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. Author manuscript; available in PMC: 2012 Jun 14.
Published in final edited form as: J Med Chem. 2010 Oct 28;53(20):7356–7364. doi: 10.1021/jm100953c

Table 3.

Tolerability and Efficacy of Intraperitoneal Treatment with Oxaliplatin Derivatives Compared to Oxaliplatin in L1210 Leukemia-Bearing Mice (Therapeutic Effects at the Respective Optimum Dose Are Marked in Bold Type)

compd dose (mg/kg/day) min body weight (%) toxic deaths ILS (%)a long-term survivorsb
oxaliplatin 9 6/6 0/6
6 (MTD)c 93.2 0/6 152 2/6
4.5 91.3 0/6 89 1/6
3 94.1 0/6 94 1/6
d-OHP 12 1/6 0/6
9 (MTD)c 85.9 0/6 63 0/6
6 93.1 0/6 73 1/6
4.5 93.6 0/6 26 0/6
3a 12 2/6 4/6
9 (MTD)c 88.6 0/6 > 200 5/6
6 97.5 0/6 119 0/6
4.5 94.6 0/6 84 1/6
3 97.3 0/6 90 0/6
3b 9 1/6 0/6
6 (MTD)c 92.0 0/6 103 1/6
4.5 93.4 0/6 68 2/6
3 97.9 0/6 68 1/6
3c 12 2/6 1/6
9 (MTD)c 86.4 0/6 122 2/6
6 87.3 0/6 78 1/6
4.5 87.9 0/6 111 2/6
4 12 83.2 0/6 144 2/6
9 (MTD)c 89.9 0/6 129 1/6
6 93.6 0/6 89 0/6
3 98.4 0/6 61 0/6
5 12 100.0 0/6 33 0/6
6 100.0 0/6 25 0/6
3 98.5 0/6 17 0/6
a

Increase in life span compared to untreated controls, based on median survival; all values indicate life prolongation with high statistical significance (p < 0.001).

b

Animals with ILS > 200% without any signs of leukemia.

c

Maximum tolerated dose.

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