2021
DOI: 10.1080/00958972.2021.1951258
|View full text |Cite
|
Sign up to set email alerts
|

Synthesis, characterization and biological applications of curcumin-lysine based schiff base and its metal complexes

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

2021
2021
2022
2022

Publication Types

Select...
3

Relationship

0
3

Authors

Journals

citations
Cited by 3 publications
(1 citation statement)
references
References 27 publications
0
1
0
Order By: Relevance
“…Metal complexes of thiosemicarbazones have been explored for nearly 50 years because of their versatile biological activity and prospective use as drugs [1]. Owing to the interest they generate through a variety of biological properties, thiosemicarbazones metal complexes have been employed in medicinal applications ranging from anticancer [2], antitumor [3], antifungal [4,5], antibacterial [6], antmalarial [7,8], antitilarial, [9], antiviral [10,11], antineoplastic [12,13], antileprotic [14], trypanocidal [15,16] and anti-HIV activities [17]. It has been proved that thiosemicarbazones block DNA synthesis in mammalian cells by inhibiting the enzyme, ribonucleoside diphosphate reductase, presumably either via chelation with iron(III) required by the enzyme or because a preferred metal chelate of the inhibitor interacts with the target enzyme [18,19].…”
Section: Introductionmentioning
confidence: 99%
“…Metal complexes of thiosemicarbazones have been explored for nearly 50 years because of their versatile biological activity and prospective use as drugs [1]. Owing to the interest they generate through a variety of biological properties, thiosemicarbazones metal complexes have been employed in medicinal applications ranging from anticancer [2], antitumor [3], antifungal [4,5], antibacterial [6], antmalarial [7,8], antitilarial, [9], antiviral [10,11], antineoplastic [12,13], antileprotic [14], trypanocidal [15,16] and anti-HIV activities [17]. It has been proved that thiosemicarbazones block DNA synthesis in mammalian cells by inhibiting the enzyme, ribonucleoside diphosphate reductase, presumably either via chelation with iron(III) required by the enzyme or because a preferred metal chelate of the inhibitor interacts with the target enzyme [18,19].…”
Section: Introductionmentioning
confidence: 99%