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. Author manuscript; available in PMC: 2016 May 20.
Published in final edited form as: Tetrahedron Lett. 2015 May 20;56(21):2832–2835. doi: 10.1016/j.tetlet.2015.04.061

Table 1.

rac-(trans-3,4)-Disubstituted pyrrolidine analogs tested against TbrPDEB1

graphic file with name nihms685683t1.jpg
Cpd R R1 TbrPDEB1 (% inh)a
10a OCH2CH3 CH3 8 ± 11
10b OH CH3 17 ± 9
11a graphic file with name nihms685683t2.jpg CH3 5 ± 5c
11b graphic file with name nihms685683t3.jpg CH3 7 ± 5c
11c graphic file with name nihms685683t4.jpg CH3 8 ± 0
11d graphic file with name nihms685683t5.jpg CH3 6 ± 6
11e graphic file with name nihms685683t6.jpg CH3 16 ± 11
11f graphic file with name nihms685683t7.jpg CH3 10 ± 5
11g graphic file with name nihms685683t8.jpg CH3 16 ± 6
11h NHCH3 CH3 8 ± 0
11i NHCH2CH3 CH3 5 ± 4
11j graphic file with name nihms685683t9.jpg CH3 1 ± 2
11k graphic file with name nihms685683t10.jpg CH3 10 ± 3
13a OCH2CH3 SO2CH3 3 ± 4
13b OCH2CH3 COCH3 15 ± 0
a

Data shown are average of 2 replicate independent experiments. Compounds were tested at 10 µM concentrations.

b

n=1

c

Replicate of 3 independent experiments.