CCC1=C(C)N2C(=C1C)C(=C1C(C)=C(CC)C(C)=[N]1[B]2(F)F)C1=CC=C(C=C1)C#C[Au]=C1N(C)C2=C(N1C)C(=O)N(C)C(=O)N2C

InChIKey=KSGXEPIIGHLGMC-UHFFFAOYSA-N

C34H38AuBF2N6O2

808.49

Organic compounds

Organoheterocyclic compounds

Imidazopyrimidines

Purines and purine derivatives

Not available

Xanthines

6-oxopurines Alkaloids and derivatives Pyrimidones Substituted pyrroles N-substituted imidazoles Benzene and substituted derivatives Vinylogous amides Heteroaromatic compounds Ureas Metal acetylides Lactams Propargyl-type 1,3-dipolar organic compounds Organic transition metal salts Organic metalloid salts Azacyclic compounds Organopnictogen compounds Organooxygen compounds Organonitrogen compounds Organogold compounds Organic oxides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Xanthine - Purinone - 6-oxopurine - Alkaloid or derivatives - Pyrimidone - Benzenoid - Substituted pyrrole - Pyrimidine - N-substituted imidazole - Monocyclic benzene moiety - Heteroaromatic compound - Vinylogous amide - Pyrrole - Imidazole - Azole - Metal acetylide - Urea - Lactam - Azacycle - Organic metalloid salt - Organic transition metal salt - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organic salt - Organooxygen compound - Organonitrogen compound - Organometallic compound - Organogold - Organic transition metal moeity - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as xanthines. These are purine derivatives with a ketone group conjugated at carbons 2 and 6 of the purine moiety.

Not available