2017
DOI: 10.5155/eurjchem.8.3.195-202.1576
|View full text |Cite
|
Sign up to set email alerts
|

Structural characterization, biological evaluation and DNA interaction of some potential drugs based on bifunctional aldehyde functionality

Abstract: Recent work aimed at evaluating the possibility of enhancing biological activities by synthetically modifying bifunctional aldehyde structures. In this article, two series of bifunctional aldehydes were synthesized, structurally characterized (M-1A, M-1C and M-2A) using single crystal X-ray diffraction analysis. Several pharmacological properties like cytotoxic, antifungal, antibacterial, antioxidant and antitumor activities were also evaluated. In addition, bifunctional aldehyde-DNA interaction assay was exam… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

0
2
0

Year Published

2023
2023
2023
2023

Publication Types

Select...
1

Relationship

0
1

Authors

Journals

citations
Cited by 1 publication
(2 citation statements)
references
References 33 publications
(46 reference statements)
0
2
0
Order By: Relevance
“…Following the method described in the preceding investigations DiAl was synthesized 46–48 . By carefully adding 1,4‐dibromobutane (0.01 mole), p‐hydroxy benzaldehyde (0.02 mole) and potassium carbonate (50 mole) to a DMF solution in a 100 mL round bottom flask fitted with a reflux condenser.…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…Following the method described in the preceding investigations DiAl was synthesized 46–48 . By carefully adding 1,4‐dibromobutane (0.01 mole), p‐hydroxy benzaldehyde (0.02 mole) and potassium carbonate (50 mole) to a DMF solution in a 100 mL round bottom flask fitted with a reflux condenser.…”
Section: Methodsmentioning
confidence: 99%
“…Following the method described in the preceding investigations DiAl was synthesized. [46][47][48] By carefully adding 1,4-dibromobutane (0.01 mole), p-hydroxy benzaldehyde (0.02 mole) and potassium carbonate (50 mole) to a DMF solution in a 100 mL round bottom flask fitted with a reflux condenser. The mixture was refluxed for 24 h at 80 C under N 2 environment, and cooled to ambient temperature, filtered and then purified by re-suspending it in 100 mL of DI water.…”
Section: Synthesis Of Dialdehyde (Dial)mentioning
confidence: 99%