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. Author manuscript; available in PMC: 2014 Apr 1.
Published in final edited form as: Chem Biol Drug Des. 2013 Apr;81(4):10.1111/cbdd.1427. doi: 10.1111/cbdd.1427

Table 2.

In vitro antileishmanial activity (L. donovani) of tricyclic guanidine derivatives

Compd.
No.
L. donovani
Compd.
No
L. donovani
IC50
(μM)
IC90
(μM)
IC50
(μM)
IC90
(μM)
12a 64.98 126 17b 14.44 29.65
12b 12.31 33.03 17c 10.13 23.85
12c 2.39 11.27 17d 59.60 112.5
12d 48.25 91.15 17e 85.69 >13
12e 73.26 >130 17f 61.06 125
12f 28.87 91.18 17h 63.09 >100
12h 29.47 72.56 17i 63.75 >100
12i 32.41 79.80 17j 62.91 >100
12j 29.34 78.24 17l 48.19 124.4
12l 13.33 55.73 20a 29.31 116
14a 34.02 106.5 20b 57.76 119
14b 9.51 19.59 20c 10.34 22.25
14c 2.78 12.76 20d 57.23 114
14d 46.51 93.02 20e 133.6 >100
14e 62.71 128.9 20f 50.90 >100
14f 10.20 20.40 20h 12.08 45.31
14h 7.23 14.91 20i 48.23 106
14i 7.71 15.90 20l 9.52 20.95
14l 10.97 21.94

IC50 and IC90 = Sample concentrations that kill 50% and 90% cells compared to the solvent controls; Pentamidine: IC50 = 2.94 μM, IC90 = 5.88 μM; Amphotericin B: IC50 = 0.173 μM, IC90 = 0.358 μM.