中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Design, synthesis, and antibacterial evaluation of vancomycin-LPS binding peptide conjugates

文献类型:期刊论文

作者Shi, Weiwei1,2; Chen, Feifei1,2; Zou, Xiangman1,3; Jiao, Shang1,2; Wang, Siqi1,2; Hu, Yu1,4; Lan, Lefu1,2; Tang, Feng1,2; Huang, Wei1,2,5
刊名BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
出版日期2021-08-01
卷号45页码:8
关键词Vancomycin analogues LPS binding peptides Vancomycin-Peptide Conjugates Antibacterial activity
ISSN号0960-894X
DOI10.1016/j.bmcl.2021.128122
通讯作者Lan, Lefu(llan@simm.ac.cn) ; Tang, Feng(tangfeng2013@simm.ac.cn) ; Huang, Wei(haungwei@simm.ac.cn)
英文摘要Developing novel antibiotics is urgently needed with emergency of drug resistance. Vancomycin, the last resort for intractable Gram-positive bacterial infections, is ineffective against Gram-negative bacteria and vancomycin resistant bacteria. Herein, we report a series of novel vancomycin derivatives carrying LPS binding peptides, vancomycin-LPS binding peptide conjugates (VPCs). The LPS binding peptides were conjugated onto 4 sites of vancomycin via CuAAC or maleimide- sulfydryl addition, and the formed VPCs were screened against VISA/VRE and Gram-negative strains. VPCs exhibited enhanced activity against vancomycin resistant bacteria and obtained the activity against Gram-negative bacteria in vitro, providing a novel strategy for vancomycin modification and glycopeptide antibiotics synthesis.
WOS关键词ANTIBIOTICS ; DETOXIFICATION ; MECHANISMS ; ANALOGS ; SITE
资助项目National Natural Science Foundation of China (NNSFC)[21877116] ; SIMM institute fund[CASIMM0120202009] ; Shanghai Action Plan of Technological Innovation[18431900700] ; National Megaproject for Innovative Drugs[2019ZX09721001004009]
WOS研究方向Pharmacology & Pharmacy ; Chemistry
语种英语
WOS记录号WOS:000661400500013
出版者PERGAMON-ELSEVIER SCIENCE LTD
源URL[http://119.78.100.183/handle/2S10ELR8/297178]  
专题中国科学院上海药物研究所
通讯作者Lan, Lefu; Tang, Feng; Huang, Wei
作者单位1.Chinese Acad Sci, Shanghai Inst Mat Med, Ctr Biotherapeut Discovery Res, CAS Ctr Excellence Mol Cell Sci,CAS key Lab Recep, 555 Zuchongzhi Rd,Pudong, Shanghai 201203, Peoples R China
2.Univ Chinese Acad Sci, 19A Yuquan Rd, Beijing 100049, Peoples R China
3.Univ South China, Hunan Prov Key Lab Tumor Microenvironm Response, Hunan Prov Cooperat Innovat Ctr Mol Target New Dr, Inst Pharm & Pharmacol, Hengyang 421001, Hunan, Peoples R China
4.Jinzhou Med Univ, Sch Pharm, Jinzhou 121001, Peoples R China
5.Univ Chinese Acad Sci, Hangzhou Inst Adv Study, Sch Pharmaceut Sci & Technol, Hangzhou 310024, Peoples R China
推荐引用方式
GB/T 7714
Shi, Weiwei,Chen, Feifei,Zou, Xiangman,et al. Design, synthesis, and antibacterial evaluation of vancomycin-LPS binding peptide conjugates[J]. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS,2021,45:8.
APA Shi, Weiwei.,Chen, Feifei.,Zou, Xiangman.,Jiao, Shang.,Wang, Siqi.,...&Huang, Wei.(2021).Design, synthesis, and antibacterial evaluation of vancomycin-LPS binding peptide conjugates.BIOORGANIC & MEDICINAL CHEMISTRY LETTERS,45,8.
MLA Shi, Weiwei,et al."Design, synthesis, and antibacterial evaluation of vancomycin-LPS binding peptide conjugates".BIOORGANIC & MEDICINAL CHEMISTRY LETTERS 45(2021):8.

入库方式: OAI收割

来源:上海药物研究所

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