CSC1=NC=NC2=C1C(Br)=CN2C1OC(CO)C(O)C1O

InChIKey=IRFZERSLBNKSOA-UHFFFAOYSA-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 Tetrahydrofurans Heteroaromatic compounds Secondary alcohols Sulfenyl compounds Azacyclic compounds Oxacyclic compounds Organopnictogen compounds Organonitrogen compounds Organobromides Hydrocarbon derivatives Primary alcohols

Aromatic heteropolycyclic compounds

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