Literature DB >> 36139935

Phytochemical Profiling, In Vitro Biological Activities, and In-Silico Studies of Ficus vasta Forssk.: An Unexplored Plant.

Hanan Y Aati1, Mariyam Anwar2, Jawaher Al-Qahtani1, Areej Al-Taweel1, Kashif-Ur-Rehman Khan2, Sultan Aati3, Faisal Usman4, Bilal Ahmad Ghalloo2, Hafiz Muhammad Asif5, Jafir Hussain Shirazi6, Aliza Abbasi2.   

Abstract

Ficus vasta Forssk. (Moraceae family) is an important medicinal plant that has not been previously investigated for its phytochemical and biological potential. Phytochemical screening, total bioactive content, and GCMS analysis were used to determine its phytoconstituents profile. Antioxidant, antibacterial, antifungal, anti-viral, cytotoxicity, thrombolytic, and enzyme inhibition activities were examined for biological evaluation. The plant extract exhibited the maximum total phenolic (89.47 ± 3.21 mg GAE/g) and total flavonoid contents (129.2 ± 4.14 mg QE/g), which may be related to the higher antioxidant potential of the extract. The extract showed strong α-amylase (IC50 5 ± 0.21 µg/mL) and α-glucosidase inhibition activity (IC50 5 ± 0.32 µg/mL). Significant results were observed in the case of antibacterial, antifungal, and anti-viral activities. The F. vasta extract inhibited the growth of HepG2 cells in a dose-dependent manner. The GCMS analysis of the extract provided the preliminary identification of 28 phytocompounds. In addition, the compounds identified by GCMS were subjected to in silico molecular docking analysis in order to identify any interactions between the compounds and enzymes (α-amylase and α-glucosidase). After that, the best-docked compounds were subjected to ADMET studies which provide information on pharmacokinetics, drug-likeness, physicochemical properties, and toxicity. The present study highlighted that the ethanol extract of F. vasta has antidiabetic, antimicrobial, anti-viral, and anti-cancer potentials that can be further explored for novel drug development.

Entities:  

Keywords:  ADMET; Ficus vasta; GCMS; HepG2 cell line; anti-viral; antibacterial; antifungal; molecular docking; thrombolytic

Year:  2022        PMID: 36139935     DOI: 10.3390/antibiotics11091155

Source DB:  PubMed          Journal:  Antibiotics (Basel)        ISSN: 2079-6382


  1 in total

1.  Metabolic Profiling by GC-MS, In Vitro Biological Potential, and In Silico Molecular Docking Studies of Verbena officinalis.

Authors:  Rabia Nisar; Saeed Ahmad; Kashif-Ur-Rehman Khan; Asmaa E Sherif; Fawaz Alasmari; Afaf F Almuqati; Chitchamai Ovatlarnporn; Mohsin Abbas Khan; Muhammad Umair; Huma Rao; Bilal Ahmad Ghalloo; Umair Khurshid; Rizwana Dilshad; Khaled S Nassar; Sameh A Korma
Journal:  Molecules       Date:  2022-10-08       Impact factor: 4.927

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.