Antioxidant and Antibacterial Activity of Sulfonamides Derived from Carvacrol: A Structure-Activity Relationship Study

被引:5
|
作者
de Oliveira, Aldo S. [1 ]
de Souza, Luiz F. S. [2 ]
Nunes, Ricardo J. [2 ]
Johann, Susana [3 ]
Palomino-Salcedo, David L. [4 ]
Ferreira, Leonardo L. G. [4 ]
Andricopulo, Adriano D. [4 ]
机构
[1] Fed Univ Santa Catarina UFSC, Dept Exact Sci & Educ, Blumenau, SC, Brazil
[2] Fed Univ Santa Catarina UFSC, Dept Chem, Florianopolis, SC, Brazil
[3] Univ Fed Minas Gerais, UFMG, Dept Microbiol, Belo Horizonte, MG, Brazil
[4] Univ Sao Paulo, Lab Med & Computat Chem, Ctr Res & Innovat Biodivers & Drug Discovery, Inst Phys Sao Carlos, Sao Carlos, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
Carvacrol; Sulfonamides; Bacterial resistance; S; aureus; E; coli; Antioxidant; ANTIMICROBIAL RESISTANCE; HYDRAZONE;
D O I
10.2174/1568026619666191127144336
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Background: Bacterial resistance to antibiotics is a growing problem in all countries and has been discussed worldwide. In this sense, the development of new drugs with antibiotic properties is highly desirable in the context of medicinal chemistry. Methodology: In this paper we investigate the antioxidant and antibacterial potential of sulfonamides derived from carvacrol, a small molecule with drug-like properties. Most sulfonamides had antioxidant and antibacterial potential, especially compound S-6, derived from beta-naphthylamine. Results: To understand the possible mechanisms of action involved in biological activity, the experimental results were compared with molecular docking data. Conclusion: This research allows appropriate discussion on the identified structure activity relationships.
引用
收藏
页码:173 / 181
页数:9
相关论文
共 50 条
  • [41] Antioxidant Structure-Activity Relationship Analysis of Five Dihydrochalcones
    Li, Xican
    Chen, Ban
    Xie, Hong
    He, Yuhua
    Zhong, Dewei
    Chen, Dongfeng
    MOLECULES, 2018, 23 (05):
  • [42] Structure-activity study of the antibacterial peptide fallaxin
    Nielsen, Sandra L.
    Frimodt-Moller, Niels
    Kragelund, Birthe B.
    Hansen, Paul R.
    PROTEIN SCIENCE, 2007, 16 (09) : 1969 - 1976
  • [43] Structure-activity relationship study on histone deacetylase (HDAC) inhibitors derived from Santacruzamate
    Hogle, Emily
    Onate, Alma
    Tucker, Janelle
    Leduc, Rachel
    Thuy Do
    Klein, Reid
    Thowfeik, Fathima
    Merino, Edward
    Ma, Lili
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2016, 251
  • [44] Anticonvulsant activity of phenylmethylenehydantoins: A structure-activity relationship study
    Thenmozhiyal, JC
    Wong, PTH
    Chui, WK
    JOURNAL OF MEDICINAL CHEMISTRY, 2004, 47 (06) : 1527 - 1535
  • [45] A structure-activity relationship study of compounds with antihistamine activity
    Brzezinska, Elzbieta
    Koska, Grazyna
    BIOMEDICAL CHROMATOGRAPHY, 2006, 20 (10) : 1004 - 1016
  • [46] Structure-activity relationship (SAR) and antibacterial activity of pyrrolidine based hybrids: A review
    Bhat, Aeyaz Ahmad
    Tandon, Nitin
    Singh, Iqubal
    Tandon, Runjhun
    JOURNAL OF MOLECULAR STRUCTURE, 2023, 1283
  • [47] Structure-activity relationship study of anoplin
    Ifrah, D
    Doisy, X
    Ryge, TS
    Hansen, PR
    JOURNAL OF PEPTIDE SCIENCE, 2005, 11 (02) : 113 - 121
  • [48] Structure-activity relationship study of myriaporones
    Roy, Myriam
    Taylor, Richard E.
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2007, 233
  • [49] Antibacterial activity of resveratrol structural analogues: A mechanistic evaluation of the structure-activity relationship
    Singh, Deepti
    Mendonsa, Rebecca
    Koli, Mrunesh
    Subramanian, Mahesh
    Nayak, Sandip Kumar
    TOXICOLOGY AND APPLIED PHARMACOLOGY, 2019, 367 : 23 - 32
  • [50] Amphiphilic cyclodextrin derivatives with antibacterial activity: chemical mutation and structure-activity relationship
    Yamamura, Hatsuo
    Kato, Ayame
    Yamada, Eri
    Kato, Hisato
    Katsu, Takashi
    Masuda, Kazufumi
    Osawa, Kayo
    Miyagawa, Atsushi
    NEW JOURNAL OF CHEMISTRY, 2024, 48 (27) : 12355 - 12361