65174-36-9Relevant academic research and scientific papers
Synthesis and antitumor activity of preactivated isophosphamide analogues bearing modified alkylating functionalities
Takamizawa,Matsumoto,Iwata,Makino,Yamaguchi,Uchida,Kasai,Shiratori,Takase
, p. 208 - 214 (1978)
In search of cancer chemotherapeutic agents with greater efficacy than cyclophosphamide, 4-hydroperoxyisophosphamide analogues bearing modified alkylating functionalities such as 2-bromoethyl, 2-iodoethyl, 2-methylsulfonyloxyethyl, and 2-ethylsulfonyloxyethyl groups were prepared by ozonolytic cyclization reaction of N,N'-substituted 3-butenyl phosphorodiamidates. Comparative cytotoxicity against L1210 cells and antileukemic life-span activity against L1210 implanted BDF1 mice of the newly synthesized compounds were tabulated. The 4-hydroperoxyisophosphamide analogues which have different alkylating groups in a molecule showed slightly greater cytotoxicity in vitro than those with the same alkylating groups. Most of the compounds having different alkylating groups also showed high antileukemic activity in vivo. Among them, the highest efficacy was found for 2-[N-methyl-N-(2-chloroethyl)]amino-3-(2-methylsulfonyloxyethyl)- 4-hydroxyperoxy-1,3,2-oxazaphosphorinane 2-oxide (NSC 280122D) whose life-span activity was also greater than that of 4-hydroxyperoxyisophosphamide, cyclophosphamide, and isophosphamide. The superiority of this compound was especially apparent by oral administration.
Cyclic phosphamide derivatives
-
, (2008/06/13)
Cyclic phosphamide derivatives of the general formula: STR1 [wherein X represents a halogen atom, Y represents a lower alkanesulfonyloxy, and R represents a lower alkyl] being useful as medicaments exhibiting antitumor and immunosuppressive activities.
