دورية أكاديمية
Introduction of pyrrolidineoxy or piperidineamino group at the 4-position of quinazoline leading to novel quinazoline-based phosphoinositide 3-kinase delta (PI3Kδ) inhibitors
العنوان: | Introduction of pyrrolidineoxy or piperidineamino group at the 4-position of quinazoline leading to novel quinazoline-based phosphoinositide 3-kinase delta (PI3Kδ) inhibitors |
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المؤلفون: | Minhang Xin, Weiming Duan, Yifan Feng, Yuan-Yuan Hei, Hao Zhang, Ying Shen, Hong-Yi Zhao, Shuai Mao, San-Qi Zhang |
المصدر: | Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 33, Iss 1, Pp 651-656 (2018) |
بيانات النشر: | Taylor & Francis Group, 2018. |
سنة النشر: | 2018 |
المجموعة: | LCC:Therapeutics. Pharmacology |
مصطلحات موضوعية: | PI3Kδ inhibitors, 4-pyrrolidineoxy, 4-piperidineamino, selectivity, anti-proliferation, Therapeutics. Pharmacology, RM1-950 |
الوصف: | Phosphoinositide 3-kinase Delta (PI3Kδ) plays a key role in B-cell signal transduction and inhibition of PI3Kδ was confirmed to have clinical benefit in certain types of activation of B-cell malignancies. Herein, we reported a novel series of 4-pyrrolidineoxy or 4-piperidineamino substituted quinazolines, showing potent PI3Kδ inhibitory activities. Among these compounds, 12d, 14b and 14c demonstrated higher potency against PI3Kδ with the half maximal inhibitory concentration (IC50) values of 4.5, 3.0, and 3.9 nM, respectively, which were comparable to idelalisib (IC50 = 2.7 nM). The further PI3K isoforms selectivity evaluation showed that compounds 12d, 14b and 14c have excellent PI3Kδ selectivity over PI3Kα, PI3Kβ, and PI3Kγ. Moreover, compounds 12d, 14b and 14c also displayed different anti-proliferative profiles against a panel of four human B cell lines including Ramos, Raji, RPMI-8226, and SU-DHL-6. The molecular docking simulation indicated several key hydrogen bonding interactions were formed. This study suggests the introduction of pyrrolidineoxy or piperidineamino groups into the 4-position of quinazoline leads to new potent and selective PI3Kδ inhibitors. |
نوع الوثيقة: | article |
وصف الملف: | electronic resource |
اللغة: | English |
تدمد: | 1475-6366 1475-6374 14756366 |
Relation: | https://doaj.org/toc/1475-6366; https://doaj.org/toc/1475-6374 |
DOI: | 10.1080/14756366.2018.1444608 |
URL الوصول: | https://doaj.org/article/a6de2c5a67fe4ee1805a686eb1048be3 |
رقم الأكسشن: | edsdoj.6de2c5a67fe4ee1805a686eb1048be3 |
قاعدة البيانات: | Directory of Open Access Journals |
تدمد: | 14756366 14756374 |
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DOI: | 10.1080/14756366.2018.1444608 |