AI-Driven De Novo Design of Ultra Long-Acting GLP-1 Receptor Agonists.

Wei, Ting et al.·Advanced science (Weinheim·2025·
RPEP-141092025RETHINKTHC RESEARCH DATABASErethinkthc.com/research

Quick Facts

Study Type
Not classified
Evidence
Not graded
Sample
Not reported

What This Study Found

Key Numbers

How They Did This

Why This Research Matters

What This Study Doesn't Tell Us

Trust & Context

Original Title:
AI-Driven De Novo Design of Ultra Long-Acting GLP-1 Receptor Agonists.
Published In:
Advanced science (Weinheim, Baden-Wurttemberg, Germany), 12(40), e07044 (2025)
Database ID:
RPEP-14109

Evidence Hierarchy

Meta-Analysis / Systematic Review
Randomized Controlled Trial
Cohort / Case-Control
Cross-Sectional / ObservationalSnapshot without intervening
This study
Case Report / Animal Study
What do these levels mean? →

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Cite This Study

RPEP-14109·https://rethinkpeptides.com/research/RPEP-14109

APA

Wei, Ting; Ma, Jiating; Cui, Xiaochen; Lin, Jiahui; Zheng, Zhuoqi; Cheng, Liu; Cui, Taiying; Lin, Xiaoqian; Zhu, Junjie; Ran, Xuyang; Hong, Xiaokun; Johnston, Luke; Yu, Zhangsheng; Chen, Haifeng. (2025). AI-Driven De Novo Design of Ultra Long-Acting GLP-1 Receptor Agonists.. Advanced science (Weinheim, Baden-Wurttemberg, Germany), 12(40), e07044. https://doi.org/10.1002/advs.202507044

MLA

Wei, Ting, et al. "AI-Driven De Novo Design of Ultra Long-Acting GLP-1 Receptor Agonists.." Advanced science (Weinheim, 2025. https://doi.org/10.1002/advs.202507044

RethinkPeptides

RethinkPeptides Research Database. "AI-Driven De Novo Design of Ultra Long-Acting GLP-1 Receptor..." RPEP-14109. Retrieved from https://rethinkpeptides.com/research/wei-2025-aidriven-de-novo-design

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Study data sourced from PubMed, a service of the U.S. National Library of Medicine, National Institutes of Health.

This study breakdown was produced by the RethinkPeptides research team. We analyze and report published research findings without making health recommendations. All interpretations are based solely on the published abstract and study data.