Suppr超能文献

发现了能刺激激肽释放酶相关肽酶 3(KLK3)活性的化合物。

The discovery of compounds that stimulate the activity of kallikrein-related peptidase 3 (KLK3).

机构信息

School of Pharmacy, Pharmaceutical Chemistry, Faculty of Health Sciences, University of Eastern Finland, P.O. Box 1627, 70211 Kuopio, Finland.

出版信息

ChemMedChem. 2011 Dec 9;6(12):2170-8. doi: 10.1002/cmdc.201100349. Epub 2011 Sep 27.

Abstract

Kallikrein-related peptidase 3 (KLK3), also known as prostate-specific antigen (PSA), is the most useful biomarker for prostate cancer (PCa). KLK3 is suggested to play a role in regulating cancer growth through anti-angiogenic activity in vivo and in vitro. This feature, together with its specificity for prostate tissue, makes KLK3 an intriguing target for the design of new therapies for PCa. 3D pharmacophores for KLK3-stimulating compounds were generated based on peptides that bind specifically to KLK3 and increase its enzymatic activity. As a result of pharmacophore-based virtual screening, four small, drug-like compounds with affinity for KLK3 were discovered and validated by capillary differential scanning calorimetry. One of the compounds also stimulated the activity of KLK3, and is therefore the first published small molecule with such an activity.

摘要

激肽释放酶相关肽酶 3(KLK3),也称为前列腺特异性抗原(PSA),是前列腺癌(PCa)最有用的生物标志物。KLK3 被认为通过体内和体外的抗血管生成活性在调节癌症生长中发挥作用。这一特征,以及其对前列腺组织的特异性,使得 KLK3 成为设计用于治疗前列腺癌的新疗法的一个有趣靶点。基于特异性结合 KLK3 并增加其酶活性的肽,生成了用于 KLK3 刺激化合物的 3D 药效团。基于药效团的虚拟筛选,发现了四个对 KLK3 具有亲和力的小型类药物化合物,并通过毛细管差示扫描量热法进行了验证。其中一种化合物还能刺激 KLK3 的活性,因此是第一个具有这种活性的已发表小分子。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验