Structure Information
Structure

Compound Identification

SMILES

OP(O)(=O)OC[C@H]1O[C@H](C[C@@H]1OP(O)(O)=O)N1C(NC2=CC3=C(C=C2)C2=CC=CC=C2C3)=NC2=C1NC=NC2=O

InChIKey

InChIKey=IMZHXGYONDJUMP-IPMKNSEASA-N

Formula

C23H23N5O10P2

Mass

591.41

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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 - Ribonucleoside 3'-phosphate - Fluorene - Hypoxanthine - 6-oxopurine - Purine - Imidazopyrimidine - Monoalkyl phosphate - Pyrimidone - Benzenoid - Alkyl phosphate - Pyrimidine - Phosphoric acid ester - Organic phosphoric acid derivative - N-substituted imidazole - Aminoimidazole - Heteroaromatic compound - Vinylogous amide - Tetrahydrofuran - Imidazole - Azole - Oxacycle - Azacycle - Organoheterocyclic compound - Secondary amine - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Amine - 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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