Structure Information
Structure

Compound Identification

SMILES

NC1=NC=NC2=C1N=CN2C1OC(COP(O)(=O)OC2CC(COP(O)(=O)OC3CC(CO)OC3N3C=NC4=C3N=CN=C4N)OC2N2C=NC3=C2N=CN=C3N)CC1O

InChIKey

InChIKey=CKZWLFLXOQDVEX-UHFFFAOYSA-N

Formula

C30H37N15O13P2

Mass

877.666

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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 - 6-aminopurine - Imidazopyrimidine - Purine - Aminopyrimidine - Dialkyl phosphate - N-substituted imidazole - Organic phosphoric acid derivative - Phosphoric acid ester - Pyrimidine - Alkyl phosphate - Imidolactam - Heteroaromatic compound - Azole - Oxolane - Imidazole - Secondary alcohol - Oxacycle - Organoheterocyclic compound - Azacycle - Hydrocarbon derivative - Organonitrogen compound - Alcohol - Organic nitrogen compound - Organic oxide - Organooxygen compound - Organic oxygen compound - Amine - Primary alcohol - Primary 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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