COC1(CCN(CC1)C1=CC(Br)=CC=C1)O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1N1C=CC(=O)NC1=O

InChIKey=ZNMPQKFDFFQHSM-NXWXRZEISA-N

C21H26BrN3O7

512.357

Organic compounds

Nucleosides, nucleotides, and analogues

Pyrimidine nucleosides

Not available

Not available

Pyrimidine nucleosides

Phenylpiperidines Glycosylamines Pentoses Aniline and substituted anilines Dialkylarylamines Pyrimidones Bromobenzenes Ketals Aryl bromides Hydropyrimidines Oxolanes Vinylogous amides Heteroaromatic compounds Secondary alcohols Ureas Lactams Oxacyclic compounds Azacyclic compounds Organopnictogen compounds Hydrocarbon derivatives Primary alcohols Organic oxides Organobromides

Aromatic heteromonocyclic compounds

Pyrimidine nucleoside - Phenylpiperidine - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - Aniline or substituted anilines - Dialkylarylamine - Tertiary aliphatic/aromatic amine - Bromobenzene - Ketal - Halobenzene - Pyrimidone - Aryl bromide - Aryl halide - Monocyclic benzene moiety - Hydropyrimidine - Monosaccharide - Piperidine - Pyrimidine - Benzenoid - Vinylogous amide - Oxolane - Heteroaromatic compound - Urea - Tertiary amine - Secondary alcohol - Lactam - Organoheterocyclic compound - Oxacycle - Azacycle - Acetal - Alcohol - Organic nitrogen compound - Organic oxide - Organopnictogen compound - Organic oxygen compound - Amine - Organohalogen compound - Organobromide - Organonitrogen compound - Organooxygen compound - Primary alcohol - Hydrocarbon derivative - 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