4030-95-9Relevant academic research and scientific papers
Synthesis and biological activity profile of novel triazole/quinoline hybrids
Azerang, Parisa,Jamshidi, Hoda,Naimi-Jamal, Mohammad Reza,RayatSanati, Kimia,Safavi, Maliheh,Tahghighi, Azar
, (2022/02/23)
Based on the significant and diverse pharmacophore features of triazole ring and considering the potent antimicrobial properties of quinoline scaffold, a novel series of 1,2,3-triazole-based polyaromatic compounds containing chloroquinoline moiety were synthesized through a well-established synthetic methodology, named click chemistry. The structure of the synthetic compounds was characterized by various spectroscopic methods. The final products of triazole/quinoline hybrids and ((prop-2-yn-1-yloxy)methyl)benzene intermediates were screened for their antibacterial (Staphylococcus aureus, Escherichia coli, Shigella flexneri, and Salmonella enterica), antifungal (Candida albicans, Saccharomyces cerevisiae, and Aspergillus fumigatus), and cytotoxic activities. The best antifungal compounds exhibited minimum inhibitory concentration (MIC), in the range of 0.35–0.63?μM, against S.?cerevisiae without any cytotoxic effect. These compounds can be selected as the potential candidates for treating invasive fungal infections caused by S.?cerevisiae, after further investigation. Preliminary in silico ADME studies also predicted the favorable pharmacokinetic attributes of most compounds.
Inhibitors against Fungal Cell Wall Remodeling Enzymes
Delso, Ignacio,Valero-Gonzalez, Jessika,Gomollón-Bel, Fernando,Castro-López, Jorge,Fang, Wenxia,Navratilova, Iva,van Aalten, Daan M. F.,Tejero, Tomás,Merino, Pedro,Hurtado-Guerrero, Ramon
supporting information, p. 128 - 132 (2018/02/06)
Fungal β-1,3-glucan glucanosyltransferases are glucan-remodeling enzymes that play important roles in cell wall integrity, and are essential for the viability of pathogenic fungi and yeasts. As such, they are considered possible drug targets, although inh
Anticancer (hexacarbonyldicobalt)propargyl aryl ethers: Synthesis, antiproliferative activity, apoptosis induction, and effect on cellular oxidative stress
Schimler, Sydonie D.,Hall, David J.,Debbert, Stefan L.
, p. 28 - 37 (2013/02/25)
While an increasing number of (hexacarbonyldicobalt)alkynes have been found to possess antiproliferative activity against a number of cancer cell lines, the role of the organometallic moiety in this bioactivity is not well understood. To gain a better und
