一个改进的TRβ选择性thyromimetic GC-1的合成
Xiaohui Chu1, Jinjun Wang1,2, Yanzhong Li3,4
1School of Food and Bioengineering, Yantai Institute of Technology, Yantai, 264003, China.
Scientific reports
|July 23, 2025
概括
研究人员开发了一种高效的合成GC-1,一个选择性甲状腺模拟剂. 这种新方法使用基保护组,提高产量,简化净化用于多克制量生产.
科学领域:
- 有机合成 有机合成
- 药用化学 医学化学
- 内分泌学 在内分泌学.
背景情况:
- 甲状腺激素受体 (TR) 调节剂对于治疗代谢性疾病至关重要.
- 选择性TRβ激动剂,或thyromimetics,提供治疗潜力,并减少副作用.
- 已知GC-1是一种TRβ选择性胸膜学药,需要高效的合成.
研究的目的:
- 开发一种新的,高效的,可扩展的合成路径,用于TRβ选择性甲状腺模拟GC-1.
- 通过利用基保护组来优化合成,以改善反应控制和净化.
- 建立一个可适应模拟设计和相关化合物的多功能合成策略.
主要方法:
- 采用合成策略,仅使用基替代剂作为保护组.
- 执行了GC-1的六步总合成.
- 在多克尺度上进行合成.
主要成果:
- 在GC-1的总合成中获得了62%的总产量.
- 由于选择的保护组策略,在最后一步证明了简化净化.
- 在多克尺度上成功生产了GC-1,表明了可扩展性.
结论:
- 开发的合成途径为生产GC-1提供了一种高效和实用的方法.
- 基保护组策略有效避免了副作用,并简化了净化.
- 这种可适应的合成方法适用于生成GC-1类同类物和其他甲基二醇.
相关概念视频
Synthesis and Regulation of Thyroid Hormones
5.1K
Low blood levels of the thyroid hormones — triiodothyronine (T3) and thyroxine (T4) — signal the hypothalamus to release the thyrotropin-releasing hormone (TRH). TRH then reaches the pituitary gland and stimulates the release of thyroid-stimulating hormone(TSH) into the bloodstream.
Upon reaching the thyroid gland, TSH stimulates the follicular cells' active uptake of iodide ions from the blood. The ions diffuse to the apical surface of the cells and are oxidized to iodine. The...
Upon reaching the thyroid gland, TSH stimulates the follicular cells' active uptake of iodide ions from the blood. The ions diffuse to the apical surface of the cells and are oxidized to iodine. The...
5.1K
Functions of Thyroid Hormones
3.2K
The thyroid hormone (TH) plays a pivotal role in the intricate orchestration of physiological processes, exerting profound effects on development, metabolism, and homeostasis throughout different life stages.
TH is indispensable for the normal development and maturation of the skeletal, muscular, and nervous systems during fetal and childhood growth. It facilitates bone mineral turnover and regulates protein synthesis in developing tissues, contributing significantly to overall growth and...
TH is indispensable for the normal development and maturation of the skeletal, muscular, and nervous systems during fetal and childhood growth. It facilitates bone mineral turnover and regulates protein synthesis in developing tissues, contributing significantly to overall growth and...
3.2K
GPCRs Regulate Adenylyl Cylase Activity
5.9K
Some GPCRs transmit signals through adenylyl cyclase (AC), a transmembrane enzyme. AC helps synthesize second messenger cyclic adenosine monophosphate (cAMP). AC catalyzes cyclization reaction and converts ATP to cAMP by releasing a pyrophosphate. The pyrophosphate is further hydrolyzed to phosphate by the enzyme pyrophosphatase, which drives cAMP synthesis to completion. However, cAMP is rapidly degraded to 5′ AMP by the enzymes phosphodiesterase (PDE), preventing overstimulation of...
5.9K
The Thyroid Gland
4.4K
The thyroid gland is a small, butterfly-shaped gland located in the neck and covers the anterior surface of the trachea. The gland has two lateral lobes connected by a thin tissue mass called the isthmus. Internally, each lobe comprises many small spherical structures known as thyroid follicles, surrounded by a network of blood vessels.
The follicles have a central cavity lined by simple cuboidal to squamous epithelial cells called follicular cells. These cells produce the glycoprotein...
The follicles have a central cavity lined by simple cuboidal to squamous epithelial cells called follicular cells. These cells produce the glycoprotein...
4.4K
TGF - β Signaling Pathway
7.7K
The TGF-β signaling pathway regulates cell growth, differentiation, adhesion, motility, and development. TGF-β ligands that induce TGF-β signaling are synthesized in their latent form. Several proteases or cell surface receptors such as integrins act upon the latent form, releasing the active ligand. There are three types of mammalian TGF-βs: (TGF-β1, TGF-β2, and TGF-β3) that bind as homodimers or heterodimers to TGF-β receptors. The TGF-β receptors...
7.7K
Adrenergic Antagonists: Chemistry and Classification of β-Receptor Blockers
770
β-adrenergic antagonists, or β-blockers, modulate the sympathetic nervous system by targeting β-adrenoceptors and inhibiting catecholamine-mediated sympathetic responses. β-blockers differ in their adrenoceptor subtype affinity, lipophilicity, and α-blocking capabilities. The history of β-blocker development began with the prototype, dichloroisoprenaline, which exhibited partial agonist activity. As a result, propranolol was developed as a pure antagonist but...
770


