Journal of Biomolecular Structure and Dynamics, ( ISI ), Volume (38), No (13), Year (2020-8) , Pages (1-15)

Title : ( Exploring 3-Hydroxyflavone Scaffolds as Mushroom Tyrosinase Inhibitors: Synthesis, X-Ray Crystallography, Antimicrobial, Fluorescence Behaviour, Structure-Activity Relationship and Molecular Modelling Studies )

Authors: Jamshaid Ashraf , Ehsan Ullah Mughal , Amina Sadiq , Maryam Bibi , Nafeesa Naeem , Anser Ali , Anam Massadaq , Nighat Fatima , Asif Javid , Muhammad Naveed Zafar , Bilal Ahmad Khan , Muhammad Faizan Nazar , Amara Mumtaz , Muhammad Nawaz Tahir , Masoud Mirzaei Shahrabi ,

Citation: BibTeX | EndNote

Abstract

To explore new scaffolds as tyrosinase enzyme inhibitors remain an interesting goal in the drug discovery and development. In due course and our approach to synthesize bioactive compounds, a series of varyingly substituted 3-hydroxyflavone derivatives (1-23) were synthesized in one-pot reaction and screened for in vitro against mushroom tyrosinase enzyme.The structures of newly synthesized compounds were unambiguously corroborated by usual spectroscopic techniques (FTIR, UV-Vis, 1H-, 13C-NMR) and mass spectrometry (EI-MS). The structure of compound 15 was also characterized by X-ray diffraction analysis. Furthermore, the synthesized compounds (1-23) were evaluated for their antimicrobial potential. Biological studies exhibit pretty good activity against most of the bacterial-fungal strains and their activity is comparable to those of commercially available antibiotics i.e. Cefixime and Clotrimazole.Amongst the series, the compounds 2, 4, 5, 6, 7, 10, 11, 14 and 22 exhibited excellent inhibitory activity against tyrosinase, even better than standard compound. Remarkably, the compound 2 (IC50 = 0.280±0.010 μg/ml) was found almost sixfold and derivative 5 (IC50 = 0.230±0.020 μg/ml) about sevenfold more active as compared to standard Kojic acid (IC50 =1.79±0.6 μg/ml). Moreover, these synthetic compounds (1-23) displayed good to moderate activities against tested bacterial and fungal strains. Their emission behavior was also investigated in order to know their potential as fluorescent probes. The molecular modelling simulations were also performed to explore their binding interactions with active sites of the tyrosinase enzyme.Limited structure-activity relationship was established to design and develop new tyrosinase inhibitors by employing 2-arylchromone as a structural core in the future.

Keywords

, 3, Hydroxyflavones; Algar, Flynn, Oyamada reaction; Antibacterial; Antifungal; Tyrosinase enzyme inhibition; Molecular docking studies.
برای دانلود از شناسه و رمز عبور پرتال پویا استفاده کنید.

@article{paperid:1080607,
author = {جمشید اشرف and احسان اولاه موغال and آمینا صدیق and مریم بی بی and نفیسا نعیم and انصر علی and آنام مصادق and نیقات فاطیما and آصف جاوید and محمد نوید ظفر and بلال احمدخان and محمد فیضان نظر and امارا ممتاز and محمد نواز طاهر and Mirzaei Shahrabi, Masoud},
title = {Exploring 3-Hydroxyflavone Scaffolds as Mushroom Tyrosinase Inhibitors: Synthesis, X-Ray Crystallography, Antimicrobial, Fluorescence Behaviour, Structure-Activity Relationship and Molecular Modelling Studies},
journal = {Journal of Biomolecular Structure and Dynamics},
year = {2020},
volume = {38},
number = {13},
month = {August},
issn = {0739-1102},
pages = {1--15},
numpages = {14},
keywords = {3-Hydroxyflavones; Algar-Flynn-Oyamada reaction; Antibacterial; Antifungal; Tyrosinase enzyme inhibition; Molecular docking studies.},
}

[Download]

%0 Journal Article
%T Exploring 3-Hydroxyflavone Scaffolds as Mushroom Tyrosinase Inhibitors: Synthesis, X-Ray Crystallography, Antimicrobial, Fluorescence Behaviour, Structure-Activity Relationship and Molecular Modelling Studies
%A جمشید اشرف
%A احسان اولاه موغال
%A آمینا صدیق
%A مریم بی بی
%A نفیسا نعیم
%A انصر علی
%A آنام مصادق
%A نیقات فاطیما
%A آصف جاوید
%A محمد نوید ظفر
%A بلال احمدخان
%A محمد فیضان نظر
%A امارا ممتاز
%A محمد نواز طاهر
%A Mirzaei Shahrabi, Masoud
%J Journal of Biomolecular Structure and Dynamics
%@ 0739-1102
%D 2020

[Download]