Topoisomerase poisons for the treatment of proliferative disorders
Methods for the treatment of a proliferative disorder are provided in which a subject in need of such treatment is administered an effective amount of a compound selected from: compounds of formula (I) or a pharmaceutically acceptable salt thereof, wherein X 1 and X 2 are independently H, Cl, F, Br, I, CN, CF 3 or NO 2 , and Ar 1 is a substituted or unsubstituted aryl or a substituted or unsubstituted heteroaryl; and compounds of formula (II) wherein X 3 and X 4 are each independently H, Cl, F, Br, I, CN, CF 3 or NO 2 ; Y is (C 2 –C 6 )alkylene or (C 2 –C 6 )heteroalkylene; and Z is Cl, F, Br, I, CN, CF 3 or NO 2 .
1. A method for the treatment of a proliferative disorder selected from the group consisting of colorectal carcinoma, ovarian cancer, small cell lung cancer and non-Hodgkin's lymphoma, said method comprising administering to a subject in need of such treatment an effective amount of a compound of formula I,
wherein
X 1 is H or Cl and X 2 is F or Cl; and
Ar 1 is a member selected from the group consisting of substituted or unsubstituted aryl.
2. A method in accordance with claim 1 , wherein X 1 is H, X 2 is Cl, and Ar 1 is selected from the group consisting of 4-chlorophenyl and 4-nitrophenyl.
3. A method for selectively inducing DNA double strand breaks in a cell in all phases of the cell cycle without inhibiting nucleotide excision repair or daughter strand gap repair in said cell, said method comprising contacting said cell with a compound of formula I,
wherein
X 1 is H or Cl and X 2 is F or Cl; and
Ar 1 is a member selected from the group consisting of substituted or unsubstituted aryl; and thereby treating a proliferative disorder selected from the group consisting of colorectal carcinoma, ovarian cancer, small cell lung cancer and non-Hodgkin's lymphoma.
4. A compound of formula I,
wherein
X 1 is H or Cl and X 2 is F or Cl; and
Ar 1 is a member selected from the group consisting of substituted or unsubstituted aryl.
5. A pharmaceutical composition comprising a pharmaceutically acceptable excipient and a compound of formula I,
wherein
X 1 is H or Cl and X 2 is F or Cl; and
Ar 1 is a member selected from the group consisting of substituted or unsubstituted aryl.