Structure Information
Structure

Compound Identification

SMILES

[H][C@]1(CO)O[C@@]([H])(N2N=CC3=C2C=C(C(C)=C3)N(=O)=O)[C@]([H])(O)[C@]1([H])O

InChIKey

InChIKey=NEWDXNFXLZRIIP-FDYHWXHSSA-N

Formula

C13H15N3O6

Mass

309.278

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Indazole ribonucleosides and ribonucleotides

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Indazole ribonucleosides and ribonucleotides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

1-ribofuranosylindazole - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - Benzopyrazole - Indazole - Nitroaromatic compound - Monosaccharide - Benzenoid - Azole - Heteroaromatic compound - Pyrazole - Tetrahydrofuran - C-nitro compound - Organic nitro compound - Secondary alcohol - Oxacycle - Azacycle - Organic oxoazanium - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organonitrogen compound - Organic nitrogen compound - Alcohol - Organooxygen compound - Organic oxygen compound - Primary alcohol - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organic zwitterion - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as indazole ribonucleosides and ribonucleotides. These are compounds in which the C-1 of a ribose (or deoxyribose) is linked to the N1-position of the indazole ring. Nucleotides have a phosphate group linked to the C5 carbon of the ribose (or deoxyribose) moiety.

External Descriptors

Not available

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