Drug screening of rhodanine derivatives for antibacterial activity

被引:45
作者
Maddila, Suresh [1 ,2 ]
Gorle, Sridevi [3 ]
Jonnalagadda, Sreekantha B. [1 ]
机构
[1] Univ KwaZulu Natal, Sch Chem & Phys, Westville Campus,Private Bag 54001, ZA-4000 Durban, South Africa
[2] GITAM Univ, GITAM Inst Sci, Dept Chem, Visakhapatnam, Andhra Pradesh, India
[3] GITAM Univ, GITAM Inst Sci, Dept Microbiol & Food Sci & Technol, Visakhapatnam, Andhra Pradesh, India
关键词
Rhodanine; anti-bacterial activity; multi drug-resistance; structure-activity relationship; drug discovery; ACID-DERIVATIVES; ANTIMICROBIAL ACTIVITY; BIOLOGICAL EVALUATION; IN-VITRO; INHIBITORY-ACTIVITIES; BACTERIAL-INFECTIONS; PRIVILEGED SCAFFOLD; ANTIFUNGAL ACTIVITY; DESIGN; DYES;
D O I
10.1080/17460441.2020.1696768
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Bacteriological infections are a major risk to human health. These include all hospital and public-acquired infections. In drug discovery, rhodanines are privileged heterocyclic frameworks. Their derivatives possess strong anti-bacterial activity and some of them have shown potent activity against multidrug-resistant pathogens, both under in vitro and in vivo conditions. To treat multi-drug resistant pathogens, the development of novel potent drugs, with superior anti-bacterial efficacy, is paramount. One avenue which shows promise is the design and development of novel rhodanines. Areas covered: This review summarizes the status on rhodanine-based derivatives and their anti-bacterial activity, based on published research over the past six years. Furthermore, to facilitate the design of novel derivatives with improved functions, their structure-activity relationships are assessed with reference to their efficacy as anti-bacterial agents and their toxicity. Expert opinion: The pharmacological activity of molecules bearing a rhodanine scaffold needs to be very critically assessed in spite of considerable information available from various biological evaluations. Although, some data on structure-activity relationship frameworks is available, information is not adequate to optimize the efficacy of rhodanine derivatives for different applications.
引用
收藏
页码:203 / 229
页数:27
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