Design of a Highly Active Peptide Inhibitor of Farnesyltransferase and Its Protective Effect Against Acute Liver Failure

Collectively, these findings demonstrate that PD081376(d2,d3,d5) could alleviate LPS/D-GaIN or TAA-induced ALF by regulating apoptosis, pyroptosis, and necrotizing apoptosis, which might provide a new therapeutic strategy and scalability challenge for ALF.

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Publication Details

Journal
Drug Design Development and Therapy
Published
2025-03-01
DOI
https://doi.org/10.2147/dddt.s505541
Citations
2
Primary Topic
Vitamin C and Antioxidants Research
Type
article
Field-Weighted Citation Impact
2.24
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article

Design of a Highly Active Peptide Inhibitor of Farnesyltransferase and Its Protective Effect Against Acute Liver Failure

Chen-Qian Ying, Yongzhi Tang, Tao‐Hsin Tung, Huazhong Chen et al.
2 citations
Drug Design Development and Therapy
Vitamin C and Antioxidants Research
2.24
article

Design of a Highly Active Peptide Inhibitor of Farnesyltransferase and Its Protective Effect Against Acute Liver Failure

Chen-Qian Ying, Yongzhi Tang, Tao‐Hsin Tung, Huazhong Chen, Anne Li, Hui Qu, Hui Shao, Chun-Lian Huang, Jiansheng Zhu
article en
2 citations

Abstract

Collectively, these findings demonstrate that PD081376(d2,d3,d5) could alleviate LPS/D-GaIN or TAA-induced ALF by regulating apoptosis, pyroptosis, and necrotizing apoptosis, which might provide a new therapeutic strategy and scalability challenge for ALF.

Drug Design Development and TherapyVol. Volume 19
Wenzhou Medical University (CN), Zhejiang Taizhou Hospital (CN)
Good health and well-being
Openalex Percentile: Top 15%
Vitamin C and Antioxidants Research
2.24
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