Structure Information
Structure

Compound Identification

SMILES

NC1=NC(Cl)=NC2=C1N=CN2[C@@H]1O[C@H](CO[N+]([O-])=O)[C@H]2OP(O)(=O)O[C@@H]12

InChIKey

InChIKey=MSQVIPBOWVFUGK-UUOKFMHZSA-N

Formula

C10H10ClN6O8P

Mass

408.65

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Purine nucleotides

Subclass

Cyclic purine nucleotides

Intermediate Tree Nodes

Not available

Direct Parent

2',3'-cyclic purine nucleotides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

2',3'-cyclic purine ribonucleotide - Ribonucleoside 3'-phosphate - 6-aminopurine - Imidazopyrimidine - Purine - 2-halopyrimidine - Aminopyrimidine - Halopyrimidine - Aryl chloride - Aryl halide - Monosaccharide - N-substituted imidazole - Organic phosphoric acid derivative - Imidolactam - Pyrimidine - Heteroaromatic compound - Azole - 1,3_dioxaphospholane - Imidazole - Alkyl nitrate - Organic nitrate - Oxolane - Organic nitric acid or derivatives - Organic nitro compound - Allyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Organoheterocyclic compound - Oxacycle - Azacycle - Organonitrogen compound - Organohalogen compound - Organic oxide - Hydrocarbon derivative - Amine - Organic oxygen compound - Organooxygen compound - Organic nitrogen compound - Primary amine - Organic salt - Organochloride - Organic zwitterion - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as 2',3'-cyclic purine nucleotides. These are purine nucleotides in which the oxygen atoms linked to the C2 and C3 carbon atoms of the ribose moiety are both bonded the same phosphorus atom of the phosphate group.

External Descriptors

Not available

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