ningnanmycin and antofine

ningnanmycin has been researched along with antofine* in 2 studies

Other Studies

2 other study(ies) available for ningnanmycin and antofine

ArticleYear
New Strategies and Methods to Study Interactions between Tobacco Mosaic Virus Coat Protein and Its Inhibitors.
    International journal of molecular sciences, 2016, Feb-26, Volume: 17, Issue:3

    Studies of the targets of anti-viral compounds are hot topics in the field of pesticide research. Various efficient anti-TMV (Tobacco Mosaic Virus) compounds, such as Ningnanmycin (NNM), Antofine (ATF), Dufulin (DFL) and Bingqingxiao (BQX) are available. However, the mechanisms of the action of these compounds on targets remain unclear. To further study the mechanism of the action of the anti-TMV inhibitors, the TMV coat protein (TMV CP) was expressed and self-assembled into four-layer aggregate disks in vitro, which could be reassembled into infectious virus particles with TMV RNA. The interactions between the anti-TMV compounds and the TMV CP disk were analyzed by size exclusion chromatography, isothermal titration calorimetry and native-polyacrylamide gel electrophoresis methods. The results revealed that assembly of the four-layer aggregate disk was inhibited by NNM; it changed the four-layer aggregate disk into trimers, and affected the regular assembly of TMV CP and TMV RNA. The four-layer aggregate disk of TMV CP was little inhibited by ATF, DFL and BQX. Our results provide original data, as well as new strategies and methods, for research on the mechanism of action of anti-viral drugs.

    Topics: Amino Acid Sequence; Antiviral Agents; Benzothiazoles; Capsid Proteins; Cytidine; Indoles; Molecular Sequence Data; Phenanthrolines; Protein Binding; Tobacco Mosaic Virus

2016
Synthesis and antiviral activities of antofine analogues with different C-6 substituent groups.
    Journal of agricultural and food chemistry, 2013, Feb-06, Volume: 61, Issue:5

    On the basis of previous structure-activity relationship (SAR) and antiviral mechanism studies, antofine analogues with different substituent groups at the C-6 position targeting tobacco mosaic virus (TMV) RNA were synthesized for the first time. The antofine analogues 1a-8a and 1b-9b were evaluated for their antiviral activity against TMV. The SAR study of antofine analogues is discussed. Most of the compounds were found to exhibit higher antiviral activity than commercial Ningnanmycin in vitro and in vivo. The groups with hydrogen donor or electron-withdrawing groups at the C-6 position were found to be favorable for antiviral activity.

    Topics: Antiviral Agents; Indoles; Magnetic Resonance Spectroscopy; Phenanthrolines; RNA, Viral; Structure-Activity Relationship; Tobacco Mosaic Virus

2013