Synthesis and biological activity of tricyclic aryloimidazo-, pyrimido-, and diazepinopurinediones

DOI: 10.1016/j.bmc.2006.06.052

Source and publish data:

Bioorganic and Medicinal Chemistry p. 7258 - 7281 (2006)

Update date:2022-08-03

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Authors:

Drabczynska, Anna

Mueller, Christa E.

Lacher, Svenja K.

Schumacher, Britta

Karolak-Wojciechowska, Janina

Nasal, Antony

Kawczak, Piotr

Yuzlenko, Olga

Pekala, Elzbieta

Kiec-Kononowicz, Katarzyna

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Article abstract of DOI:10.1016/j.bmc.2006.06.052

Syntheses and physicochemical properties of N-aryl-substituted imidazo-, pyrimido-, and 1,3-diazepino[2,1-f]purinediones are described. These derivatives were synthesized by the cyclization of 7-haloalkyl-8-bromo-1,3-dimethyl- or 1,3-dipropyl-xanthine der

Full text of DOI:10.1016/j.bmc.2006.06.052

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Product name:1,3-dimethyl-8-p-tolyl-7,8-dihydro-1H,6H-imidazo[2,1-f]purine-2,4-dione

Cas No:32086-94-5

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