Anti-α-Glucosidase, SAR Analysis, and Mechanism Investigation of Indolo[1,2-b]isoquinoline Derivatives DOI Creative Commons
Mengyue Li, Lin Li, Li Lu

et al.

Molecules, Journal Year: 2023, Volume and Issue: 28(13), P. 5282 - 5282

Published: July 7, 2023

To find potential α-glucosidase inhibitors, indolo[1,2-b]isoquinoline derivatives (1–20) were screened for their inhibitory effects. All presented effects with IC50 values of 3.44 ± 0.36~41.24 0.26 μM compared to the positive control acarbose (IC50 value: 640.57 5.13 μM). In particular, compound 11 displayed strongest anti-α-glucosidase activity, being ~186 times stronger than acarbose. Kinetic studies found that compounds 9, 11, 13, 18, and 19 all reversible mix-type inhibitors. The 3D fluorescence spectra CD results revealed interaction between changed conformational changes α-glucosidase. Molecular docking molecular dynamics simulation indicated addition, cell cytotoxicity drug-like properties also investigated.

Language: Английский

Synthesis and biological evaluation of indole derivatives containing thiazolidine-2,4-dione as α-glucosidase inhibitors with antidiabetic activity DOI
Chunmei Hu,

Bingwen Liang,

Jinping Sun

et al.

European Journal of Medicinal Chemistry, Journal Year: 2023, Volume and Issue: 264, P. 115957 - 115957

Published: Nov. 24, 2023

Language: Английский

Citations

61

Comprehensive Insights into Medicinal Research on Imidazole-Based Supramolecular Complexes DOI Creative Commons

Shu-Rui Li,

Yi-Min Tan,

Ling Zhang

et al.

Pharmaceutics, Journal Year: 2023, Volume and Issue: 15(5), P. 1348 - 1348

Published: April 27, 2023

The electron-rich five-membered aromatic aza-heterocyclic imidazole, which contains two nitrogen atoms, is an important functional fragment widely present in a large number of biomolecules and medicinal drugs; its unique structure beneficial to easily bind with various inorganic or organic ions molecules through noncovalent interactions form variety supramolecular complexes broad potential, being paid increasing amount attention regarding more contributions imidazole-based for possible application. This work gives systematical comprehensive insights into research on complexes, including anticancer, antibacterial, antifungal, antiparasitic, antidiabetic, antihypertensive, anti-inflammatory aspects as well ion receptors, imaging agents, pathologic probes. new trend the foreseeable near future toward chemistry also prospected. It hoped that this provides help rational design drug agents effective diagnostic pathological

Language: Английский

Citations

43

Novel thiosemicarbazide-based β-carboline derivatives as α-glucosidase inhibitors: Synthesis and biological evaluation DOI

Bingwen Liang,

Di Xiao, Shao‐Hua Wang

et al.

European Journal of Medicinal Chemistry, Journal Year: 2024, Volume and Issue: 275, P. 116595 - 116595

Published: June 12, 2024

Language: Английский

Citations

32

Thiazolidine-2,4-dione derivatives as potential α-glucosidase inhibitors: Synthesis, inhibitory activity, binding interaction and hypoglycemic activity DOI
Mengyue Li, Jinping Sun,

Bingwen Liang

et al.

Bioorganic Chemistry, Journal Year: 2024, Volume and Issue: 144, P. 107177 - 107177

Published: Feb. 6, 2024

Language: Английский

Citations

28

Exploring the synthesis, molecular structure and biological activities of novel Bis-Schiff base derivatives: A combined theoretical and experimental approach DOI
Sana Gul, Aftab Alam,

Zainab Zainab

et al.

Journal of Molecular Structure, Journal Year: 2024, Volume and Issue: 1306, P. 137828 - 137828

Published: Feb. 17, 2024

Language: Английский

Citations

28

Synthesis, anti-α-glucosidase activity, inhibition interaction, and anti-diabetic activity of novel cryptolepine derivatives DOI

Mei Feng,

Bingwen Liang,

Jinping Sun

et al.

Journal of Molecular Structure, Journal Year: 2024, Volume and Issue: 1310, P. 138311 - 138311

Published: April 11, 2024

Language: Английский

Citations

22

Inhibitory mechanisms of galloylated forms of theaflavins on α-glucosidase DOI
Mengting Wang,

Wenwen Guo,

Zhijian Ke

et al.

International Journal of Biological Macromolecules, Journal Year: 2025, Volume and Issue: 294, P. 139324 - 139324

Published: Jan. 4, 2025

Language: Английский

Citations

2

Exploring Fluorine-Substituted Piperidines as Potential Therapeutics for Diabetes Mellitus and Alzheimer’s Diseases DOI
Ehsan Ullah Mughal, Mohammed B. Hawsawi, Nafeesa Naeem

et al.

European Journal of Medicinal Chemistry, Journal Year: 2024, Volume and Issue: 273, P. 116523 - 116523

Published: May 21, 2024

Language: Английский

Citations

12

Unveiling the Chemistry of Citrus Peel: Insights into Nutraceutical Potential and Therapeutic Applications DOI Creative Commons
Hussan Munir, Sanabil Yaqoob, Kanza Aziz Awan

et al.

Foods, Journal Year: 2024, Volume and Issue: 13(11), P. 1681 - 1681

Published: May 27, 2024

The recent millennium has witnessed a notable shift in consumer focus towards natural products for addressing lifestyle-related disorders, driven by their safety and cost-effectiveness. Nutraceuticals functional foods play an imperative role meeting nutritional needs offering medicinal benefits. With increased scientific knowledge awareness, the significance of healthy lifestyle, including diet, reducing disease risk is widely acknowledged, facilitating access to diverse safer diet longevity. Plant-based rich phytochemicals are increasingly popular effectively utilized management. Agricultural waste from plant-based being recognized as valuable source nutraceuticals dietary interventions. Citrus peels, known flavonoids, emerging promising health-promoting ingredient. Globally, citrus production yields approximately 15 million tons by-products annually, highlighting substantial potential utilizing phyto-therapeutic nutraceutical applications. peels with concentrations ranging 2.5 5.5 g/100 g dry weight, depending on variety. most abundant flavonoids peel include hesperidin naringin, well essential oils monoterpenes like limonene. extracts exhibit high antioxidant capacity, DPPH radical scavenging activities 70 90%, comparable synthetic antioxidants BHA BHT. Additionally, present have been found properties, which can help reduce oxidative stress 30% cardiovascular 25%. Potent anti-inflammatory effects also demonstrated, inflammatory markers such IL-6 TNF-α up 40% cell culture studies. These findings highlight diet-based therapies.

Language: Английский

Citations

12

Novel isatin–triazole based thiosemicarbazones as potential anticancer agents: synthesis, DFT and molecular docking studies DOI Creative Commons
Alia Mushtaq,

Rabbia Asif,

Waqar Ahmed Humayun

et al.

RSC Advances, Journal Year: 2024, Volume and Issue: 14(20), P. 14051 - 14067

Published: Jan. 1, 2024

Synthesis of mono- and bis-thiosemicarbazones 4a–h 5a–h isatin–triazole hybrids 3a 3b in turn accessed via CuAAC, their DFT studies potential as phosphoinositide 3-kinase (PI3K) inhibitors has been evaluated this study.

Language: Английский

Citations

11