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. 2016 Jan 28;2016:1523691. doi: 10.1155/2016/1523691

Table 1.

Effect of CCBs and standard drugs on parasites and mammalian cells.

Drug IC50 (μM) ± SDa
L. (L.) infantum
promastigotes
L. (L.) infantum
amastigotes
L. (L.) amazonensis
promastigotes
L. (V.) braziliensis
promastigotes
T. cruzi
trypomastigotes
LLC-MK2
cytotoxicity
Amrinone neb neb neb neb neb >500
Fendiline 16.15 ± 4.20 12.20 ± 1.74 8.66 ± 1.27 9.15 ± 0.78 12.13 ± 2.97 49.85 ± 8.16
Lidoflazine 17.67 ± 0.93 16.29 ± 4.45 11.54 ± 1.49 14.48 ± 1.08 10.39 ± 1.87 106.54 ± 57.99
Mibefradil 3.60 ± 0.11 neb 2.23 ± 0.42 2.75 ± 0.39 2.99 ± 0.43 11.96 ± 1.03
Pentamidine 1.06 ± 0.12 ndc 1.14 ± 0.15 0.69 ± 0.04 ndc 23.48 ± 3.53
Glucantimed ndc 30.15 ± 1.18 ndc ndc ndc >500
Benznidazole ndc ndc ndc ndc 440.18 ± 39.14 >500

aIC50: 50% inhibitory concentration ± standard deviation (SD).

bne: not effective.

cnd: not determined.

dConcentrations for Glucantime are expressed as µg/mL, as the molecular weight is unknown.