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. Author manuscript; available in PMC: 2021 Apr 7.
Published in final edited form as: J Med Chem. 2019 Mar 29;62(7):3524–3538. doi: 10.1021/acs.jmedchem.8b02009

Figure 5.

Figure 5.

Stability of 6 in the presense of human recombinant enzymes. 6 was spiked in incubations containing no enzyme, cathepsin B, cathepsin L, a mixture of cathepsin B and L, or HDAC2, and prodrug disappearance was measured over a period of 3 h via LC–MS. 6 showed the highest rate of disappearance in the presense of combined cathepsin B and L. HDAC2 did not cause prodrug metabolism. Negative control without enzymes showed no metabolism, confirming 6 to be chemically stable.