Synthesis and Biological Evaluation of Ruthenium Polypyridine Complexes with 18β-Glycyrrhetinic Acid as Antibacterial Agents against Staphylococcus aureus

2021 ◽  
Author(s):  
Qin Zhang ◽  
Yan-Shi Xiong ◽  
Jianxin Chen ◽  
Yanhui Tan ◽  
Xiangwen Liao ◽  
...  

Abstract Four new ruthenium (II) polypyridine complexes bearing 18β-glycyrtinic acid derivatives, [Ru(bpy)2L](PF6)2 (Ru1), [Ru(dmb)2L](PF6)2 (Ru2), [Ru(dtb)2L](PF6)2 (Ru3) and [Ru(phen)2L](PF6)2 (Ru4) (bpy = 2,2-bipyridine, dmb = 4,4'-dimethyl-2,2'-bipyridine, dtb = 4,4'-di-tert-butyl-2,2'-bipyridine, phen...

2019 ◽  
Vol 15 ◽  
pp. 1468-1474
Author(s):  
Leticia Monjas ◽  
Peter Fodran ◽  
Johanna Kollback ◽  
Carlo Cassani ◽  
Thomas Olsson ◽  
...  

The synthesis and antibacterial activity of two new highly truncated derivatives of the natural product abyssomicin C are reported. This work outlines the limits of structural truncation of the natural product and consequently provides insights for further structure–activity relationship studies towards novel antibiotics targeting 4-amino-4-deoxychorismate (ADC) synthase. Specifically, it is demonstrated that the synthetically challenging bicyclic motif is essential for activity towards methicillin-resistant Staphylococcus aureus (MRSA).


2008 ◽  
Vol 5 (5) ◽  
pp. 353-357 ◽  
Author(s):  
Ahmed Kamal ◽  
S. Ahmed ◽  
M. A. Khan ◽  
Rajesh Shetty ◽  
B. Siddhardha ◽  
...  

ACS Omega ◽  
2021 ◽  
Author(s):  
Matej Zore ◽  
Shella Gilbert-Girard ◽  
Inés Reigada ◽  
Jayendra Z. Patel ◽  
Kirsi Savijoki ◽  
...  

2013 ◽  
Vol 56 (20) ◽  
pp. 8112-8138 ◽  
Author(s):  
Roger B. Clark ◽  
Minsheng He ◽  
Yonghong Deng ◽  
Cuixiang Sun ◽  
Chi-Li Chen ◽  
...  

2017 ◽  
Vol 2017 ◽  
pp. 1-8 ◽  
Author(s):  
Vu Van Vu ◽  
Trinh Thi Nhung ◽  
Nguyen Thi Thanh ◽  
Luu Van Chinh ◽  
Vu Dinh Tien ◽  
...  

A series of 14 new (-)-gossypol Schiff bases and hydrazones have been synthesized via an in situ procedure in high yields. Structural data showed that all target compounds exist as the enamine tautomer. Bioassays showed that several compounds exhibited cytotoxic effects against three human cancer cell lines. Compound 8a showed the greatest cytotoxic effect against hepatocellular carcinoma (HepG2), lung carcinoma (LU-1), and breast cancer (MCF-7) cell lines with IC50 values of 20.93, 13.58, and 9.40 μM, respectively. However, in an antibacterial test, compounds 8a and 8b inhibited Staphylococcus aureus and Bacillus cereus and compound 8e inhibited only Staphylococcus aureus at the same MIC values of 1024 μg/ml.


2016 ◽  
Vol 9 ◽  
pp. S1875-S1883 ◽  
Author(s):  
Sayan Dutta Gupta ◽  
Ganga Balaji Rao ◽  
Manish Kumar Bommaka ◽  
Nulgumnalli Manjunathaiah Raghavendra ◽  
Swapna Aleti

2015 ◽  
Vol 58 (11) ◽  
pp. 4703-4712 ◽  
Author(s):  
Cuixiang Sun ◽  
Diana K. Hunt ◽  
Chi-Li Chen ◽  
Yonghong Deng ◽  
Minsheng He ◽  
...  

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