(Alkylsulfonyl)methanesulfonates as anticancer agents
申请人:Southern Research Institute
公开号:US04611074A1
公开(公告)日:1986-09-09
Compounds of the formula: ##STR1## wherein R is methyl or other lower alkyl group; X and X' individually are hydrogen or lower alkyl; and R' is a 2-haloethyl group or other halogenated lower alkyl group are useful in the treatment of neoplastic diseases.
2-Chloroethyl (methylsulfonyl)methanesulfonate and related (methylsulfonyl)methanesulfonates. Antineoplastic activity in vivo
作者:Y. Fulmer Shealy、Charles A. Krauth、W. Russell Laster
DOI:10.1021/jm00371a019
日期:1984.5
2-Haloethyl and ethyl (methylsulfonyl)methanesulfonates were prepared via sulfene intermediates. 2-Chloroethyl (methylsulfonyl)methanesulfonate is highly active against P388 leukemia in vivo; the majority of leukemic mice treated with this compound at 50 mg/kg per day, qd 1-5, survived more than 30 days and about 37% survived for more than 60 days. 2- Fluoroethyl (methylsulfonyl)methanesulfonate is also