Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Amina Sadiq

Showing results (11-20 of 48) with videos related to

Pageof 5
Sort By:
Future Medicinal Chemistry|August 1, 2025
Piperidines as dual inhibitors of tyrosinase and pancreatic lipase: <i>in vitro</i> and <i>in silico</i> mechanistic insightsNafeesa Naeem, Ehsan Ullah Mughal, Bushra Shakoor, et al.
Journal of Biomolecular Structure & Dynamics|November 30, 2020
Synthetic flavonoids as potential antiviral agents against SARS-CoV-2 main proteaseFarwa Batool, Ehsan Ullah Mughal, Komal Zia, et al.
Future Medicinal Chemistry|October 21, 2025
Thioflavonols as potent α-glucosidase inhibitors: <i>in vitro</i>, <i>in vivo</i>, and computational analysisEhsan Ullah Mughal, Nafeesa Naeem, Bushra Shakoor, et al.
Bioorganic & Medicinal Chemistry|April 11, 2006
Synthesis and antibacterial activity of substituted flavones, 4-thioflavones and 4-iminoflavonesEhsan Ullah Mughal, Muhammad Ayaz, Zakir Hussain, et al.
RSC Advances|April 28, 2022
Natural and synthetic flavonoid derivatives as new potential tyrosinase inhibitors: a systematic reviewRami J Obaid, Ehsan Ullah Mughal, Nafeesa Naeem, et al.
RSC Advances|May 2, 2022
Scholl reaction as a powerful tool for the synthesis of nanographenes: a systematic reviewRabab S Jassas, Ehsan Ullah Mughal, Amina Sadiq, et al.
Bioorganic & Medicinal Chemistry|October 27, 2016
Synthesis, structure-activity relationship and molecular docking of 3-oxoaurones and 3-thioaurones as acetylcholinesterase and butyrylcholinesterase inhibitorsEhsan Ullah Mughal, Amina Sadiq, Shahzad Murtaza, et al.
Journal of Biomolecular Structure & Dynamics|October 18, 2022
Synthesis and biological evaluation of substituted aurone derivatives as potential tyrosinase inhibitors: <i>in vitro</i>, kinetic, QSAR, docking and drug-likeness studiesNajla A Alshaye, Ehsan Ullah Mughal, Eslam B Elkaeed, et al.
RSC Advances|August 3, 2022
Inhibitory potential of nitrogen, oxygen and sulfur containing heterocyclic scaffolds against acetylcholinesterase and butyrylcholinesteraseRami J Obaid, Nafeesa Naeem, Ehsan Ullah Mughal, et al.
RSC Advances|May 28, 2026
Chalcone-sulfonate ester derivatives as dual urease and α-amylase inhibitors: synthesis, biological evaluation and integrated computational studiesZobia Noreen, Amina Sadiq, Nafeesa Naeem, et al.
Pageof 5

Showing results (11-20 of 48) with videos related to

Sort By:
Pageof 5
Future Medicinal Chemistry|August 1, 2025
Piperidines as dual inhibitors of tyrosinase and pancreatic lipase: <i>in vitro</i> and <i>in silico</i> mechanistic insightsNafeesa Naeem, Ehsan Ullah Mughal, Bushra Shakoor, et al.
Journal of Biomolecular Structure & Dynamics|November 30, 2020
Synthetic flavonoids as potential antiviral agents against SARS-CoV-2 main proteaseFarwa Batool, Ehsan Ullah Mughal, Komal Zia, et al.
Future Medicinal Chemistry|October 21, 2025
Thioflavonols as potent α-glucosidase inhibitors: <i>in vitro</i>, <i>in vivo</i>, and computational analysisEhsan Ullah Mughal, Nafeesa Naeem, Bushra Shakoor, et al.
Bioorganic & Medicinal Chemistry|April 11, 2006
Synthesis and antibacterial activity of substituted flavones, 4-thioflavones and 4-iminoflavonesEhsan Ullah Mughal, Muhammad Ayaz, Zakir Hussain, et al.
RSC Advances|April 28, 2022
Natural and synthetic flavonoid derivatives as new potential tyrosinase inhibitors: a systematic reviewRami J Obaid, Ehsan Ullah Mughal, Nafeesa Naeem, et al.
RSC Advances|May 2, 2022
Scholl reaction as a powerful tool for the synthesis of nanographenes: a systematic reviewRabab S Jassas, Ehsan Ullah Mughal, Amina Sadiq, et al.
Bioorganic & Medicinal Chemistry|October 27, 2016
Synthesis, structure-activity relationship and molecular docking of 3-oxoaurones and 3-thioaurones as acetylcholinesterase and butyrylcholinesterase inhibitorsEhsan Ullah Mughal, Amina Sadiq, Shahzad Murtaza, et al.
Journal of Biomolecular Structure & Dynamics|October 18, 2022
Synthesis and biological evaluation of substituted aurone derivatives as potential tyrosinase inhibitors: <i>in vitro</i>, kinetic, QSAR, docking and drug-likeness studiesNajla A Alshaye, Ehsan Ullah Mughal, Eslam B Elkaeed, et al.
RSC Advances|August 3, 2022
Inhibitory potential of nitrogen, oxygen and sulfur containing heterocyclic scaffolds against acetylcholinesterase and butyrylcholinesteraseRami J Obaid, Nafeesa Naeem, Ehsan Ullah Mughal, et al.
RSC Advances|May 28, 2026
Chalcone-sulfonate ester derivatives as dual urease and α-amylase inhibitors: synthesis, biological evaluation and integrated computational studiesZobia Noreen, Amina Sadiq, Nafeesa Naeem, et al.
Pageof 5