7025-24-3Relevant academic research and scientific papers
In Silico Driven Design and Synthesis of Rhodanine Derivatives as Novel Antibacterials Targeting the Enoyl Reductase InhA
Slepikas, Liudas,Chiriano, Gianpaolo,Perozzo, Remo,Tardy, Sébastien,Kranjc, Agata,Patthey-Vuadens, Ophélie,Ouertatani-Sakouhi, Hajer,Kicka, Sébastien,Harrison, Christopher F.,Scrignari, Tiziana,Perron, Karl,Hilbi, Hubert,Soldati, Thierry,Cosson, Pierre,Tarasevicius, Eduardas,Scapozza, Leonardo
, p. 10917 - 10928 (2016/12/30)
Here, we report on the design, synthesis, and biological evaluation of 4-thiazolidinone (rhodanine) derivatives targeting Mycobacterial tuberculosis (Mtb) trans-2-enoyl-acyl carrier protein reductase (InhA). Compounds having bulky aromatic substituents at position 5 and a tryptophan residue at position N-3 of the rhodanine ring were the most active against InhA, with IC50 values ranging from 2.7 to 30 μM. The experimental data showed consistent correlations with computational studies. Their antimicrobial activity was assessed against Mycobacterium marinum (Mm) (a model for Mtb), Pseudomonas aeruginosa (Pa), Legionella pneumophila (Lp), and Enterococcus faecalis (Ef) by using anti-infective, antivirulence, and antibiotic assays. Nineteen out of 34 compounds reduced Mm virulence at 10 μM. 33 exhibited promising antibiotic activity against Mm with a MIC of 0.21 μM and showed up to 89% reduction of Lp growth in an anti-infective assay at 30 μM. 32 showed high antibiotic activity against Ef, with a MIC of 0.57 μM.
Synthesis of new potential anticancer agents based on 4-thiazolidinone and oleanane scaffolds
Kaminskyy, Danylo,Bednarczyk-Cwynar, Barbara,Vasylenko, Olexandr,Kazakova, Oxana,Zimenkovsky, Borys,Zaprutko, Lucjusz,Lesyk, Roman
, p. 3568 - 3580 (2013/03/13)
The synthesis and evaluation of the anticancer activity of new acylated oximes derivatives of oleanolic acid with 4-thiazolidinone-3(5)-carboxylic acid moieties were described. Newly synthesized compounds were elucidated on the basis of elemental analyses
