OCC1=NOC(=C1)[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC2=C(NC3=CC=CC=C3F)N=C(Cl)N=C12

InChIKey=KHQDLRSLCRTLGO-LUXYFRNMSA-N

C19H16ClFN6O5

462.82

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Glycosylamines

6-aminopurines Aniline and substituted anilines 2-halopyrimidines Aminopyrimidines and derivatives Fluorobenzenes N-substituted imidazoles Imidolactams Aryl chlorides Aryl fluorides Oxolanes Isoxazoles Heteroaromatic compounds Secondary alcohols Oxacyclic compounds Azacyclic compounds Hydrocarbon derivatives Aromatic alcohols Organochlorides Organofluorides Amines Organopnictogen compounds Primary alcohols

Aromatic heteropolycyclic compounds

N-glycosyl compound - 6-aminopurine - Imidazopyrimidine - Purine - Aniline or substituted anilines - Aminopyrimidine - 2-halopyrimidine - Fluorobenzene - Halobenzene - Halopyrimidine - Aryl chloride - Aryl fluoride - Aryl halide - Monocyclic benzene moiety - N-substituted imidazole - Imidolactam - Pyrimidine - Benzenoid - Oxolane - Azole - Heteroaromatic compound - Isoxazole - Imidazole - Secondary alcohol - Organoheterocyclic compound - Azacycle - Oxacycle - Amine - Hydrocarbon derivative - Organopnictogen compound - Organohalogen compound - Organonitrogen compound - Organochloride - Primary alcohol - Organic nitrogen compound - Alcohol - Organofluoride - Aromatic alcohol - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as glycosylamines. These are compounds consisting of an amine with a beta-N-glycosidic bond to a carbohydrate, thus forming a cyclic hemiaminal ether bond (alpha-amino ether).

Not available