Structure Information
Structure

Compound Identification

SMILES

O[C@@H]1[C@@H](COP(O)(O)=O)O[C@H]([C@@H]1O)N1C=NC2=C1N=CN=C2NCCNC(=O)C1=C2C(=O)OC3(C2=CC=C1)C1=C(OC2=C3C=CC(O)=C2)C=C(O)C=C1

InChIKey

InChIKey=OQZNCXYUGPMCRH-HYHFPRINSA-N

Formula

C33H29N6O13P

Mass

748.598

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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-5-phosphate - Pentose phosphate - Xanthene - Dibenzopyran - 6-alkylaminopurine - Diaryl ether - N-glycosyl compound - Glycosyl compound - 6-aminopurine - Benzofuranone - 1-benzopyran - Benzopyran - Monosaccharide phosphate - Isobenzofuranone - Pentose monosaccharide - Phthalide - Purine - Isocoumaran - Imidazopyrimidine - Isobenzofuran - Aminopyrimidine - 1-hydroxy-2-unsubstituted benzenoid - Monoalkyl phosphate - Phenol - Monosaccharide - N-substituted imidazole - Organic phosphoric acid derivative - Alkyl phosphate - Imidolactam - Benzenoid - Pyrimidine - Phosphoric acid ester - Azole - Heteroaromatic compound - Imidazole - Oxolane - Secondary carboxylic acid amide - Carboxylic acid ester - Lactone - Secondary alcohol - Carboxamide group - 1,2-diol - Ether - Oxacycle - Azacycle - Carboxylic acid derivative - Organoheterocyclic compound - Amine - Organic oxygen compound - Organic nitrogen compound - Organic oxide - Hydrocarbon derivative - Organonitrogen compound - Organooxygen compound - Alcohol - 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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