Leupeptazin, a highly modified tripeptide isolated from cultures of a Streptomyces sp. inhibits cathepsin K

Bioorg Med Chem Lett. 2017 Mar 15;27(6):1397-1400. doi: 10.1016/j.bmcl.2017.02.007. Epub 2017 Feb 5.

Abstract

Using a human cathepsin K-targeting inhibitor screen, a new leupeptin analogue, leupeptazin (1), containing an unprecedented piperidinotriazine moiety, was isolated from a liquid culture of soil Streptomyces sp. IS2-4 collected in northern Italy. The structure of leupeptazin was established using HRESIMS as well as 1D and 2D NMR data. The inhibitory activity of the compound towards the collagenase cathepsin K was tested in vitro to reveal moderate activity with an inhibition constant, Ki, of 44μM.

Keywords: Leupeptin; Protease inhibition; Streptomyces; Structure elucidation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cathepsin K / antagonists & inhibitors*
  • Humans
  • Magnetic Resonance Spectroscopy
  • Oligopeptides / pharmacology*
  • Spectrometry, Mass, Electrospray Ionization
  • Streptomyces / chemistry*

Substances

  • Oligopeptides
  • Cathepsin K

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