银屑病JAK/STATs通路潜在抑制剂植物化学物质的硅筛选

IF 1.6 4区 医学 Q4 BIOCHEMICAL RESEARCH METHODS
Lokendra Singh Rathor, Divya Sahu, Manju Singh, Deependra Singh
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引用次数: 0

摘要

皮肤是一个由不同层组成的动态组织,如角质层,角质层是角质细胞发育和皮肤自然变化的成熟部位。在牛皮癣中,角质形成细胞的自然发育受到干扰,有核角质形成细胞聚集在皮肤表皮,导致鳞状皮肤的出现,从而使患者在身体、社会和心理上都出现疾病。各种天然的、半合成的和合成的处理方法是可用的。然而,半合成或合成主要用于治疗对身体不同部位产生副作用的牛皮癣,这是危及生命的。银屑病中各种分子靶点如Janus激酶/信号转导和转录激活因子(JAK/STATs)、磷酸二酯酶4 (PDE4)、丝裂原活化蛋白激酶(MAPK)、血小板选择素(Pan selectin)、肿瘤坏死因子α (TNF-α)、白细胞介素-23 (IL-23)、白细胞介素-17 (IL-17)、酪氨酸激酶2 (Tyk2)等均出现上调。植物及其类黄酮类、生物碱类、树脂类、单宁类、糖苷类和萜类的生物活性化合物以外用、口服和生物形式用于治疗牛皮癣。利用计算方法,可以研究这些分子靶点的抑制作用,并可以识别潜在分子。本研究旨在寻找潜在的抑制分子位点的分子,并且比人工合成的分子更有效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
In Silico Screening of Phytochemicals as Potential Inhibitors of the JAK/STATs Pathway in Psoriasis.

The skin is a dynamic tissue that consists of different layers such as stratum corneum, the site for keratinocyte development and maturation for the natural changeover of skin. In psoriasis, this natural development of keratinocytes gets disturbed and aggregation of nucleated keratinocytes takes place in the epidermis of the skin, leading to the presence of scaly skin, which makes the patient physically, socially, and psychologically ill. Various natural, semisynthetic, and synthetic treatments are available. Still, semisynthetic or synthetic are mainly used to treat psoriasis with side effects on different parts of the body, which is life threatening. Various molecular target sites are getting upregulated such as Janus kinase/Signal transducer and activator of transcription (JAK/STATs), phosphodiesterase 4 (PDE4), mitogen-activated protein kinase (MAPK), platelet selectin (Pan Selectin), Tumor Necrosis Factor Alpha (TNF-α), Interleukin-23 (IL-23), Interleukin-17 (IL-17), and Tyrosine Kinase 2 (Tyk2) in psoriasis. Plants and their bioactive compounds of flavonoids, alkaloids, resins, tannins, glycosides, and terpenoids category are used in the treatment of psoriasis as topical, oral, and biological forms. Using a computational approach, the inhibition of these molecular targets can be studied and potential molecules can be identified. This research article aims to find out the potential molecules that can inhibit the molecular sites and are effective than synthetic ones.

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来源期刊
Assay and drug development technologies
Assay and drug development technologies 医学-生化研究方法
CiteScore
3.60
自引率
0.00%
发文量
33
审稿时长
>12 weeks
期刊介绍: ASSAY and Drug Development Technologies provides access to novel techniques and robust tools that enable critical advances in early-stage screening. This research published in the Journal leads to important therapeutics and platforms for drug discovery and development. This reputable peer-reviewed journal features original papers application-oriented technology reviews, topical issues on novel and burgeoning areas of research, and reports in methodology and technology application. ASSAY and Drug Development Technologies coverage includes: -Assay design, target development, and high-throughput technologies- Hit to Lead optimization and medicinal chemistry through preclinical candidate selection- Lab automation, sample management, bioinformatics, data mining, virtual screening, and data analysis- Approaches to assays configured for gene families, inherited, and infectious diseases- Assays and strategies for adapting model organisms to drug discovery- The use of stem cells as models of disease- Translation of phenotypic outputs to target identification- Exploration and mechanistic studies of the technical basis for assay and screening artifacts
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