2020
DOI: 10.1080/00958972.2020.1852223
|View full text |Cite
|
Sign up to set email alerts
|

Multifunctional 1,10-phenanthroline derivative and its metal complexes as an anti-Alzheimer’s agent: structure-based drug design, synthesis, characterization and pharmacological studies

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1

Citation Types

0
3
0

Year Published

2021
2021
2022
2022

Publication Types

Select...
6

Relationship

0
6

Authors

Journals

citations
Cited by 7 publications
(3 citation statements)
references
References 45 publications
0
3
0
Order By: Relevance
“…Therefore, in recent years a plethora of studies support the use of metal-based complexes as potential drugs with a wide range of pharmacological properties, such as anticancer [24][25][26], antimicrobial [27][28][29], antiparasitic [30][31][32], anti-neurodegenerative [33][34][35], or antidiabetic [36][37][38] activities.…”
Section: Metal-based Compounds As Therapeutic Agentsmentioning
confidence: 99%
See 1 more Smart Citation
“…Therefore, in recent years a plethora of studies support the use of metal-based complexes as potential drugs with a wide range of pharmacological properties, such as anticancer [24][25][26], antimicrobial [27][28][29], antiparasitic [30][31][32], anti-neurodegenerative [33][34][35], or antidiabetic [36][37][38] activities.…”
Section: Metal-based Compounds As Therapeutic Agentsmentioning
confidence: 99%
“…Recently, cadmium (Cd) complexes bearing selenazoyl-hydrazones (33)(34)(35) in Fig. 3) as anticancer agents were reported, along with their S analogs for comparison [111].…”
Section: Metal Complexes Based On Ni Zn and CDmentioning
confidence: 99%
“…Zhou et al (2018) developed a series of 2‐aryl‐9‐methyl‐β‐carbolinium bromides for anti‐AChE activity with IC 50 values in the range of 0.11–0.76 μM, higher than standard drug galantamine and high selectivity toward AChE. 1,10‐phenanthroline derivative was synthesized by group Gladis et al (2020), and AChE inhibitory effect was examined. The synthesized ligands showed selective inhibition against AChE and BuChE with IC 50 values of 0.20 and 3.20 μM as compared to references, galantamine and rivastigmine.…”
Section: Primary Drug Therapies For Admentioning
confidence: 99%