Antiviral Potential of Selected N-Methyl-N-phenyl Dithiocarbamate Complexes against Human Immunodeficiency Virus (HIV)

被引:7
|
作者
Mufhandu, Hazel T. T. [1 ]
Obisesan, Oluwafemi S. S. [1 ]
Ajiboye, Timothy O. O. [2 ]
Mhlanga, Sabelo D. D. [2 ]
Onwudiwe, Damian C. C. [3 ,4 ]
机构
[1] North West Univ, Fac Nat & Agr Sci, Sch Biol Sci, Dept Microbiol, Mafikeng Campus,Private Bag X2046, ZA-2735 Mmabatho, South Africa
[2] Nelson Mandela Univ, Chem Dept, Univ Way, ZA-6019 Gqeberha, South Africa
[3] North West Univ, Fac Nat & Agr Sci, Mat Sci Innovat & Modelling MaSIM Res Focus Area, Mafikeng Campus,Private Bag X2046, ZA-2735 Mmabatho, South Africa
[4] North West Univ, Fac Nat & Agr Sci, Sch Phys & Chem Sci, Dept Chem, Mafikeng Campus,Private Bag X2046, ZA-2735 Mmabatho, South Africa
基金
新加坡国家研究基金会;
关键词
dithiocarbamate complexes; human immunodeficiency virus; cytotoxicity; antiviral efficacy; pseudovirus; inorganic compounds; HG(II) COMPLEXES; NANOPARTICLES; CD(II); DESIGN; ZN(II); RNA;
D O I
10.3390/microbiolres14010028
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Despite the use of highly active antiretroviral therapy approved by the United States Food and Drug Administration (FDA) for the treatment of human immunodeficiency virus (HIV) infection, HIV remains a public health concern due to the inability of the treatment to eradicate the virus. In this study, N-methyl-N-phenyl dithiocarbamate complexes of indium(III), bismuth(III), antimony(III), silver(I), and copper(II) were synthesized. The complexes were characterized by thermal gravimetric analysis (TGA), differential scanning calorimetry (DSC), and Fourier transform infrared spectroscopy (FTIR). The N-methyl-N-phenyl dithiocarbamate complexes were then evaluated for their antiviral effects against HIV-1 subtypes A (Q168), B (QHO.168), and C (CAP210 and ZM53). The results showed that the copper(II)-bis (N-methyl-N-phenyl dithiocarbamate) complex had a neutralization efficiency of 94% for CAP210, 54% for ZM53, 45% for Q168, and 63% for QHO.168. The silver(I)-bis (N-methyl-N-phenyl dithiocarbamate) complex showed minimal neutralization efficiency against HIV, while indium(III) and antimony(III) N-methyl-N-phenyl dithiocarbamate complexes had no antiviral activity against HIV-1. The findings revealed that copper(II)-bis (N-methyl-N-phenyl dithiocarbamate), with further improvement, could be explored as an alternative entry inhibitor for HIV.
引用
收藏
页码:355 / 370
页数:16
相关论文
共 50 条
  • [31] DESIGN OF A 4-HELIX-BUNDLE PROTEIN AS A POTENTIAL VACCINE AGAINST HUMAN-IMMUNODEFICIENCY-VIRUS (HIV-1)
    EROSHKIN, AM
    ZHILKIN, PA
    SHAMIN, VV
    MOLECULAR BIOLOGY, 1993, 27 (03) : 321 - 329
  • [32] Potential Antiviral Activity of Lactiplantibacillus plantarum KAU007 against Influenza Virus H1N1
    Rather, Irfan A.
    Kamli, Majid Rasool
    Sabir, Jamal S. M.
    Paray, Bilal Ahmad
    VACCINES, 2022, 10 (03)
  • [33] Polyanionic N-donor ligands as chelating agents in transition metal complexes: synthesis, structural characterization and antiviral properties against HIV
    Garcia-Gallego, Sandra
    Sanchez Rodriguez, Javier
    Luis Jimenez, Jose
    Cangiotti, Michela
    Ottaviani, Maria Francesca
    Angeles Munoz-Fernandez, M.
    Gomez, Rafael
    Javier de la Mata, F.
    DALTON TRANSACTIONS, 2012, 41 (21) : 6488 - 6499
  • [34] Antiviral activity of diterpenes isolated from the Brazilian marine alga Dictyota menstrualis against human immunodeficiency virus type 1 (HIV-1)
    Pereira, HS
    Leao-Ferreira, LR
    Moussatché, N
    Teixeira, VL
    Cavalcanti, DN
    Costa, LJ
    Diaz, R
    Frugulhetti, ICPP
    ANTIVIRAL RESEARCH, 2004, 64 (01) : 69 - 76
  • [35] Identification of potential antiviral compounds from Egyptian sea stars against seasonal influenza A/H1N1 virus
    Okasha, Nadia I.
    Rahman, Mohamed Abdel
    Nafie, Mohammed S.
    Shama, Noura M. Abo
    Mostafa, Ahmed
    El-Ebeedy, Dalia A.
    Azeiz, Ahmed Z. Abdel
    JOURNAL OF GENETIC ENGINEERING AND BIOTECHNOLOGY, 2024, 22 (01):
  • [36] Human immunodeficiency virus (HIV) subtype surveillance of African-born persons at risk for group O and group N HIV infections in the United States
    Sullivan, PS
    Do, AN
    Ellenberger, D
    Pau, CP
    Paul, S
    Robbins, K
    Kalish, M
    Storck, C
    Schable, CA
    Wise, H
    Tetteh, C
    Jones, JL
    McFarland, J
    Yang, CF
    Lal, RB
    Ward, JW
    JOURNAL OF INFECTIOUS DISEASES, 2000, 181 (02): : 463 - 469
  • [37] Potential antiviral activity of rhamnocitrin against influenza virus H3N2 by inhibiting cGAS/STING pathway in vitro
    Chen, Zexing
    Wang, Wanqi
    Zeng, Kefeng
    Zhu, Jinyi
    Wang, Xinhua
    Huang, Wanyi
    SCIENTIFIC REPORTS, 2024, 14 (01):
  • [38] SYNTHESIS AND ANTIVIRAL ACTIVITY OF VARIOUS 3'-AZIDO ANALOGS OF PYRIMIDINE DEOXYRIBONUCLEOSIDES AGAINST HUMAN IMMUNODEFICIENCY VIRUS (HIV-1, HTLV-III-LAV)
    LIN, TS
    GUO, JY
    SCHINAZI, RF
    CHU, CK
    XIANG, JN
    PRUSOFF, WH
    JOURNAL OF MEDICINAL CHEMISTRY, 1988, 31 (02) : 336 - 340
  • [39] Mutation D30N is not preferentially selected by human immunodeficiency virus type I subtype C in the development of resistance to nelfinavir
    Grossman, Z
    Paxinos, EE
    Averbuch, D
    Maayan, S
    Parkin, NT
    Engelhard, D
    Lorber, M
    Istomin, V
    Shaked, Y
    Mendelson, E
    Ram, D
    Petropoulos, CJ
    Schapiro, JM
    ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2004, 48 (06) : 2159 - 2165
  • [40] Construction and enhanced cytotoxicity of a [Cyanovirin-N]-[Pseudomonas exotoxin] conjugate against human immunodeficiency virus-infected cells
    Mori, T
    Shoemaker, RH
    McMahon, JB
    Gulakowski, RJ
    Gustafson, KR
    Boyd, MR
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1997, 239 (03) : 884 - 888