Structure Information
Structure

Compound Identification

SMILES

[H]C1(COP(=O)(NCCOC)OC2([H])C([H])(COP(O)(O)=O)OC([H])(N3C=NC4=C3NC(=N)N=C4O)C2([H])OC)CC([H])(O)C([H])(O1)N1C=CC(=N)N=C1O

InChIKey

InChIKey=BFXZXCWPXVGQPP-UHFFFAOYSA-N

Formula

C23H35N9O14P2

Mass

723.53

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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 - Pentose phosphate - Pentose-5-phosphate - Glycosyl compound - N-glycosyl compound - Monosaccharide phosphate - Imidazopyrimidine - Purine - Phosphoric diester monoamide - Monoalkyl phosphate - Hydroxypyrimidine - Organic phosphoric acid amide - Alkyl phosphate - Hydropyrimidine - Pyrimidine - Monosaccharide - Phosphoric acid ester - N-substituted imidazole - Organic phosphoric acid derivative - Imidazole - Heteroaromatic compound - Oxolane - Azole - Secondary alcohol - Azacycle - Oxacycle - Ether - Organoheterocyclic compound - Dialkyl ether - Hydrocarbon derivative - Alcohol - Organic oxygen compound - Organic nitrogen compound - Organic oxide - Organonitrogen compound - Organooxygen compound - 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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