CSC1=NC=NC2=C1C(Br)=CN2C1O[C@H](CO)[C@@H](O)[C@H]1O

InChIKey=IRFZERSLBNKSOA-PUXKXDTASA-N

C12H14BrN3O4S

376.23

Organic compounds

Nucleosides, nucleotides, and analogues

Pyrrolopyrimidine nucleosides and nucleotides

Not available

Not available

Pyrrolopyrimidine nucleosides and nucleotides

Glycosylamines Pentoses Pyrrolo[2,3-d]pyrimidines Alkylarylthioethers Aryl bromides Substituted pyrroles Pyrimidines and pyrimidine derivatives Oxolanes Heteroaromatic compounds Secondary alcohols 1,2-diols Oxacyclic compounds Sulfenyl compounds Azacyclic compounds Organonitrogen compounds Organobromides Hydrocarbon derivatives Primary alcohols

Aromatic heteropolycyclic compounds

Pyrrolopyrimidine ribonucleoside - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - Pyrrolopyrimidine - Pyrrolo[2,3-d]pyrimidine - Aryl thioether - Alkylarylthioether - Pyrimidine - Substituted pyrrole - Aryl bromide - Aryl halide - Monosaccharide - Oxolane - Heteroaromatic compound - Pyrrole - 1,2-diol - Secondary alcohol - Oxacycle - Azacycle - Organoheterocyclic compound - Sulfenyl compound - Thioether - Organonitrogen compound - Organobromide - Organohalogen compound - Alcohol - Organic nitrogen compound - Organooxygen compound - Organosulfur compound - Organic oxygen compound - Hydrocarbon derivative - Primary alcohol - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as pyrrolopyrimidine nucleosides and nucleotides. These are nucleoside derivatives containing a ribose derivative which is n-glycosylated to a pyrrolopyrimidine. Also called deazapurine nucleosides, they are analogs of purine nucleosides with the N atom of the purine being replaced by a C atom at position 7.

Not available