ClC1=CC=C(SC2=NC(NC(=O)CC3=CC=CC=C3)=NC3=C2N=CN3C2CC(COCC3=CC=CC=C3)C2)C=C1

InChIKey=GMWJMZIEZHFVER-UHFFFAOYSA-N

C31H28ClN5O2S

570.11

Organic compounds

Nucleosides, nucleotides, and analogues

Nucleoside and nucleotide analogues

Cyclobutyl nucleosides

Not available

Cyclobutyl nucleosides

Diarylthioethers Phenylacetamides 6-thiopurines Benzylethers Thiophenol ethers N-arylamides Chlorobenzenes Pyrimidines and pyrimidine derivatives Aryl chlorides N-substituted imidazoles Heteroaromatic compounds Secondary carboxylic acid amides Sulfenyl compounds Azacyclic compounds Dialkyl ethers Carbonyl compounds Hydrocarbon derivatives Organic oxides Organochlorides

Aromatic heteropolycyclic compounds

Cyclobutyl purine nucleoside - Cyclobutyl nucleoside - Diarylthioether - Phenylacetamide - 6-thiopurine - Benzylether - Imidazopyrimidine - Purine - Aryl thioether - N-arylamide - Thiophenol ether - Chlorobenzene - Halobenzene - Monocyclic benzene moiety - Benzenoid - Pyrimidine - Aryl halide - Aryl chloride - N-substituted imidazole - Heteroaromatic compound - Azole - Imidazole - Carboxamide group - Secondary carboxylic acid amide - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Sulfenyl compound - Dialkyl ether - Ether - Thioether - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organic nitrogen compound - Carbonyl group - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organohalogen compound - Organochloride - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as cyclobutyl 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 or pyrimidine base.

Not available