دورية أكاديمية
New horizons in drug discovery of lymphocyte-specific protein tyrosine kinase (Lck) inhibitors: a decade review (2011–2021) focussing on structure–activity relationship (SAR) and docking insights
العنوان: | New horizons in drug discovery of lymphocyte-specific protein tyrosine kinase (Lck) inhibitors: a decade review (2011–2021) focussing on structure–activity relationship (SAR) and docking insights |
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المؤلفون: | Ahmed Elkamhawy, Eslam M. H. Ali, Kyeong Lee |
المصدر: | Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 36, Iss 1, Pp 1572-1600 (2021) |
بيانات النشر: | Taylor & Francis Group, 2021. |
سنة النشر: | 2021 |
المجموعة: | LCC:Therapeutics. Pharmacology |
مصطلحات موضوعية: | lck inhibitors, structure-activity relationship (sar), src family kinase, lymphocyte-specific protein tyrosine kinase (lck), molecular modelling, Therapeutics. Pharmacology, RM1-950 |
الوصف: | Lymphocyte-specific protein tyrosine kinase (Lck), a non-receptor Src family kinase, has a vital role in various cellular processes such as cell cycle control, cell adhesion, motility, proliferation, and differentiation. Lck is reported as a key factor regulating the functions of T-cell including the initiation of TCR signalling, T-cell development, in addition to T-cell homeostasis. Alteration in expression and activity of Lck results in numerous disorders such as cancer, asthma, diabetes, rheumatoid arthritis, atherosclerosis, and neuronal diseases. Accordingly, Lck has emerged as a novel target against different diseases. Herein, we amass the research efforts in literature and pharmaceutical patents during the last decade to develop new Lck inhibitors. Additionally, structure-activity relationship studies (SAR) and docking models of these new inhibitors within the active site of Lck were demonstrated offering deep insights into their different binding modes in a step towards the identification of more potent, selective, and safe Lck 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: | 10.1080/14756366.2021.1937143 |
URL الوصول: | https://doaj.org/article/d6a27ac3eecf47fda47655e77608feac |
رقم الأكسشن: | edsdoj.6a27ac3eecf47fda47655e77608feac |
قاعدة البيانات: | Directory of Open Access Journals |
تدمد: | 14756366 14756374 |
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DOI: | 10.1080/14756366.2021.1937143 |