)OCC(COC(=O)CCC(=O)OC[C@@H]1C[C@@H](OP(O)(=O)OC[C@@H]2C[C@@H](OP(O)(=O)OC[C@@H]3C[C@@H](O)[C@@H](O3)N3C=NC4=C3N=CN=C4N)[C@@H](O2)N2C=NC3=C2N=CN=C3N)[C@@H](O1)N1C=NC2=C1N=CN=C2N)OC(=O)CCCCCCCCCCCCCCC

InChIKey

InChIKey=DNJGEDOZQDNLJW-UGCJHBIKSA-N

Formula

C69H107N15O20P2

Mass

1528.648

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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 bisphosphates

Direct Parent

Purine deoxyribonucleoside 2',5'-bisphosphates

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine deoxyribonucleoside 2',5'-bisphosphate - Purine 3'-deoxyribonucleoside monophosphate - Triacyl-sn-glycerol - Tetracarboxylic acid or derivatives - 6-aminopurine - Imidazopyrimidine - Purine - Aminopyrimidine - Fatty acid ester - Dialkyl phosphate - Glycerolipid - Fatty acyl - Alkyl phosphate - N-substituted imidazole - Organic phosphoric acid derivative - Pyrimidine - Imidolactam - Phosphoric acid ester - Imidazole - Heteroaromatic compound - Azole - Oxolane - Carboxylic acid ester - Secondary alcohol - Amino acid or derivatives - Azacycle - Carboxylic acid derivative - Organoheterocyclic compound - Oxacycle - Amine - Alcohol - Organic oxygen compound - Organonitrogen compound - Carbonyl group - Organooxygen compound - Organic nitrogen compound - Primary amine - Organic oxide - Hydrocarbon derivative - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine deoxyribonucleoside 2',5'-bisphosphates. These are purine ribobucleotides with one phosphate group attached to each of two different hydroxyl groups of the ribose moiety, which lacks a hydroxyl group at position 3.

External Descriptors

Not available

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