Synthesis and antitumor activity of a series of sulfone analogs of 1, 4-naphthoquinone
MH Holshouser, LJ Loeffler, IH Hall
Index: Holshouser, Mark H.; Loeffler, Larry J.; Hall, Iris H. Journal of Medicinal Chemistry, 1981 , vol. 24, # 7 p. 853 - 858
Full Text: HTML
Citation Number: 40
Abstract
A series of novel substituted thiochromones and thiochroman-4-ones was synthesized. Compounds were designed as analogues of naphthoquinone and as potential “bioreductive alkylating agents” and were tested for antitumor activity. The lead compound, 3- (chloromethyl) thiochromone 1, l-dioxide (4), inhibited Ehrlich ascites tumor growth by 100% in CF1 male mice at 10 (mg/kg)/day ip. Similarly, 18 of the 29 related compounds ...
Related Articles:
[Zhang, Youlai; Tanimoto, Hiroki; Nishiyama, Yasuhiro; Morimoto, Tsumoru; Kakiuchi, Kiyomi Synlett, 2012 , # 3 p. 367 - 370]
[Patonay; Adam; Levai; Koever; Nemeth; Peters Journal of Organic Chemistry, 2001 , vol. 66, # 7 p. 2275 - 2280]
[Nakazumi, Hiroyuki; Asada, Akira; Kitao, Teijiro Bulletin of the Chemical Society of Japan, 1980 , vol. 53, # 7 p. 2046 - 2049]
[Coombes, Richard C.; Fenton, David E. Phosphorus and Sulfur and the Related Elements, 1982 , vol. 14, p. 139 - 142]
[Kumar, Pradeep; Bodas, Mandar S Tetrahedron, 2001 , vol. 57, # 48 p. 9755 - 9758]