Unknown

Dataset Information

0

Dual activity of indolin-2-ones containing an arylidene motif: DNA and BSA interaction.


ABSTRACT: Applying a multistep approach, novel indolin-2-ones (IND) that possess an arylidene motif have been synthesized. Eight compounds were chosen for different biological tests (antimicrobial and cytotoxicity). IND containing 2-thienyl (4h) fragment have been found to exhibit good antimicrobial activity against B. cereus. Molecules that have 3-aminophenyl (4d) or 2-pyridyl (4g) groups have shown the best antifungal activities against all tested fungi. These compounds have also been noticed as promising pharmaceuticals against MCF-7 cancer cell lines. Experimental outcomes from the investigation of the interaction of 4d with DNA implied its moderate binding to DNA (KSV = 1.35 × 104 and 3.05 × 104 M-1 for EB and Hoechst binder, respectively). However, considerably stronger binding of 4d to BSA has been evidenced (Ka = 6.1 × 106 M-1). In summary, IND that contains m-aminobenzylidene fragment (4d) exhibits a good dual biological activity making it a promising candidate for further investigation in the drug discovery sector.

SUBMITTER: Bukhari SNA 

PROVIDER: S-EPMC10518658 | biostudies-literature | 2023 Sep

REPOSITORIES: biostudies-literature

altmetric image

Publications

Dual activity of indolin-2-ones containing an arylidene motif: DNA and BSA interaction.

Bukhari Syed Nasir Abbas SNA   Alsahli Tariq G TG   Ejaz Hasan H   Ahmed Naveed N   Ahmad Waqas W   Ahmad Waqas W   Elsherif Mervat A MA   Alotaibi Nasser H NH   Junaid Kashaf K   Janković Nenad N  

RSC advances 20230925 40


Applying a multistep approach, novel indolin-2-ones (IND) that possess an arylidene motif have been synthesized. Eight compounds were chosen for different biological tests (antimicrobial and cytotoxicity). IND containing 2-thienyl (4h) fragment have been found to exhibit good antimicrobial activity against <i>B. cereus</i>. Molecules that have 3-aminophenyl (4d) or 2-pyridyl (4g) groups have shown the best antifungal activities against all tested fungi. These compounds have also been noticed as  ...[more]

Similar Datasets

| S-EPMC4335313 | biostudies-literature
| S-EPMC7864298 | biostudies-literature
| S-EPMC6274071 | biostudies-literature
| S-EPMC6432916 | biostudies-literature
| S-EPMC10493310 | biostudies-literature
| S-EPMC7511821 | biostudies-literature
| S-EPMC9531837 | biostudies-literature
| S-EPMC8982289 | biostudies-literature
| S-EPMC8464069 | biostudies-literature
| S-EPMC5549488 | biostudies-other