CCNC(=O)[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC2=C1N=C(Cl)N=C2NNC(=O)C1=C(C)C=CS1

InChIKey=CMHQDWHZIUMRGC-VZVWNTEVSA-N

C18H20ClN7O5S

481.91

Organic compounds

Nucleosides, nucleotides, and analogues

Purine nucleosides

Not available

Not available

Purine nucleosides

Glycosylamines Purines and purine derivatives Thiophene carboxamides 2-halopyrimidines Aryl chlorides Imidolactams N-substituted imidazoles Oxolanes Heteroaromatic compounds Secondary carboxylic acid amides 1,2-diols Carboxylic acid hydrazides Secondary alcohols Oxacyclic compounds Azacyclic compounds Organonitrogen compounds Hydrocarbon derivatives Carbonyl compounds Organic oxides Organochlorides

Aromatic heteropolycyclic compounds

Purine nucleoside - Glycosyl compound - N-glycosyl compound - Purine - Imidazopyrimidine - Thiophene carboxamide - Thiophene carboxylic acid or derivatives - 2-halopyrimidine - Halopyrimidine - Aryl chloride - Aryl halide - Pyrimidine - N-substituted imidazole - Imidolactam - Azole - Heteroaromatic compound - Imidazole - Thiophene - Oxolane - 1,2-diol - Carboxamide group - Carboxylic acid hydrazide - Secondary carboxylic acid amide - Secondary alcohol - Organoheterocyclic compound - Azacycle - Oxacycle - Carboxylic acid derivative - Organic nitrogen compound - Hydrocarbon derivative - Alcohol - Carbonyl group - Organic oxide - Organic oxygen compound - Organohalogen compound - Organochloride - Organonitrogen compound - Organooxygen compound - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as purine nucleosides. These are compounds comprising a purine base attached to a ribosyl or deoxyribosyl moiety.

Not available