2019
DOI: 10.1007/s11094-019-01968-3
|View full text |Cite
|
Sign up to set email alerts
|

Synthesis, Biological Evaluation and Ligand Based Pharmacophore Modeling of New Aromatic Thiosemicarbazones as Potential Anticancer Agents

Abstract: Two series of new aromatic thiosemicarbazone derivatives were synthesized by condensation of N-(4-cyanophenyl)hydrazine carbothioamide (I) and N-(4-methylsulfanylphenyl)hydrazine carbothioamide (II) with appropriate aromatic aldehydes in order to investigate their antiviral and cytostatic potency. The chemical structures of all compounds were fully characterized by elemental analysis and spectroscopic techniques. The results of the bioassays indicated that compounds Id, Ie, If and IIf proved inhibitory against… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2

Citation Types

0
1
0

Year Published

2021
2021
2025
2025

Publication Types

Select...
6
1

Relationship

0
7

Authors

Journals

citations
Cited by 9 publications
(2 citation statements)
references
References 15 publications
0
1
0
Order By: Relevance
“…[11][12][13][14][15]. Thiosemicarbazones of aliphatic [16][17][18], aromatic [19][20][21], hetero aromatic aldehydes and ketones (22)(23)(24), various derivatives of hetero aromatic carbonyl compounds, generally exhibit the most pronounced pharmacological activities [25][26]. N-substituted thiosemicarbazone of aromatic carbonyl compounds acts as tridentate ligands with NNS set of donor atoms due to the central position of nitrogen atom the ligand [27].…”
Section: Introductionmentioning
confidence: 99%
“…[11][12][13][14][15]. Thiosemicarbazones of aliphatic [16][17][18], aromatic [19][20][21], hetero aromatic aldehydes and ketones (22)(23)(24), various derivatives of hetero aromatic carbonyl compounds, generally exhibit the most pronounced pharmacological activities [25][26]. N-substituted thiosemicarbazone of aromatic carbonyl compounds acts as tridentate ligands with NNS set of donor atoms due to the central position of nitrogen atom the ligand [27].…”
Section: Introductionmentioning
confidence: 99%
“…1). They are active and interesting arrangement structures for many scientists [1,2]. The C(=S)-NH group and -NH-NH-hydrazide fragment play a very important role in pharmaceutic chemistry due to their potentially high anti-fungal, anti-bacterial [3], anti-viral (HIV-1) and anti-malarial activities [4].…”
Section: Introductionmentioning
confidence: 99%