Structure Information
Structure

Compound Identification

SMILES

CC1=C2C=CC3=C(C(NC4=NC=NC5=C4N=CN5C4CC(O)C(COP(O)(O)=O)O4)C(O)C(O)C3O)C2=CC2=CC=CC=C12

InChIKey

InChIKey=UDCYUSDDQBLFLF-UHFFFAOYSA-N

Formula

C29H30N5O9P

Mass

623.559

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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 monophosphates

Direct Parent

Purine 2'-deoxyribonucleoside monophosphates

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine 2'-deoxyribonucleoside monophosphate - Phenanthrol - Anthracene - Phenanthrene - 6-alkylaminopurine - 6-aminopurine - Tetralin - Imidazopyrimidine - Purine - Aminopyrimidine - Monoalkyl phosphate - N-substituted imidazole - Organic phosphoric acid derivative - Phosphoric acid ester - Pyrimidine - Imidolactam - Alkyl phosphate - Benzenoid - Azole - Imidazole - Oxolane - Heteroaromatic compound - Secondary alcohol - Polyol - Azacycle - Oxacycle - Organoheterocyclic compound - Amine - Organooxygen compound - Organonitrogen compound - Alcohol - Organic nitrogen compound - Organic oxide - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine 2'-deoxyribonucleoside monophosphates. These are purine nucleotides with monophosphate group linked to the ribose moiety lacking a hydroxyl group at position 2.

External Descriptors

Not available

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