Antitumor Agents. II: Regio- and Stereospecific Syntheses of 1-β-Alkyl-1-desoxypodophyllotoxin Derivatives and Biological Activity

Abstract

1-β-Alkyl derivatives of 1-desoxypodophyllotoxin were synthesized, and their cytotoxicity and inhibitory effects on DNA topoisomerase II (Topo-II) and tubulin polymerization were examined. The reaction of epipodophyllotoxin derivatives (la—c) with trimethylallylsilane in the presence of boron trifluoride etherate gave 1-β-allylated compounds (2a—c). The regiochemistry and the β-stereochemistry of the 1-allyl group were confirmed by comparison of the 13C-NMR spectra and NOE’s (%) of 2c, podophyllotoxin (POD) and epipodophyllotoxin (1b). 1-β-Alkyl-1-desoxypodophyllotoxin derivatives (3—8) were prepared from 2b. None of the tested compounds (3—8) showed any inhibitory effect on Topo-II. 1-β-Propyl compound (3) and its 4’-demethyl compound (4) inhibited tubulin polymerization and the cytotoxicities of these compounds were equal to that of VP-16. 1-β-(2,3-Dihydroxypropyl) compounds (5 and 8) and 1-β-(2,3-diacetoxypropyl) compounds (6 and 7) showed no inhibitory effect on tubulin polymerization. Although 5 did not inhibit either Topo-II activity or tubulin polymerization, it showed a high cytotoxicity against sarcoma 180. © 1993, The Pharmaceutical Society of Japan. All rights reserved.