Structure Information
Structure

Compound Identification

SMILES

O.[Rh++].[Rh++].CC([O-])=O.CC([O-])=O.CC([O-])=O.CC([O-])=O.CN1C=NC2=C(N=CN2C2OC(CO)C(O)C2O)C1=N.CN1C=NC2=C(N=CN2C2OC(CO)C(O)C2O)C1=N

InChIKey

InChIKey=ANQJZXBSQMWCRL-UHFFFAOYSA-J

Formula

C30H44N10O17Rh2

Mass

1022.546

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Purine nucleosides

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Purine nucleosides

Alternative Parents

Molecular Framework

Not available

Substituents

Purine nucleoside - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - Imidazopyrimidine - Purine - Monosaccharide - N-substituted imidazole - Pyrimidine - Imidolactam - Azole - Imidazole - Heteroaromatic compound - Tetrahydrofuran - Acetate salt - Secondary alcohol - Carboxylic acid salt - Organoheterocyclic compound - Carboxylic acid derivative - Organic transition metal salt - Carboxylic acid - Monocarboxylic acid or derivatives - Oxacycle - Azacycle - Organic oxide - Carbonyl group - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organonitrogen compound - Organooxygen compound - Alcohol - Primary alcohol - Organic salt - Organic zwitterion - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine nucleosides. These are compounds comprising a purine base attached to a ribosyl or deoxyribosyl moiety.

External Descriptors

Not available

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