Structure Information
Structure

Compound Identification

SMILES

CSC1=CC=C(OP(=O)(OC[C@H]2O[C@H](C=C2)N2C=NC3=C2NC=NC3=O)OC[C@H]2O[C@H](C=C2)N2C=NC3=C2NC=NC3=O)C=C1

InChIKey

InChIKey=ZMWJKPSTPUWLSU-FMWKFLBASA-N

Formula

C27H25N8O8PS

Mass

652.58

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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',3'-dideoxyribonucleoside monophosphates

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine 2',3'-dideoxyribonucleoside monophosphate - 6-oxopurine - Hypoxanthine - Purine - Imidazopyrimidine - Phenoxy compound - Aryl thioether - Thiophenol ether - Alkylarylthioether - Dialkyl phosphate - Pyrimidone - N-substituted imidazole - Benzenoid - Alkyl phosphate - Organic phosphoric acid derivative - Pyrimidine - Phosphoric acid ester - Monocyclic benzene moiety - Imidazole - Azole - Vinylogous amide - Heteroaromatic compound - Dihydrofuran - Oxacycle - Azacycle - Organoheterocyclic compound - Sulfenyl compound - Thioether - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organopnictogen compound - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Organic oxide - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine 2',3'-dideoxyribonucleoside monophosphates. These are purine nucleotides with monophosphate group linked to the ribose moiety lacking a hydroxyl group at positions 2 and 3.

External Descriptors

Not available

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