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. Author manuscript; available in PMC: 2009 Jun 8.
Published in final edited form as: ChemMedChem. 2008 Aug;3(8):1250–1268. doi: 10.1002/cmdc.200800047

Table 2.

Ba ENR inhibition and antibacterial activity for modification of ring B.

graphic file with name nihms96579f12.jpg
Compound ortho meta para IC50 (μM) or %inhibition at 1μM MIC[b] (μg/mL)
Triclosan Cl --- Cl 0.6 ± 0.0 3.1
55 --- --- --- 0.5 ± 0.1 32
3 --- --- OH 2.6% >64
20 --- --- NH2 7.1 ± 1.2 12
18 --- --- graphic file with name nihms96579t2.jpg 1.6% 111
19 graphic file with name nihms96579t3.jpg --- --- 0% 111
22 --- --- graphic file with name nihms96579t4.jpg >12[a] 4.9
4 --- --- NO2 7.2% 3.3
5 NO2 --- --- 7.7 ± 0.7 13.3
6 Cl --- NO2 0.3 ± 0.0 <0.1 – 3.1
7 --- --- Ph >6.25 1.9
32 --- --- graphic file with name nihms96579t5.jpg 15.5% >145
33 --- graphic file with name nihms96579t6.jpg --- 9.9% 2.3
[a]

Saturation with inhibitor was not obtained over the concentration range tested. The percent inhibition of BaENR showed a linear response to increasing inhibitor concentrations.

[b]

MIC values are against ΔANR B. anthracis.