COC1=CC=C(C=C1)C(OC[C@H]1O[C@H](C[C@@H]1O)N1C=NC2=C1N=CN(SC(C1=CC=CC=C1)(C1=CC=CC=C1)C1=CC=CC=C1)C2=N)(C1=CC=CC=C1)C1=CC=C(OC)C=C1

InChIKey=LMWQAZHJMFYPJG-DZRFKLJISA-N

C50H45N5O5S

828.0

Organic compounds

Benzenoids

Triphenyl compounds

Not available

Not available

Triphenyl compounds

Purine 2'-deoxyribonucleosides Benzylethers Purines and purine derivatives Anisoles Phenoxy compounds Methoxybenzenes Alkyl aryl ethers Pyrimidines and pyrimidine derivatives Imidolactams N-substituted imidazoles Oxolanes Heteroaromatic compounds Secondary alcohols Dialkyl ethers Sulfenyl compounds Azacyclic compounds Oxacyclic compounds Hydrocarbon derivatives Organonitrogen compounds

Aromatic heteropolycyclic compounds

Triphenyl compound - Purine 2'-deoxyribonucleoside - Purine nucleoside - Benzylether - Imidazopyrimidine - Purine - Anisole - Phenoxy compound - Phenol ether - Methoxybenzene - Alkyl aryl ether - Imidolactam - Pyrimidine - Monocyclic benzene moiety - N-substituted imidazole - Heteroaromatic compound - Oxolane - Azole - Imidazole - Secondary alcohol - Sulfenyl compound - Oxacycle - Azacycle - Organoheterocyclic compound - Dialkyl ether - Ether - Hydrocarbon derivative - Organonitrogen compound - Organic nitrogen compound - Organooxygen compound - Organosulfur compound - Alcohol - Organic oxygen compound - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as triphenyl compounds. These are aromatic compounds containing a triphenyl moiety.

Not available