CC(C)(C)C1=NN=C(O1)[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC2=C1N=CN=C2NC1=C(F)C=C(Cl)C=C1

InChIKey=ZQYJPMPXQLNTPQ-QCUYGVNKSA-N

C21H21ClFN7O4

489.89

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Glycosylamines

6-aminopurines Aniline and substituted anilines Aminopyrimidines and derivatives Chlorobenzenes Fluorobenzenes Aryl chlorides Aryl fluorides N-substituted imidazoles Imidolactams 1,3,4-oxadiazoles Oxolanes Heteroaromatic compounds 1,2-diols Secondary alcohols Azacyclic compounds Oxacyclic compounds Organofluorides Organonitrogen compounds Organopnictogen compounds Organochlorides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

N-glycosyl compound - 6-aminopurine - Imidazopyrimidine - Purine - Aniline or substituted anilines - Aminopyrimidine - Halobenzene - Chlorobenzene - Fluorobenzene - Benzenoid - Imidolactam - Pyrimidine - Monocyclic benzene moiety - Aryl halide - Aryl fluoride - Aryl chloride - N-substituted imidazole - 1,3,4-oxadiazole - Heteroaromatic compound - Azole - Oxolane - Oxadiazole - Imidazole - Secondary alcohol - 1,2-diol - Organoheterocyclic compound - Azacycle - Oxacycle - Alcohol - Organic nitrogen compound - Hydrocarbon derivative - Organopnictogen compound - Organonitrogen compound - Organofluoride - Organohalogen compound - Organochloride - 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