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Structure Information
Structure

Compound Identification

SMILES

CCCCCCCCCCCCCCCCOCC(COC(=O)CCC(=O)O[C@@H]1C[C@@H](COP(O)(=O)O[C@@H]2C[C@@H](COP(O)(=O)O[C@@H]3C[C@@H](CO)O[C@H]3N3C=NC4=C3N=CN=C4N)O[C@H]2N2C=NC3=C2N=CN=C3N)O[C@H]1N1C=NC2=C1N=CN=C2N)OCCCCCCCCCCCCCCCC

InChIKey

InChIKey=QZLNVTHCMWROAS-CLLUHGPVSA-N

Formula

C69H111N15O18P2

Mass

1500.682

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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 - 1,2-dialkyl,3-acyl-sn-glycerol - Dialkylmonoacylglycerol - 6-aminopurine - Imidazopyrimidine - Purine - Aminopyrimidine - Fatty acid ester - Glycerol ether - Dialkyl phosphate - Glycerolipid - Dicarboxylic acid or derivatives - N-substituted imidazole - Organic phosphoric acid derivative - Phosphoric acid ester - Fatty acyl - Pyrimidine - Alkyl phosphate - Imidolactam - Azole - Oxolane - Heteroaromatic compound - Imidazole - Amino acid or derivatives - Carboxylic acid ester - Organoheterocyclic compound - Azacycle - Oxacycle - Carboxylic acid derivative - Dialkyl ether - Ether - Organic nitrogen compound - Organic oxygen compound - Organooxygen compound - Primary amine - Carbonyl group - Primary alcohol - Organic oxide - Organonitrogen compound - Hydrocarbon derivative - Alcohol - Amine - 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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