Discovery of BT-114143, a Novel and Potent Phosphoric Acid-Containing Small-Molecule Plasminogen Activation Inhibitor for Hyperfibrinolysis

Fibrinolysis, the natural process of blood clot dissolution regulated by plasmin, plays a crucial role in preserving vascular health. Nevertheless, if this process becomes hyperactive, it can lead to severe bleeding episodes, particularly in instances of traumatic injuries. Conventional antifibrinolytics such as ε-aminocaproic acid (<b>EACA</b>) and tranexamic acid (<b>TXA</b>) exhibit limited impact attributed to their modest potency. The substantial dosage volume necessary for effectiveness, along with safety concerns, especially when administered in high doses, further constrains their usage. In response to these challenges, we have engineered <b>BT-114143</b>, an innovative plasminogen activation inhibitor featuring a phosphoric acid functional group. Crafted through structure-based drug design and nonclassical bioisosteres, <b>BT-114143</b> has demonstrated significant antifibrinolytic activity and target selectivity in extensive preclinical studies. Presently, <b>BT-114143</b> is in Phase Ib clinical trials in China (<b>CTR20222910</b>), representing a noteworthy progression in antifibrinolytic therapy.

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Publication Details

Journal
Journal of Medicinal Chemistry
Published
2025-03-18
DOI
https://doi.org/10.1021/acs.jmedchem.4c03190
Citations
2
Primary Topic
Blood Coagulation and Thrombosis Mechanisms
Type
article
Field-Weighted Citation Impact
3.54
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article

Discovery of BT-114143, a Novel and Potent Phosphoric Acid-Containing Small-Molecule Plasminogen Activation Inhibitor for Hyperfibrinolysis

Jianzong Li, Xiaodong Zhang, Jun Qi, Yan Wang et al.
2 citations
Journal of Medicinal Chemistry
Blood Coagulation and Thrombosis Mechanisms
3.54
article

Discovery of BT-114143, a Novel and Potent Phosphoric Acid-Containing Small-Molecule Plasminogen Activation Inhibitor for Hyperfibrinolysis

Jianzong Li, Xiaodong Zhang, Jun Qi, Yan Wang, Hao Wang, Xiao Wang, Zhiqiang Li, Min Li, Xiao Hu, Shaomei Zeng, Jun Tang, Sen Ji
article en
2 citations

Abstract

Fibrinolysis, the natural process of blood clot dissolution regulated by plasmin, plays a crucial role in preserving vascular health. Nevertheless, if this process becomes hyperactive, it can lead to severe bleeding episodes, particularly in instances of traumatic injuries. Conventional antifibrinolytics such as ε-aminocaproic acid (<b>EACA</b>) and tranexamic acid (<b>TXA</b>) exhibit limited impact attributed to their modest potency. The substantial dosage volume necessary for effectiveness, along with safety concerns, especially when administered in high doses, further constrains their usage. In response to these challenges, we have engineered <b>BT-114143</b>, an innovative plasminogen activation inhibitor featuring a phosphoric acid functional group. Crafted through structure-based drug design and nonclassical bioisosteres, <b>BT-114143</b> has demonstrated significant antifibrinolytic activity and target selectivity in extensive preclinical studies. Presently, <b>BT-114143</b> is in Phase Ib clinical trials in China (<b>CTR20222910</b>), representing a noteworthy progression in antifibrinolytic therapy.

Journal of Medicinal ChemistryVol. 68(6)
Mochida Pharmaceutical (Japan) (JP), Taiho Pharmaceutical (Japan) (JP)
Openalex Percentile: Top 9%
Blood Coagulation and Thrombosis Mechanisms
3.54
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