COC1=CC=C(CSC2=NC(N)=NC3=C2N=CN3[C@H]2C[C@H](O)[C@@H](CO)O2)C=C1

InChIKey=XCYBLEKOXLNHSE-BFHYXJOUSA-N

C18H21N5O4S

403.46

Organic compounds

Nucleosides, nucleotides, and analogues

Purine nucleosides

Purine 2'-deoxyribonucleosides

Not available

Purine 2'-deoxyribonucleosides

6-thiopurines Anisoles Methoxybenzenes Phenoxy compounds Alkylarylthioethers Alkyl aryl ethers Aminopyrimidines and derivatives N-substituted imidazoles Oxolanes Heteroaromatic compounds Secondary alcohols Oxacyclic compounds Azacyclic compounds Sulfenyl compounds Hydrocarbon derivatives Primary alcohols Primary amines

Aromatic heteropolycyclic compounds

Purine 2'-deoxyribonucleoside - 6-thiopurine - Imidazopyrimidine - Purine - Phenoxy compound - Aryl thioether - Anisole - Methoxybenzene - Phenol ether - Alkyl aryl ether - Aminopyrimidine - Alkylarylthioether - Monocyclic benzene moiety - N-substituted imidazole - Benzenoid - Pyrimidine - Azole - Heteroaromatic compound - Imidazole - Oxolane - Secondary alcohol - Organoheterocyclic compound - Thioether - Sulfenyl compound - Ether - Oxacycle - Azacycle - Primary alcohol - Organonitrogen compound - Amine - Organooxygen compound - Organic nitrogen compound - Alcohol - Hydrocarbon derivative - Primary amine - Organosulfur compound - Organic oxygen compound - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as purine 2'-deoxyribonucleosides. These are compounds consisting of a purine linked to a ribose which lacks a hydroxyl group at position 2.

Not available