Structure Information
Structure

Compound Identification

SMILES

COC(=O)C1=C(NN=C1C(N)=O)C1OC(COCC2=CC=CC=C2)C(OCC2=CC=CC=C2)C1OCC1=CC=CC=C1

InChIKey

InChIKey=VTMKWUYUPBKWNM-UHFFFAOYSA-N

Formula

C32H33N3O7

Mass

571.63

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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 - Glycosyl compound - C-glycosyl compound - Pentose monosaccharide - Benzylether - Pyrazole-5-carboxamide - Pyrazole-4-carboxylic acid or derivatives - 2-heteroaryl carboxamide - Monocyclic benzene moiety - Benzenoid - Monosaccharide - Azole - Pyrazole - Tetrahydrofuran - Vinylogous amide - Heteroaromatic compound - Methyl ester - Carboxamide group - Carboxylic acid ester - Primary carboxylic acid amide - Carboxylic acid derivative - Oxacycle - Dialkyl ether - Ether - Azacycle - Monocarboxylic acid or derivatives - Organoheterocyclic compound - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organonitrogen compound - Organooxygen 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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