A discovery of potent kaempferol derivatives as multi-target medicines against diabetes as well as bacterial infections: an <i>in silico</i> approach-Reference-Cited by-同舟云学术

A discovery of potent kaempferol derivatives as multi-target medicines against diabetes as well as bacterial infections: an in silico approach

Published:2024-02-09 Issue: Volume: Page:1-23
ISSN:0739-1102
Container-title:Journal of Biomolecular Structure and Dynamics
language:en
Short-container-title:Journal of Biomolecular Structure and Dynamics

Author:

Parveen Shagufta¹,Shehzadi Saman¹,Shafiq Nusrat¹,Rashid Maryam¹,Naz Sadaf²,Mehmood Tahir³,Riaz Rabia¹,S. Almaary Khalid⁴,Nafidi Hiba-Allah⁵,Bourhia Mohammed⁶

Affiliation:

1. Synthetic and Natural Product Drug Discovery Laboratory, Department of Chemistry, Government College Women University, Faisalabad, Pakistan

2. Department of Chemistry, The University of Lahore, Lahore, Pakistan

3. Centre for Applied Molecular Biology (CAMB), University of the Punjab, Punjab, Pakistan

4. Department of Botany and Microbiology, College of Science, King Saud University, Riyadh, Saudi Arabia

5. Department of Food Science, Faculty of Agricultural and Food Sciences, Laval University, Quebec, QC, Canada

6. Department of Chemistry and Biochemistry, Faculty of Medicine and Pharmacy, Ibn Zohr University, Laayoune, Morocco

Funder

Pakistan Science Foundation

King Saud University, Riyadh, Saudi Arabia

Publisher

Informa UK Limited

Link

https://www.tandfonline.com/doi/pdf/10.1080/07391102.2024.2308773

Reference107 articles.

1. Quantum computational studies, spectroscopic (FT-IR, FT-Raman and UV–Vis) profiling, natural hybrid orbital and molecular docking analysis on 2,4 Dibromoaniline

2. Density functional theory investigation of the physical properties of dicyano pyridazine molecules;Ajeel F. N.;International Journal of Science and Research,,2015

3. Tackling Virulence of Pseudomonas aeruginosa by the Natural Furanone Sotolon

4. The Flavonoid Kaempferol Ameliorates Streptozotocin-Induced Diabetes by Suppressing Hepatic Glucose Production

5. Genetic programming for computational pharmacokinetics in drug discovery and development