Structure Information
Structure

Compound Identification

SMILES

CCSC1=NC2=C(N=CN2C2CC(OP(O)(O)=O)C(COP(O)(O)=O)O2)C(NC)=N1

InChIKey

InChIKey=DZGOMQYNNHDHEU-UHFFFAOYSA-N

Formula

C13H21N5O9P2S

Mass

485.34

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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 - 6-alkylaminopurine - 6-aminopurine - Purine - Imidazopyrimidine - Aryl thioether - Aminopyrimidine - Monoalkyl phosphate - Alkylarylthioether - Secondary aliphatic/aromatic amine - Pyrimidine - Phosphoric acid ester - Imidolactam - Organic phosphoric acid derivative - N-substituted imidazole - Alkyl phosphate - Oxolane - Heteroaromatic compound - Imidazole - Azole - Oxacycle - Azacycle - Organoheterocyclic compound - Sulfenyl compound - Thioether - Secondary amine - Organic oxygen compound - Amine - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Organic oxide - Hydrocarbon derivative - 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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