fig3

<i>In silico</i> design of novel gold-phosphate containing compounds as selective inhibitors of cathepsin B in neuroinflammation

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

Neuroimmunology and Neuroinflammation
ISSN 2349-6142 (Online) 2347-8659 (Print)

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Portico

All published articles are preserved here permanently:

https://www.portico.org/publishers/oae/