Overview: PAI-1 inhibitors and clinical applications

Plasminogen activator inhibitor-1 (PAI-1) is a protein involved in the fibrinolytic system and has been reported to be involved in various pathologies such as fibrosis and inflammation. We have developed small molecule inhibitors of human PAI-1 for clinical applications. A clinical candidate compound (TM5509) was finally identified among over 1400 derivatives of a hit compound (TM5275) searched by the X-ray crystal structure information of human PAI-1 and the in silico approach on a big virtual chemical library. From pre-clinical studies using our PAI-1 inhibitors, new therapeutic concepts for clinical applications, such as anti-cancer and anti-aging, have been conceived, some oh which have been tested in various investigator-initiated clinical trials.

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Publication Details

Journal
Biomedical Journal
Published
2025-05-20
DOI
https://doi.org/10.1016/j.bj.2025.100874
Citations
4
Primary Topic
Protease and Inhibitor Mechanisms
Type
article
Field-Weighted Citation Impact
3.75
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article

Overview: PAI-1 inhibitors and clinical applications

Toshio Miyata
4 citations
Biomedical Journal
Protease and Inhibitor Mechanisms
3.75
article

Overview: PAI-1 inhibitors and clinical applications

Toshio Miyata
article en
4 citations

Abstract

Plasminogen activator inhibitor-1 (PAI-1) is a protein involved in the fibrinolytic system and has been reported to be involved in various pathologies such as fibrosis and inflammation. We have developed small molecule inhibitors of human PAI-1 for clinical applications. A clinical candidate compound (TM5509) was finally identified among over 1400 derivatives of a hit compound (TM5275) searched by the X-ray crystal structure information of human PAI-1 and the in silico approach on a big virtual chemical library. From pre-clinical studies using our PAI-1 inhibitors, new therapeutic concepts for clinical applications, such as anti-cancer and anti-aging, have been conceived, some oh which have been tested in various investigator-initiated clinical trials.

Biomedical JournalVol. 49(1)
Toho University (JP), Tohoku University (JP)
Openalex Percentile: Top 7%
Protease and Inhibitor Mechanisms
3.75
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