Cl.Cl.CC(C)[C@H](N)C(=O)O[C@@H]1[C@@H](CO)O[C@@H](N2C=CC(N)=NC2=O)[C@]1(C)O

InChIKey=XENHXZMAOSTXGD-DSMKLBDQSA-N

C15H26Cl2N4O6

429.3

Organic compounds

Nucleosides, nucleotides, and analogues

Pyrimidine nucleosides

Not available

Not available

Pyrimidine nucleosides

Valine and derivatives Alpha amino acid esters Glycosylamines Pyrimidones Aminopyrimidines and derivatives Fatty acid esters Hydropyrimidines Imidolactams Monosaccharides Tertiary alcohols Heteroaromatic compounds Oxolanes Carboxylic acid esters Oxacyclic compounds Monocarboxylic acids and derivatives Azacyclic compounds Monoalkylamines Primary alcohols Hydrochlorides Hydrocarbon derivatives Carbonyl compounds Organic oxides

Aromatic heteromonocyclic compounds

Pyrimidine nucleoside - Alpha-amino acid ester - Valine or derivatives - Glycosyl compound - N-glycosyl compound - Alpha-amino acid or derivatives - Aminopyrimidine - Fatty acid ester - Pyrimidone - Hydropyrimidine - Monosaccharide - Fatty acyl - Imidolactam - Pyrimidine - Heteroaromatic compound - Oxolane - Tertiary alcohol - Amino acid or derivatives - Carboxylic acid ester - Organoheterocyclic compound - Carboxylic acid derivative - Oxacycle - Monocarboxylic acid or derivatives - Azacycle - Organic oxygen compound - Primary aliphatic amine - Hydrochloride - Alcohol - Hydrocarbon derivative - Organonitrogen compound - Organooxygen compound - Carbonyl group - Organic oxide - Organic nitrogen compound - Amine - Primary amine - Primary alcohol - 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