7DF5

Human Galectin-3 CRD in complex with novel tetrahydropyran-based thiodisaccharide mimic inhibitor

7DF5 の概要

• エントリーDOI: 10.2210/pdb7df5/pdb
• 関連するPDBエントリー: 7DF6
• 分子名称: Galectin-3, MAGNESIUM ION, CHLORIDE ION, ... (5 entities in total)
• 機能のキーワード: inhibitor, complex, galectin-3 crd, carbohydrate
• 由来する生物種: Homo sapiens (Human)
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 19367.88

構造登録者

Ghosh, K.,Kumar, A. (登録日: 2020-11-06, 公開日: 2021-06-23, 最終更新日: 2023-11-29)

主引用文献

Xu, L.,Hartz, R.A.,Beno, B.R.,Ghosh, K.,Shukla, J.K.,Kumar, A.,Patel, D.,Kalidindi, N.,Lemos, N.,Gautam, S.S.,Kumar, A.,Ellsworth, B.A.,Shah, D.,Sale, H.,Cheng, D.,Regueiro-Ren, A.
Synthesis, Structure-Activity Relationships, and In Vivo Evaluation of Novel Tetrahydropyran-Based Thiodisaccharide Mimics as Galectin-3 Inhibitors.
J.Med.Chem., 64:6634-6655, 2021

PubMed Abstract: Galectin-3 is a member of a family of β-galactoside-binding proteins. A substantial body of literature reports that galectin-3 plays important roles in cancer, inflammation, and fibrosis. Small-molecule galectin-3 inhibitors, which are generally lactose or galactose-based derivatives, have the potential to be valuable disease-modifying agents. In our efforts to identify novel galectin-3 disaccharide mimics to improve drug-like properties, we found that one of the monosaccharide subunits can be replaced with a suitably functionalized tetrahydropyran ring. Optimization of the structure-activity relationships around the tetrahydropyran-based scaffold led to the discovery of potent galectin-3 inhibitors. Compounds , , and were selected for further in vivo evaluation. The synthesis, structure-activity relationships, and in vivo evaluation of novel tetrahydropyran-based galectin-3 inhibitors are described.

PubMed: 33988358
DOI: 10.1021/acs.jmedchem.0c02001

実験手法

X-RAY DIFFRACTION (1.08 Å)