Structure Information
Structure

Compound Identification

SMILES

CNC1=NC(Cl)=NC2=C1N=CN2[C@H]1C[C@@H](OP(O)(O)=O)[C@@H](COP(O)(O)=O)O1

InChIKey

InChIKey=AWSMOXWWSLFSCL-FSDSQADBSA-N

Formula

C11H16ClN5O9P2

Mass

459.67

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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 - Imidazopyrimidine - Purine - Aminopyrimidine - Monoalkyl phosphate - 2-halopyrimidine - Secondary aliphatic/aromatic amine - Halopyrimidine - Organic phosphoric acid derivative - Aryl chloride - Aryl halide - Imidolactam - Alkyl phosphate - N-substituted imidazole - Pyrimidine - Phosphoric acid ester - Imidazole - Oxolane - Azole - Heteroaromatic compound - Oxacycle - Azacycle - Organoheterocyclic compound - Secondary amine - Organic nitrogen compound - Organic oxygen compound - Amine - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organohalogen compound - Organonitrogen compound - Organochloride - 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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