Structure Information
Structure

Compound Identification

SMILES

CCOC(=O)C1=C([C@@H]2O[C@H](COC(=O)C3=CC=CC=C3)[C@@H](OC(=O)C3=CC=CC=C3)[C@H]2OC(=O)C2=CC=CC=C2)N(CC2=CC=CC=C2)N=C1C(=O)OCC1=CC=CC=C1

InChIKey

InChIKey=HYVHMGAAKVPGLX-PWWGNSHJSA-N

Formula

C47H40N2O11

Mass

808.84

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Nucleoside and nucleotide analogues

Subclass

3-ribofuranosylpyrazoles

Intermediate Tree Nodes

Not available

Direct Parent

3-ribofuranosylpyrazoles

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

3-ribofuranosylpyrazole - C-glycosyl compound - Glycosyl compound - Benzoate ester - Benzyloxycarbonyl - Pentose monosaccharide - Benzoic acid or derivatives - Benzoyl - Pyrazole-5-carboxylic acid or derivatives - Pyrazole-4-carboxylic acid or derivatives - Pyrazole-3-carboxylic acid or derivatives - Monocyclic benzene moiety - Monosaccharide - Benzenoid - Azole - Heteroaromatic compound - Oxolane - Vinylogous amide - Pyrazole - Carboxylic acid ester - Organoheterocyclic compound - Azacycle - Ether - Dialkyl ether - Carboxylic acid derivative - Oxacycle - Hydrocarbon derivative - Organonitrogen compound - Organooxygen compound - Organic nitrogen compound - Organic oxygen compound - Organic oxide - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as 3-ribofuranosylpyrazoles. These are nucleoside and nucleotide analogs with a structure that consists of a pyrazole ring system which is N-substituted at the 3-position with a ribose moiety. Nucleotide analogues contain a phosphate group linked to the C5 carbon atom of the furanose.

External Descriptors

Not available

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