901414-72-0Relevant academic research and scientific papers
Synthesis and bioactivity evaluation of rhodanine derivatives as potential anti-bacterial agents
Song, Ming-Xia,Zheng, Chang-Ji,Deng, Xian-Qing,Wang, Qing,Hou, Shao-Pu,Liu, Ting-Ting,Xing, Xiao-Lan,Piao, Hu-Ri
experimental part, p. 403 - 412 (2012/10/08)
Five series of (Z)-5-(4-(2-oxo-2-phenylethoxy)benzylidene)-2- thioxothiazolidin-4-one derivatives (I-V) were synthesized, characterized, and evaluated for their anti-bacterial activity. Most of the synthesized compounds showed potent inhibition against several Gram-positive bacteria (including multidrug-resistant clinical isolates) with MIC values in the range of 1-32 μg/mL. Compounds IIIi, Vb and Vc presented the most potent activity, showing four-fold more potency than norfloxacin (MIC = 8 μg/mL and 4 μg/mL) and 64-fold more activity than oxacillin (MIC > 64 μg/mL) against MRSA CCARM 3167 and 3506 strains with MIC values of 1 μg/mL, and 64-fold more potency than norfloxacin (MIC > 64 μg/mL) and comparable activity to oxacillin (MIC = 1 μg/mL) against the QRSA CCARM 3505 and 3519 strains. None of the compounds exhibited any activity against the Gram-negative bacteria Escherichia coli 1356 at 64 μg/mL.
A convenient synthesis of some new 5-substituted-4-thioxo-thiazolidinones and fused thiopyrano[2,3-d]thiazole derivatives
Metwally, Nadia Hanafy
experimental part, p. 2073 - 2085 (2009/07/18)
The new Z-5-arylmethylene-4-thioxo-thiazolidine derivatives have been synthesized by condensation of ω -(4-formylphenoxy)acetophenone derivatives with 4-thioxo-thiazolidine derivatives, in good yields. The cycloaddition of the newly synthesized compounds
