首页> 外文OA文献 >Epinecidin-1, an Antimicrobial Peptide Derived From Grouper (Epinephelus coioides): Pharmacological Activities and Applications
【2h】

Epinecidin-1, an Antimicrobial Peptide Derived From Grouper (Epinephelus coioides): Pharmacological Activities and Applications

机译:Epinecidin-1,衍生自Grouper(Epinephelus Coioides)的抗微生物肽:药理学活动和应用

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Epinecidin-1 is an antimicrobial peptide derived from the orange-spotted grouper (Epinephelus coioides). The mature epinecidin-1 peptide is predicted to have an amphipathic α-helical structure and a non-helical hydrophilic domain at the C-terminal RRRH. The majority of work studying the potential pharmacological activities of epinecidin-1, utilize synthesized epinecidin-1 (Epi-1), which is made up of 21 amino acids, from the amino acid sequence of 22–42 residues of Epi-1—GFIFHIIKGLFHAGKMIHGLV. The synthetized Epi-1 peptide has been demonstrated to possess diverse pharmacological activities, including antimicrobial, immunomodulatory, anticancer, and wound healing properties. It has also been utilized in different clinical and agricultural fields, including topical applications in wound healing therapy as well as the enhancement of fish immunity in aquaculture. Hence, the present work aims to consolidate the current knowledge and findings on the characteristics and pharmacological properties of epinecidin-1 and its potential applications.
机译:Epinecidin-1是衍生自橙色斑点的石斑鱼(Epinephelus Coioides)的抗微生物肽。预计成熟的环保式素-1肽在C末端RRRH处具有两亲性α-螺旋结构和非螺旋亲水结构域。研究Epinecidin-1的潜在药理活性的大多数作品利用合成的Edececidin-1(EPI-1),其由21个氨基酸组成,来自EPI-1-Gfifhiikglfhagkmihglv的22-42个残基的氨基酸序列。已证明合成的EPI-1肽具有不同的药理学活性,包括抗微生物,免疫调节,抗癌和伤口愈合性能。它还已被用于不同的临床和农业领域,包括伤口愈合治疗的局部应用以及水产养殖中鱼免疫的增强。因此,本工作旨在巩固目前关于Epinecidin-1及其潜在应用的特征和药理学性质的知识和结果。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号