In silico studies and biological evaluation of chalcone-based 1, 5-benzothiazepines as new potential H1N1 neuraminidase inhibitors

N Frimayanti, M Yaeghoobi, H Namavar… - Journal of applied …, 2020 - japsonline.com
Benzothiazepines are benzo-fused seven-membered heterocycles. Due to their biological
activities against a wide spectrum of targets, they are of particular interest for drug discovery …

[PDF][PDF] Insight on the in silico study and biological activity assay of chalcone-based 1, 5-benzothiazepines as potential inhibitor for breast cancer MCF7. CMUJ

N Frimayanti, M Yaeghoobi, I Ikhtiarudin, DRW Putri… - Nat. Sci, 2021 - cmuj.cmu.ac.th
In silico study was performed to twelve 1, 5-benzothiazepine chalcone derivatives with the
protein target from the crystallographic structure modeling of the enzyme tyrosine kinase …

6‐Octadecenoic and Oleic Acid in Liquid Smoke Rice Husk Showed COVID‐19 Inhibitor Properties

I Arundina, N Frimayanti, MDC Surboyo… - Advances in …, 2024 - Wiley Online Library
In recent years, liquid smoke rice husk (LSRH) has shown its therapeutic potency to
diabetes, wound healing, stomatitis, and periodontitis. The phenol, 6‐octadecenoic acid …

[PDF][PDF] Insight into the in silico Study and Biological Evaluation of Curcumin Analogue Compounds as New Potential Inhibitors for Dengue DEN2 NS2B/NS3 Serine …

N Frimayanti, N Herfindo, S Aisyah, E RAHMAWATY - Sains Malaysiana, 2024 - ukm.my
Dengue is an infectious disease caused by a virus and it is a rapidly emerging pandemic
disease in many parts of the world. However, to date, one licensed tetravalent Dengvaxia …

In Silico Analysis for Exploring the Potential Inhibitors Against Breast Cancer (MCF7) Using Curcumin Analogue Compounds

N Frimayanti, A Zamri, Y Eryanti - Jurnal Kimia Sains dan …, 2024 - ejournal.undip.ac.id
Breast cancer is one of the most problematic diseases in the world. Currently, there are no
potential vaccines for the treatment of this disease. Therefore, finding effective compounds …

IAI SPECIAL EDITION: In silico approach through molecular docking and study ADME on imine derivative compounds as a potential antibacterial agent against …

N Frimayanti, MR Nasution… - Pharmacy …, 2024 - pharmacyeducation.fip.org
Background: Antibiotics are drugs or compounds that inhibit or kill bacteria. Most natural and
synthetic pharmacophores have been reported to be antimicrobial agents. One of these is …

Synthesis, docking, and molecular dynamic study of hydrazones compounds to search potential inhibitor for breast cancer MCF-7

Y Nurulita, N Afriana, I Ikhtiarudin… - The Thai Journal of …, 2021 - digital.car.chula.ac.th
Introduction: Hydrazones have been reported for various biological activities, such as
anticancer. The presence of the azomethine group (-NHN= CH-) makes these compounds …

Estimation of Hydrazone Derivative Compounds as Anti-Bacterial Agents Against Staphylococcus aureous Through Molecular Docking and Self Consisted Field

N Frimayanti, M Octaviani, G Wulandari, A Zamri - Trends in Sciences, 2023 - tis.wu.ac.th
Molecular docking is an important computational method for drug design. It can be used to
predict the binding interaction of receptor with the ligand. Hydrazone were reported as …

[PDF][PDF] Synthesis and Molecular Docking Study of 4-(3-(2-Chlorophenyl)-5-(2-Methoxyphenyl)-4, 5-Dihydro-1H-Pyrazol-1-yl) Benzenesulfonamide as Antibreast …

EM Putri, N Herfindo, G Guntur… - ALCHEMY Jurnal …, 2022 - academia.edu
Breast cancer is a disease in which cells in the breast tissue change and divide in an
uncontrolled way. Pyrazoline is a promising agent reported against cancer. In this work, we …

Synthesis, Docking and Molecular Dynamic Study of Hydrazones Compounds to Search Potential Inhibitor for Breast Cancer MCF7:(TJPS-2020-0222. R1)

J Jasril, Y Nurulita, N Afriana… - Thai Journal of …, 2021 - tjps.pharm.chula.ac.th
Introduction Hydrazones have been reported for various biological activities, such as
anticancer. The presence of azomethine group (-NHN= CH-) makes these compounds as …