Structure Information
Structure

Compound Identification

SMILES

CN(CCCl)C1=CC=C(CNP(O)(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)N2C=NC3=C2N=CN=C3N)C=C1

InChIKey

InChIKey=HZJTWAKQXMPJCT-WVSUBDOOSA-N

Formula

C20H27ClN7O6P

Mass

527.9

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Purine nucleotides

Subclass

Purine ribonucleotides

Intermediate Tree Nodes

Not available

Direct Parent

Purine ribonucleoside monophosphates

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine ribonucleoside monophosphate - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Pentose monosaccharide - Imidazopyrimidine - Purine - Aniline or substituted anilines - Dialkylarylamine - Tertiary aliphatic/aromatic amine - Aminopyrimidine - Phosphoric monoester monoamide - Monosaccharide - N-substituted imidazole - Organic phosphoric acid derivative - Monocyclic benzene moiety - Phosphoric acid ester - Pyrimidine - Imidolactam - Benzenoid - Organic phosphoric acid amide - Imidazole - Heteroaromatic compound - Azole - Oxolane - Secondary alcohol - Tertiary amine - 1,2-diol - Azacycle - Organoheterocyclic compound - Oxacycle - Hydrocarbon derivative - Organohalogen compound - Organochloride - Organic oxygen compound - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Primary amine - Amine - Alkyl halide - Alkyl chloride - Alcohol - Organic oxide - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine ribonucleoside monophosphates. These are nucleotides consisting of a purine base linked to a ribose to which one monophosphate group is attached.

External Descriptors

Not available

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