Structure Information
Structure

Compound Identification

SMILES

CC1=CN([C@H]2C[C@H](OP(O)(=O)OC[C@H]3O[C@H](C[C@@H]3OP(O)(=O)OC[C@H]3O[C@H](C[C@@H]3OP(O)(=O)OC[C@H]3O[C@H](C[C@@H]3O)N3C=NC4=C3N=CN=C4N)N3C=CC(N)=NC3=O)N3C=NC4=C3N=CN=C4N)[C@@H](COP(O)(=O)OCCNC(=O)C3=CC=CC4=C3C3=CC=CC=C3C4=O)O2)C(=O)NC1=O

InChIKey

InChIKey=MZBOYLOQFCXPOY-KXXFLWHRSA-N

Formula

C55H62N16O26P4

Mass

1487.082

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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 3',5'-bisphosphates

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine deoxyribonucleoside 3',5'-bisphosphate - Pyrimidine deoxyribonucleoside 3',5'-bisphosphate - Pyrimidine deoxyribonucleoside bisphosphate - Purine 2'-deoxyribonucleoside monophosphate - Ribonucleoside 3'-phosphate - Fluorene - 6-aminopurine - Imidazopyrimidine - Purine - Aryl ketone - Phosphoethanolamine - Aminopyrimidine - Dialkyl phosphate - Pyrimidone - Imidolactam - Benzenoid - Alkyl phosphate - Hydropyrimidine - N-substituted imidazole - Organic phosphoric acid derivative - Pyrimidine - Phosphoric acid ester - Vinylogous amide - Azole - Imidazole - Oxolane - Heteroaromatic compound - Carboxamide group - Urea - Ketone - Lactam - Secondary carboxylic acid amide - Secondary alcohol - Amino acid or derivatives - Carboxylic acid derivative - Azacycle - Organoheterocyclic compound - Oxacycle - Organic oxide - Organic nitrogen compound - Amine - Hydrocarbon derivative - Organic oxygen compound - Alcohol - Primary amine - Organonitrogen compound - Organooxygen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine deoxyribonucleoside 3',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 2.

External Descriptors

Not available

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