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. 2015 Jul 18;80:710–724. doi: 10.1016/j.ijbiomac.2015.07.029

Fig. 6.

Fig. 6

Lineweaver–Burk plots for inhibition of substituted chalcones (1a–1j; a), chalconesemicarbazone isomers (2a–2j; b), (2a′–2j′; c) and diarylpyrazolines (3a–3j; d) on cathepsin H at fixed concentration (10−4 M) of inhibitor and varying substrate i.e. Leu βNA concentration (2.5, 2.0, 1.5, 1.0, 0.5, 0.3, 0.25 mM).