CC1=CC(CN2C=C(CCNC3=NC=NC4=C3N=CN4[C@@H]3O[C@@H]([C@@H](O)[C@H]3O)C(N)=O)C3=CC=CC=C23)=C(C)C=C1

InChIKey=ANZDCOZQPXKIRO-APSVEGKFSA-N

C29H31N7O4

541.612

Organic compounds

Nucleosides, nucleotides, and analogues

Purine nucleosides

Not available

Not available

Purine nucleosides

6-alkylaminopurines Glycosylamines 3-alkylindoles N-alkylindoles p-Xylenes Aminopyrimidines and derivatives Substituted pyrroles Imidolactams N-substituted imidazoles Oxolanes Heteroaromatic compounds Secondary alcohols 1,2-diols Primary carboxylic acid amides Oxacyclic compounds Azacyclic compounds Carbonyl compounds Amines Hydrocarbon derivatives Organic oxides

Aromatic heteropolycyclic compounds

Purine nucleoside - Glycosyl compound - N-glycosyl compound - 6-alkylaminopurine - 6-aminopurine - N-alkylindole - 3-alkylindole - Indole or derivatives - Indole - Purine - Imidazopyrimidine - P-xylene - Xylene - Aminopyrimidine - N-substituted imidazole - Monocyclic benzene moiety - Pyrimidine - Imidolactam - Substituted pyrrole - Benzenoid - Oxolane - Pyrrole - Azole - Heteroaromatic compound - Imidazole - 1,2-diol - Carboxamide group - Secondary alcohol - Primary carboxylic acid amide - Organoheterocyclic compound - Azacycle - Oxacycle - Carboxylic acid derivative - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Alcohol - Amine - Organooxygen compound - Organonitrogen 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