Trivaric acid, a potent depside human leukocyte elastase inhibitor.

Biol Pharm Bull

New Drug Research & Development Center, North China Pharmaceutical Group Corporation, No. 388 Heping East Road, Shijiazhuang 050015, Hebei, China.

Published: May 2013

Human leukocyte elastase (HLE) is a serine protease implicated in several inflammatory diseases, and represents a major target for anti-inflammatory drug development. In the present study, nordivaricatic acid (1), divarinyl divarate (2), and trivaric acid (3), three depsides isolated from the culture of a soil derived fungal strain were identified as inhibitors of HLE. Two didepsides 1 and 2 showed low inhibitory activity. In contrast, trivaric acid, a para-tridepside, exhibited highly potent inhibitory activity with an IC(50) value of 1.8 µM and a K(i) of 0.6 µM. Kinetic investigations with trivaric acid showed that this inhibition is reversible, competitive pattern. Further studies on the selectivity of three depsides toward serine proteases showed that they did not inhibit chymotrypsin, trypsin and thrombin even at 150 µM.

Download full-text PDF

Source
http://dx.doi.org/10.1248/bpb.b12-00642DOI Listing

Publication Analysis

Top Keywords

trivaric acid
16
human leukocyte
8
leukocyte elastase
8
three depsides
8
inhibitory activity
8
trivaric
4
acid potent
4
potent depside
4
depside human
4
elastase inhibitor
4

Similar Publications

Varic acid analogues from fungus as PTP1B inhibitors: Biological evaluation and structure-activity relationships.

Bioorg Med Chem Lett

August 2017

School of Life Science, Biotechnology, Dalian University of Technology, Dalian, Liaoning 116024, China. Electronic address:

Protein tyrosine phosphatase 1B (PTP1B) inhibitors as potential therapies for diabetes and obesity have attracted much attention in recent years. Six varic acid analogues were isolated from two strains of fungi and evaluated for PTP1B inhibition activities. The structure-activity relationships were also characterized and predicted by molecular modeling.

View Article and Find Full Text PDF

Aim: To screen a potential PTP1b inhibitor from the microbial origin-based compound library and to investigate the potential anti-diabetic effects of the inhibitor in vivo and determine its primary anti-diabetic mechanism in vitro and in silico.

Methods: PTP1b inhibitory activity was measured using recombination protein as the enzyme and p-NPP as the substrate. The binding of the inhibitor to PTP1b was analysed by docking in silico and confirmed by ITC experiments.

View Article and Find Full Text PDF

Trivaric acid, a potent depside human leukocyte elastase inhibitor.

Biol Pharm Bull

May 2013

New Drug Research & Development Center, North China Pharmaceutical Group Corporation, No. 388 Heping East Road, Shijiazhuang 050015, Hebei, China.

Human leukocyte elastase (HLE) is a serine protease implicated in several inflammatory diseases, and represents a major target for anti-inflammatory drug development. In the present study, nordivaricatic acid (1), divarinyl divarate (2), and trivaric acid (3), three depsides isolated from the culture of a soil derived fungal strain were identified as inhibitors of HLE. Two didepsides 1 and 2 showed low inhibitory activity.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!