CC1=CC=C(SCNC2=NC=NC3=C2N=CN3[C@@H]2O[C@H](CO)C[C@H]2O)C=C1

InChIKey=BNLUHVFEABNXQY-WPKBUWHJSA-N

C18H21N5O3S

387.46

Organic compounds

Nucleosides, nucleotides, and analogues

Purine nucleosides

Purine 3'-deoxyribonucleosides

Not available

Purine 3'-deoxyribonucleosides

6-alkylaminopurines Thiophenol ethers Toluenes Alkylarylthioethers Pyrimidines and pyrimidine derivatives Imidolactams N-substituted imidazoles Oxolanes Heteroaromatic compounds Secondary alcohols Sulfenyl compounds Azacyclic compounds Oxacyclic compounds Primary alcohols Hydrocarbon derivatives Organonitrogen compounds

Aromatic heteropolycyclic compounds

Purine 3'-deoxyribonucleoside - 6-alkylaminopurine - Purine - Imidazopyrimidine - Aryl thioether - Thiophenol ether - Toluene - Alkylarylthioether - Pyrimidine - Monocyclic benzene moiety - N-substituted imidazole - Benzenoid - Imidolactam - Heteroaromatic compound - Azole - Oxolane - Imidazole - Secondary alcohol - Oxacycle - Azacycle - Organoheterocyclic compound - Sulfenyl compound - Thioether - Organooxygen compound - Organonitrogen compound - Alcohol - Organosulfur compound - Organic nitrogen compound - Primary alcohol - Organic oxygen compound - Hydrocarbon derivative - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as purine 3'-deoxyribonucleosides. These are compounds consisting of a purine linked to a ribose which lacks a hydroxyl group at position 3.

Not available