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A similar tendency in activity was also observed for related compounds. Deoxypodophyllotoxin cyclic ether, where the lactone carbonyl group of 4-deoxypodophyllotoxin was substituted by a methylene unit, was 8-11 times more cytotoxic than the 4-deoxypodophyllotoxin analogue having a cyclopentane ring D structure
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A similar tendency in activity was also observed for related compounds. Deoxypodophyllotoxin cyclic ether, where the lactone carbonyl group of 4-deoxypodophyllotoxin was substituted by a methylene unit, was 8-11 times more cytotoxic than the 4-deoxypodophyllotoxin analogue having a cyclopentane ring D structure. Gensler, W. J.; Murthy, C. D.; Trammel, M. H. J. Med. Chem. 1977, 20, 635; Loike, J. D.; Brewer, C. F.; Sternlicht, H.; Gensler, W. J.; Horwitz, S. B. Cancer Res. 1978, 38, 2688.
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