CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O[Si](C)(C)C(C)(C)C)C(CO)=C[C@H]1N1C=NC2=C1N=CN=C2NC(=O)C1=CC=CC=C1

InChIKey=UPTKAFHJJTZBRI-GPXOXTDOSA-N

C30H45N5O4Si2

595.891

Organic compounds

Nucleosides, nucleotides, and analogues

Nucleoside and nucleotide analogues

Cyclopentyl nucleosides

1,3-substituted cyclopentyl nucleosides

1,3-substituted cyclopentyl purine nucleosides

Purines and purine derivatives Benzamides Benzoyl derivatives Pyrimidines and pyrimidine derivatives N-substituted imidazoles Imidolactams Trialkylheterosilanes Heteroaromatic compounds Silyl ethers Secondary carboxylic acid amides Azacyclic compounds Organic metalloid salts Hydrocarbon derivatives Organic oxides Organonitrogen compounds Primary alcohols

Aromatic heteropolycyclic compounds

1,3-substituted cyclopentyl purine nucleoside - Purine - Benzamide - Benzoic acid or derivatives - Imidazopyrimidine - Benzoyl - Pyrimidine - Monocyclic benzene moiety - N-substituted imidazole - Benzenoid - Imidolactam - Azole - Trialkylheterosilane - Heteroaromatic compound - Imidazole - Silyl ether - Carboxamide group - Secondary carboxylic acid amide - Organoheterosilane - Azacycle - Carboxylic acid derivative - Organic metalloid salt - Organoheterocyclic compound - Alcohol - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organosilicon compound - Organic metalloid moeity - Organonitrogen compound - Organooxygen compound - Primary alcohol - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as 1,3-substituted cyclopentyl purine nucleosides. These are nucleoside analogues with a structure that consists of a cyclobutane that is substituted a the 1-position with a hydroxyl group and at the 3-position with either a purine base.

Not available