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. Author manuscript; available in PMC: 2007 Jun 29.
Published in final edited form as: Bioorg Med Chem Lett. 2006 Sep 1;16(22):5773–5777. doi: 10.1016/j.bmcl.2006.08.078

Table 1.

Inhibitory activities of the adamantane-based ureas 1{1}, 2{1}, 3{1}, and 4{1} derived from the amines 1 to 4

graphic file with name nihms21272f5.jpg

Compounda R2-NH2 IC50b(nM) % inhibitionc
1{1} 1 0.5 86 ± 9
2{1} 2 0.5 75 ± 12
3{1} 3 30 19 ± 7
4{1} 4 100 10 ± 3
a

The notation for the compound number: amine number {isocyanate number}, for example, 2{1} indicates a compound made by the combination of amine 2 with isocyanate 1.

b

As determined via a kinetic fluorescent assay.10

c

Determined via an end-point fluorescent assay, results are means ± SD of three separate experiments.11