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Novel indole-based indoleamine 2,3-dioxygenase-1 (IDO1) inhibitors: design, synthesis, and antidepressant evaluation

delete2025-12-02
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PRE
AI
J
Juan Zhang
W
Wenjing Gao
Y
Yu-Xi Zheng
J
J. Shao
N
Nai-Yu Zhang
W
Wei Guo
S
Shuai Wang
朱孔凯 (Kongkai Zhu) *
M
Ming Gao *
J
Jin‐Hai Yu *
甯濛 (Ning Meng) *
江成世 (Cheng‐Shi Jiang) *
DOI:10.1016/j.bmc.2025.118503delete
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Abstract

Abstract

En 中文
• Scaffold hopping of known benzimidazole IDO1 inhibitors yielded novel potent indole-based leads. • Indole derivatives 9f and 10f achieve sub-10 nM IDO1 inhibition in cell-based bioassay. • Compound 10f suppresses neuroinflammation in LPS-stimulated BV-2 microglia. • Compounds 9f and 10f show improved plasma stability and extended in vivo half-life. • Both compounds rescue depressive-like behavior in LPS-induced mouse models.

Journal

B
Bioorganic and Medicinal Chemistry
IF:
3
Papers:
1.7W
Citations:
2.7W

Organization

U
University of Jinan
Scholars:
1.6W
Papers: 1.1W
Citations: 1.4W
S
shandong university
Scholars:
9.1W
Papers: 6.3W
Citations: 94
C
cambrian neuroscience inc.
Scholars:
2
Papers: 1
Citations: 0
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