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. Author manuscript; available in PMC: 2014 May 1.
Published in final edited form as: ChemMedChem. 2013 Mar 18;8(5):847–857. doi: 10.1002/cmdc.201300007

Table 3.

Antiprion potency for AMT analogs with amide C-groups.

graphic file with name nihms523172u3.jpg
Cmpd R1 = R2 = EC50 ± SEM(nM)[a] n[B]
34 phenyl cyclopropyl 248 ± 67 4
35 phenyl CH3 119 ± 10 3
36 phenyl MeOCH2- 1588 ± 295 3
37 phenyl i-Pr >10,000 3
38 phenyl phenyl >10,000 3
39 pyridin-4-yl cyclopropyl 173 ± 16 3
40 2-Me-pyridin-3-yl cyclopropyl >10,000 3
41 4-Me2N-pyridin-3-yl cyclopropyl 109 ± 12 3
42 graphic file with name nihms523172t3.jpg cyclopropyl >10,000 3
43 graphic file with name nihms523172t4.jpg cyclopropyl >10,000 3
44 graphic file with name nihms523172t5.jpg cyclopropyl 1315 ± 233 4
45 graphic file with name nihms523172t6.jpg cyclopropyl 682 ± 100 3
46 graphic file with name nihms523172t7.jpg cyclopropyl 118 ± 11 3
47 graphic file with name nihms523172t8.jpg cyclopropyl 70 ± 23 4
[a]

antiprion potency in ScN2a-cl3 cells by ELISA; SEM is calculated as standard deviation divided by the square root of n.

[b]

number of repetitions.