Compound Identification
SMILES
NC(=S)C1=C2C=CC=CC2=NN1C1OC(CO)C(O)C1O
InChIKey
InChIKey=IIAFAZNQIWSUBY-UHFFFAOYSA-N
Formula
C13H15N3O4S
Mass
309.34
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Nucleosides, nucleotides, and analogues
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Class
Nucleoside and nucleotide analogues
- Subclass 2-ribofuranosylindazoles
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Class
Nucleoside and nucleotide analogues
-
Superclass
Nucleosides, nucleotides, and analogues
Kingdom
Organic compounds
Superclass
Nucleosides, nucleotides, and analogues
Class
Nucleoside and nucleotide analogues
Subclass
2-ribofuranosylindazoles
Intermediate Tree Nodes
Not available
Direct Parent
2-ribofuranosylindazoles
Alternative Parents
Glycosylamines Pentoses Indazoles Benzenoids Thioamides Heteroaromatic compounds Pyrazoles Oxolanes Secondary alcohols Azacyclic compounds Thiocarboxylic acid amides Oxacyclic compounds Organonitrogen compounds Primary alcohols Hydrocarbon derivatives Thiocarbonyl compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
2-ribofuranosylindazole - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - Benzopyrazole - Indazole - Monosaccharide - Benzenoid - Azole - Heteroaromatic compound - Oxolane - Pyrazole - Thioamide - Secondary alcohol - Azacycle - Oxacycle - Thiocarboxylic acid amide - Organoheterocyclic compound - Organic nitrogen compound - Primary alcohol - Alcohol - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organic oxygen compound - Thiocarbonyl group - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as 2-ribofuranosylindazoles. These are nucleoside and nucleotide analogs with a structure that consists of an indazole ring system which is N-substituted at the 2-position with a ribose moiety. Nucleotide analogues contain a phosphate group linked to the C5 carbon atom of the furanose.
External Descriptors
Not available