Structure Information
Structure

Compound Identification

SMILES

CCOC(=O)C1=NN(CC2=CC=CC=C2)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)=C1C(=O)OC(C)(C)C

InChIKey

InChIKey=SYZOGJUXRWJXJD-VQSITJFTSA-N

Formula

C44H42N2O11

Mass

774.823

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