Structure-Based Discovery of the First Inhibitor Targeting the Talin2-β-integrin Interaction with Potent <i>In Vivo</i> Antitumor Activity in Breast Cancer Models

pharmacokinetic characteristics. In conclusion, Peptide-2 is a novel inhibitor that offers a potential new strategy for breast cancer therapy.

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Publication Details

Journal
Journal of Medicinal Chemistry
Published
2026-04-22
DOI
https://doi.org/10.1021/acs.jmedchem.5c03539
Primary Topic
Cell Adhesion Molecules Research
Type
article
Field-Weighted Citation Impact
0.00
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article

Structure-Based Discovery of the First Inhibitor Targeting the Talin2-β-integrin Interaction with Potent In Vivo Antitumor Activity in Breast Cancer Models

Yunjiang Zhou, Miaomiao Niu, Yi Zhou, Weiwei Hu et al.
Journal of Medicinal Chemistry
Cell Adhesion Molecules Research
article

Structure-Based Discovery of the First Inhibitor Targeting the Talin2-β-integrin Interaction with Potent In Vivo Antitumor Activity in Breast Cancer Models

Yunjiang Zhou, Miaomiao Niu, Yi Zhou, Weiwei Hu, Mengting Lou, Shuting Li, Lixia Guan, Shutong Chen
article en

Abstract

pharmacokinetic characteristics. In conclusion, Peptide-2 is a novel inhibitor that offers a potential new strategy for breast cancer therapy.

Journal of Medicinal Chemistry
China Pharmaceutical University (CN), Genesis Laboratories (US), Changzhou No.2 People's Hospital (CN), Nanjing Medical University (CN)
Good health and well-being
Openalex Percentile: Top 8%
Cell Adhesion Molecules Research
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