CO[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1N1C=CC(NC(=O)OCCC2=CC=C(C=C2)[N+]([O-])=O)=NC1=O

InChIKey=ZILRMMXGJRLXFU-MWQQHZPXSA-N

C19H22N4O9

450.404

Organic compounds

Nucleosides, nucleotides, and analogues

Pyrimidine nucleosides

Not available

Not available

Pyrimidine nucleosides

Glycosylamines Nitrobenzenes Nitroaromatic compounds Pyrimidones Hydropyrimidines Imidolactams Monosaccharides Carbamate esters Heteroaromatic compounds Oxolanes Secondary alcohols Oxacyclic compounds Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds Dialkyl ethers Organic oxoazanium compounds Organic oxides Organonitrogen compounds Carbonyl compounds Primary alcohols Hydrocarbon derivatives Organic salts Organic zwitterions

Aromatic heteromonocyclic compounds

Pyrimidine nucleoside - Glycosyl compound - N-glycosyl compound - Nitrobenzene - Nitroaromatic compound - Pyrimidone - Monocyclic benzene moiety - Hydropyrimidine - Monosaccharide - Pyrimidine - Benzenoid - Imidolactam - Carbamic acid ester - Heteroaromatic compound - Oxolane - Secondary alcohol - Organic nitro compound - C-nitro compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Dialkyl ether - Oxacycle - Azacycle - Organoheterocyclic compound - Ether - Organic oxoazanium - Organic zwitterion - Organic oxide - Organonitrogen compound - Alcohol - Organic oxygen compound - Organic nitrogen compound - Organic salt - Organooxygen compound - Primary alcohol - Hydrocarbon derivative - Carbonyl group - Aromatic heteromonocyclic compound

This compound belongs to the class of organic compounds known as pyrimidine nucleosides. These are compounds comprising a pyrimidine base attached to a ribosyl or deoxyribosyl moiety.

Not available