CC(=O)NC1=NC(=O)C2=C(N1)N([C@H]1C[C@H](OCC3=CC=CC=C3)[C@@H](COCC3=CC=CC=C3)[C@@H]1Br)C(=O)N2

InChIKey=ZFRVWCOWGILUFL-MLNNCEHLSA-N

C27H28BrN5O5

582.455

Organic compounds

Nucleosides, nucleotides, and analogues

Nucleoside and nucleotide analogues

Not available

Not available

Nucleoside and nucleotide analogues

6-oxopurines Hypoxanthines Benzylethers N-acetylarylamines Pyrimidones N-substituted imidazoles Acetamides Heteroaromatic compounds Vinylogous amides Ureas Secondary carboxylic acid amides Dialkyl ethers Azacyclic compounds Organobromides Organic oxides Hydrocarbon derivatives Carbonyl compounds Alkyl bromides

Aromatic heteropolycyclic compounds

6-oxopurine - Purinone - Hypoxanthine - Imidazopyrimidine - N-acetylarylamine - Purine - Benzylether - N-arylamide - Pyrimidone - N-substituted imidazole - Monocyclic benzene moiety - Pyrimidine - Benzenoid - Imidazole - Heteroaromatic compound - Acetamide - Azole - Vinylogous amide - Secondary carboxylic acid amide - Carboxamide group - Urea - Azacycle - Carboxylic acid derivative - Dialkyl ether - Ether - Organoheterocyclic compound - Alkyl halide - Alkyl bromide - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Organobromide - Organohalogen compound - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as nucleoside and nucleotide analogues. These are analogues of nucleosides and nucleotides. These include phosphonated nucleosides, C-glycosylated nucleoside bases, analogues where the sugar unit is a pyranose, and carbocyclic nucleosides, among others.

Not available