fig3
Figure 3. Orientations of the most potent reference enzymatic activity inhibitors P(CH2CH3)3 (A), P(CH2CH3)(C6H5)2 (B), and P(C6H5)3, P(C6H4NH3+)(C6H5)2 (C) in the active site of cathepsin B
Figure 3. Orientations of the most potent reference enzymatic activity inhibitors P(CH2CH3)3 (A), P(CH2CH3)(C6H5)2 (B), and P(C6H5)3, P(C6H4NH3+)(C6H5)2 (C) in the active site of cathepsin B
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