CC1=CC=C(C=C1)S(=O)(=O)N1N=C(C2OC(CO)C(O)C2O)C(O)=C1C(N)=O

InChIKey=DQJVUTFHPZANHB-UHFFFAOYSA-N

C16H19N3O8S

413.4

Organic compounds

Nucleosides, nucleotides, and analogues

Nucleoside and nucleotide analogues

3-ribofuranosylpyrazoles

Not available

3-ribofuranosylpyrazoles

C-glycosyl compounds Tosyl compounds Benzenesulfonamides Pentoses Benzenesulfonyl compounds 2-heteroaryl carboxamides Pyrazole-5-carboxamides Vinylogous acids Sulfonyls Oxolanes Organosulfonic acids and derivatives Heteroaromatic compounds Secondary alcohols Primary carboxylic acid amides Dialkyl ethers Oxacyclic compounds Azacyclic compounds Organonitrogen compounds Primary alcohols Hydrocarbon derivatives Organic oxides

Aromatic heteromonocyclic compounds

3-ribofuranosylpyrazole - C-glycosyl compound - Glycosyl compound - Pentose monosaccharide - Tosyl compound - Benzenesulfonamide - Benzenesulfonyl group - 2-heteroaryl carboxamide - Pyrazole-5-carboxamide - Toluene - Benzenoid - Monocyclic benzene moiety - Monosaccharide - Oxolane - Vinylogous acid - Heteroaromatic compound - Pyrazole - Sulfonyl - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Azole - Carboxamide group - Secondary alcohol - Primary carboxylic acid amide - Organoheterocyclic compound - Azacycle - Oxacycle - Ether - Dialkyl ether - Carboxylic acid derivative - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Alcohol - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Primary alcohol - Organic nitrogen compound - Aromatic heteromonocyclic compound

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.

Not available