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. Author manuscript; available in PMC: 2008 Oct 16.
Published in final edited form as: FEBS Lett. 2007 Sep 24;581(25):4955–4959. doi: 10.1016/j.febslet.2007.09.031

Table 1.

Effect of BA derivatives on the chymotrypsin-like activity of 20S proteasome.

graphic file with name nihms-32673-t0006.jpg
Compounds Structures IC50# (μg/ml)
R1 R2
DSB*1 (2) graphic file with name nihms-32673-t0007.jpg OH 4.0
A15*1 (3) graphic file with name nihms-32673-t0008.jpg OH 8.2
A16*1 (4) graphic file with name nihms-32673-t0009.jpg OH >20
A18*1 (5) graphic file with name nihms-32673-t0010.jpg OH >20
LH68*1 (6) graphic file with name nihms-32673-t0011.jpg OH 6.5
LH141*2
(7)
graphic file with name nihms-32673-t0012.jpg graphic file with name nihms-32673-t0013.jpg >20
IC9564*2
(8)
H graphic file with name nihms-32673-t0014.jpg >20

The chemical structures and characteristics of these compounds are described in reference 16 (*1) and 22 (*2).

#

The IC50 values in the table are the average of three experiments.